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What are you experiences with this these meds?
She wrote:
None sound like fun to take but for some patients who have progressive hair loss, they are eager to try anything. I completely understand your lack of interest in these medications however.
The least worrisome treatments are topical steroids, injected steroids, and Excimer laser. Excimer laser is UVB light in higher concentrations that is delivered through a wand that we shine on the particular area of involvement. It is painless and has helped many people but it is very time intensive and requires twice weekly visits which many people are unable to do. Further, it is costly and needs to be authorized by insurance.
Any thoughts or experiences with any of this?
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I have been on plaquenil and Erythromycin (because Doxy upset my stomach) for the past 2 years with monthly steroid injections in my scalp. my LPP is nearly burned out. very little active areas and I still have hair. I have a new short cut that is styled forward and it pretty much camouflages my receded hairline from ear to ear. Working very closely with dermatologist who has experience treating FFA (mine is LPP), has really helped me. I am optimistic! I had a brow transplant 3 yrs ago and those are still growing strong. There are a lot of baseline tests that have to be performed to make sure you are a good candidate for plaquenil. I have had no negative side effects. I was hell bent on fighting this. Good luck! My dermatologist says there is more clinical success with Plaquenil and either doxy or erythromycin than there is with Actos or cellcept.
Thanks for the info on the laser therapy and your friend's experience!!
I have been losing hair for 5 years... was diagnosed with alopecia areata in 2011. After years of losing hair at hairline - and it not coming back (and clearly seeing the "white" band of skin)... My derm recommended we biopsy for scarring alopecia - officially diagnosed in January, 2015... have been taking meds ever since.
Believe me - I (and every one on this forum) understand that frustration whole-heartedly. It plays with our minds/emotions/self esteem. My sides (above my ears) are back 2 inches, and my temples as well... I thought it had stopped, but then about a year ago I started to see these red dots and pink scalp along front hair line... at which point my diagnosis changed from alopecia areata (original mis-diagnosis) to FFA. I started treatment a year ago - but it has not seemed to stop the frontal hair loss. I always think to myself if the front hairline recedes back as much as the sides (temples and above year), I will easily have a 2 plus inch "band" around my whole face. That, sadly, seems to be what happens with many. That said, I read posts from people like Katy M (above), who have had great success with medicine stopping/slowing the progress. If only there could be some consistency/certainty. I think that would alleviate so much of our worry. On that note, do you just push your hair forward, or wear bangs to try to disguise the loss?
Oh BBQueen! Your post really spoke to my heart. I know you feel like you look like a freak, but I bet you don't, AT ALL! I've been telling my hairdresser (friend) that if and when my top hair thins so much, the bangs are not going to "cut it" (no pun intended) anymore, we need to come up with some idea's for some new super funky cuts like shaved on one side and long on the other, or something. I just the other day had to explain to my sister that I appreciate it when people say, "you can't tell!" But, it doesn't change the fact that I have to work hard on my bangs working well and that it's not enough I'm aging and have to work hard to not get too overweight, I also have to worry about my hair, my beautiful hair...saying goodbye to my once beautiful hair is very difficult. I hear your pain and despair. I hope you can find a solution that will help you feel a bit better and not like a "freak!" Don't give up!
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