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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
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But autoimmune alopecia can be triggered by stress, menopause, pregnancy or other hormonal factors. It's still alopecia, and if this treatment works on autoimmune alopecia, why wouldn't it work on autoimmune alopecia in some people and not others?
I mean, I don't plan to try an immune suppressant ever as I don't believe having hair back is worth having a higher risk of getting cancer, tuberculosis or any other disease but it's unfortunate that the treatment is not a sure fire hair-grower.
You’d be surprised to know that Jak inhibitors do in fact work for androgenetic alopecia. It’s like anything else, some people will respond and some others won’t.
A huge number of people are getting growth and for the rest I believe it is just a matter of time.
Hi Guys,
Just a quick little update .
I had another haircut in a proper style which I fill in with hair fibers. I am amazed at how different life is like this especially with the opposite sex. It's absolutely amazing to feel desirable and an equal to others. It feels very strange to have hair (almost like a dream) I often think I will just wake up one day and be back to where I was but no, It's real and it's happening.
Every day I look at the mirror no longer filled with dread , worry and despair but actually looking forward to seeing what new hairs are coming through. To not have to worry about losing anything any more is a immense load of my shoulders.
It's very odd but because I've had virtually nothing for so long I subconsciously still feel I have AU.
I will have some new pictures of my new haircut up shortly .
Thanks Singh ,
How is your treatment going?
At the 7th month before I had anything significant.
On most people who have had alopecia for a long period of time it will normally start out as white , wispy vellus hairs that are hard to see and then progress onto full terminal hairs.
You'l get there eventually :)
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