I was diagnosed with MS about 6 months ago and my neurologist put me on Rebif. I immediately noticed that my hair started to fall out in clumps. I was taken off Rebif and placed on Copaxone with the hopes that the hair loss would stop. It hasn't. I've been on Copaxone for 2 months and if anything, the hair loss has gotten worse. I am only 18 years old and my hair is extremely thin. I used to have so much hair and now it's all gone. Is this something related to the Copaxone or could it be the MS itself? My neurologist does not seem to give this issue much importance, but I'm extremely worried, especially after hearing that many people lose the majority of their hair because of these medications. Is there something I could do to reduce this? Any supplements or medications out there? Thanks in advance for any help.
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Copaxone and hair?
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found a link from the Mayo Clinic on the relationship between stress and hair loss: http://www.mayoclinic.com/health/str...r-loss/AN01442
Sounds like it could be a possibility.
Yogs, meditation, guided meditations (chopra.com) might help.
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hair loss
I have been on copaxone since january 1st 2011 and for the last 6 months i have been losing hair a lot. I took it as my normal "shedding" in the summer time but i'm still losing it and its all the time. I can wash, brush/dry my hair and its tons of hair. I can brush my hair walk away and brush it 5 mins later and i just shed each and every time i brush my hair. I can't find anywhere that is a side effect of copaxon...but i'm not taking anything else.
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Hi!
I just posted a similar question in the nutrition section. I'm on Copaxone (and have been for several years), and my hair has become so thin. Like you, I started losing hair on Rebif (which is listed as side effect) and steroids. So I thought Copaxone would let my hair regrow. Sadly, it's only gotten worse on the Copaxone. I'm going to check into these suggestions!
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posting update: I had hair loss from mid-July til the first week in Oct. It then returned to normal. My first call to SS, they said it was not a side effect. I called a second time, spoke with the pharmacist and yes, it has been recorded as a side effect. My last check-in call, I asked that they officially report my experience.
No, you´re not nuts and yes, for me, it stopped.
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Gilenya does the same thing??
My hair loss stopped after I stopped the Copaxone. I have been on Gilenya for 3 months now and the hair loss seems to be returning....I hope it's not associated with the Gilenya because I have been tolerating it pretty well otherwise.Diagnosed Feb. 2011
Rebif 3/11-5/11;Copaxone 6/11-10/11;Gilenya 10/11-present
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Originally posted by Temagami View Postposting update: I had hair loss from mid-July til the first week in Oct. It then returned to normal. My first call to SS, they said it was not a side effect. I called a second time, spoke with the pharmacist and yes, it has been recorded as a side effect. My last check-in call, I asked that they officially report my experience.
No, you´re not nuts and yes, for me, it stopped.
I'm sorry to hear that some of you are in the small group of hair loss patients.
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My doc said
Get extra seliennium in your diet or try to take supplement. It helps the scalp. Also try Nioxin shampoo and Conditioner. My cousin is a hair dresser for 30 years and says it is the best.
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