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I have been on Ruxolitinib (Jakafi) for 1 month now and have seen some small white hairs on scalp and arms. I have been universalis for about 12 years, I am 22. Dr. King prescribed it on a whim thinking it would not get covered but they did it. My dad is a doctor so I think his health insurance is just good like that. It is called Amerihealth.
I tried xeljanz for 8 months, saw a little regrowth but then it kind of stalled out and faded away. Jakafi seems to be responding much quicker. I am very interested to hear if anyone is on Jakafi or has been. The published studies are so small that its hard to get an accurate read on how the medication works.
Anyway I will keep everyone posted
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Are you still taking the Ruxolitinib and how is the hair coming?
My dermatologist was willing to prescribe it until this article was published:
https://www.ncbi.nlm.nih.gov/pubmed/28628689
"Aggressive Skin Cancers Occurring in Patients Treated With the Janus Kinase Inhibitor Ruxolitinib"
As a result, he no longer feels that the potential for benefit outweighs the risk with this medication. That's unfortunate, of course, but so is aggressive malignancy.
I discontinued Xeljanz for the same reason as Joey--it stalled, even after raising the dose to 20mg / day. I also suspect that it might have been responsible for some symptoms I developed such as fatigue and anemia, but that's difficult to know for certain.
I'm curious what the long-term results will be for someone who was an inadequate responder to Xeljanz, but make sure you're checking out your skin regularly, and have your dermatologist do the same.
Here you go.
I don't know rules of this forum but ...
Maybe someone have used (open) box Ruxolitinib for sale.
I am from Ukraine, but have post adress in US.
Thanks.
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