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Thread: keratosis pilraris rubra faceii section

  1. #1
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    Default keratosis pilraris rubra faceii section

    Hello,

    I would like to make a suggestion of a sub forum for Keratosis Pilraris Rubra Faceii.

    There used to be a dedicated subforum from a Keratosis Pilaris forum, but unfortunately the whole forum was discontinued.

    As the symptoms are similar to Rosacea, I feel it could be useful for sufferers to post. I mistakenly thought for years I had Rosacea until a specialist informed me otherwise.

    Being a long time sufferer and big computer nerd I would be happy regularly check it and reply to inquiries

    It suddenly just came across my mind to make this request, no worries if not of course!

    Thanks,

    realwork

  2. #2
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    I support this proposal
    Suffering from Keratosis Pilaris Rubra Faceii (KPRF)

  3. #3
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    Quote Originally Posted by realwork View Post
    Hello,

    I would like to make a suggestion of a sub forum for Keratosis Pilraris Rubra Faceii.

    There used to be a dedicated subforum from a Keratosis Pilaris forum, but unfortunately the whole forum was discontinued.

    As the symptoms are similar to Rosacea, I feel it could be useful for sufferers to post. I mistakenly thought for years I had Rosacea until a specialist informed me otherwise.

    Being a long time sufferer and big computer nerd I would be happy regularly check it and reply to inquiries

    It suddenly just came across my mind to make this request, no worries if not of course!

    Thanks,

    realwork
    Hmm.. turns out i'm too dumb/lazy to even notice there's already a Similar and co-existing conditions section ;( Apologies.

  4. #4
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    hey guys,

    how your keratosis pilraris face started?

    Did u have it since kid or one day u woke up and were red?

  5. #5
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    Quote Originally Posted by ricfazers View Post
    hey guys,

    how your keratosis pilraris face started?

    Did u have it since kid or one day u woke up and were red?
    Hello ricfazers,

    When I was very young it was very mild, once I hit puberty it really kicked in, and has started calming down in my late 20s.

    Do you need advice on how I control it? Or just wanted to know?

    Thanks,

    realwork

  6. #6
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    Quote Originally Posted by realwork View Post
    Hello ricfazers,

    When I was very young it was very mild, once I hit puberty it really kicked in, and has started calming down in my late 20s.

    Do you need advice on how I control it? Or just wanted to know?

    Thanks,

    realwork
    hello,

    supposedly i have this told by derm.

    one day i woke up and my skin was peeling both sides face (cheeks and "under it") i tought i was having some allergic reaction to a cream i was using for acne, but 7 months later im still red from that "situation" not really sure what i got, if rosacea or keratosis (i have a bit of if on my triceps)

    im already 22 years old. the derm gave me some cream and said that vbeam should solve this.
    the redness is very mild (i cant even find pictures on internet similar to mine) but i really hate to have this on my face. it looks like keratosis but another derm told me i had a "erythema" and gave me mirvaso, not really sure who i can trust...

    at night, sometimes, i feel my face a little hot but nothing special. i can go run for 45m/1hour after i came home my redness is bit worse but i dont feel any burn sensations, really strange...
    more frustrating than redness is not having 100% what i have on my face. im thinking consulting another derm.

    ps: its possible to have rosacea and keratosis rubra face at same time? cuz my nose is a bit pink too and my chin just under the mouth is bit red with skin peeling. maybe seb derm?

    im just using moisturizer and differin to control some pimples i have.

  7. #7
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    my derm subscribed me this for keratosis:

    leti-at-4-crema-panal-pasta-al-agua-75-g.jpg

    said it would help, but not solve the redness...

  8. #8
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    realwork, do u think its possible to get kprf in adulthood?

  9. #9
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    UP!

    there's basically no website / forum for KPRF, nowhere in the Internet. No research (only one or two papers), no people looking for a cure, even most of dermatologists don't know even the existence..

    A sub-section in this forum would be great because creating a forum from zero would have zero visibility.. and this last thing is what we need

    Thanks

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