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I have been on levoxyl for 3 month and losing quite a bit of hair still. I have hashimotos and doc wanted to start treatment to see if it would help my prior symptoms (hair loss, brain fog, interrupted sleep). When is it supposed to stop the hair loss?? My question for you all is if I stop taking this medicine(I wouldn't do so unless dr says it's ok) will the hair loss get even worse? It seems that the hair loss is worse on the medicine. I'm only 36 and my hair is getting so very thin around the bangs and temples!! I used to have the thickest hair of anyone I knew!! I need some advice from you all!!!!
Thindy, I have been on levoxyl for 3 months and my hair is falling out by the handful. I also had superSuper aytinal 50 plus Super aytinal for active adults Super b complex Super b complex with c Super b-50 Super calcium Super high vitamins and minerals Super plenamins thick hair... it's the only feature I ever had confidence in b/c most women would love to have as much hair as I had. I wish I could tell you it will get better but it's too soon in my treatment to know that. I do know that I saw a new doctor last week and she said that it was time to try something else b/c I shouldn't be losing this much hair still. She added T3 to my levoxyl... no improvement yet, but it's been less than one week. She said 8-10 weeks should show a difference.
Now... that being said, I also FREAKED out about my hairloss in the beginning... did some searches online, joined a couple yahoo threads and it seems to be pretty common to see hairloss with thyroid meds. While the literature says that "rarely" people will lose hair in the first few months but it's USUALLY temporary, I have found in my research about 50/50 on people who say that the hairloss stopped vs. people who said the hairloss never got better. TIme will tell.
I am sorry you're going through this. It's very frustrating and scary. I get pretty bummed when I think about how my favorite barrett now just slides out of my hair (it was my favorite b/c it was the only one I'd ever found that would hold ALL my hair without breaking... I've had it since I was in highschool... back in the early 90s). Now those barrets that would only hold part of my hair can easily hold all of my hair... it's depressing.
Thanks for your comments. It's always encouraging to know you're not the only one going thru something like this. That's what I like about this forum-we can all share our experiences and feelings and other people listen and respond. It's very therapeutic at times for me!! Shaerich you need to let me know if the T3 helps you eventually. I sure hope it does!!
I too am on levoxyl. I just started a month ago. My hair had just started falling out before I started taking the levoxly and it still is coming out by fist fulls. Its annoying to look on the bathroom floor and see bunches of hair or even gross when its clumped up in the shower drain. Let us know what the endo tells you at your appt. Good luck to you.
Good luck!
Darla
Now... that being said, I also FREAKED out about my hairloss in the beginning... did some searches online, joined a couple yahoo threads and it seems to be pretty common to see hairloss with thyroid meds. While the literature says that "rarely" people will lose hair in the first few months but it's USUALLY temporary, I have found in my research about 50/50 on people who say that the hairloss stopped vs. people who said the hairloss never got better. TIme will tell.
I am sorry you're going through this. It's very frustrating and scary. I get pretty bummed when I think about how my favorite barrett now just slides out of my hair (it was my favorite b/c it was the only one I'd ever found that would hold ALL my hair without breaking... I've had it since I was in highschool... back in the early 90s). Now those barrets that would only hold part of my hair can easily hold all of my hair... it's depressing.