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-   Reflex Sympathetic Dystrophy (RSD and CRPS) (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/)
-   -   Problem with hair on legs... (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/125485-hair-legs.html)

RUReady 06-20-2010 04:37 AM

Problem with hair on legs...
 
This may come across as a strange question , but here goes . The hair on my left leg (RSD spread from LUE to chest , abdomen and LLE) is very coarse . The hair is very short , but very wiry with like little barbs . The problem I am running into is the hair is shredding my sheets on the bed after a short period of time . I have put down a comforter on top of the sheets , but it is taking a beating and will need replacing before long . The leg is sensitive so long pant pajama bottoms are out of the question , or should I say I haven't found any I can tolerate . And yes I am a male , so shaving is not an option as the other leg looks perfectly fine , hair and all LOL . I realize this is sort of a strange topic , but wanted to see if anyone else had any suggestions or this problem themselves and how they deal with it . Take care !!! :confused:

hannah1234 06-21-2010 09:32 AM

I have nooooo idea what to say. Except that sucks!!! best of luck to you and your sheets!!! I cant even think of ANYTHING that could fix that, except buying new sheets all the time!!! Good Luck!!!

Jimking 06-21-2010 10:35 AM

The only thing that comes to mind, and may sound goofy, is to apply hair conditioner on your legs, let stand for 5 minutes and rinse. It may soften the hair and not be so rigid.

Kakimbo 06-21-2010 01:29 PM

I have the same problem. The hair is very coarse and sharp. I am female, so I have options. Same place, left leg. My nails on the left side have become quite hard and rigid also. Just another perk for us RSD sufferers.

daniella 06-22-2010 08:05 AM

I did not have this with hair but did with my skin. Not just dry but shedding off. I never had skin problems pre rsd. The skin has gotten a lot better though I still have flares. Though I feel it was from rsd cause I see connections in flares sometimes anyhow I did go to the dermatologist who rx some meds and it did help to a degree. Now I manage it with lotions mostly. Though it is from RSD have you thought of seeing a dermatologst? Maybe they have seen similar in non rsd patients but the treatment may help you. Hopefully maybe your dermatologist will know about rsd though if you go. Sorry I wish I had more answers. The body with rsd does some odd things that before I faced them would of never thought of. Feel better


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