hair loss: Has anyone noticed they have... - Cure Parkinson's

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hair loss

uvmmom05 profile image
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Has anyone noticed they have been losing their hair while using cardilopa-levodopa? or Mirapex?

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uvmmom05
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14 Replies
GymBag profile image
GymBag

I used to have hair on the back of my hands, arms ,legs, chest , top of my feet. It all disappeared 6 or 7 years ago. I have been slowly reducing the amount of Requip (Ropinerole) over the last 2 years and 6 months ago I started getting some hair back. Not sure but I think Requip is similar to Mirapex. I am fairly sure that my hair loss is not due to Leva/Carb or Amantadine because I have increased them as I drop the Requip. My younger brother (Alzheimer ) likes to comment on my smooth Girly legs. Of course typical of PD , my eyebrows, and the hair in my ears and nose and facial hair that I shave is growing at 2 or 3 times the old normal rate.

uvmmom05 profile image
uvmmom05 in reply to GymBag

Thank you for your reply.

ge1shh profile image
ge1shh

My hair has thinned since taking Madopar. It also thinned when I took pills for high blood pressure, but recovered growth when I stopped that medication. I was happy for a while, but then I started the Madopar having been recently diagnosed with PD, and have lost hair thickness again.

uvmmom05 profile image
uvmmom05 in reply to ge1shh

I am on both carbidopa-levodopa and mirapex. not sure which one or both is causing the hair loss. they have cut me off of carbidopa-levodopa and PI have an appointment in a couple days.

ge1shh profile image
ge1shh in reply to uvmmom05

It's difficult to be sure of the cause - could be other factors too. I hope your hair loss is not too noticeable. I assume you are female? I bought a wig, which I wear fairly often for social occasions when I dont have time to wash my hair or go to hairdresser. I wouldnt like to wear it all the time, but am really pleased with it, and most people don't realize it's a wig. I got it free of VAT tax (in UK), as my reason for purchase was accepted as medical. It will take a month or two before you can be sure if levadopa is the cause.

uvmmom05 profile image
uvmmom05 in reply to ge1shh

I am female and on other medications as well with other diagnosis. I have an upcoming dental procedure or all teeth removed and dentures in, so this adding a wig would be just the icing on the cake.

ge1shh profile image
ge1shh in reply to uvmmom05

I have just read your Profile, so I see you have a lot to deal with. I don't have those other conditions, but I have osteoporosis, which will increase my risk of frailty with the Parkinsons - if my balance gets affected there is the risk of falls and fractures. Also prone to sciatica. I am finding that walking and exercise is beneficial - I started a PD 'Boxercise' class! Still in early stage of Parkinsons, age 70 (it's still a shock not to be 60something any more ... Hope all goes well for you.

uvmmom05 profile image
uvmmom05 in reply to ge1shh

I am glad you are finding the exercise helping you.

I try to get out and walk as much as I can with "my buddy" (my walker). haha

Beckey profile image
Beckey

While I was taking sinemet my hair started coming out in bunches. I stopped sinemet and went to dopa mucuna about 3 months ago but never regained my normal amount of hair.

Bouffere85 profile image
Bouffere85

Yes yes ! I have been diagnosed 7 years ago and indeed have been loosing hair everyday ! Did not make the relation with Sinemet, that’s interesting! Would there be a study on that?

Good luck,

Chantal

Bouffere85 profile image
Bouffere85

Forgot to add I am on Sinemet but not on Mirapex

Ajssister profile image
Ajssister

My bro keeps complaining about losing his hair. He’d been on CL for about 3 yrs so maybe there is a connection. But... he’s also on 2 blood pressure meds as well. So I’m just sayin 🤔

reneep profile image
reneep

Yes, I have experienced it also. I believe it is the carbo/ Levi. I started taking hair vitamins and it seems to have stopped shedding. The shaft even seems thicker but I have not regained what I lost.

uvmmom05 profile image
uvmmom05 in reply to reneep

I have found out from my neurologist that depakote has a bigger chance of causing hair loss (I have bipolar also). I lowered teh dosage of depakote and hair loss is a lot less.

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