My Journey to halt/end my psoriasis

[Sheila]

Yes it's true there are a lot of comorbidities with psoriasis.

*I think you will find the site you visited is not like Psoriasis Club and run by patients, it's run by money and we are the only psoriasis website run by patients. Just saying. 

Yes, Fred, you are quite correct. The ask for donations with pop ups and are sponsored by several of the big pharma's. So yes, I agree. Even though it says it's patient run, it is heavily influenced by companies.

Any other comorbidities that I should be aware of?

Wintrman.

Well that is about it. (There is more, but we will not tell you…. Hihihi )

There was a webinar yesterday evening, organised by the Dutch psoriasis association. I was surprised, it was amazingly good. Still lots of things that I didn’t agree with, but there seems to start a change to a more patient driven approach.
Anyway, what I saw over there was that the doctor who was interviewed  showed a very interesting figure of a tree. A psoriasis tree.
Above the ground the stylistic crown of psoriasis flakes, but under the ground there was a whole root system which showed the possible comorbidities. Maybe the will place a version of the webinar on the website, then I will try to make a picture in orde to show it to you.
He stated also: “It is possible that you can get a comorbidity, but there no ‘must or will’. “

Hi Caroline,

With all my other diagnoses, it would take a genius doctor to figure what symptoms I am experiencing is related to psoriasis or another disease. I just hope they can help alleviate the symptoms, regardless of the source. If I am lucky, they might be able to figure out this mess I call a body.


cheers

Wintrman