FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
|
Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
|
Thread Tools | Display Modes |
![]() |
#1 | ||
|
|||
Member
|
Hi
This may seem like a bizarre question, but Im very interested in your responses! My mum pointed out to me a few days ago that there is something wrong with my finger nails and I have been fascinated by this ever since! Over the last few years I have developed vertical ridges on my nails and I have pitting (small pits that look like the surface of a thimble). I also have small splinter heamorrages under my nails. None of this has been caused by trauma to the nail bed as I really dont do anything! I do the dishes with rubber gloves as I have sensitive skin, I also wear gloves if and when I do any cleaning! Has anyone else noticed a change in their nails since becomming ill? Has anyone ever spoken to their Dr about a change in the condition of their nails? Has a Dr ever examined your nails? Im really keen to hear your responses. I have really only just noticed how much worse they are. Ive certainly never had a Dr look at them. Ive never said to the Dr that my nails have changed. Thanks.....I know it seems nuts but it could be very interesting and I do want to hear from the guys as well as the girls! Love Rach |
||
![]() |
![]() |
|
|
![]() |
||||
Thread | Forum | |||
Hair and Nails, | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
Unhealthy finger nails | Vitamins, Nutrients, Herbs and Supplements | |||
Nails | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
Nails, fingers and toes | Peripheral Neuropathy |