I was diagnosed with Grave's Disease in February and opted for the RAI treatment and was hypothyroid within a month. My endo started me on .1 mg of Synthroid and then increased it about a month later to .125 mg and then again a month later to .15 mg. But within 4 weeks of being on the .15 mg (which is what I am on now because my TSH levels are in the range) I started to lose my hair by the masses. I know that Synthroid can cause some hair loss but I have been on it for over 5 months and just starting losing my hair withn the last month and a half. I dread taking showers and combing my hair. Has anyone switched to another thyroid hormone replacement drug, such as Thyrolar because of hair loss? I have also begun to notice other side effects and want to know if there are other options besides Synthroid.
I am not telling you to switch to my brand, but I take Armour and have never had ANY side effects but I did when I took Synthroid, Each person is different and Armour may not be as kind to you as it has been to me, plus many Docs, due to Pharmaceuticle Companies competing have convinced many Dr.s that Armour is bad. Armour is over 100 years old and has successfully treated peoplec with hypothyroidism for all that time.
If you hear hype about dosage inconsistancy (each pill in a bottle has a different amount), this has been dicovered with Synthroid as well as Armour in the past but both manufacturers have gone to great lengths to make sure this does not happen. In spite of this, you'll hear advocates from both sides try to use this to downgrade the other.
My opinion is that both synthetic and natural hormone replacement are beneficial but some patients simply benefit a little better with one than the other.
I have read a little about Armour on the web. Is this a prescription medication? Would I need to see my endo to get the medication? What side effects does the Armour have, if any? I am just deseperate to stop my hair from falling out and just to feel good in general but it seems as though none of the doctors want to help. Thanks for your response, I really appreciate it!
I got my lab results yesterday and my TSH was 0.77, and my FT4 was 118 (the nurse said that was on the hyper side). So they have now reduced my Synthroid level from .150 to .137 and my doctor seems to think this will reduce the hair loss. I am very skeptical but guess I will give it a try for a month and if I don't see any results I am going to request a change in medication. I just really want to see results now because I am beginning to become very depressed over this whole thing. Thanks for your post JimLow!
Hi, I too have massive hair loss, and am so curious what is the cause. I started losing it after the birth of my twins 5 years ago, to where you see bald on top, real bad. I had been suffering from thyroid problems, and have Hashimoto's, just didn't know it until last year. Since starting my Synthroid, my hair loss, has stopped, but all the hair i've lost already never grew back. I guess I assumed once I started treatment, it would grow back, any suggestions? Like I mentioned, I think the synthroid helped me because it stopped falling out, but I have heard many many stories of people losing their hair on Synthroid. Am currently being checked for adrenal problems, maybe treatment of this, will return my hair, we'll see.
Have you been checked for Alepecia (I hope I spelled that right). I have a friend who has this disorder. It appeared out of nowhere and over time she has developed so many bald spots that she now wears wigs.
When I went in on Monday to see me endo and I had a ton of blood work done and everything looks good (no adrenal problems, anemia, etc.) I went to the dermatologist and she said that my hair loss would slow once I got used to the Synthroid but it has only gotten worse over as the months go by. Because I too thought that maybe something else was causing my hair loss. I have even asked the pharmicist and she said the same thing as the docotrs, "Give it a month". I am tired of hearing that. I cry every morning because my hair falls out so bad. I just want the doctor to listen and not assume that one medication is the cure for everyone. I have been reading on the Armour that JimLowe suggested and also Thyrolar. I am hoping to switch to one of those medications. If the doctor will switch my medication, I will definitely let you know if I see good results.
I'm checking in on that last question about the hair loss. Did you ever stop losing hair? I recently (2 months) had a dose increase and am starting to lose my hair. I'm afraid to comb it. It comes out in clumps when I do. I've been on Synthroid for 11 years after RAI. Maybe the dose change was just too high. That is what I'm hoping for.
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