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-   -   Psoriasis / Skin Inflamation (https://www.neurotalk.org/multiple-sclerosis/50017-psoriasis-skin-inflamation.html)

Kitty 07-15-2008 12:57 PM

Psoriasis / Skin Inflamation
 
The year before I was dx with MS I had a terrible case of dermatitis/psoriasis on the palm of my right hand.

I tried every OTC remedy that was for sale and even saw a dermatologist who gave me a prescription for Temovate which didn't help much. I used it nonetheless and it eventually cleared up after nearly 10 months.

After I was dx with MS I mentioned it to my Neuro and he said it would have been considered a "flare up" had I been dx with MS at the time. It was a flareup - I just didn't know it at the time...:rolleyes:

Well, I now have a tiny patch on the palm of my left hand. About the size of a pencil eraser. It doesn't itch all the time but it's not going away, either.

Has anyone here had this with any exacerbation? I don't get this anywhere else except the palms of my hands.

SandyC 07-15-2008 01:25 PM

Jim gets it on his face periodically. He uses Lotrisone, the generic, on a daily basis to keep it under control. It's for treating fungal infections but works well for Jim's skin condition pretty good.

SallyC 07-15-2008 01:30 PM

That's where my Psoriosis is, too, on the palms of my hands. It came years after my MS DX and, at first, I thought it was a fungus or something..:eek:

I never considered the Psoriasis as a MS attack, but it may have been part of a MS attack? Psoriasis is an auto-immune disease just as, they also think, is MS, so they are related to each other.

:hug:

FinLady 07-15-2008 07:06 PM

My brother uses the same thing Jim does. Thanks Sandy for mentioning it. He has a severe and rare case of psoriasis. He's had to use TGel shampoo forever.

Kitty 07-15-2008 07:19 PM

Well, it's not spreading and doesn't itch too badly. I think I'll get some of the stuff Sandy suggested. The last time I had this it was my entire palm....not fun! Everything irritated it....:mad:

I'd trade the spasticity in my legs and the ringing in my ears for a mild case of this....but I don't want them all!!!!!!! :eek: :rolleyes:

Erin524 07-15-2008 11:37 PM

I had a long and weird experience with psoriasis in the mid-90s with psoriasis. I always thought it was an allergic reaction to the stupid McDonald's hat that I had to wear for nearly the entire 8yrs I worked for McDonald's.

Then I thought that it was from all the sweating I did in the heat of the McD's that I worked at.

I finally decided it was my shampoo and after using T-Gel for a long time, I found a decent shampoo and never really had a problem with the psoriasis since then. (altho, I think I have a little patch of it on my neck near the pulse point for the past few weeks)

GladysD 07-16-2008 05:52 AM

I developed my first episode with psoriasis the fall before I developed ON. Looking back, I guess I'd consider it my first 'flair'? I noticed I get little flare ups during times of stress. Usually all over my scalp and sometimes my legs. :(

SandyC 07-16-2008 09:16 AM

Kelly, the med Jim uses is by prescription. Maybe your doctor can just call in the script for you like Jim's doctor did.

Kitty 07-16-2008 09:44 AM

Quote:

Originally Posted by SandyC (Post 324840)
Kelly, the med Jim uses is by prescription. Maybe your doctor can just call in the script for you like Jim's doctor did.


Thanks - I was thinking "generic" as in OTC and it's not!! :o I'm going to call him today just so I'll have some on hand.

Luckily the little patch is staying calm and quiet - and not getting any bigger. I think stress has something to do with it, too. Anybody know how to keep stress out of life??? :p

Debbie D 07-16-2008 03:26 PM

I think the answer to stress is called valium...:thud:


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