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I have received a lot of interest from others on here in my involvement with the Xeljanz trials at Yale.
I thought it would be nice for everyone if I documented my progress on here.
Xeljanz is a Jak3 inhibitor and is believed to work with alopecia by turning off the distress signal relayed by the hair follicle to the attacking immune system which is the cause of the hairs falling out. Xeljanz comes in a strength of 5mg per pill and a full box contains 60 tablets. The recommended dosage for arthritis is 1 tablet in the morning and another in the evening each day.
The trial is set in a series of stages and there are requirements before participating. These include monthly visits and blood tests every 2 weeks. Dr Brett King is absolutely fantastic and is an inspiration to me. His positivity and enthusiasm gives me the much needed hope I have craved for over a decade. I have been put on a low dose to start with which is 1 tablet every other day. My dosage has now been increased to 1 tablet every day and next month it could be increased to 2 tablets per day depending on the results.
I have completed my first month and have already noticed my alopecia has stabilised . I have not lost any existing hairs. In addition to this I have seen little hairs growing in my chest area as well as eyebrows. Fingers crossed! To date, I have experienced no side effects.
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AW: Other discussions on Xeljanz / Tofacitinib
https://alopeciaworld.com/main/search/search?q=Tofacitinib
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She desappaired i hope she good...i hope no heatlh problems
Hi Friends -
I have been on Xeljanz now since July 2, 2015. I have ALL my eyelashes, most of my body hair, and I had a full head of white fluff with some dark hairs growing in...and then in march, the hair on my head began to fall out. I still have white hair mostly on my head (although I look kind of like a troll doll with this long, diffuse white hair sticking straight up about 3 inches long.) At this point, it still has not all fallen out from my head... but it doesn't seem to be coming back either. Meanwhile, 6 weeks ago I got a set of injections in my eyebrows (where I had only soft white hair) and they grew in FAST. Dark, terminal hairs!
Has anyone else had an experience like this? Is there anyone who can give me some hope to hang onto? Thanks!
Football Fan,
Would it be possible to communicate this concern at any Alopecia Areata conference?
I have recently finished a 12 week trial using topical JAK inhibitors, if I am to respond to these drugs it will happen from now, I will post any reaction in the weeks coming up, if nothing I will consider oral Xel next year
Another pharmaceutical company developing a JAK solution for AA, looks like this one is a modified oral ruxolitinib:
http://www.businesswire.com/news/home/20160504006458/en/Concert-Pha...
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