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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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Merry.
I have been on 2 pills a day for a year. My spots just came back wondering if I should increase to 3 pills. How long have you been on it?
I too have Hashimoto's thyroid disease, Vitaligo, RA, and Gluten Intolerance. I'm a hot damn mess! Lol!
Hi, I was just prescribed Xeljanz. My insurance company just denied coverage as I knew they would. I appealed their decision, but I am not counting on them reversing their decision. I have heard of Xelsource and the patient assistant program. I am sure that I qualify, but I think that still comes to about 24,000 a year out of my pocket that I cannot afford. I am not sure what I should do. I am excited just to have gotten to this point, as finding a doctor to prescribe me the medication was difficult enough. But, I am afraid I am out of options to afford it. I was just wondering if any of you knew more, or afford the medication with additional assistance that may be available. Thank you for any of your help or insight.
Hi Alo-mom,
I just sent you a friend request. Thank you for offering to help!
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