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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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Will this be safer (regarding side effects) than Ruxolitinib and Xeljanz?
Has anyone managed to claim the tax back on Xeljanz brought in Turkey?
Does anyone wonder if these posts regarding biologics might be a "bait". Spend a lot of time researching things you read about. Not everything is going to work. If you study people who have been around this site for long times, you might be able to save a lot of money and repeated grief by losing more than our hair. Trust me, losing kidney function, liver crapping out and being in horrific pain makes a person think more than once about putting more poison in my body than whatever caused AA, AU, or AT in the first place. Some things just don't add up! My opinion only.
I think you have a point, but that's also a very pessimistic POV. Without research, trying to figure it out, trial and error, no one knows what will or will not work. But even a pessimist can benefit if something good comes out of it, like a cure or treatment, so, why would anyone spend more time posting about how bad they feel having a disorder when we can spend time forging forward, offering positive POV and perhaps sharing positive results when we have them? Imo
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I took this faithfully for over a year with no results.
Hi Starshine, how many mg were you taking a day?
After speaking with Dr King most people respond but there has been a few who have not unfortunately. Not within a year time frame at any rate.
My next step at that stage would be a combination treatment of minoxidil, cortisone injections and xeljanz.
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