Flaym – An Awesome New Platform for People with Psoriasis
Flaym – a lil corner of the internet just for flakers
Psoriasis is not a social media-friendly thing. No one posts about their flaky penis on Facebook. Or updates their friends on that 10cm buildup of skin crust on their elbow. It’s just not something you tend to share – unless you’re on Flaym that is!
I first learned about Flaym a few weeks ago when Lasse, the community manager, gave me the heads-up. And now, one week after using it, I have to say its pretty awesome. Here’s why.
So, what’s Flaym?
Flaym is like a mash-up of Twitter and Facebook for the psoriasis community. You set up a profile – anonymously, if you want – and start bashing away at the keyboard! The main page is a scrolling timeline of posts, much like Twitter. New posts are limited to 250 characters to keep the conversations flowing, and posts are categorized into different topics such as sex, diets, exercise, treatment etc.
Its simple, but what makes it really special is the people.
A funny and inspiring bunch
Many flakers don’t feel like sharing their stories because its so poorly understood (no, its not contagious, no, I don’t have leprosy), so when you have a community of people all in the same boat, the results are pretty cool. People feel comfortable and open up about their experience, that flare-up they’re struggling with, the latest shampoo they’re trying, the flake-covered bed sheets. It’s pretty awesome to have a hangout on the internet just for P.
Plus, the users on there are plain hilarious. I try to be upbeat about psoriasis and have to say, I haven’t had as many psoriasis-related LOL moments as on Flaym over the past week. The people are really supportive and most have a dark sense of humour about it, just like I do. This story really cracked me up:
But of course, people share the dark stuff too, one girl spoke about her ex who told her she was disgusting and he wanted to shower after having sex. He sounds like a massive asshole and many people rallied around her to say so. Others speak about their flare-ups and difficulties. But the common thing is people are not afraid to talk openly about psoriasis whatever the topic.
Come check it out!
In a nutshell, its a really cool platform that I can see myself using a lot. My blog posts on here tend to take a while to write and research but on Flaym I can share my experience and connect with others in a few minutes. If you wanna check it out, my Flaym profile is on here. I’ve just started a new conversation on Valentine’s Day sexy tips, come share yours!
About the Author
redblob I'm just an average 28 year old living with psoriasis. Over the last decade, I've tried everything, from real snake poison to rubbing banana peels over my body. I've finally found an approach that's working for me, and I'm sharing it with all the flakers out there. But Psoriasis Blob is not about one man, it's a growing community of great, red people.
3 Responses to Flaym – An Awesome New Platform for People with Psoriasis
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Hi, I'm Jack. I had psoriasis for over ten years before I managed to tame it. Now my skin's as smooth as a baby's. On most days! 
Hi Jack this is Clive , from South Africa , i am very new to all this P business and in a stupid attempt at alleviating my embarrassing scalp P i washed my head with our garden type variety of Apple Cider Vinegar , now i seem to be in a world of inflammation and infection as all the glands in my neck and head are swollen and extremely painful , any possible advice , and have any other readers experienced anything similar ?? Thank you for your blog it is so helpful .
Sorry to hear about your experience Clive, has the inflammation died down? I’ve never had that happen with ACV before and its considered to have strong anti-inflammatory properties (at least the organic kind).
I have psoriases and have tried many products–no cures tho. sometimes its worse than other times..myn is mostly around my ankles and partly on my legs,,my hands and my back..If I have someone around to give me constant back rubs its not itchy–its controlled with a mosturiser—I have tryed natural stuff but so far Im always going back to corizone creams. When I get very iychy//Iv had it for about 13 years. and hate it..Nothing I can do to cure it..don`t know the ingredient..Thats my story.