I went to pluck my eyebrows earlier. With tweezers in hand I took off my glasses, peered myopically into the mirror... and realised it wasn't worth the effort. The even, defined arcs I had are a thing of the past; all I have left are a pair of stunted catkins.
I'm taking Levo religiously, yet seem to be exhibiting more hypo symptoms as the treatment progresses.
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Joburton
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Yes dear Flower, I would consider showing up at the endo appointment after not, ahem, attending to the rather exuberrant growth of said migrant problem on my chin. However, they'd probably wonder if I needed some quality time in the psych ward. Don't think I have not considered a two week hiatus of my not inconsiderable attention to these nasty sprouts. I'd need to wear a scarf over my face like a Wild West train robber while out in public.
What annoys me most is after plucking it all, then they grow back in waves. So there's always soldiers getting up from the battlefield. It's like 'Whack a Mole'.
My eyebrows are growing like weeds since Ive been on T3, I'm starting to look like Dennis Healey, except thst hes dead. If I didnt crop them on a fegukar basis I wouldnt be able to see wgere I was going. Now, my moustache is thinning out and slowly disappearing.
I am tempted to try T3 too, but will be giving Levo a fair trial first... finding it frustrating that at present I seem worse than I was before diagnosis and treatment.
I will be investing in a good eyebrow pencil... I'm never going down the tattoo route. Have you seen some of the horror stories permanently inked on some people!? {{Shudder}}
I have lost mine for over 15 years now and it is awful to have to constantly draw on your eyebrows...one help was BIOTIN which helps you hair and nails grow so you might want to try that. Other than that, being on T3 only...which works for me...but is no cure...what else can you do? Some say rub coconut oil on them every evening and that helps them grow back...good luck.
I'm looking at getting my hip replaced how are you the surgeon knows I need it done but doesn't like the fact I'm 56 yes old he wants me to wait but he says its up to me ??
Hi! The down side of surgery-waiting for your body to heal etc. plus I was very sick for a week-was down to the pain killers but don't know how much of my NDT I've managed to hang onto so pretty tired but getting there!
I had my first hip replaced at 61 and no one said it's too soon but that they are lasting longer these days. I think you have to weigh up the quality of life. I was in so much pain with the first one it wasn't funny and I'm not good with pain killers! I vowed the next one I wouldn't wait as long as it helps if you are good to aid your recovery. This time my walking wasn't too bad but I was in pain getting out of the car. The surgeon asked me why did I think I want it done as already said not as bad as before so I said for years I had struggled with a thyroid problem and now I have changed my meds to NDT I'm raring to go but my hip is dragging me back so he sent me for an X-ray which showed bone on bone so ready to be done anyway! Send me a PM when you make a decision and we can chat more.
It feels quite strange but it doesn't hurt as an anaesthetic cream is applied. It takes a good couple of hours and you have to look after them very well for a week or so, no water or touching the slight stabbing etc. It makes a big difference
makes one wonder how beneficial thyroxine can be.. having progressively got more and more unpleasant symptoms could it be completely toxic and killing us??
YES is the answer so look it up at drugs.com and check out "side effects" of Levothyroxine and any drug you are on....that was enough for me as I had most of them when I was on Levo for 12 years and felt terrible! It is also filled with fluoride which is toxic to the thyroid, perhaps not in the UK but most certainly in the States which is Big Pharma nicely keeping you ill....making sure they get rich off your misery! Do check out Drugs.com to be in the know with what you are actually putting in your body!
I lost mine almost overnight too. But I found a brilliant medical Tattooist and now they look better than ever. I was Hypo but now I have sub Hyperthyroidism but no medication as yet. They want to remove my thyroid but I am fighting that as it is not cancerous.
Hi there - where/how did you find your medical tattooist and can you give me an idea if costs - i've been thinking about this for a while and when I have some spare cash will invest - I hate my eyebrow loss!
It was £200 for the first 2 treatment sessions. Now I have a top up about once every 6/8 months at £100. It isn't cheap but they don't come off overnight so you have no need to feel silly in the morning. I googled and found her in Ashford.
I couldn't help but be interested in this subject... I have Graves Disease ... only diagnosed in Sept. 2016 ... and had ALL the classic symptoms of such .. but
I unfortunately have lost almost every hair in my eyebrow line .... How so ?
who can tell me why please ... and how to get them back .
I hope yours do grow back in for you Jo... as we feel bad enough without losing
Diagnosed Oct 2010, had B&R for 18 mths. Started to go hyper within a month of stopping. I was never well on it anyway.
Lost faith in Endo at that point as she started pushing for either RAI (are you serious? I have TED!) or surgery (I have right sided heart failure so not keen on having too many ops!)
Persuaded her to let me titrate the Carbimazole which she let me do. I went slow and steady and she had me do blood tests roughly every 12 weeks.
Stopped Dec 2014 and have 'clinically' been in remission since. Although my bloods show Im euthyroid I feel slightly hypo. Worse symptoms - tiredness and muscle weakness.
I could be worse but I could be a damn sight better!!
Oh ladies you've done me good this morning, I thought it was just me who was starting to think I could join the circus as the bearded lady! It's driving me mad and I'm sure it's getting worse. I tried laser treatment which didn't work, burned my face and left me with chronic hives, because my very difficult immune system thought I was being attacked apparently!
Ellyblue, I had wondered about laser for dark chin hairs, but stopped and thought about whether there may be scarring and soreness, from having Hashi's. I wondered if the autoimmune thins would cause a reaction. Thanks for sharing that information, I will try other methods!
Mine fell out completely and never grew back. Ended up going for semi permanent make-up, namely natural hair stroke brows. After 12-18 months they'll need a refresh.
Really pleased with them. Also had semi permanent eye liner, now that was painful!
Me too on losing outer third of eyebrows. One sort of positive ............. No underarm shaving anymore. Ermm, I curled up with migration to chin 😂 As reported by other ladies replies. Done me a world of good knowing I'm not the only one with these hairy/less issues. On a more serious note Joburton, I do hope you get your eyebrows back to how you want them. X
I spent the best part of five decades plucking and shaping what was thick bushy brows, now they're the fashion well .......... least said soonest mended. Now other areas need the attention. 😀. I'm on t3 and I have to say mine have grown back slightly, so, I hope yours will too. X
i have learnt something new today as i didn't realise that this was a symptom. My eyebrows and eyelashes have got very sparse but. Just put it down to ageing as i am naturally fair haired. Thankfully Clinique and Bobbi Brown have some wonderful products, but without the makeup i do look expressionless! No whiskers yet tho...😜😳
I have had good results with a product called Revitabrow . Topical application once a day takes a few weeks to kick in but worth it. I had virtually no eyebrows for last 20 years can't believe I now have growth and reasonable shape.cant say the same for the chin though, daily check needed!
Have used Revitabrow since mid August and each one lasts me around 8 weeks. Been an amazing difference, pity I didn't have a before pic.still thickening up on the inner bits towards the nose but has grown in dark which is great and good condition.
This is a great thread! I've used "Rapidbrow Enhancing Eyebrow serum" from Boots, Amazon etc. Or cheaper on ebay usually. It's really effective. They recommend using it twice a day, but I've now got it down to once, just to keep them as I want them. And save money!
I may have to try this, I'd given up trying to do anything with mine to be honest.
Hahaha.. Laughter is good therapy!! From hobbit feet to Gandalf beards and bald eyebrows.. You have all made me laugh.. Probably as all of it fits me too but I usually am so embarrassed by it all. Bought myself an expensive facial laser, after spending years paying for electrolysis which obviously hasn't worked) which comes out for chin and moustache (even neck!) every couple of weeks. Eyebrows usually not too bad but my youthful daughter has lost the last third of hers. I asked old doc to test her thyroid and of course it came back in normal range as did mine. Wondering to advise her to try back with new doc given she has has just started me on thyroxine. My daughter already displays many of the features I have suffered from for years. would hate her to go through the pain and hoops I have had to!
There is another laser on the market ladies which I might have bought if I'd known about it before forking out my savings in my Philips one. Think it's called the Nono and you can buy in in chemists. Happy hair removal or relocation of unwanted hair to your missing bits! Soo funny! Thank you 😂😂😂
I have been brushing on my eye brows for years! I'm 58 and been hypo since age 14! Tried lots of different products over the years, pencils too harsh! I have found the ideal product for me and stocked up on a few just in case they stop making it! I use BareMinerals brow powder in Taupe (they do lots of different colours not just black or brown!) you can put it on lightly and build it up to look natural. My favourite eyebrow brush is from smashbox cosmetics, I never go anywhere with out both these products and never go out with out makeup!
I must have spent loads over the years trying to find the best product and been too embarrassed to ask for help! If you find a good BareMinerals stockist you could try the different shades to see which suits. A good brush helps too I've tried loads smashbox brow brush gets my vote!
Levo doesn't treat many symptoms well. My hair grew back on t3. Eyebrows are not full like they used to be since loosing them initially. Take note of other symptoms that you are having like puffiness etc.. see if you can pinch and lift your skin too. no offense, but your eyes look puffy, i think you may be improperly treated. My eyes look worse.
Yes I'm constantly puffy Faith. Believe it or not, it's not too bad in this photo because it was taken at night. Fingers, knees and ankles look like overstuffed sausages. When I saw the endo initially he wasn't very helpful, said I had angioedema with no suggestions to help.
Am having bloods done next week, but regardless of the results will be asking for an increase in 25mcg increments until no longer symptomatic.
This has really made me laugh this morning. I initially went to doctor because my face was puffy and my eyebrows were falling out. He gave me levo and I felt much, much worse. Actually, having done all of my bloods they then went off down an another autoimmune route ( I have hashis and lupus). However, I am CONVINCED that I felt fine until I started taking levo and that the issue is my thyroid. Even when they raised my dose of levo, I didn't feel any better. Recently, somebody suggested I take some t3 to see if symptoms improved. For 2 months I've had more energy since this all started last April. The t3 is brilliant (although apparently my bloods don't show that I need it) and my eyebrows have grown back a bit.
That was until the weekend. I had a very stressful day on Friday, on Saturday I felt dizzy and really not well, and now I'm back to moving like a snail and puffy eyes. I am hoping and praying that this is just a blip!
Ask about t3. Even if your bloods apparently show you are converting ok, it might help. My doctor is very good and listens to symptoms to prescribe.
just like mine have been for years! I have had never ending trouble with levo and been up or down for 30 years. Just a few months ago started t3 slow release and even though I am still overweight feel the best i have in years!!!!! try to get a doctor with some expertise in thyroid issues who also practices wholistic health. I am in Australia so no good to refer my doctor. all the best, cheers Sue
You have way more than me!!! I have to use an eyebrow pencil. I have a couple hairs at the end of my brows, a few more on the beginning of the brows, and NOTHING in the middle! The hardest thing was trying to cover the once very dark and defined brows with a color that wouldn't contrast against my fair skin and blonde (bottle) hair. It took me months, but I have finally gotten an "acceptable" brow look.
I'm lucky to still have coverage on the inner edge and middle, I was just shocked how the outer edge literally disappeared overnight! Bit worried that it's the beginning of further loss. Beimmunewise, I really feel for you with so few brows left x
I hope you get some regrowth with better thyroid treatment.
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