Hello from Quest4Cure

[Kat]

Hi just made a mistake and another post was posted as me..it repeated the other post... It starts out I'm 37 year old and thought psoriasis was hereditary ... I hope it can be delegated!

Just getting the hang of this new site.

Any way I hope to get this straightened out. Sorry for the mistake.


I hope I haven't caused too much trouble.

Hi, I am the snorkel horse my name is Quest4Cure .
I have psoriasis and psoriatic p. Have a whole mixed bad. The plaque P. I've had since a child, it isn't quite as bad and palmoplanter P. Hand and feet are the worse . Also just this year developed Inverse P. So 4 out of 6 types of P . Sun shine helps this time of year for plaque . I just look like I have white freckles.
Palmoplanter It comes every winter like clock work . Water is my biggest enemy.. For Hands and feet. So sharing ideas and talking with others & sharing what they do to help control their P. Or palmoplantar. Or al types of P. PustularP and plaque P.

Thank goodness Derms have become better at treating this disease and better meds have come along the past few years.

My right hand had surgery last yr for one finger as it turned out it caused what they call the Keobler effect and and caused a flair from surgery causing all my fingers to curl and remain stiff. Has anyone else experienced the Keobler effect ?

I highly recommend a hand spa with wax to keep hands and feet moisturizers during cold dry winters.

Looking foreword to meeting new people and sharing experiences with living with P.
Thanks Quest4Cure

Hello
This will be my first winter after getting my p-diagnosis. How does the hand spa with wax work? I'm definitely looking into some good moisturizers. I have an appointment with a medical spa to get some moisturizer for my face. I'm hoping to be far enough along in my treatment before the coldness of winter sets in as I've heard it can be a tough time.

Glad to have you on board here