Hyper Thyroid/Graves Disease And Hair Loss... How It DRASTICALLY Changed My Life
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- čas přidán 6. 05. 2023
- Graves Disease and hair loss often go hand-in-hand. At least for me it did. I also had the protruding eyes. Hyperthyroidism is something I struggled with on the daily. Not only does Graves Disease affect your body, your thyroid, but it also affects your mental wellbeing. I remember feeling as though I was going crazy.... Like my body wasn't mine... So many things were happening that felt wrong. This is my story and how Graves Disease and hair loss drastically changed my life.
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✨ I purchased Mesmerized from here with my own funds: wigs.pxf.io/mesmerized_shadedsand
💁♀JOIN MY EMAIL LIST: Send me an email (wigswithsteph@gmail.com) with the Subject Line saying "Add Me To Your Email List", and let me know your name in the description of the email! (I love getting to know YOU)
😍 What does my email list receive? I send out emails with important Wiggy information, I sell my wigs that I don't wear anymore and tell you about awesome discounts! What can I say... It's a fun place to be 😁😃
Losing hair is really soul crushing. I am still trying things on my scalp to maintain the hair I do have while wearing wigs in the meantime.
I use coconut oil for this =) My hair really lacks moisture these days, and I find it really helps me XO
Yes,me to trying rosemary tonic after washing,and magnesium oil pre wash two times a week don`t know..but not to do anything would drive me nuts:(
My hair was also beautiful thick and long I lost a lot and it shrinks all the time I miss my thick beautiful hair 🥲
I have experienced major hair loss for decades via Hashimoto’s Thyroiditis/Hypothyroidism. One cannot emphasis enough the important ramifications of thyroid autoimmune diseases and their impact on hair loss. I do have many lovely wigs and use them often although I can still (barely) get by without them with my very short, white hair plus scalp cover-up powder. Thank you for sharing your story and raising both awareness and confidence!
I feel you on the comments. After that I took the initiative to start medications. Funny how I came across your channel before in regards to wigs. Now it’s for hyperthyroid. I too am wearing one 😅
I went straight to wigs. I didn't try toppers or extensions because I was afraid that they would pull too much at the hair that I do have.
Wow, can't believe in this day and age that you went undiagnosed for so long. So unfortunate! My mom had Graves disease in the 70's. No exophthalmus though. She did have iodine therapy and was on meds for hypothyroid after. It's sad physicians still don't listen to women and try to blame real health concerns on mental health issues. I am retired from the medical field and specialized in cardiology. A lot of women's heart issues were blamed on nerves, anxiety and mental health issues. I'm glad you got dx. BTW, I'm originally from Peterborough, Ontario, but have lived many years in the states for work. I found your channel when researching alternative hair for ?? post menopausal hair thinning. I have 5 wigs. They can be addicting. I've started to notice some new hair growth with the change of my blood pressure pill, spironolactone. Didn't realize it helped with hair loss. Thanks for the inspiration.
Thank you so much for sharing your story. Autoimmune disease is so hard . You are helping so many with your honesty and sincerity. ❤
Thank you for your comment and your kindness ❤️
Hi Steph....I don't normally comment on many videos, but after hearing a little about your story, I can't believe how much I relate! I too, was diagnosed with Grave's Disease about 5 years ago. I had that same long list of things happening to me that didn't seem right. In fact, one day before going to the doctor, I wrote down every symptom I was having. He actually had the nerve to tell me to seek a psychiatrist! I was stunned. I'm not sure about you, but my hair loss and hand tremors were the worst symptoms. My Mom suggested I go to a neurologist because she thought I may have had Parkinson's. I am happy to say that the neurologist is who ended up diagnosing me and saying that my thyroid was beyond high and that I needed an endocrinologist right away. Pretty scary stuff....well after a radiation treatment and eventually switching to a naturopathic doctor, I'm happy to say that my numbers went down dramatically and more often now, I'm usually 'hypo'. After all that hair loss, wigs eventually changed my life too. I enjoy not having to take hours to do my hair and still have it looking like crap. LOL! I want to thank you for your video and sharing with us. I look forward to viewing many of your others. ❤🧡💛💚💙💜
Donna!!! Hello!! ❤️❤️❤️ I was so very happy reading your comment 🥰 You’re the first comment to mention that you too were diagnosed with Graves Disease! I had totally forgotten about the hand tremors… yes, mine was really bad too. I remember it was so hard to even hold a coffee cup, because I would shake the coffee right out of the cup!! Another one of my symptoms, a big one, was my mental state. I didn’t go too much into it in the video…. But I felt crazy at times… like actually thought I was losing my mind. I explained it to my partner at the time that it was like ‘everything was wrong’…. Everything felt wrong… and then I would ask myself, “what exactly is it that’s wrong right now?” And I couldn’t answer it…. It’s such a tough thing to explain. I feel like only someone else who’s been through it will know what I’m talking about. Did you experience this symptom? 💕 so happy we’ve connected!!! I look forward to reading more of your comment XO
@@WigsWithSteph…Thanks for your sweet reply. 💜💜💜 And yes, I definitely felt like I was losing my mind or that my body was being taken over! I was actually so grateful to finally be diagnosed because it validated that I’m not crazy! Lol! But the road to where I am today has been long. As I mentioned earlier, I see a Naturopath now. That changed my life. Instead of being on all that Synthroid that was actually making me sicker, I now take a medication designed specifically for me. It’s made at a special Compounding Pharmacy that includes the stuff geared towards fixing my high and low TSH and T3 numbers. I feel so much better now. I’m no doctor,but if you ever feel like you’re not feeling stable, you should check out a Naturopath. She got my health back to a very manageable place. I go to her every 4 mos. to get my labs checked. But believe it or not, I still lose handfuls of my stringy bio hair. I should probably shave it, but far too scared to take that step, so for now, I just throw up the ugly and put on a very beautiful wig! I’m waiting for my hair mail now….trying out Simmer! I love Raquel Welch wigs! Hope you have a great nite! Keep putting out great content….I look forward to it. Sorry for the chatty long msg! Lol! 😊
@@donnavilhauer9014 Hi Donna! Don't ever be sorry for a long, chatty message! This is why I'm on CZcams- to connect with like-minded people like yourself ☺ Thank you for being so open and honest and sharing your story. I know that you will have touched the hearts of so many on here who will also read your comment. I know you've touched my heart.
I also see a Naturopath and we found that I was severely deficient of Vit D. Now I get Vit D shots. That's what actually allowed me to go into remission and not have to get rid of my thyroid. I feel so balanced now, THANK GOODNESS, because it took me 6 years of being on medication for hyperthyroid to get to this point. I am so grateful to finally not have to be on meds and feel like a person again. Although, I too still have the stringy, thin hair, that falls out.
I have heard that about the synthetic thyroid, that often times people don't feel great on it. I love your story and that you were able to see a Naturopath and figure out a way to remain balanced, while not having to take exactly what the doctors were initially telling you to take. I hope others see this comment from you because I think it would be very helpful!
I feel the same as you do... Wigs are the best. I will never go back to wearing my own hair because trying to get it to look some-what decent is a waste of my time... it's just not manageable. LOL. Thank goodness for wigs!!! 💜💖💛❤
I can so relate. I used to have thick curly hair so when my hair started falling out it was so devastating. I don't have Graves disease, but I have scarring alopecia . I can so relate. Thanks for sharing Steph.
Thanks for being vulnerable. I've been Losing My beautiful long hair for over 30 years now it's fine but a lot of it. Now I see my scalp in more ways than one.
I'm a woman. I struggle with hyper thyroid.Test come back normal well something is not normal that with the depression and brain fog etc... I can't stand anything on my head my head. Barrett's or rubber bands or everything just hurts my head. Thanks for this channel. Nobody I know gets it. It's a Lot more than being Vain.
Steph, thank you so much for sharing your story!
Thank you so much! You have given me hope to deal with this hair loss in my life.
Very very very inspiring! Thanks a lot for sharing ❤
Thank you so very much for sharing your experience. That was very helpful and inspiring ❤
Thanks for sharing!
Thank you, I'll try a wig now
Thank you so much for sharing!! I struggle with hyperthyroidism too so I can relate
Thank you so much for sharing your experience! You are very helpful & needed.
The one you're wearing looks incredible, and the style is gorgeous on you.
Aah Steph, another wonderful video. Thanks for sharing your experiences and feelings with us. I love listening to you, for some reason you make me feel really calm 😅
Loved what you said about not commenting on other people's bodies. So important! 🌷🩷
Awww thank you for your comment, Christina!!! ❤️ So happy to have you hear!! XO
I have been having eye pressure and retroorbital pain and the ophthalmologist told me it was just dry eyes and really was just dismissive of my symptoms and that is so disappointing and I feel lost as I can't function with the eye pressure and pain. Thank you for posting your videos as I feel I'm not alone in this.
Wow! Amazing. I woke up thinking about this topic and then I was looking at character wigs for a party and then found myself here. I've been "skinny" for ever and now I'm going to research Graves disease. I've been diagnosed with diabetes, but I've always questioned other health issues. And the eye situation. Makes me wonder.Thanks.
Great video my hair loss is so bad I can't go out without a topper or a hat now it sucks but so grateful for wigs and toppers 💃
I was at that point too, and totally understand. It does suck!!!! Thank goodness for wigs and toppers!!! ❤️❤️❤️❤️ Sending you so much love, Clara!!! Thank you for your comment xo
Thanks for sharing, i am currently undergoing chemo. I have ovarian cancer stage 4. I purchased a simmer which i luv but being petite its really too large , just ordered my first upstage petite yay. Can't wait! Luv your chanel very helpful! Thanks again ❤
I'm also have a Petite head and I have a similar struggle in which most wigs are big on me. I find Upstage Petite to be better. Have you tried the Ellen Wille brand before? I find her wigs fit the BEST on me (they're a smaller fit). I'm sooo excited for you to get your Upstage! I hope you love her!!! When I first got mine, she was a little poofy, but with the heat from my hands and wearing her out on a hot day, she settled down, and now she's perfection!!! XO
New subscriber Thank you so much I feel so alone I started out with hypo then hyper with medication and it's still going strong I can so relate I feel like I'm losing my mind along with hair loss so many other symptoms especially in my hands shaking so bad everybody ask why are you shaking and all these other questions makes me stay inside and not want to go out anywhere especially with my hair falling I've been dealing with this for about a year was undiagnosed during the pandemic so I truly understand you are so beautiful it gives me confidence to move forward in this journey Thank you God bless you your friend always Wendy 💜
Wendy, I totally understand what you're saying here. I used to feel the very same. My shakes were so bad that when I tried to drink tea, I would literally shake the liquid out of the cup. I also had a hard time leaving the house for fear of people seeing me like this. I want you to have hope though because it does get better! And wigs have given me so much confidence again, that I finally do feel like myself. I wish this for you too 💜
@@WigsWithSteph Thank you Steph you are so kind this channel is the best that I have ever found not only with the wigs with the disease itself they still haven't gotten me under control yet I might have to do radiation I'm not sure they have me on levothyroxine all kinds of different crazy dosages off one week and then skip Sunday and Saturday it's just been so complicated and I am age 52 but I still have hope Thank you for responding just knowing I am not alone gives me the strength and the courage to carry on Thank you so much this channel is life-changing I get so depressed and I truly understand about the shakiness bless your heart words are not enough to express this disease and they don't understand why I've tried studying so much and it's just a non-stop circle of articles I've been through now I find your channel I'm so blessed sorry if I'm running in circles the medication they tried was levothyroxine but they say medicine itself will make you lose hair I don't have totally bald spots yet but my pony is so tiny it is definitely stress and I think the more stress that we are the worst it can get to Thank you so much for responding your friend always wendy 💜
I also have Grave’s Disease in remission and so very much grateful hearing you sharing your struggles.
Presently I am wearing a synthetic topper bought two months ago. It’s heat friendly with highlights and looks very attractive when combed and sprayed but falls down into my face soon after. I like to have it styled or purchase a new one. I live in Toronto and don’t know where to go to get the right topper. I need advice, I need direction. Please help!
anither fab video..which wig are you wearing 😊x
bless you.xx
I had Graves’ disease too. It was caught early and cured. People would always tell me I’m too skinny as well - those comments didn’t come from a nice place. People can be down right mean. Thanks for sharing your story, experience and feelings.
Hi Molly! 💕 it is so nice to hear from someone whose had a similar experience. You’re so right- people can be mean. I’m so glad to hear you are feeling better now and cured ☺️💕
Did you take medicine or have surgery?
@@jomr4249 I took methimazole for about a year. I hand to get blood work done every three months and my doctor tapered down the dosage based my blood levels of tsh.
My hair has thinned to point i am now wearing wigs and loving it, look so natural and can wear different colors and lengths, styles
Have you found a good wig line?
Agreed. In my case, my alternative hair is definitely an enhancement.
The hair is awful, the body changes suck.Thyroid Eye Disease is devastating. I am going through it now. God Bless you. You are a lovely lady!
Thanks for sharing your story. My sister has graves disease, she's 9 years older than me. I have had hypothyroidism since I was 35 and developed multiple sclerosis about the same time but wasn't diagnosed for 15 more years! The fatigue from both have taken so much of my ability to live!! Within the past 10 years I have lost my eyebrows and so much of my hair! I am 67 now and really want to wear a wig! My hair is dry and brittle along with my nails. All I want is a straight Bob similar to my hair color. I don't have grey yet so it's blond with highlights. It needs to be reasonably priced. I am on disability with no help. Any suggestions?
Go on girl
Steph I always learn something new when I watch your videos. As I stated on another video I have stage 1 breast cancer. I’m having a lumpectomy tomorrow. I’ll meet with my oncologist and surgeon again on the 21st to discuss my chemo treatments. My doctor already told me I will loose my hair. My question is where to go to find this beautiful wig you have on in this video? I’m in the USA and I don’t know of any wig shops around me. The web sites I have looked at show wigs are very expensive. I would definitely spend money for a good wig but how do you tell the good ones from the not so good ones.
Hi Tammy!! I am only seeing this message you left now! At this point, you must have had your lumpectomy already. How are you doing?? I hope you are feeling okay, and I'm sending you all the positive, healing vibes. ❤💛💗
@@WigsWithSteph Thank you Steph. Yes I had my lumpectomy. Also my doctor said she got good margins and the lymph nodes are clear. No further surgery needed. I go back to see my oncologist this coming Tuesday so I’ll know more about the chemo treatments then. I’ll keep you posted
@@WigsWithSteph Hi Steph. I thought I left you a message but anyway here goes. Yes I had my lumpectomy and my doctor said my pathology report came back with good news. No more surgery needed. She got good margins and there are no signs of any cancer in the limps nodes. I have to go see her and my oncologist tomorrow so I’ll find out when chemo status abs let you know
@@tammypalmer9185 Hi Tammy! YAY! That is WONDERFUL news!!! Yes please keep me updated 💕
Thanks for sharing your story! I had thin hair my entire life from Hashimotos but then I got Alopecia Universalis, so I have no hair at all. I've been wearing wigs for 12 years. I am embarrassed that people can see the tracks from the wefts so clearly against my pale scalp. I haven't tried a lace front in years since I'm so intimidated by cutting the lace so I keep buying ones with bangs, but I feel very out of style. Do you have any videos on how to deal with the lace, I couldn't find one, maybe you could make one in the future? Thank you!
Not gonna lie, most websites at this point that ive seen have both pre-cut and glueless lace. The only thing with the lace is that after a couple of years some of the hairs fall out and you'll have to either put new ones in (similar to hand-sewing if youve done that, but smaller) or replace the lace front with a similar one, such as one of the units on hairvivi where the wig is $300 CAD and the hairline replacement part is $100. cutting the lace isn't that bad, its actually the plucking of the hairline that takes a lot of time and is easy to screw up, but again most places do that before shipping it to you.
I started taking T3 as an adjunct to my antidepressant , my thyroid levels and TSH are normal levels but I'm getting very dry skin, I can't sleep and I'm starting to get thinning hair on the temples and sides.
Thank you for sharing your story. Similar to you, I have a health condition that causes hairloss and it has been a journey for me as well. I wanted to ask about the wig you have on now: with it being a heat friendly synthetic, and also being a long, straight style, have you experienced it knotting up more than with a wavy or curly shorter style? I would love to get that wig, but I am concerned that it will tangle easily. Also, I would love for you to do more videos on how you heat style your wigs. Specifically, on how you heat style this wig.
Hi Jenna!! This is an excellent question. I have both long styles and short styles in heat friendly wigs and non heat friendly wigs. Speaking just of longer wigs in general, yes they do tangle more easily. In my opinion it doesn’t have to do with it being heat friendly or just a regular synthetic, because I find just longer wigs in general will tangle more easily. So yes, that is true. In the summertime, if I were to wear a tank top for example, she doesn’t tangle as much as if I’m wearing a sweater or full shirt. Wigs tangle due to friction and rubbing against clothes, so it very much depends on when you think you’d be wearing it. In the wintertime, for example, I tend to wear shorter synthetics, or longer human hair wigs, allowing myself to avoid terrible tangles. In the summertime, because of what I wear (wearing less, LOL), I can get away with both long and short styles. 😊 Even with the added effort to keep her looking nice, she has been SO worth it in my opinion. She’s so light, and even when she’s tangly, she still looks beautiful. She’s one of my husbands favourites too!!
That is a great video idea!!!! I will definitely create one very soon with you in mind ☺️
By the way, this is how I like to heat style every heat friendly wig I have BEFORE I decide to either put wave or curl into her: czcams.com/video/0584kktwk6E/video.html
I find by doing it this way, all the clumping goes away, she becomes tangle free and she feels like a brand new wig again.
I have the same illness, I made a decision to shave my head. I can’t save my hair anymore. I have people telling me that same thing about my weight as well. I know the feeling.
I had TT last November, I’m happy that I don’t have Graves Disease symptoms but It’s hard to lose weight without thyroid though
Could you go over how you went into remission
I just made a video on it 🤗 czcams.com/video/EsaLn0p9xpo/video.html&feature=sharea
I have had my bloods taken on Thursday for my thyriod and i am so so anxious for Wednesday incase i do/don’t have it, the reason I’m afraid incase i DONT have it is because i’m not sure what else would possibly be wrong with me, my anxiety has been terrible and its making me depressed and miserable but yet i do not suffer from anxiety or depression, i definitely feel it’s something deeper than that, this anxiety is not only affecting me but also my relationships as i am constantly causing issues and problems because of these anxietys, i have physical weakness, loss of appetite, constant sweating and i feel my hormones have been put completely out of place, i feel like a completely different person, i’ve lost interest in things i used too love such as painting, video games and animating which is concerning as that is my job, i want to ask for some advice, how did you cope with thyroid anxiety? I want to know so i can do that to cope until my results on Wednesday as i am struggling EXTREMELY BADLY. And i also wanted to talk and see if you had any of my specific symptoms, did you lose interest in hobbies and stuff like that? (Obviously i have much more symptoms than the ones i just mentioned but these are the specific ones i see nobody talk about)
I had one of my eyes bulge years ago after I was discharged / diagnosed with MS... I've got HypOthyroid symptoms - freezing extremities and hair loss. Started ordering and using thyroid pills from Amazon which do help me with menses and not gaining weight. PS, I started using shampoo from China's eBay and there is a mere 2% of hair loss of the previous shedding each time I was my hair. And I use Minoxidil 5% too but not often as there is a temporary water weight gain.
Got severe hairloss,and wear wigs..not sure what it is anymore..got hashimotos in my family so I will need to get it tested(when I find a new doc..)......got sibo...got lots of symptoms of a slow metabolism but my bmi is normal,and my left eye seems a little bigger than my right eye it was not something I thought much about before now will keep an eye on that to..fear my hairloss is not reversibla bc its been thin for a long time now suffer from sebopsoriasis also but if it was just that I should have seen regrowth a long time ago:(
Hi Steph, I like long hair and I've been thinking about wearing a long hair wig as man. Is that weird?
Yep! We should never comment on other’s looks!!!!
❤️❤️❤️❤️❤️❤️❤️
Agree! People are so judgmental, but they’re the ones who have worst lives.
Can you suggest anyone n lace front toppers Vs wigs pls I’m confused I hv to buy one
Ho dear how many mg of carbimazole tabs were u taking and did u take them
I was hoping to have some insight that how you reversed your eye condition and also healed the hyper Thyroid, if you've left medications how are you managing your thyroid. ..... Please make a video on this topic.
I’m working on that video :) coming soon! Xo
I also made this video, maybe this will help ❤️ czcams.com/video/EsaLn0p9xpo/video.htmlsi=DBg5AR_Qu4qaGUj2
@@WigsWithSteph Thanks you so much for video suggestion, I've seen it and I am waiting for your in-detailed video of how you reversed your eye condition, because I've started noticing the same change in my left eye and there's not much videos on CZcams who are addressing this particular issue x
Hi Steph, I just found out a couple of weeks ago, I have hyper too and lost a lot of weight!? Familiar comments from family and friends....how did you recover from that and not have to take meds..... please advise, ty
Hello 💕 I had to take meds for about 6 years before my my hyperthyroid would go into remission. (Meaning, function on its own without meds). I focused on lowering my stress, working out, going for walks, and eating well. I also started getting Vit D shots after finding out I was severely deficient. I don’t think it was just one thing in particular I did that helped me go into remission, but a combination of everything. I believe the body is connected to everything. I now think of food as fuel and try to only eat things that I know are good for me (limiting sugars) and really try to live a stress-free life!! (As best I can- sometimes it’s not easy because life… is life… and can be stressful). But I’ve pulled myself out of stressful situations and environments on purpose to protect myself. I always felt my hyperthyroidism and Graves’ disease flare up when I became really stressed
@@WigsWithSteph
Steph, thank you so much... I've kind of been walking around in the dark... no one to share with!!
When I heard you say hyper ..I froze and found someone who understood and expressed it!!!
I appreciate you 💕😊
@@opalsmith7030 Awww I'm here for you!!! And I appreciate you too!!! XOXO
Wait, are you wearing a wig in this video? It looks so real?
Yes I am 🥰 this is the review video I did on the wig I’m wearing: czcams.com/video/ARYCmQJHPd0/video.htmlsi=Z2HMNNGU_Xbsdeiw
❤️ And this is where I purchased it: wigs.pxf.io/mesmerized_shadedsand
I had these to took my meds I was ok free my hair back, been off meds now my hair fell back again again, thin asl, brittle, just ugly
Hi! New sub here. You’re gorgeous and your wigs look natural to you. I could relate to what people tell you being skinny. Btw, if you go to Asia;East Asia- Southeast Asia… You’re won’t be referred to as skinny. Just normal. 😊
I have this disease 15 years and I have lots of vomiting and nausea now and depend on drug to sleep!I am 51!Someone help me🚨
I have Graves too, diagnosed 2 months ago. I have cut out gluten, sugar, dairy, caffeine and all refined foods. It has helped. I also take herbs and supplements to ease symptoms. I am going to work with a naturopath in a couple of weeks to help more. You need to see a doctor right away if you are vomiting and have nausea. You could have thyroid storm.
@@JoanneRose22 I am barely clean of Zolpedam sleeping pill now .I certainly am more than open to possibly treatment your using!I wish I was with you strictly following the protocols but you being off gluten and just about everything that's really relatively convenient to get and eat how are you managing this!You cant eat any fast food!I had a few chicken nuggets today!I didn't have many choices but you probably have so many more!Regarding the storm my heart rate is 85 on average and I often check my temperature which seems fine!
@@JoanneRose22 Frankly wish 😭I was also married to a Hyperthyroid on a nature path treatment but God wasn't so kind to me and you know I never smoked and never really been drunk and generally didn't even like staying up too much and I limited sweets junk food and fast food but I was still struck by this severe disease also insomnia and other unfortunate symptoms as you can see.I have to worry about all kinds of foods effecting me that I didn't before.I have Bugle weed and Lemon balm tinctures but they don't seem very effective and even Methimazole after 15 years started to look less effective until I just noticed that I am holding on some weight in the mid 200 teens.I m 6 ft 3 in
@@JoanneRose22 The good news is that I had 4 erection last 4 nights consecutively thus stimulating some sleep!It's a sign my body has some level of function!
I'll never find the right wig lupus was bad enough this is worse
Hi..how r u madam?
I never comment someone body because i have thyroid problem..even if they are fatter or skinnier we don't know what they are going through... I always was normal but call they called me chubby,but when i got skinnier they called me sick !! That's more difficult because they are assuming that if you are losing weight you are so sick and unhealthy that you are about to die !! 😂😮😢
Neither comments help either...
It is not something you always have. You can be cured.
Actually, Graves’ disease is not cured. It is something you always have. It’s the symptoms you control and then it lies dormant, but can always flare up with its symptoms. Hyperthyroid was a symptom I had from my Graves Disease
You are a pretty women. Try your luck in Hollywood
A spent way too much money on this already...