Thinning hair : Hi just wondering if... - Scleroderma & Ray...

Scleroderma & Raynaud's UK (SRUK)

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Thinning hair

Mirv profile image
Mirv
7 Replies

Hi just wondering if anyone has experience of thinning hair? Was diagnosed about 4 years ago with scleroderma and secondary raynauds. I take hydroxychloroquine and painkillers for sore joints. Have always had fine hair but over the last couple of years it has become worse. I dye it a lighter colour as it makes the sparseness less obvious but just now I haven't been using dye and I look really baldy! Did try a cheap wig just to see what it was like but was too warm. Anyone got any suggestions that might help?

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Mirv
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Verily profile image
Verily

Are you on any medication for your condition as this could be playing part in your hair loss

Mirv profile image
Mirv in reply toVerily

Hi thanks for replying. Apart from Seven Seas joint care with Tumeric and vitamin D, its really only hydroxychloroquine. I have ibuprofen and occasional cocodamol but have cut back on those when I can. I am wondering if it is linked to hormone changes (55) and the fact I have always had fine hair. It's just that there is less of it than baby hair! It feels like grabbing a handful of nothing!

Verily profile image
Verily in reply toMirv

You could try alpecin caffeine shampoo a friend of mine losted lumps of hair and had a bald patch after a road accident and she used this and her hair is back to it's usual thickeness 🌈

Jen3131 profile image
Jen3131

I have thinning hair - when I look at old pictures, I must have less than half of what I had before. It’s sometimes difficult to know the cause - meds (Methotrexate and then mycophenolate) or age. I have limited scleroderma and Raynauds and was diagnosed more or less the same time as you. It definitely is looking worse since the colour has faded - I can see my scalp 😩

Dargomom profile image
Dargomom

I also have very fine hair but I used to have a lot of it. I have Diffuse Scleroderma overlapping into Limited Scleroderma. I have severe Raynaud's. My first sign of Scleroderma was my hands turning blue in 2010. I am not on any Scleroderma medications. About 2 years later, a hairdresser commented that my hair was thinning at my crown. I would say that I have about half the hair I had and you can definitely see my scalp. The thing that works the best is a good quality, human hair "topper." No one can tell that it's not my hair.

Lucinda227loz profile image
Lucinda227loz

Hi I wear wigs no one said anything so now I’ve got longer hair and keeps my head warm when it’s cold very good

Meg42 profile image
Meg42

I suggest trying hair regrowth shampoos or hair densifying shampoos. That's where I'm at right now. I'm still researching, so I can't recommend any unfortunately,but a google search turned up a few, and I definitely read customer reviews (best & worst). One trick I use to conceal areas where my scalp is showing, I dab a matching eye shadow right onto my scalp with the makeup applicator and it looks very natural. I only do this if I'm going out for the day, as I feel it's healthier to let my scalp breathe.

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