Finally Addressing My Hair Loss… (While I Do My Skincare)

Finally Addressing My Hair Loss… (while I do my skincare with Isntree)

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Addressing my hair loss and talking about my dry skin and kind of the weird things that are happening with my body. While we do a k-beauty morning, routine, a lot of people have been commenting about hair loss or about my dry skin and i've even spoken about. Why that's weird and why i've been seeing doctors a little bit more recently outside of people that i work with actually going in as a patient to talk about certain things and boy has some stuff been uncovered so today i wanted to do a morning skincare routine. I wanted to put some of my favorite products on my face and just have an open, sit-down conversation about this, because it is my personal medical information. It is mine, hello, it is nobody's business unless i make it their business, and you know i find these things personally fascinating. They are things that you know have kind of obviously been carried with me throughout my entire life, especially as we talk more about genetic conditions or syndromes or things of that nature. But it's also something that is kind of cathartic to talk about. You know it's cathartic to not go through it alone, and sometimes talking about it is when we can uncover things that other people have experienced or brainstormed together collectively about hey. This is what's going on. This is what's new. Have you heard of anything like this? Before? Have you experienced anything? What do you think and again this is not medical advice. I am not telling you to take the same prescriptions that i am or ask your doctor about the same things i just wanted to speak openly and honestly about kind of what's been going on, because for the first time in my life, my oily acne-prone skin has Been a little bit more dry, it wasn't even until the pandemic that i realized. I have eczema and psoriasis. I had seen patches on my skin. That'S what i thought and then i got it clinically diagnosed and on top of that hair loss. It'S actually thanks to the beautiful butterflies that a lot of people started, commenting they're like wait. Why is your hairline, like so large, like it's getting bigger like what is happening over here and um? I i want to talk about that, because it's something that i haven't experienced before. I don't think that there's a shame or a stigma in living inside of our bodies and going through what they do to us. But i also believe that discussing some of these things can be helpful, if not even necessary. This mask is the real mugwort clay mask from isn't true, who we're actually partnering with on this video. They are one of my favorite k-beauty brands and they're actually having a sale on amazon from december 23rd through 26th. One of our beautiful butterflies shiny is actually a doctor who got me obsessed and hooked and falling in love with this. This was my first introduction to isn't tree and they are hands down one of my favorite k-beauty lines for their products, their formulas and just what they stand for, and i mean it's just so surreal even being able to work with some of the brands that i Love the most who support this content and all of the people, the amazing people that i get to work with to make these happen, which yes includes the cats who edit and the fact that a brand is willing to. Let me talk about you know the personal things um, creating a safe space to open up, but also make the regular content that we do even possible. It is flippin fantastic, so, yes, they're having an amazing sale. All of those details are below and i will be using, isn't treat today, but let's let this soak into the skin. While we talk about vitamin d levels - and you know the drill we got to put the skincare headband on, i do think it's important to discuss how we got here. Some of the other things that you might not know that i deal with such as one kidney and other reproductive issues as well as epilepsy. I'Ve gone through a lot of issues with anxiety and depression. Throughout my entire life, there are genetic predispositions and family history of these sorts of things, as well as hypothyroidism, basically a whole bunch of stuff in the family and by the way this mugwort mask mugwort is actually a plant. It'S antibacterial and anti-fungal. This one specifically, is amazing for sebum care. So if you do have you know an oily area such as i do in my t-zone, really really helpful, but again. This is why everything for me is kind of weird, because i'm having these little dry patches, where i'm having eczema and psoriasis flares on areas of my body, that up until the past two years had never been an issue. Even during times of like stress. In my life this does mildly exfoliate, which is why we're going to be applying a sunscreen. But look i actually brought a whole thing of water with me instead of, like forgetting the water and she has a towel, so she doesn't have to wipe on her legs or on the floor, which is what usually happens so now. This has been on for a little while i'm just going to kind of wash this off and go in with our cleanser. But essentially, when i was growing up, i was diagnosed with premature rheumatoid arthritis, because my knees would swell my joints would swell, and this was probably in the fourth or fifth grade. It was actually quite debilitating for me because here i was, you know, a young kid and i couldn't even walk or run, and i was in physical pain and they would remove 50 to 100 ccs of fluid from each knee. Basically, my knees were like the size of footballs and it was very, very painful, and i was just told you have this premature rheumatoid arthritis. You basically have the swelling, really unfortunate. You know you can be on certain medications, but you just kind of hope. It'S gon na go away, and thankfully, after you know being on crutches and taking some time away from that, it relatively did up until high school and i had another little flare. But overall it was not as debilitating for me long term as other people who have rheumatoid arthritis or things of that nature. But we didn't really realize that. Oh, could this be related to my connective tissue or to my skin, to acne to all of these different things, and a lot of these questions are what i'm currently, you know, trying to work to uncover and um there's a lot of unknowns. Also, when i was growing up, we did not know that i had one kidney psoriasis, slash eczema among dermatographia and other things. If you ever notice that my face gets really red, that's erythema, eryth means red and dermatographia is basically it's a hystemic response. It'S almost like a hive, and it causes me even when i just touch my skin a little bit to really really flush and flare. There'S also some subclinical rosacea as well. My dad has that it's just a whole host of fun things speaking of fun things, this bubble foam is phenomenal. This is a sensitive skin, balancing bubble foam, it's the derma clara and this is formulated to be slightly acidic, but it's an actual bubble. Cleanser that doesn't overly strip the skin and if you do have sensitive skin, but you want something that actually works. If you actually have a damaged skin barrier or even eczema, psoriasis, that's being treated by a dermer doctor and just want a nice k-beauty gentle cleanser. This actually has ceramides in it. The foaming doesn't come just from the formula. It actually comes from the little pump top so that it's not as stripping as you know, traditional foaming, cleansers or even shampoos or things of that nature, and i normally don't cleanse my skin. Every morning but um i will admit, i did not cleanse my skin very well last night, thankfully no sleeping and makeup, no, no, no, no, but just making sure that i'm cleaning today and removing any remnants of sunscreen. This has arginine alanine, tyrosine, basically a bunch of amino acids, and it is moisturizing which again weird dry skin things me likey. So a couple of years ago i had a family member who was diagnosed with psoriasis, with seborrheic dermatitis with atopic dermatitis. Basically, a combination of psoriasis and eczema and for those who know psoriasis, usually runs in families. There is a large genetic component to it and you know it often shows up in parents or siblings or extended cousins etc, and this family member has really bad seborrheic dermatitis, especially behind the ears and it's to the point that it splits it fissures and warning a Graphic image incoming, but it's actually gotten infected before as well and obviously ketoconazole nizoral, topical steroids, have really helped, but haven't really solved the problem. But again, this was a problem for that family member and not really for me now in late 2020, i started to get this weird patch on my kneecap and normally things like eczema happen in the axillary areas or kind of in skin folds, and not really on The knee, but i looked at it and i was like i am not a doctor - i do not diagnose, but this looks to me like psoriasis, or this looks like an eczema flare, and i currently have a couple of other ones right here and especially underneath certain Areas you know in some skin folds, so yes saw a dermatologist as a patient and yes, it is psoriasis and apparently just the way my other family member has it. So do i and we just didn't know of it now. This also brings up the conversation around you know, kind of systemic body stuff, as well as inflammation of joints, because remember when i was younger, we had this joint swelling, but one thing that many people don't realize about psoriasis is that it's not just a skin condition. It can impact your entire body and there's something called psoriatic arthritis, which can be extremely painful and that can really impact the spine joints etc. Now i have not done genetic testing, i'm kind of worried about data and security and data privacy, but at the same time i'm like. I would really like to know exactly what's going on, not only when it comes to psoriasis, but when it comes to other syndromes and genetic disorders of connective tissue, such as marfan syndrome or marfan's disease, which we're going to talk about in just a second. Because this again got very interesting, i'm also going to go in with a gentle exfoliant this morning. Isn'T tree has always had this clear skin eight percent, aha essence, but they actually just launched this. It'S the two percent bha clear liquid from chestnut, and i have to say this is probably the most gentle bha that i've ever used. I feel like i can use this before i go out during the day. It is a really light liquid. It just soaks in the skin so well and it doesn't irritate a lot of bhas can be overly drying or overly irritating and k. Beauty in general is a bit more gentle, but this is just so soothing and it doesn't irritate the skin uh. The way that a lot of other bha products do this one does have that salicylic acid, but it also has this chestnut extract, which is wonderful as well as sodium hyaluronate, which you know is related to hyaluronic acid. It'S the salt form, which can be really nice and hydrating to skin. Now. Asentry also has this: it's the hyaluronic acid plus. This is a really great toner, but this one is just the hyaluronic acid, whereas this one is hydrating, this one is relatively new. It came out in november if you have sensitive skin and you need a bha. This is one of the best one of the others that i just love. So much is this one, the green tea on days that you're not exfoliating? I would definitely recommend this and again it's all thanks to shiny that i became obsessed one of the best antioxidant toners i've ever used, but now what is this marfan syndrome? How does this relate to hair loss? What is going on with the skin, etc? Well, marfan syndrome is a genetic connective tissue disorder. Basically, your connective tissue can impact your joints. Your heart, yes, other areas of your skin and this syndrome is a defect in how the body creates a specific protein fbn1 and that can again affect a lot of things throughout the body and it's usually characterized by a tall lanky build an elongated face. Yes, i have been called a horse before i don't take offense to it, but you know some people think that i look like a horse. It'S also characterized by unusually long fingers and toes, which i do have even as a baby. My parents would look at my fingers and toes and be like what the heck very very long and i do have scoliosis and sometimes that is associated now. There are other things like pigeon chest, which i don't personally have and, as you know, if you've watched this channel for a while, i had meningitis in the beginning of 2020, and i also struggled with seizures and atypical epilepsy end of 2019-2012. And we think that that may have you know some correlation to heart issues. I have a large inferior, vena cava. Basically, the big vein that takes blood from your body and pushes it back to the heart mind is big and so sometimes blood pools up. There doesn't get to the heart, then doesn't get to my brain triggers a seizure, because your brain needs blood and oxygen in order to function right, but here's the question a lot of people with marfan syndrome do have issues with their aorta with their mitral valve. Basically in their heart and how it works, and unfortunately, the most common death for people with this are issues with their aorta, either in aortic dissection, which is basically imagine the big ol uh hose that is attached to your heart. It almost kind of splits in two and blood is flowing two different places or a triple a which is terrifying. It'S an abdominal aortic aneurysm and it's basically pop goes the weasel um to one of the most important arteries in your entire body and um. If you can't pump blood to your entire body and your brain, you can't stay around that long, so it is a little bit concerning and i don't have all of the clinical criteria again. I saw some doctors about it, but i'm actually scheduled to go, see someone who specializes in genetics, which is really exciting, especially because i feel like i've waited my entire life for answers and i feel like we're. Finally, uncovering them - and you know there are other tests which i do pass, such as how long your fingers are or how hyper mobile your joints are now. This also brings up questions like what about eds ehlers-danlos syndrome or what about other connective tissue disorders. That may be related and again that's why i do not self-diagnose, nobody should be self-diagnosing. You should see a doctor, you should do specific tests or look at specific clinical criteria to try to get that evaluated. Now, while we were kind of going through the preliminary stages of looking at this, i of course also brought up. You know the weird kind of dry skin patches that i've never dealt with as well. As you know, some of this hair loss hair kind of falling out in the shower. You know we have this running joke of. I look down and there's a chinchilla at my feet. It'S not a joke and i've been through some very stressful periods of my life, but i've never lost as much hair as i did in the past two years. All from you know making some major changes in my job and career, making some major changes in school. Being diagnosed with atypical epilepsy, having meningitis um pandemic, all of the things it's a lot and um. I didn't talk about this, but my father was diagnosed with cancer. My grandmother has a very rapidly progressing dementia and alzheimer's and there's just a lot and the sasquatch upstairs. Doesn'T shut up, but you know, even when those things get to me, i have skin care as a form of self-care, which i love. This right here is the tw real bifida ampule. This is probably one of the most luxurious products i've ever used from isn't tree. It doesn't cost a luxury price, especially when it's on sale, which again, i think, they're having um from the 23rd to the 26th. But this just feels luxurious. It'S this beautiful little white bottle and the entire formula is this clear liquid that just smooths on the skin? So well - and this is vegan and cruelty free, but it has hydrolyzed collagen in it, so it's actually quite moisturizing and nourishing to the skin. It'S also got some different peptides in here and the main ingredient, which is why it's called the bifida ampule is because it does have bifida ferment lysate. This is, basically, you can think of it as a probiotic that is supposed to help kind of balance out the barrier of skin or potentially help with balancing a microbiome, especially if your skin is irritated or stripped which hi psoriasis, weird patches of dry and oily skin. That'S what's been going on for me, this also has a pumpkin extract as well as a bunch of peptides. We do have acetyl hexapeptide, eight, that's for like anti-wrinkle and kind of helps with fine lines. We have palmital tripeptide, one really good for kind of wound healing and then copper tripeptide, one which is used quite interestingly, all the time and again it's for wound healing for skin suppleness, for kind of barrier, support, etc. I absolutely love this. I don't know how they're not charging way more for this i feel like this is one of the most luxury isn't tree products. There is and just k, beauty in general. It says it's a high functioning ampule, which contains bifida fermented, lysate and triple peptides for skin. Tightening which i don't know you tell me another amazing serum - that i love from isn't tree. Is this one? It'S the hyaluronic acid water essence. This was one of my first. This was my first isn't tree product that i tried back in 2020. It has eight types of hyaluronic acid, and this is a non-drying, hyaluronic, acid, serum, it's milky and creamy and i don't need to go in with two different types of um, serum or extra hyaluronic acid. But i'm going to because i love this one. So basically, when kind of looking at these different things trying to get set up with specialists, of course you want to do. Blood tests want to make sure everything is looking good for those who don't know, i do choose to follow a plant-based lifestyle. I also love my sunscreen and, as mentioned thyroid issues run in my family, specifically hashimoto's disease, which is like a non-functioning thyroid and kind of goiters right and hypothyroidism, or a low functioning thyroid is throughout my family, like on both sides, and so i've always been extremely Worried do i have a low thyroid? Is there an issue etc, and some actual medical studies show that i think 75 percent of people who have low thyroid or hypothyroidism complain of dry skin, and especially seeing as this kind of changed i was like ooh are my thyroid levels intact? Like am i, okay? Is something changing, etc, especially in hashimoto's disease, where your body basically attacks your own organs, it attacks your own thyroid and stops it from working. Is that related? And then many years ago i was not eating gluten, because there was this concern that if someone has celiac disease the way certain proteins work inside of the body we didn't want to trigger any hypothyroidism stuff. That'S no longer an issue for me. I still have ibs irritable bowel syndrome still have some issues with diarrhea, but this is also related to my one. Kidney and my duplicated reproductive system, which is also very, very fascinating and kind of goes into. Some discoveries that i've made and tried to take to gynecologists. But i think i need some new gynecologists, because again we love doctors, we love care, but not all doctors operate the same and i just think i've had really bad luck with gynecologists, thus far. So basically, my skin is changing my body's changing we're trying to look. If there are specific genetic connective tissue disorders etc, but my hair is also changing and i said you know i want a blood test. I want to look at thyroid stuff, t4, tsh, etc. I also want to look at all of my nutrient levels to see. What'S going on and lo and behold guess what happens? Come back vitamin d deficient now it's not severe, but my vitamin d was pretty low and again about 50 percent of the population is, and vitamin d is arguably one of the most important hormones or vitamins in the body. Basically, almost every single cell in our bodies has a vitamin d receptor and vitamin d acts as a hormone. It'S one of the fat soluble vitamins and it impacts your thyroid. It impacts your heart health. It impacts your bones: it impacts basically everything and seeing as mine was low, it was like okay could this be contributing to hair loss, because there are some potential connections and correlations between hair loss and vitamin d, as well as things like anxiety and depression and psychological Conditions now i come from a family who has struggled with depression, anxiety, potential schizophrenia. Like a lot of stuff and people have been institutionalized. I had to go, get help as well and um. For me, that was one of the best things, but my depression and anxiety and like adhdness, like that's, always been there that i don't think, is anything new, but looking at current vitamin d levels and kind of trying to assess how has this changed over time? Could those vitamin d levels be causing, you know a little bit of hair loss and then for those who are familiar with vitamin d and how it's used in the body? Your kidneys are essential to making sure that vitamin d is put into an active form. That is used in the body and can bind to those receptors on all of the cells in your body now, seeing as i only have one kidney, the question becomes: am i just low because of lifestyle factors? Is there something genetic such as these other things that we've discussed, that could be impacting how my body creates stores or absorbs vitamin d also having ibs vitamin d is often absorbed in the gut as well, because you can get it through sunlight and through food, but In the gut in the intestines is mine being absorbed or not, and then hi hello, one solitary kidney. Could there be an issue with the 125 dihydroxy vitamin d and processed in the rest of my body and as we apply this moisturizer? Let'S talk about how vitamin d works in the body because it is really fascinating. Our body basically uses uvb rays from the sun to create vitamin d and mushrooms as well. You can get it from your diet. It normally comes from things like liver or fish, but being plant-based. I don't consume those so getting them from plant sources like mushrooms that also use vitamin d from uvb rays or getting them from uvb or dietary supplements is important. This right here is the hyaluronic acid aqua gel cream. This is a moisturizer. You know the insentry sunscreen is so good that i really don't need a moisturizer underneath it, but for the sake of playing with things today and having a relaxing morning, i am going to do so because skincare is self-care. But when it comes to how vitamin d works in the body, there are so many different steps, and basically, if something goes wrong in any step along the way someone could be deficient or someone could have problems. Think of this, like aladdin just run with me here, aladdin is actually a movie i've seen, but i don't know if i remember it at all. I think i saw it like once think of jasmine as the uvb rays, the sunlight right. We have the sunlight outside of our body and then we have our internal body, our skin. You know that barrier and everything protects it. Think of aladdin and his magical world, as the inside of the body. So jasmine is out here, she's, bright and sunny. She can kind of burn. She can be a little sassy she's that uvb well. What happens when uvb hits the skin? There is a cholesterol inside of our skin. That says: oh, i like this and think of that as aladdin right aladdin. This cholesterol is like a me likey. The problem is these: two people come from different worlds, so they kind of have to come together and when they do, they actually create a baby. I don't actually know if aladdin and jasmine ever had a child did they. I don't know but play with me here: they have a baby and that baby is in the skin, so in aladdin's magical world and that baby is vitamin d3 colo calciferol. Now this is not the active form that can go. Do amazing things in the body think about it? A baby can't rule a kingdom a baby, you know can't be a king. So what happens and this baby vitamin d3 goes on an adventure. It jumps on a magic carpet which is a protein, and this baby d3 takes a magic carpet ride to the liver. Now the liver is where this d3 is stored, but something interesting happens here. It actually meets a genie. This genie is an enzyme, and what do genies do they grant wishes? And what does this enzyme do? Well, it grants this vitamin d3's wish of getting an extra hydrogen. So it's actually transformed you know just the way if a dream or a wish of ours comes true, it can have impactful things on our life. You know when you make a wish and something changes. Well, this vitamin d3 gets changed by this enzyme, the genie while it is being stored in the liver, 25 hydroxylase to be exact, but think of this as growing up right. Just because you're, a baby doesn't mean that you're ready to run a kingdom to be king. You need to learn things. You need to have a mentor like the genie, these enzymes right and once this form of vitamin d kind of grows up, hangs out in the liver for a while. Then it's time to get sent to the kidney or the kidneys. If you're not me - and you have more than one now - you can think of being in the kidneys as kind of like the king training right, you need to have a crown to be a king, and what is that crown that crown is yet again another hydrogen And that usually happens in the kidneys. It can also happen like in the lungs and lymph nodes in other areas as well, but once that form of vitamin d gets its crown, it's actually ready to start making change in the world right. It needs to kind of grow up change, a little bit be responsible, and then it's got it's crown it's a king. It can go, and that is the form of vitamin d that our body can readily use. It can actually do things in our body. It can help with our bones and our health etc. In this form, it's called 125 dihydroxyvitamin d or calcitriol, but this is what our body actually uses and it's again really really important for literally all of our cells, especially in our bodies to regulate things like calcium and phosphate. And if those go out of whack things get bad now, thankfully, my blood levels and my cbc came back really good. My calcium and my phosphate are looking lovely and also look at those liver, markers, okay, low liver inflammation. Again, it's nobody's business. What my blood work results are, but you know a lot of people like to pick on me for being plant-based or vegan and they're like you, can't possibly be healthy. You'Re gon na wither away, vegan deterioration and i'm like look at my cbc in fasting lipid panel. Tell me what's wrong here: show me, your cholesterol, also, my resting heart rate, while talking is what 68 68, while talking and fidgeting okay and again, it's nobody's business, and i'm not here to prove this to anyone, and you should never be comparing your results. Your blood work to mine, you know every single body is different, but i am choosing to share this publicly because i want to - and i think it's interesting and yes, that opens me up for criticism, and that opens me up for discussion and i'm totally. Okay with that, but basically with this entire vitamin d process from getting from these uvb rays, all the way to calcitriol what happens if there's a problem along the way, what happens if that genie or that enzyme doesn't show up what happens if there's a problem in The kidney or, if you only have one kidney and again that crown that kind of final step to making vitamin d ready to go throughout the body and rule the world in a sense isn't working properly. We are going to be looking into my one kidney to see if there is something going on now again, vitamin d does come from uvb rays again from the sun and people who stay indoors or 50 of the population. Don'T always get enough sun. It also depends on where you live. You know if you live like in the arctic or in a nordic country, you're much farther from the equator, depending on your skin color. This can also impact how you absorb vitamin d, people who have black or ebony skin. Generally, don't absorb vitamin d as well as those who have you know, white or more pale. Skin and vitamin d comes from food and for those who don't eat, salmon or liver. You know that could have an impact as well and yes, i do have some of the lifestyle factors that could contribute to low vitamin d. Now, personally, i'm on 50 000 ius of ergocalciferol. That'S a lot! That'S a lot and again you should never be taking vitamin d supplements or supplements without speaking to your doctor, especially if they're oil soluble, because vitamin d toxicity is extreme. 50. 000 iu's is a lot most. People need about 900 to 1200 a day and, if you're, supplementing, maybe a thousand to two thousand but again don't take that from me. Take it from your doctor but to get my levels back up to a normal amount. It'S been about two months and i'm on fifty thousand international units of ergocalciferol or vitamin d2, because again vegan vegetarian vitamin d3 is the animal form which i'm choosing not to take. Now, of course, once we get those levels a little bit more back up to normal, i'm going to be transitioning to a lower dose, but the question is: will those levels even get up to normal? Are my intestines absorbing this vitamin d properly? Is it actually a nutrition or uvb exposure thing, or is it something else inside of my body or is my kidney kind of not you know doing its job, we don't know and that's what we're trying to figure out and vitamin d can lead to so many Things throughout the body again, you literally have a vitamin d receptor on almost every single cell in your body, it's essential for bone health for heart health, which again my heart, is pretty healthy, but we should look at my aorta and some mitral valves in case. You know i have this weird genetic connective tissue thing, but some studies have shown that the vitamin d can impact hair loss and, let's actually take this off before we apply our sunscreen. If you'll notice, i had kind of this widening part. Now there are many things that can cause hair loss, and that includes stress high pandemic. All of these things with my dad's cancer, my grandma work stuff that i've that i've spoken about i've worked night shifts before that can be really stressful. Making changes in my professional life outside of youtube is very stressful issues with family members and friends, and not getting back to people or having issues of anxiety or depression that are always there. All of that is stressful and that can definitely lead to telogen effluvium. Now telogen effluvium is basically this hair fall it's basically when your hair falls out and it's normally six months after a traumatic or stressful event, and i feel, like we've all been going through traumatic and stressful events, especially for the last you know year and a half To two, but now telogen effluvium normally happens kind of everywhere and if you'll notice, a lot of this hair loss, for me at least, has been you know just kind of starting in this part, as well as in these two areas. Now, what that's actually more indicative of is something like androgenetic alopecia. Now what is alopecia or this hair loss or androgenetic alopecia? I know that's a big word: it's basically male sex hormone, hair loss or male pattern, baldness or male pattern, hair loss right and, as you can see, as this part kind of widens a lot of people, don't catch it or don't realize it or kind of as The hairline recedes here or even here in the back a lot of people, don't notice it. Now. Thankfully, we have the beautiful butterfly community, who was kind enough. Some people were rude, but again i put myself out here on the internet like i expected at this point. I'M okay with it um, but some people pointed it out in a kind way and we're like hey. What'S going on with your hair, like do you have hair loss and i was like do i have hair loss? And then i look at myself and i say: okay, i actually have to speak to people that i know about this, so i've asked dermatologists and trichologists that i work with. I have not seen a dermatologist as a patient since my psoriasis diagnosis, but i actually have an appointment for about a week from now to actually take a look at things and to see could this be related to vitamin d again, hair loss can be caused by So many different things is this: just stress: is there something going on with my thyroid outside of what blood tests are showing with tsh and with free t4 and all these other things? But it is, you know, stressful and then you're sitting here like pulling your hair out and you're like what's going on and then you know you start to kind of blame yourself, or at least i do and so then i'm sitting here and thinking. Well, what did i switch up? You know i used uh scene, hair care, which is created by i think, a harvard dermatologist, which i love. I don't think that was an issue and that was actually really helpful for my scalp. Then i was also using function of beauty. I use that for like a year and a half - and i was okay with that. I know some people reported hair loss, but i've been really happy with it recently. I did switch to what was it: love, beauty and planet and um something started happening, but again i'm not blaming the shampoo or conditioner at this point because there are so many other things internally, maybe genetically, maybe stress and lifestyle related that could impact this. But at the end of the day it is happening. I am aware of it, and i want to do something about it and understand it a bit more, and that also brings us to what i found out about myself. You know about having a duplicated reproductive system and one kidney and again is the one kidney related to this is the one kidney not creating enough vitamin d in the form of calcitriol, which therefore is causing issues in hair loss. I don't know, but we are gon na find out. So let's put up our hair and let's put on some sunscreen as we talk about my one, kidney because, yes for those who don't know, i was born with one kidney - and we didn't know this until about halfway through my life and not only was i born With one kidney i was also born with a duplicated reproductive system. I basically have two uteruses or uteri, and then i also have a regular amount of fallopian tubes and two vaginas or what's called a hemi vagina, which means it's kind of split. So everything from the outside looks normal, but from the inside it's genetically messed up and speaking of sunscreens, these are two of my favorites. This is amazing, if you do like that james welsh dewy, skin glow. This is the hyaluronic acid watery sun gel it's an spf 50 with eight types of hyaluronic acid does prevent against uva and uvb rays and as we're on the topic of sunscreens. A lot of people are worried about sunscreens because they're like oh my gosh, does it stop vitamin d production? No vitamin d production has actually shown to be better when you use a broad spectrum, sunscreen fyi, so just getting that out of there and again links references and medical studies are in the description below. But if you don't want that james welsh glow, they also have this one. You know, maybe i can do half and half today. This is the hyaluronic acid airy sun stick. This is very light and pillowy can kind of feel a little bit tacky. But i say this is great for sport, if you're someone who wants something that doesn't flash back at all this just kind of goes on in a stick. It is completely sheer. This works for literally every skin tone and color like even if you were purple, even if you were green. This would work because it is completely sheer, whereas this one takes a touch of rubbing in, but it does go in sheer after a while. They also have this one. This is the natural sun cream. I like this one too, but i don't find this one to be as sheer as this one or as these. So these are what i'm going to be using today. But yes, i was born very, very weird now a part of my life that i don't always speak about on youtube and that i'm choosing not to are things when it comes to school and career, etc, and for some of those purposes. I was learning about embryonic and fetal development and basically, all of the changes that go through a little baby, fetus as it grows up and all the things that can go wrong. You know which doctors should know about or which a gynecologist should know about, or a geneticist should know about, and as i was learning you know about these different things and kind of brushing up on genetics and some of these things just for education purposes and not Even you know, from a self-centered point of view, i came across a very interesting syndrome: the herlin werner, wunderlich syndrome or hww syndrome. Try saying that five times fast, it is basically an ipsilateral renal, agenesis and obstructed hemi vagina. Now, what the frick is that that's a big mouthful, let's break it down right, ipsilateral, renal, agenesis, ipsilateral, one-sided renal, kidney agenesis not being created so basically missing a kidney on one side and an obstructed; hemi vagina, an obstructed or kind of closed off, henny or half Of vajayjay and i sat there and my jaw freaking dropped. This is a very, very rare syndrome. Only a couple handful have been reported and it's not even in all textbooks or in all literature, but it is basically this hww syndrome where young women are born with an obstructed, hemi, vagina or hemi, uterus or uterus didelphys, which is what i have as well as Ipsilateral renal agenesis, or only having one kidney and being born that way, not losing it due to a surgery or an accident or anything else, and i sat there and i was like oh my god, i'm looking at these scans basically radiology and i am just like Shocked and like wait, this perfectly describes me and what this is is a malaria, family, congenital abnormality, again very rare, but basically again big fancy words. What that means is that, while a little baby, what that means is that cassandra needs to charge her microphone and camera batteries because they both died and she sat here and spoke for an hour and none of it was recorded. So i apologize for that, but basically what this means as a malaria abnormality is that while a baby is being created, so while i was in my mom's womb, things did not progress as normal things did not form the way they should have, and it basically ended Up with no kidney being there on one side and um, you know with a duplicated hemi vagina and duplicated uterus or uterine didelphus, and, as i was reading this, it was so shocking and almost refreshing to me to see this on paper. My entire life. I'Ve struggled with dysmenorrhea, basically extremely painful periods. I get two a month and they've lasted 21 to 28 days, and when i was a kid i would sit there and i would complain to my mom or to doctors or to whoever and they'd be like oh yeah. I know honey being a woman sucks. Oh it's painful. I know i felt like no one really understood the pain and um. It was so devalidating right. It'S like, i know it hurts, but like i'm, i can't focus. I can't concentrate i'm on tram at all. For my periods, it's basically related to morphine and i'm not telling anyone else to do that but, like i need severe painkillers because of said pain, and i it's ridiculous and they're not regular, and all these things actually more recently, i thought you know. Potentially, i have endometriosis basically tissue in that area grows in places it shouldn't. It can grow attached to other tissues and be really painful. I'Ve also looked at pcos. You know. Are these things related because of hair growth, all this stuff, questioning that i was supposed to go in for imaging 2019-2020, for you know kind of looking at endometriosis, which is really hard, even with imaging to find without laparoscopic surgery, but pandemic happened. It'S like! I don't want to go in for elective things if i don't have to, and also who has time, it was really really rough, but just seeing all of this written down, realizing that i'm not the only one realizing that i'm not crazy, okay! Well, that's actually a very subjective, um statement, but realizing that my pain is not fake, like this is real, and this dysmenorrhea is something that's experienced by so many other people. It was just so refreshing to see and um. You know for some people, you know. Imagine every single month we we people who were born with a uterus. We lose that lining right, imagine having a closed off cavity that that cannot be lost. It can't escape the body. Right can actually grow up, create like this big old blockage in there and it has to be removed surgically. Thankfully, i think mine is not like that, because i do have two a month, but for some people they literally have to go into surgery, infertility issues, endometriosis, a lot of problems - and this is very rare, so just kind of seeing it was like wow. I can't believe i just came across this, especially because i've seen ob gyns before i've spoken to care practitioners, that i know that i'm friends with that i've worked with and been like hey. What do you think of my one, kidney and so far no one's ever mentioned this syndrome to me, and even in many medical textbooks in curriculum, this usually isn't taught. And again i get that it's rare. I get that it's unusual, but even when it comes to ob gyns, you know i don't think i've had the best obstetric care. Um doctors are humans, right and uh. Humans are human, and doctors are amazing and every doctor is going to do their best. But you know some naturally are better fits than others and as a patient, it's my right. It'S your right to seek a care provider that works for us. Well, um. I feel like. I need a new ob gyn, just because i haven't really gotten the care that i've needed even before finding this hww syndrome. But as i see this, i'm like wow, i really want to go in for another round of imaging. I want to speak to someone who knows about this speak to someone who's worked in fetal development or in genetics, or you know in gynecology who can understand this and what it means. For me, it's almost relieving in a way to know that it's not just in my head, not being hypochondriacs here you know, but is this stuff related, is me being born with one kidney and potentially having connective tissue disorder stuff? Could that relate to how my body either absorbs or processes or creates this vitamin d this calcitriol and could that be related to other genetic things in my body like psoriasis or thyroid, and therefore could that all be impacting my hair loss or my dry skin? Or these things that are very evident to me that i care about and again we are not self-diagnosing here. This is why, even outside of talking to people that i know or that i consider myself friends with i'm speaking to specialists and doctors as a patient, not saying that you should compare your blood work to mine or that you should get on the same prescriptions that I do please don't do that, i'm just saying, as your acne big sister who's been going through stuff. I want to talk to you as my skincare sibling and share, what's been going on, it's almost like a path of further self-discovery and again not being a hypochondriac. Not having anxiety about medical conditions or things like that, it's just that i'm trying to uncover these things and i finally feel, like i - have a team of care providers who's really in my court to help do that. It'S refreshing, you know, is this stuff all related, and even when i was a child, i remember you know i would sit in um cooking class and i would sit here and my scalp would bleed and people would tease me and at the time i thought it Was acne because i had acne all over my face, but looking back you know they kind of looked like psoriasis, or was it atopic dermatitis? Is it what my other family member is dealing with, and it would just bleed - and i would itch at it because it was itchy and what i'm currently going through with just kind of little dry, patches or dry patches on my skin? Is this the same and related to what i had as a child, or is this something different um? I don't actually know, but with all of this, it's just it's interesting and it's kind of cool to finally feel like i'm getting some answers, and you know hopefully in sharing this with others. Listen. I know that it opens me up for criticism by speaking online. I recognize that people can form judgments or opinions or speculate about me and by speaking about this openly. I am basically making that a thing, but i do feel that it's important because a it matters to me and b you my little skincare siblings and i is your acne big sister, i'm going through it, and i want to talk about that in case. It'S just eye opening or if it's interesting to anyone else and like all of these things, a lot of them. Don'T have a clear-cut answer. You know, and even if we do, you know blood work. You know we have to look at clinical symptoms to make a definitive diagnosis or even a field diagnosis, and some things maybe won't, have answers or aren't definitive, but i am trying to get my hair loss a little under control trying to catch it. While it's early, you know, i have not yet used something topical like minoxidil, that's something i'm considering or like you know, a vegan cruelty, free minoxidil or like a rogaine um, basically something that can help to stop the hair from falling out further. Dr dre uses this uh little helmet. This eye restore helmet. I'Ve been considering that as well. I'M not looking at a transplant at this point, but i mean whatever you know when i was younger um, my hair used to be so long. I literally didn't trim it. So my ends were super dead. I have photos of my hair being down to my waist with a super dead ends, and there were multiple reasons that i didn't trim my hair, that were personal reasons as well as hair elsewhere. On my body more recently, i've been trimming it and i'm trying to get it to grow out further and again. There are many reasons why hair might not grow out. I'M not blaming it. On my shampoo, sometimes it's genetic, some people have different rates of hair growth and therefore hair fall and how long it takes for their hair to fall out and hair cycles are six to seven years right. But i do want to find out if these things are related and really what this means for me, what this means for me to be healthy and happy, hopefully long term and not die of a triple a you know if i do have a marfan's disease. If there's a way to be aware of this and to keep an eye on it and know that it's there, instead of just like blindly go through life, not understanding, you know why my fingers are extra long. Why? I have scoliosis, you know and why i, you know, have two periods a month because that's nice and frustrating as mentioned. We are not self-diagnosing, we are not being hypochondriacs. If you want me to keep, you updated, potentially i'm kind of an open book at this time. I feel comfortable doing that and um. If that's something you're interested in, maybe we can do more skincare little k-beauty routines and talk about these updates in the future. But another huge thanks to isn't tree for actually allowing me to create a video like this and for helping us create content regularly. They have amazing products and, as you can see, this site is like nice and dewy kind of that james welsh glow, whereas this one, i wouldn't call it mattified. But it's definitely you know it doesn't have that same glow, that this does so this for the oily skin this for the dry skin. If you have both, you know, you can do this in your different oily versus dry patches. All of their products are amazing and relatively inexpensive, they're even more affordable when they're on sale, which again, i believe, is from the 23rd to the 26th. But i will leave all of the links for these and my favorite isn't tree products below, as well as some links to just some medical studies that i've read or some of the textbooks that i've been studying from or some of the other things that i've kind Of looked up and tried to understand, or even some of the references that doctors and specialists have given me or if they give me interesting things in the future, because, again i understand this is nobody's business, but my own, i'm choosing to open up about it. I want to have these conversations. I do find them somewhat interesting and almost relieving just to know that i'm finally, on my way to getting some answers, you know, and hopefully those answers will allow me to deal with hair loss and you know dry skin, but also just help me be. You know the healthiest and happiest version of myself, so do always remember to stay hydrated both orally and topically, especially if you only have one kidney make sure to reapply your sunscreen and produce that vitamin d and also remember to be youtiful both inside and out. Thanks for understanding that my camera battery died, thank you for putting sunscreen on and doing this little k-beauty routine with me, and i can't wait to see you in this next video love. You guys bye, you

Pamela Kammer: CASSANDRA!! I was also born with uterine didelphys!! 2 cervix AND ONE KIDNEY! I am 48 years old and have had 12 surgeries since I was 12 years old... I GET IT I did end up having to have a hysterectomy at 24 years old. I am also a registered nurse for the last 17 years... I understand your pain and can help if you would like

Babs X: Such an amazing job of taking a very complicated topic and providing an epic narration! This is exactly why I watch you!!! You can conquer any topic, and most definitely figure out what is going on with your health. ❤

Hedwig: I've been shedding for the past 3 months and lost more than half of my hair. And I must say that even though I have an ED the hair loss was too much to be only due to my ED, I've literally taken every vitamin and multivitamin. So I went to the dermatologist and apparently I have seborrheic dermatitis and I started treating this, and when i brush my hair now I don't see as much hair as before! Now we're waiting for the blood exams results to do anything else!

Lainey Wakeman: my boyfriend recently got diagnosed with marfans syndrome, after an emergency surgery on an abdominal aortic aneurysm which was terrifying to go through. if you suspect you have marfans, it's definitely a good idea to get it looked into further sooner rather than later, so i'm glad you're seeing a specialist asap

t.: I started spironolactone about 3 months ago due to hair loss- which unfortunately my doctor ignored for years. This video definitely makes me feel not as alone, so thank u for sharing your experiences Cassandra ❤️

Cicely: I am a doctor and have struggled with hair loss since my early twenties. At one point I thought I would lose my hair and need to use wigs or other ways to camouflage. I am now 40 and it is better than it was then, I can wear it long and does not show. My two cents - minoxidil helps, even if it is telogen effluvium - nizoral and exfoliating lactic acid shampoos for the inflammatory part of hair loss (I have some dandruff and seborrheic dermatitis) - nutrition: vitamin D, iron (look at your ferritin stores and if they are less than 60-70 supplement- take the supplement with something with vitamin C like a tangerine, and away from tea, coffee or dairy) - make sure your vegan diet includes lots of protein : eat a good portion of pulses every day (chickpeas, beans, lentils) and a good portion of tofu. - marketed hair supplements and vitamins are usually not very helpful and simple brewers yeast tops them all (with IRON and PROTEIN) xxxxxx Iron and protein may be another two things to supplement.

linmonPIE: Thank you for explaining all this. I can’t imagine having to go through all you’re going through. You seem to be handling it all like a champ, though! I’m actually going through hair loss too. It’s such a frustrating condition! Please keep us updated!

Sharon Cormier: I'm enthralled by all this science in this video. As a medical professional this kind of content keeps my attention and excites me. I appreciate your courage to put so much of your PMI out to the public, and appreciate that it will allow someone with similar issues to hopefully feel not so alone and maybe help them understand better.

Becky Collins: We thought my son had Marfans syndrome because he was 6'2 and skinny at 12. After genetic testing we found out he has Ehlers-danlos. The genetic testing was worth it. Good luck and hoping you get the answers you need. Thanks for all your wonderful videos! You have really helped me so much. ❤

Samantha Blanchard: Everything in my body started going haywire once I got around 30. I know exactly how you’re feeling.

Kaylee Weber: I feel you girl. I too have rheumatoid arthritis as well as Hasimoto's thyroiditis, very low Vit D3 levels. In my late 20's to early 30's, I experienced hair loss that left me nearly bald. I tried everything to get it to regrow. Then, just as suddenly as it started, it got better and back to nearly normal. I'm now 60 yr old. My hair has gone thru ups and downs since the original loss. It has never regained the fullness it had before all this started. But it has never gotten as bad as it was during the first loss either. I had patches that were completely bald and it thinned everywhere. I wish I could tell you what stopped it. I tried everything, vitamins, massage, clean living, no dyes. I had given up and turned it over to God in prayer. I do advise to get a liposomal Vit D3. I take a prescription vitamin D but it wasn't enough to get my levels where the doctor wanted them, so she told me to take an OTC vitamin as well.

Tina Sampley: I have EDS so I understand the testing, skin issues, heart problems and so many other things. I hope you find your answers soon and I hope your dad’s cancer will be in remission soon!!

Lagina Lutz: I can't pretend to know exactly what you're going through, but I do know these words come straight from my heart. We are here for you -- to listen, to help, to care, because you mean so much to us.

Lila Durán: Every time another person comes out and says their reproductive system is different-than-expected I feel 2 years younger. I'm not alone!

Victoria E: I totally hear you on the pain. Endo Stage 4, doctors didn’t catch it and just said I was crazy Now my cervix is connected to my colon and they can’t fix it. Plus PCS it’s really tough. I took morphine when I had insurance. I’ve had horrible obgyns this world hates vaginas!

Megan Taft: Keep us updated! Stay strong and thank you for sharing your story with us. You've helped so many. You're so wise and thank you for educating us on different topics❤ You are very loved within this community!

Natalie Delong: Chronic telogen effluvium & AGA patient here (who is sending hugs & greatly appreciates your bringing awareness to the topic of hair loss). I was previously vitamin D deficient, but had a lot of luck with prescription vitamin D/now a liquid OTC supplement. Also had a great experience with low dose oral minoxidil after using topical for a few years, and added spironolactone and Nutrafol on as well two years ago, also with success and some regrowth. If you can find a derm who specializes in hair loss, I 1000% recommend it. It made all the difference in the world, as I think many derms have been trained to assume most forms of hair loss respond poorly to treatment/are a bit dismissive of wanting to intervene early. I hope that you can stabilize your vitamin D levels/find the answers you're looking for soon! <3

Kimber Martin: You are so well informed! I am pre PA with intent to specialize in derm and this was so fun to listen to because you have a knack for explaining complex interactions within the body. Thank you for demonstrating how interconnected our body systems are and being an excellent example of self-advocacy in healthcare ♥️

A C Gilbert: Hair loss seems to be quite prevalent in this stressful Covid time. Dr Dray also has addressed this issue on YouTube. I know many women who have noticed an increase in 'shedding' and less fullness in their hair . I relate to the painful periods. Too personal for comments but.. I understand.

Yeet: Despite the pain and suffering you have experienced, it’s a sight to behold your strength in choosing the narrative and choosing to live your beautiful skincare life how you want to. Your positivity and knowledge has been a huge blessing on more people than you can count. Thank you for being you. Wishing you the very best and happy holidays! :)

Allie H.: i have EDS and this video off top made me feel something. regardless of what it is, thank you for braving up & sharing your health journey. i’m sure it makes a lot of us feel less alone.

Khavya: When I come to know abt wat you've been through I genuinely feel blessed for having this body...I always felt tat my body isn't perfect...I always felt bad for my health conditions...but seeing you have all those health conditions nd still being able to pull off things is making me feel confident...thank you cas...sending you so much love my pretty lady❤

Anita Rókás: I wish you the best. I have hypothyreosis, and because of that my iron levels are not the best. I always had fine hair that had a really slow growth, but recently I also noticed that I'm having a bigger gap up there. I started to use the Ordinary's Multi-Peptide Serum for Hair Density, and I'm seeing great results. Someone said it perfectly that what this serum does is, it helps your hair to grow healthy. Maybe try that until your full diagnosis.

August Ice: I worry you might be not absorbing nutrients especially minerals. I also have ibs and gut damage. I cant absorb certain things so i have to supplement. For eczema (which i used to have) i recommend a liquid b complex, liquid zinc, iron, and vitamin d3 to increase immune and wound healing ability. I got blood tested and was very deficient in d3. I guessing since ive been inside a lot during thid pandemic. I got a rash on my cheek, added d3 into my diet, and it healed! Magnesium is also important too. I put cashew powder in my overnight oats! It has zinc/iron/magnesium in high amounts. Please take supplements cassandra! Trust me. Some people just don't absorb it well or need more due to their body types! There are studies for example that show we lose the ability to absorb b12 as we age so we must supplement! Try it out and see how you feel! Im also vegan! I try to get as much of these minerals from my food. I am consistently taking d3 and b12. Iron was a one time thing and it was enough to cure my anemia (i was anemic even on a meat diet). Protien with each meal is also important and omegas. Only eat organic legumes and breads as the pesticides can damage intestinal lining! Anyhoo, i just wanted to help!

Chloe Demure (Save The Victory Roll): That is a lot to go through, you got this! . My Grandmother passed away due to Alzheimer’s, its awful. Hugs

xoRitz727xo: As someone who has lived with psoriasis for almost 30 yrs, my skin is a hot mess. I love that isntree bifida ampule...my skin loves it. I absolutely applaud you for being so open and transparent with us. ❤ I hope you have an amazing Christmas.

TheTinyTitan92: I experienced hair loss twice in my life (due to anorexia nervosa). It was very traumatic for me, and for years later I would get anxious about seeing normal hair loss in the drain or from brushing. The only good thing out of it was that I decided I liked having shorter hair (during both times my hair was long).

Katie: I started losing hair in the same areas you are a year or so ago. it’s been so hard and I’m glad you’re talking about it.

K LL: I am just so sorry for everything you've been going through... Much love to you Cassandra. ☃️

Lauzzzy: This is an amazing video Cass, thank you for sharing! Validation is so important when dealing with lengthy mysterious illness. I have recently received answers to a major health issue and I was told multiple times in the past that it was all in my head or that I was just lazy when in reality, I have quite a debilitating illness! The validation is REAL!! Love you guys

Lisa Miller: In love with how you explain things. Your analogies are so fun! Thank you for all you do!

Kristen R: Hugs to you. This is a lot to handle, and it’s amazing you shared with us. I have an autoimmune condition that took some time to diagnose, so I appreciate anyone using their platform to discuss their health.

May June: I’m so sorry you’re dealing with all this stress. I’m sending so much good energy, you inspire me :) I also lost 40% of my hair over COVID from working, but I started vitamins and it’s coming back. The people commenting can suck it!

keerthana changat: Sending you all the love Cassandra ❤️ really appreciate your hard work inspite of everything going on in your life..thanks for educating us on several issues and reminding us to be kind to other.

Anastasia B: I’ve been watching you for around 10 years now and although I knew of some of your health concerns I had no idea the battles you were fighting behind the scenes. You are so strong for sharing your story and helping so many other people in the process. When you kept listing conditions I was almost getting angry - why would such a wonderful person have to fight through so much?? We are here for you and i hope you get the answers you need soon and find a team of doctors who truly respect and listen to you.

Melissa Midian: Thank you so much for sharing your story. I have been watching your videos for quite some time and i really appreciate the thought and insight you put into your content, you are amazing!!

Emma McConnell: Cassandra, I have always found you absolutely gorgeous & so authentic. While I do not have the same condition youve opened up about, I have struggled with other severe chronic conditions and can sympathize. Finding an expert who coulf actually provide a diagnosis after 30+ months was LIFE CHANGING. Sending tons of thoughts your way & hope you find a physician who can change your life too!

C Russell: I just want to say thank you for this post. I too have felt “crazy” when not properly understood by doctors. I would love to see this be a series and I personally would love to follow this journey with you. ❤️❤️

roxi_lovesmakeup: I do have endometriosis, and struggle with it for 11 years. Took me 4 years to diagnose it, and changed about 10 gynecologists, and finally got one that knows what this is. The journey was very painful, physical and emotional, I even been told that this was in my head, till became life threatening, and went to the ER, with internal bleeding. My endometriosis was so advanced, that was affecting my daily life: couldn't sit on my belly, I was in pain while climbing stairs, or doing daily chores like hoovering, every involving bending over that obstruct my belly, was painful. Then was the severe acne, very painful periods till the point of fainting, really bad stomach cramps, and my rectum used to heart while sitting. Had surgery twice, 1 year apart, because on my first surgery they confused it with appendicitis, and that's why they thought the blood in my abdomen was from. But boy, they were wrong! Managed to find a good doctor, and now is been 7 years since I had my second surgery, I'm under hormonal treatment since then, because without it will come back, so I'm keeping it under control with that. Side effects from that? I've gained a lot of weight : 50 lbs in a few years. Still have breakouts, especially when I'm stressed, but is not as bad as it used to be. My face was bleeding every time I washed it, had scabs all the time, tried not to picked them , but used to break and bleed on the minimal touching. I've grown a lot since then, especially with my skin care. I use more gentle products that help heal my skin

Lillian Zach: Good for you for staying optimistic despite all the medical drama and staying curious. We should all strive to get answers for medical issues with such passion- from experience, it's exhausting but so worth it. Hope you get the answers you're looking for

Sandra Witkowski: Casandra you are the most amazing person I have ever seen on you tube. To go through all these issues and still have such a great attitude and provide content for us it’s so admirable. Sending lots of love and prayers for you!

JBOT Jo Southall: Short term obsessive viewer, first time commenter. I found this video really interesting and my partner laughed at me while I watched. He's convinced that my hypermobile Ehlers Danlos Syndrome is contagious since I seem to find hypermobile folks everywhere I go. In my day job I'm an Occupational Therapist and I specialise in supporting people with complex long term conditions. I work with a LOT of people who have connective tissue disorders. Watching your video there were a few things I just wanted to mention so you can research and follow up with your Docs. Theres a trio of conditions that often run together with connective tissue disorders like EDS and Marfan. The first is PoTS (postural orthodontic tachycardia syndrome) which links to dizziness, autonomic dysfunction, digestion, sweating and urination. The second one is Mast Cell Activation Syndrome (MCAS). Common symptoms of which are histamine responses, oral allergies, food intolerances, urticaria, flushing, skin irritation, dry skin, eczema and other allergic reactions. These three conditions combined often work together to cause IBS-like symptoms. Partly stretchy gut, partly autonomic wonkiness, partly allergic responses. The downside of these combined issues is poor absorption of some vits and minerals. Often vit D, B and Magnesium. Not everyone with a hypermobility disorder will have obvious symptoms of all 3 conditions. But elements of each are common. I lean much more heavily towards the autonomic dysfunction than the MCAS but when unwell or stressed in particular I find my skin gets dry or irritated, my food intolerances get worse and my hair falls out more and my scalp gets flaky. It's really common with a hypermobility disorder to find each condition plays off each other and in times of stress or illness (hello global pandemic stress) flare ups of one of more condition cause a kind of cascade decline in all conditions. Fatigue and "burn out" are a common end result. I worked most of this out the hard way and spent ages seeking out the right healthcare team. When I qualified as an OT I was determined to let others have the same struggles. So I hope some of that was useful!

Marie Helene Chéreau: Thank you Cassandra for being our "teacher" in a very entertaining way. You help us, you deserve the best advice too. A huge HUG from France

Lova Shadowkin: With so many heath issues im thankful you’re healthy as you are. Much love to you ❤️

Michelle Michitsch: Cassandra, I love your channel, but after you sharing this, I love you even more! You are handling all this with so much grace and strength.

Ida: A great video again, Cassandra. Thank you for sharing an being so open. I've been feeling like something is wrong and my body isn't working as it should for years already, but all I've gotten is medical gaslighting. My bloodwork seems fine, but I'm very sure I have some sort of hormonal imbalance and something with my gut, maybe IBS. I'm always fatigued, I have to eat a lot and still struggle to maintain my weight and my periods are very irregular and come too often or last for a month or two straight at its worst. I'm at a point where I'm considering starting birth control, because that's the only thing I'm getting from every doctors visit. I'm always told I'm too young for there to be anything wrong with me. Also, could you please add links about research on vitamin D and sunscreen in the description? x

Dana Say: I just love you so much ❤ Thank you for always being so open and honest and for educating people. You have taught me so much and this video in particular has made me go hmm about my own experience. After I had my twins, I have had some significant changes in both my skin and hair. It may be age related as I turned 40 this year, but now I am more motivated than ever to find out what's really going on. I went from being very oily to having dry hair and somewhere between normal to dry skin. It's been kind of nice since I don't have to wash my hair as often and have been able to enjoy heavier moisturizers but I am definitely wondering about the why behind it. Thank you for being you and for being one of the best parts of my and so many other's 2021

Amber Fountain: I’m so sorry for your struggles! I love how open you are and I think it’s incredibly brave to put yourself out there. I hope you find answers h go or your questions. Much love and hugs! ❤️❤️❤️❤️

Lovebird: I just love hanging out with you talking about things going on in your life like this Cassandra. I hope you're doing well. I appreciate you and I learn so much just from watching/listening.

Irina M: Thank you for being so honest and real! Lots of love to you and please stay healthy!!! Merry Christmas!

Annie Oops: I'm going through hair loss as well..and now I have covid so I'm hoping that doesn't make it worse. My loving thoughts to everyone going through this..or anything ❤❤

Skincare and Beauty with PerkiPerkins: Thank you so much for sharing what you’ve been going through and the proper terms I’ve been dealing with sever hair loss and I’ve been having several Vit D deficit… I had been seening a specialist at Stanford and used to get infusion 1 or 2x per year which helped but COVID hit and all my on going studies and treatments were stopped since I was being treated at the cancer center… (I was told I have Endo but I kinda feeling might be PCOS). I need to reschedule and get seen by my last doctor the new one I have doesn’t listen properly and I was always an advocate to fight to be heard by doctors because sadly in the Bay Area my family and I have dealt with dismissive doctors.

Ara: Cassandra you are an amazing , natural teacher. I learned so much from this video, and as someone who just lost my last grandparent who also suffered with dementia, it is very nice and comforting to know I'm not the only one dealing with that, and things of that manner. People don't discuss these sorts of medical subjects a lot and it is so important and vital to open convos to make it more acceptable to talk about medical issues/situations. Thank you seriously from the bottom of my heart this vid helped calm me x

C J: Thank you for this post and your channel in general. It helps everyone to know we are not alone with medical issues. Lots of hugs to you.

The Skincare Concierge: Oh my gosh. You have been through so much! I am so glad that you found skincare that helps you deal with everything you have genetically going on. My thoughts and love go out to you. I will pray for some resolution and release for you physically and mentally. Thank you for sharing such personal information that can help so many other people. Way to go talking about your IBS.! You are incredible! Keep it up and be my friend! I am the best friend that happens to not have acne. Still love me?

Demm Dem: my ex literally has all these conditions she was born with two uterus and only one kidney... also she does have long fingers and used to complain about dry patches.. will surely share this with her, there's really a few of you unique people ❤️ and you're definitely not alone in any of this

Mel The Muppetslayer: I love you Cass. In terms of isntree that I’ve been wanting to try for the last 6 months plus: the 8% aha essence (4+4 glycolic lactic blend) and isntree hyaluronic acid low ph cleansing foam (creamy amino acid face wash)

Ash2theB: This should be a whole series. It’s really nice to see how physical issues manifest in to the mental are really connected. I’m currently dealing with impacted ear which I had to find out is more common as you get older. My mom had eczema but she suffers from the other skin common skin condition.

Dominique The easy minimalist: Whoa, so much information, so many conditions that you have to deal with…. I hope that you find the answers that you are looking for Cassandra. You have a long life ahead of you, it matters that you understand what is going on with your body. Wishing you a good team of experts that can accompany you in this “genetic” journey, with knowledge and empathy

lila l: hey girl merry christmas~ have you ever tried slugging? i recently started using alba botanicals’ unpetroleum all purpose jelly on my face every night as my final step and i have been waking up with baby soft skin. i also have super sensitive and dry skin though

Taylor Made Beauty by Kris: Thank you for sharing your story and knowledge. I think it is so important that we all share what we’re comfortable with about our struggles in life. Here’s to keeping it real

Mayana W.: I really loved this video because it IS interesting and it's also refreshing because people just don't discuss their health - it's personal and private and there are good reasons why we don't (people can be shitty, bad unsolicited advice, - the works) but when you're experiencing something abnormal it can be so, so, so isolating. And finding a diagnosis sometimes isn't better because you almost feel hesitant to address other issues you have bc you feel like you'll be seen as a hypochondriac/won't be taken seriously. You almost start to think you have too much going on for it to all be true - but no, human bodies are incredibly complex. I was diagnosed with lupus last summer and already have a small collection of other issues (PCOS, 1 kidney, insulin resistance - untreated anxiety and I am 97% sure I have ADHD). But it is so nice to not feel alone out here navigating the medical system figuring out what's going on.

Diogenes II: Low vitamin D is associated with low magnesium. Too much vitamin D also decrease magnesium. I recommend you get your vitamin D from lichens, which is plant based. And please start taking magnesium malate or glycinate. Also watch out for oxalates in leafy greens

Anna Mehrabyan: This was such an informative, fascinating, and gentle video. I learned a tremendous amount, and I appreciate your knowledge, meticulousness, and vulnerability. You also look lovely here!

Mikayla Jenkins: I know one of the first things you probably got tested for was vitamin levels. And I'm only a few minutes into the video, I hope you're doing alright!

nicole stewart: Thanks for being so raw with all of us. I'm currently going through investigations with my health as something is terribly wrong and they can't find me answers. Like you I need to change doctors 100%. We love you

JassiJo: Thank you for sharing. I have been researching Vit D3 as well in relation to kidney stones, gall stones, saliva duct stones, gut and bowel issues, White hair by age 23 - etc. Your video has been timely with what I have been researching. What you have researched was VERY interesting and your reasons for sharing have been astutely helpful.

Catherine Goulet: I sympathize with you Cassandra! I have experienced both types of tolegene effluvium in my life. The two types are: the one that gradually spreads over several years and the one that is sudden and intense. I also have IBS and a slow thyroid gland as well as multiple vitamin and mineral deficiencies. I have lost more hair in the last year and am trying to improve the situation. You could also consider photobiomodulation for your scalp and your thyroid! Good luck with all of this!

Libby S: I have endometriosis. It took years before I was officially diagnosed with it after a laparoscopy. The pain is horrible. But it was such a relief to have that diagnosis, from people telling you it's normal to have the pain and bleeding. And you almost start to believe them, but you know your body, you know when something is wrong. Keep fighting for you health.

Marie O' Dwyer: Thank you for sharing this difficult information. I am so sorry about what’s happening to your family, you’re so good to share your knowledge and wonderful personality at this unimaginably tough time. I wish you happiness and fantastic health.

sandysutube63: Your an amazingly strong and beautiful woman. Your soul is so awesome and sweet. I am so sorry for all your health issues. I have some health issues also / thyroid (hypo) and heart issues. I can’t believe how amazing you look at these issues, study and fight them all. So sorry about your father’s cancer and your Grandmothers dementia diagnosis. I also have that in the genetics too. Keep strong Cassandra ♥️

Elizabeth Torres: WOW! Still beautiful with an awesome personality. Around 2010 while experiencing physical changes without a clue on lab test, and Xrays. A TSH test was requested. My dr asked me to come in, she had my results and refused to tell on the phone. I sat in front of her and she started holding my hands, I did not think anything of it, and thought.. Oh how cute.. She stated that there was a women in the hospital in a coma with a TSH of 100.. Then she looks at me and said, your TSH was 315.. how the hell are you alive and walking around? Now I know why she was holding my hands, then she tells a colleague of hers, "this is 315." Recently diagnosed with Vitamin d, B12 deficiency and gain weight. Hypothyroidism tends to do that while Hyperthyroidism works the opposite. Not everyone will gain or lose weight, but my dr tried to increase the dosage and still my blood work shows my TSH is low? TIME FOR NEW DOCTORS! Hope they find all the answers needed, that clarifies everything you have gone through. For my doctors are still confused as well. Thank you for sharing

Arielle Siler: This couldn’t have come at a better time. My hair has been falling out in patches and I need to find a doctor that I feel safe with to get to the bottom of it. I love that you have so many informed questions that you can take in with you when you see your specialists. Selfishly, I’d love to hear more about this part of your journey so that I feel like I have a buddy in this. But I understand that you’re just sharing that you’re kind of going thru it right now, and to that I say, HANG IN THERE SIS! YOU’RE NOT ALONE!

Laura Kenney: Healthcare is such a difficult road to travel without rare conditions. Congratulations to your discovery in that book that was meant for you to see! Thank you for your openness & your incredibly good teaching skills. We are all better informed thanks to you. ❤

Jam Kwasowski: I also love the green tea toner! As it's full of antioxidants, is it ok to use with a peptide product? Really glad you're getting more understanding of your health so you can take the best possible care ❤️

kimberlee: I’m sorry you’ve had to deal with so many things and that people have been unkind to you. Your openness on social media will surely help others in similar circumstances to feel less alone. Best wishes to you. I hope you find answers and solutions.

Marlo Williams: Wow! Yes please keep us updated. I appreciate you sharing your knowledge and letting people know where to go for help and information. For example, I wouldn't have thought to see a dermatologist regarding hair loss but it makes total sense now. Please let us know what resources/specialists end up helping you best with your more complex issues as well; I know a lot of people kind of go in circles for many years with these things before they find out where they need to go. Maybe your journey can show others where to begin.

Kristina Ward: I had te and it was so hard on me. I didn't realize how much my hair was a huge part of my self esteem. I got my hair back within a year I was also diagnosed with a blood disorder and other things. Thank you for sharing your medical information because I find it so informative. Also, I had endometriosis and pcos with the worst pain and having a period for so long that I couldn't even remember when my last one ended my doctors would prescribe me with tylenol and send me on my way. Wishing you luck on figuring out what is going on

Khanyakwethu Dlamini: Our health, our bodies being spoken about is cathartic Cass and thank you for your candidness.

Clara Lope: Advice here: I have suffered several hair lose at the age of 15-18 due to bleaching and stress I am currently 20 and CASTOR OIL has been a mayor help for me. I put it in my hair line overnight and wash the day after. 3 months in and I have seen several baby hairs growing and my hair is recovering super fast. Hope it helps ❤️

Leslie holmes: I was diagnosed with juvenile Rheumatoid arthritis when I was in 6th grade and have struggled with pain and swelling in my joints my whole life. It's nice to know I wasn't alone in that.

sarah cooper: Thank you for sharing and the clearest explanation of why we need Vitamin D. It really helps to feel not alone whether with depression or physical ailments. Feel Doctors do assume we know our bodies and do not spend time on explaining how these ailments came about or understand their impact. Know too well how vindicating a diagnosis is regarding pain. You really went through a lot growing up and as another weird and very isolated person am full of admiration for the way you have survived so much pain. The help you have given is priceless.

Tammy 💖 𝐹**СК МЕ - СНЕ𝒞𝒦 𝑀𝒴 Р𝑅𝟢𝐹𝐼𝐿Е: CASSANDRA!! I was also born with uterine didelphys!! 2 cervix AND ONE KIDNEY! I am 48 years old and have had 12 surgeries since I was 12 years old... I GET IT I did end up having to have a hysterectomy at 24 years old. I am also a registered nurse for the last 17 years... I understand your pain and can help if you would like

April Neilson: How do you stay so positive and funny. I wish I could be so upbeat when struggling with so many issues.

Tiffany Brust: I'm so proud of you.

f1zzypop: I also suffer from crazy hair loss. I've been using the inkey list caffeine solution and actually works. My hair don't fall as it used to. I recommend you to give it a try.

Sarah Schall: Thank you for sharing your journey with us! I love your videos and your honesty and transparency. I hope you get some answers to guide your healthcare and skin care!

v: For those experiencing new hair loss and eczema/dermatitis, it's worth considering the possibility of having had covid at some point in the last two years. Hair loss and eczema are proving to be closely linked to post covid responses. Covid seems to be triggering autoimmune and inflammatory conditions, especially in those who are predisposed or susceptible to autoimmune issues. And yes, Vit D plays a huge part in it! Vit D supplementation is so important, especially in this pandemic.

Diana Isajeva: I have kidney failure and it shows on my skin. Thank you for talking about this I relate so much

thatswhatshesaid: So sorry your going through this! I pray your journey to better health is as stress free as possible. I just found out doing nutritional testing, that my ferritin levels were defficient, on top of vit. D, and found thats what was causing my hair to thin and fall out, and my super oily face to have dry patches, on top of other issues. Its crazy how things like that can have an effect on the body. I was diagnosed with EDS and a bunch of other comorbidites, so I feel ya on the craziness of the never ending weirdness that our bodies are. Love to you

Tina Rasmussen: I shed incredible amounts every day. Fortunately, I can also see growth. My daughter is now suffering covid hair loss.

Peco Picante: I have Ehler-Danlos syndrome and have some of the same conditions that you. I have struggled with all of the things and the chronic pain that comes with it. I'm sorry that you're having so many unanswered questions with it...it took multiple large hospital systems to get diagnosed and even still new syndromes are still being diagnosed.

Sandra Irene: Thank you for sharing Cassandra. I have RA and that along with the meds caused my hair loss. I was also diagnosed with low vitamin D levels so doctor has prescribed D supplements along with folic acid. Edited to add that I am also a huge fan of Isntree products!!

Li-san: I am on that part over obgyn and I just wanted to share my own frustration, woman's health is still very neglected. This is sad but we keep hearing "sucks to be a woman", "it's part of being a woman" but NO! STOP, we want doctors to listen to our problems and actually do research. I was barely in time to find my androgenetic alopecia because my doctor didn't want to look into my hormonal unbalance... I still have pain because apparently everything is fine with my cervix but I keep going back and forth with discharge and occasional pain. But doctors almost say "man up!" Woman health is neglected.

Bobbie Deniker: Thank you, video editor, for recognising that, if Cassandra were any kind of horse, she'd be a unicorn! You're beautiful

Becky Olivia: I so appreciate you opening up about your health. I'm sure it will help our Beautiful Butterflies! Happy Holidays! Much love to you & yours!

Gretchen Isasquirrel: So much gratitude, appreciation, respect and Love sending to you. Thank you for all you study and share.

Olivia Fagin: Thank you for sharing your journey thus far, for not self-diagnosing, and for being exactly who you are! I would love updates as you get them. I can't relate to your exact story as it's only yours and no one truly understands what we've gone through but ourselves. I can relate to lot of what you said though.. the self-doubt, the feelings of going crazy... My mom's side of the family has a ton of autoimmune disorders (my mom, grandma, uncle, 2 of my cousins...) and although I've never gone to get diagnosed with anything I've struggled with IBS, symptoms, joint pain, acne, headaches/migraines, a crooked spine, menstrual cramps that would wake me up from a dead sleep, hyper-sensitivity to touch, and worse of all: severe muscles aches/cramps in my legs and back. I was about 11 when everything started and I tried everything to naturally "fix" it through my teen years from yoga to going gluten free and these things only made my ED worse because the only thing that seemed to lower my inflammation and take away my painful periods was eating less and less. As anorexia became orthorexia which became anorexia again... my life felt so overwhelming and eventually the muscle aches in my legs got so bad I could hardly stand to walk. All that said, my mental health is at an all time best, my skin is clear, my digestion is regular, and I'm completely pain free most days. I still have a few bad days here and there but I can now say I now feel like a "normal" person. What I changed: I went fully vegan, I got my anxiety issues addressed, I started managing my sleep schedule more than ever, I greatly limit caffeine, I cut out all the major stressors in my life that I reasonably could, and I 100% surrendered my mind, body, and spirit to Yahweh and received true grace instead of just practicing surface-level religion out of guilt. The more I prayed with faith and the more I let go of my need for control and answers the more I felt the Holy Spirit guiding my intuition to all the things I didn't know were my triggers. Of course what works for one person doesn't work for everyone, but I wanted to share my story to tell whoever is reading this that there is hope and that you're not alone. "Come to me, all you who are weary and burdened, and I will give you rest. Take my yoke upon you and learn from me, for I am gentle and humble in heart, and you will find rest for your souls. For my yoke is easy and my burden is light." Matt. 1:1 "Fear not, for I am with you; be not dismayed, for I am your God; I will strengthen you, I will help you, I will uphold you with my righteous right hand." -Isaiah 41:10 "Bless the Lord, O my soul, and forget not all his benefits, who forgives all your iniquity, who heals all your diseases, who redeems your life from the pit, who crowns you with steadfast love and mercy, -Psalm 103:2-4 God bless Cassandra! You are dearly loved

Sharon Cormier: Secondly I relate to your menstrual issues as my complaints of pain have been dismissed all my life. 3 years ago I tried again to see what would be the 8th gyn to get an answer. For context I am 37. Thankfully he was willing to do surgery to see if I had endo, and he doubted that I did. After surgery he touched my leg and with so much compassion validated me. I had endo. I had it bad. So bad that I basically had frozen pelvis, all my organs were glued together with scars. He was able to cut through and release some of it so it can free float again however my left fallopian tube and ovary are so encased like cement it was too risky to explore. He said they have most likely been strangled and may not even be there anymore. He said the damage was so extreme I would not be able to have children. I don't and didn't want kids so I had ablation, burning in the inside of my uterus to stop my periods. It has been a blessing, tho not for everyone. I still get emotional about the battle I and so many women have to go through regarding gyn issues. I sympathize and am sorry you've struggled too.

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