I have created this web site simply not to be alone with my condition – a variant of Folliculitis Decalvans called Tufted Folliculitis. If you suffer from this disease you know what I am talking about, when doctors just shrug their shoulders not having a clue of what is going on with you and you felt hopeless. When you are reading these lines you already know that there is at least two of us with the same thing happening to us.
I believe together we can get this monkey of our backs, or shall I say scalps.
Your ideas are always welcome and I will be glad to hear from you. So do not be shy and drop me a line.