Psoriasis

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Does anyone else get pain and tenderness in their finger tips/pads?

Does anyone else get pain and tenderness in their finger tips/pads?

Mine have been so tender at times it's painful to just use my phone. Just wondering if anyone else has experienced the same?

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A MyPsoriasisTeam Member said:

I do. My fingers hurt all the time.

posted about 12 hours ago
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Risankizumab-rzaa

Risankizumab-rzaa

This is a new shot for Plaque Psoriasis. The doctor said I would be taking this the rest of my life every 3 months. I guess I will be a test subject. I only have one Kidney left and don't know enough about this product. Do you know anout this medicine?

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Diets and vitamins?

Diets and vitamins?

So I heard certian diets can help with flare ups.
Being gluten free, vegan, eating a keto diet.
Celery and aloe juice.
Vitamin D or B12.
What are some foods to avoid, foods that are safe and vitamins that help?

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A MyPsoriasisTeam Member said:

I have found fish oil or krill oil helps with inflammation

posted 2 days ago
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Anyone here have pustular psoriasis?

Anyone here have pustular psoriasis?

I have plague psoriasis since I'm 12 and recently got pustular

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A MyPsoriasisTeam Member said:

Yes, but I only get a couple of the blisters at a time anymore. I read several studies that linked pustular psoriasis to nicotine use (it's also… read more

posted about 16 hours ago
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CBD for Pain

CBD for Pain

Tomorrow im going to get a cbd vape in hopes it will help with the constant pain of walking and joint and muscle pain. Also hoping it helps with my anxiety and will help relax me and make me less stressed. Anyone have any luck using it?

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A MyPsoriasisTeam Member said:

I've tried cbd and the vape didn't really help much. I got a (eddible) extract which seemed to help a little. I do use a THC balm (it's kinda like Tiger… read more

edited, originally posted 31 minutes ago
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Has anyone used a medicine called Domeboro? Pros and cons

Has anyone used a medicine called Domeboro? Pros and cons

Ive been using it here and there. But im wondering if its better or worse for pustular psoriasis. Its a bit drying but its also good for rashes so im not sure if its a good soak or not

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Joint pain

Joint pain

I used biofreeze for joint pain when I was on biologics. Now when I use it my joints feel like they are freezing and brittle. I can’t use lidocaine allergic to it and can only use Tylenol. What does everybody use for pain?

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A MyPsoriasisTeam Member said:

Wish I could help but do not deal with pain, fortunately

posted 3 days ago
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Results taking Otezla?

Results taking Otezla?

My doctor perscribed me Otezla. Im currently on day 5. So far no changes but its only been 5 days. Wondering how its worked for anyone.
I get huge blisters on my feet that prevent me from walking the first 2 days. Then i basically limp and hop for the next couple and by day 6-7 im able to walk. But its extreamly itchy and i have dry chunks of skin peeling off. Looks like burned ham
Hands get coved in tiny blisters. Eventually they peel and become flakey and crusty. Insanley itchy the whole… read more

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A MyPsoriasisTeam Member said:

It took about 2 weeks to see results. Hang in there p

posted about 4 hours ago
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What can I do to prevent all his itching all over my body face

What can I do to prevent all his itching all over my body face

I wake up every morning with itching all over my body my face my arms my neck my ears my head my stomach all over my body is frustrated and I cannot stand the Sun or the sweat I always want to put cold water hates being around people

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A MyPsoriasisTeam Member said:

It seems like no one understands. I was always so active and loved being in the sun . Now I barley go outside! Jst got to hang in there day by day.

posted 7 days ago
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What can I do to prevent all his itching all over my body face

What can I do to prevent all his itching all over my body face

I wake up every morning with itching all over my body my face my arms my neck my ears my head my stomach all over my body is frustrated and I cannot stand the Sun or the sweat I always want to put cold water hates being around people

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A MyPsoriasisTeam Member said:

Ohh, I’ll have to try that. My head is the worst and nearly drives me mad

posted 6 days ago
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