Just got diagnosed...
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Just got diagnosed...
Just got back from the derm and she said i have psorasis, and my entire scalp is inflamed. I suppose i ahve mpb too, but she said the psoraisis is making it worse. Do you guys think LLLT with my OMG helmet will help me at all with my hairloss anymore? im begining to lose hope, but am still using the helmet.
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just starting out
Re: Just got diagnosed...
what treatments did she recommend?medstudent 21 wrote:Just got back from the derm and she said i have psorasis, and my entire scalp is inflamed. I suppose i ahve mpb too, but she said the psoraisis is making it worse. Do you guys think LLLT with my OMG helmet will help me at all with my hairloss anymore? im begining to lose hope, but am still using the helmet.
http://www.mayoclinic.com/health/scalp- ... is/AN01177
that source lists light treatment as a possible treatment for psoriasis. I think that I too have an inflamed scalp, but nizoral every few days seems to be helping.
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Re: Just got diagnosed...
She told me to use this corticosteriod for inflamation. i used it last night and it seems to help a lot i dont itch as much. Idk, i think the lasers with his will help
- hapyman
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Re: Just got diagnosed...
The lasers will help with the inflammation and the itch. The itch can take a while to fully heal and disperse. For example it took OMG 3 months to get rid of the itch fully. Unfortunately it took me much longer.
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Re: Just got diagnosed...
Hey med student,
My doctor told me in April that I had psoriasis as well. I am not sure that was the correct diagnosis as I was able to get rid of alot of the inflammation. I used the corticosteroid/anti-psoratic topical he gave me a grand total of 4 times - what a sticky, gooey mess it was. It did help after a day or two but initially made it itch more. At the same time I started the IH top 6 and I think that has had an impact on bringing my inflammation under better control. Lasers help too but at the time they were unable to deal with the inflammation alone.
I think I exacerbated my inflammation with poor choices in topicals. The one that hurt me the most was the A&G hair complex which had propylene glycol in it. It made my scalp a red, inflamed mess that felt almost like it was sunburned. I lost a lot of hair because of that. I think I have started to gain it back except perhaps in my crown. My hair is pretty long right now so it is hard to tell. I'm gonna buzz it way down soon just for kicks so I'll know more then.
I do not recommend paying $50 to try out Scalpure but I do recommend trying a home made clay topical like OMG is playing with. Add some oil to it which should be soothing to your scalp. I have been experimenting with it and if my scalp is itchy and feeling inflamed it sure helps. There is a very informative site http://www.aboutclay.com that jdp710 referenced that, if I remember correctly, talks about the benefits of clay for psoraisis. Anyway, all I am saying is you may not actually have psoriasis. A lot of doctors and derms are quick to diagnose the itching of mpb as psoraisis because they don't fully understand mpb. I'd try the clay, some soothing oils like emu or coconut, some anti-inflammatory supplements (see immortalhair.com), an all natural shampoo (like Aubrey's) and keep lasering.
Good luck!
My doctor told me in April that I had psoriasis as well. I am not sure that was the correct diagnosis as I was able to get rid of alot of the inflammation. I used the corticosteroid/anti-psoratic topical he gave me a grand total of 4 times - what a sticky, gooey mess it was. It did help after a day or two but initially made it itch more. At the same time I started the IH top 6 and I think that has had an impact on bringing my inflammation under better control. Lasers help too but at the time they were unable to deal with the inflammation alone.
I think I exacerbated my inflammation with poor choices in topicals. The one that hurt me the most was the A&G hair complex which had propylene glycol in it. It made my scalp a red, inflamed mess that felt almost like it was sunburned. I lost a lot of hair because of that. I think I have started to gain it back except perhaps in my crown. My hair is pretty long right now so it is hard to tell. I'm gonna buzz it way down soon just for kicks so I'll know more then.
I do not recommend paying $50 to try out Scalpure but I do recommend trying a home made clay topical like OMG is playing with. Add some oil to it which should be soothing to your scalp. I have been experimenting with it and if my scalp is itchy and feeling inflamed it sure helps. There is a very informative site http://www.aboutclay.com that jdp710 referenced that, if I remember correctly, talks about the benefits of clay for psoraisis. Anyway, all I am saying is you may not actually have psoriasis. A lot of doctors and derms are quick to diagnose the itching of mpb as psoraisis because they don't fully understand mpb. I'd try the clay, some soothing oils like emu or coconut, some anti-inflammatory supplements (see immortalhair.com), an all natural shampoo (like Aubrey's) and keep lasering.
Good luck!
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Re: Just got diagnosed...
I would highly recommend following an anti-inflamatory diet and taking anti-inflamatory supps.
Some supplements to look into that really help with inflammation are fish oil, krill oil, Circumin, Vitamin E, Vitamin C, MSM, Boswellia Serrata, Quercetin & Vitamin B. Also may help to start using topical emu oil, grapefruit seed extract, tea tree oil etc etc...Also could look into killing Demodex to help out as well with Sea Buckthorn soap/oil.
And of course, LLLT will kick inflammation's ass too.
Some supplements to look into that really help with inflammation are fish oil, krill oil, Circumin, Vitamin E, Vitamin C, MSM, Boswellia Serrata, Quercetin & Vitamin B. Also may help to start using topical emu oil, grapefruit seed extract, tea tree oil etc etc...Also could look into killing Demodex to help out as well with Sea Buckthorn soap/oil.
And of course, LLLT will kick inflammation's ass too.
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