Psoriasis Club

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would like to say a big thanks for the support I have received n new friends I have met  I don't feel so alone anymore Smile
(Thu-18-08-2016, 10:43 AM)numpty23 Wrote: [ -> ]would like to say a big thanks for the support I have received n new friends I have met  I don't feel so alone anymore Smile

Hi Linda the genuine support here comes from a great community, which as a member you are now part of, we can all empathise with each other, that's what makes this place special to so many of us.
feel free to add your comments to other members posts if you wish. I know they will be appreciated ( not compulsory  Big Grin )

(Thu-18-08-2016, 10:43 AM)numpty23 Wrote: [ -> ]would like to say a big thanks for the support I have received n new friends I have met  I don't feel so alone anymore Smile

thanks for your kind words Linda.
You certainly are not alone, there are a lot of us. Not all on psoriasisclub of course, but this is one of the most pleasant sites I have ever found, and not only on the subject of psoriasis. Over here there are just nice people. Rolleyes Big Grin
yeah it feels good to be able to share r worries and concerns x
(Thu-18-08-2016, 14:47 PM)numpty23 Wrote: [ -> ]yeah it feels good to be able to share r worries and concerns x

Five
Blush Smile
(Thu-18-08-2016, 10:43 AM)numpty23 Wrote: [ -> ]would like to say a big thanks for the support I have received n new friends I have met  I don't feel so alone anymore Smile

You are very welcome. And I am pleased as I'm sure all our members are that you no longer feel alone.

Thank you for the kind words about Psoriasis Club, it's the people (like you) that make it what it is and we are all in it together.

I'm trying to catch up, so if I haven't already said so. "Welcome to Psoriasis Club".



I'll move this thread to Feedback if you don't mind so others can read your comments.
You'll never be alone on here Numpty.

We all share a common bond on here.

As painful and itchy as this horrible disease is, we swap and share horror stories and it helps.

A couple of us put photos up on here in our journals to show our progress with our treatments.

So, if you want a giggle or share your experiences Numpty, you'll be sure we will do our best to help or maybe even make you laugh.

Enjoy yourself on here Numpty Thumb

GB
If you are looking for new posts in this thread I have moved them to a new thread where they are better suited.

You can find the new thread here: Acitretin and imune system problems

I will lock this thread to save any further confusion.