Chronic disease experiences galore.
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 02:48
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 :)
09 May 15:21
Does anyone workout and have a hard time due to flare ups and needle like stabbing sensations with the slightest bit of heat and sweat? If so how do you manage or deal with It?
05 May 06:41
Hello People,, Well i found out that my hurnia operation has caused an immune response, i had the hunia mesh put in 2 and half years ago and always feel pain, fairly severe in some areas, So i have to have it taken out which poses more risks,
26 Apr 11:49
My lovely Flaymers. I'll be going to England soon. My question to all of you: How do you treat your P in a cold country?
26 Apr 11:43
Hi my lovely Flaymers. Hope you are all doing well during this COVID-19 experience? My question to you : Do you think our immune system can withstand this virus?
19 Apr 05:00
Been a while since last post, I hope everyone is doing okay through this covid 19 crisis ?,I have decided for a while to let my hair down quite a bit now, skin still the same joints are still the same all good at this moment , Hope all is well :)
17 Apr 05:03
My psoriasis is going away but I am not quite sure why, I noticed it a week in quarantine.
27 Mar 15:07
COVID 19:Do you think you are safe? And Why? What do you do to keep yourself safe from this virus?
23 Mar 13:25
Hi my lovely Flaymers. Hope you are all well? How do you feel about this Covid 19 virus? Do you think it will affect us more than others because of our Immune system?
Look after yourself and keep the immune system up! xx
21 Mar 02:18
Im unable of taking my meds the one I mentioned in my previous post! I keep getting stomachache after consuming it and nauseous throughout the day! I felt the more i have stomachache the more my P increased ! What i did is wrong stopping the med?
07 Mar 23:55
Has anyone tried med called
Tine - fcon my doctor recommended them all that I know about them is that they’re made out of natural ing and manufactured in india? Did anyone try it?
29 Feb 03:25
What is the impact of psoriasis and Corona virus?
25 Feb 12:16
I saw a nutritionist who also do Keniology. I found out that my psoriasis is caused by deficiency in Zinc.. I’m gluten sensitive and need to take probiotics for the gut. In addition I take codliver oil or hemp oil. My skin has noticeable improved.
Stuff worth talking about.
I'm writing from the middle of ...
- feeling hopeful
Has anyone been home during Cov...
- feeling insecure
Hey my lovely Flaymers. All has...
- feeling okay
What's hot right now.
Hello Everyone! I am glad to jo...
- feeling hopeful
Hi guys I would like to ask if ...
- feeling afraid
I probably shouldn't be surpris...
- feeling hopeful
Sign up to get advice and support from people who understand.
Start 1-minute signup
Always free. No advertising. No requests for donations.
Get support and advice on life with Psoriasis from our friendly Community Forum.
Already a member? Log in