RainyCloud said...
Hi destiny,
First, let me say that I feel bad for you and understand how difficult this is. I lost a LOT of hair and at this point the only way to deal with it is by going bald.
However, if I look back at the process of losing my hair, I do have one regret. Which is that I never went to a dermatologist or similar and had one of those biopsies done on my hair/follicle to zoom in on what is going on.
Maybe a derm could have stopped it before the hair follicles closed, which I suspect happened at this point.
I'm just telling you this so you don't make the same mistake I did. They might not have all the answers but there's not much to lose by trying.
Thanks RainyCloud, I appreciate your response.
I've always had incredibly thick, dark, strong hair and a perfect hairline, so it has been very traumatic to lose so much hair in a matter of months. I just find it so strange that it all started after I developed this 'crawling' sensation in my scalp/face, as if there are bugs/mites eating my hair follicules. If my theory/research is right it could be demodex mites and/or morgellons, which is why I'm reaching out to see if anyone has experienced anything similar.
What interests me is that the shedding has reduced considerably (although not completely) from it's worst, since I started the MMS.. Also the tingling/crawling sensation has reduced. It's all very suspicious to me.
I have booked the earliest dermatologist appointment that I can get, which is in 4 months. I know it's not the worst symptom in the world, but losing 50% of my hair in a matter of months, and eyelashes, body hair, and facial hair has destroyed my self-confidence and sent me into a bad bout of depression. Just trying to remain positive and hoping for the best..