Chronic disease experiences galore.
22 Jan 12:48
Lately I've been getting tiny dots that turn into welts. They feel like mosquito bites, they itch really bad but after a few hours of not touching them, they disappear. Does anyone else haves this issue? I can't figure out if its part of psoriasis.
17 Jan 11:42
Covid was downgraded to the flu in March 2020. You may all think I am crazy but you can get the truth at drcharlieward. Do your own research before taking the vaccine, don't take my word for it.
17 Jan 11:26
Anyone went for the vac and if you have, how do you feel? Been reading up on it and a bit weary to go for it. It's safe for us to go for it? I heard that should I decide to take the vac, I should take the Oxcord jab as its not as strong?
17 Jan 11:24
Hi my lovely Flaymers. Haven't been on here in months. Moved to the UK to be with hubby and I'm surprised to say my skin still looks good. I hope you are all well?
05 Jan 23:08
Hey There! I am uninsured & have both Psoriasis and Psoriatic Arthritis. I'm wondering if anyone else is trying to navigate Psoriatic Arthritis, which is currently flaring out of control, with no insurance.
22 Dec 14:21
Got the covid19 vaccine at work today nhs nurses came in to do it have any of u had it yet any side effects?
17 Dec 09:06
Hi everyone, I'm new here! I'm a 16 year old female in the UK and I'm taking methotrexate for my scalp and body psoriasis. Does anyone know how strong this medication is, I've been taking it for 10 months and want to know any other stronger options?
10 Dec 21:29
At work we have been given letters to call up to book appointments for the covid19 vaccine has anyone heard how psoriasis sufferers react to this or have any information on it ?
20 Oct 01:23
Its the cold weather season and it always flares up at this time anyone any ways to sooth it can be awful ive had it since i was 8 and its only gotten worse not better
18 Oct 22:00
I hope life is treating everyone well as we stay safe from Covid. I was on Stelara but due to a lay-off, I am without insurance. I am seeking alternatives. Does anyone have any recommendations that have worked for them for behind the ear psoriasis?
01 Oct 07:08
Hello everyone! Hope you are doing well.
Just joined the Flaym Community. Glad to meet you, people :)
18 Aug 16:36
Hi my lovely Flaymers. I haven't been on here for a long time but I do hope you all are well? Our lockdown has moved from level 3 to level 2 so I'm happy. How are you all keeping?
26 Jun 15:45
I’ve been on methotrexate for over 25 years and it works for me I have 3 monthly blood checks
06 Jun 01:48
I'm writing from the middle of California where Covid-19 is blooming. My family has immune issues so we've been home for 84 days. I officially have psoriatic arthritis. I've started on methotrexate. How have any of you found that to work?
06 Jun 01:42
Has anyone been home during Covid-19 and find themselves worried to go back out into the world?
05 Jun 15:20
Hey my lovely Flaymers. All has been quiet. Tell me about your struggle with Psoriasis. I hope you are all keeping well? We are here for you .
01 Jun 15:59
Rheumatoid arthritis.: Who is the best doctor to see in the UK?
01 Jun 15:50
So in South Africa we can now buy alcohol . It was banned for the covid 19- lock down until level 3. It is now legal to buy alcohol. Yes...I bought my wine :).but how does alcohol impact your life? I'm not bothered with it as I'm a smoker.
28 May 15:56
Hi my Lovely Flaymers. Been a while since I've been on Flaym. I hope you are all doing well under the COVID-19 circumstances? It's winter here in South Africa and man, is it cold. I can feel my skin burning from it. Feels like frost bite. :)
10 May 06:14
Hello all, I been through hell last 3 days, I have developed ruematiod arthrits because of this mesh in me, 4 problems to deal with,trying be positive,Maybe more problems when mesh out, My wife is the best in the world, so supportive to me,Thanks :)
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