How Did You Find Psoriasis Club

[Fred]

Please take a moment to tell us how you found Psoriasis Club. We are self funded and it helps to know where our new members are coming from.

Please choose an option on the Pole Above. Members can tell us more on this thread if they wish, Guests can also vote but why not come and join us you will find a friendly bunch of people here.

Thank You.

[mickyfinn007]

Please take a moment to tell us how you found Psoriasis Club. We are self funded and it helps to know where our new members are coming from.

Please choose an option on the Pole Above. you can also tell us more on this thread.

Thank You.

I stumbled upon the site completely by accident after returning from the hospital one day, after having topical treatment (which didn't work), and registered immediately. Although I have not been too active on the site this year (too busy) I hope to remedy that now.
I have also just started on Methotrexate, so will let you know how I get on with that.
In summary, the site has helped me greatly and has pushed me into demanding better treatment for my Psoriasis.
Thanks especially to Fred.
Regards to all.....

[Fred]

Bump!

[Caroline]

I was searching on twitter for psoriasis. You find all kinds of things over there, also I found this frog-green logo and started to look what was behind it.
And so I became an (ir)regular visitor on the site.

The site is nice and friendly, with humorous people, and of course also with lots of information on psoriasis, of which I sometimes agree upon

[Fred]

I was searching on twitter for psoriasis. You find all kinds of things over there, also I found this frog-green logo and started to look what was behind it.
And so I became an (ir)regular visitor on the site.

The site is nice and friendly, with humorous people, and of course also with lots of information on psoriasis, of which I sometimes agree upon

[Susie Thompson]

I have been looking for ages to find out why I get a lot of shivering with my PPP, with no result as yet. I came across your original site and followed the link to here. If anybody has any answer to my original question, I'd love to know. Thanks [/font]

[Fred]

I have been looking for ages to find out why I get a lot of shivering with my PPP, with no result as yet.  I came across your original site and followed the link to here.  If anybody has any answer to my original question, I'd love to know.  Thanks

Hello Susie and welcome to the forum, thanks for letting us know how you found us.

Re shivering with PPP try starting a new thread here: Psoriasis And Psoriatic Arthritis Topics

Regards.

Fred.

[Krissie_Wright]

I've been following the twitter account for a while and was registered on the previous forum but have not really been online on the PC to get registered to this shiny new one and couldn't do it via my mobile...

Krissie

[Fred]

I've been following the twitter account for a while and was registered on the previous forum but have not really been online on the PC to get registered to this shiny new one and couldn't do it via my mobile...

Krissie

Thanks for letting us know, can you use the forum on a mobile?

[Caroline]

I've been following the twitter account for a while and was registered on the previous forum but have not really been online on the PC to get registered to this shiny new one and couldn't do it via my mobile...

Krissie

Thanks for letting us know, can you use the forum on a mobile?

Of course you can Fred, as long as it's Android of iOS...