Anyone get the “regular” skin around a patch of P going a dark grey colour. The patch on my right knee has this, just went like that in the past couple of weeks. It’s not painful or itchy.

I did a 3 month course UV at the start of the year gaining almost 100% clear but its gradually came back, not nearly as bad as before though. Around that time the course finished, I became vegan. Im wondering if that made the return less traumatic.

Its been a while since Ive been here. It seemed like the place had been abandonded but Ive just noticed emails from Flaym and I had loads of notifications when I opened the app. So if we spoke before, Hi again and if we never, Hi.

In my opinion, the cheapest way to get rid of plaques is by using soft white parafin cream. You don’t need a script and can buy it on Amazon. It doesn’t cure or even deal with the underlying P, but to get rid of unsightly plaque it’s great.

Although my body is fairly clear after the UV, I have a little at the sides of my nose and behind my ears. I got some cream from my doc. I just noticed the info sheet says not for use on the face. Where does she think the sides of my nose are?

Between two and three months finished UV and still good. However, I have an outbreak at the sides of my nose, behind my ears and downstairs. Going to the doc on Friday.

Out of curiosity, when you finish a successful course of treatment, how long does the fear factor last, the fear that now it’s finished, the P is coming straight back, or maybe you had no fear factor. Right now I’m bricking it.

Anyone else not getting to their activity page? I have a bunch of them but for three days now I can't open that page on either the app or website.

I've been persuaded to move to a whole food plant based diet (slightly different from a vegan diet I've been told). Anyways, I was also advised to watch a Netflix show called What the Health. I in turn, pass that advice to you.

Given the goggles and clear visor they make us wear during a UV session, has anyone felt like they have had too much sun on their face later in the day?

Given that like psoriasis, ibs is also an autoimmune condition, I'm guessing some here are also dealing with that?

A quick question for iPhone users, is there a Flaym app for iPhone, I'm thinking of trading in my current Android phone.

John's latest post has me wondering. He mentioned scarring. Anyone else have scars or maybe left overmarks. They told me at the UV clinic that some of the discolouration might never go away.

For the record, good skin care products made from all natural ingredients, Burt's Bees. I had cause to get some lip balm this week, the pharmacist recommended Burt's Bees. Best one I've ever used. Turns out, they do lots of products.

Anyone use avocado oil? I just bought a bottle because of its high smoke point, but I'm now reading it has a lot of nutritional qualities plus is good for both P and arthritis.

A quick UV update.

A while back someone spoke of an all natural antiperspirant / deodorant. Can anyone recall the name?

I noticed that although my P is fading all over, it's going faster higher up, chest, arms etc, and slower on my legs. I mentioned this to the clinic nurse and she said that's the way it usually goes.

Still no links allowed so check the BBC news site today (18th). A story about the dangers of inflammable skin creams.

Not been on for a while, work has been brutal then sick. Still managing the UV though (apart from this week) I'm at 2 minutes 36 seconds now. It's working superbly well, no plaque and skin down from red to pink.