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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Related Post on Alopecia World:  

Xeljanz / Tofacitinib

Olumiant

Jak Inhibitors

 

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Aladdin, why don't you start a new discussion on PRP? What is it? Also include your progress with Barticinib from China and PRP on it. Thanks

i have other questions sorry :

how i can calculate 10 mc every day..and i must take them in a pill or in another way? 

how have you made?

can you help?

the site where are factories that sell baricitinib is amazon or alibaba?

i read this study made whit a lot of people(1000) ony one let the cure and in palcebo half also one let the cure so this drougs HAS NOT SIDES EFFECT ...

Also in this study they give to people 1 time a day cuase the drougs is not like xelijanz that work 12 hours it work 24 hours so better you take it a time a day no 2 times

it's in italian but sure a lot of other trials made in Usa or other countries 

http://www.lilly.it/it/area-stampa/articoli/baricitinib-un-innovati...

Hi,

Thank you for sharing your experience and creating this forum. I have AU, RA and Lupus...oh the joy! My Doctor prescribed Xeljanz for my RA. Bonus, I have been on Xeljanz since December 18th. By March 26th I could feel hair growing in and on March 28th, I saw hundreds of hairs on my head. I have had AU for 33 years since age 12. The only thing that has worked previously was prednisone which destroyed my body. I can see other areas coming in and feel eyelashes. I will keep you posted on progress.
I'm so glad to heard that from you . good job blessing
and how many pills you take Xeljanz ?
thanks
I am on 2 pills...10mg per day. For less than 3 and a half months and the longevity of my AU, this is a miracle!
Blessing, wonderful! So happy for you. And I like blyour moniker (name). We are all blessed to have a drug that WORKS with little or minor side effects.
Amen Brother, Amen!
Sister, lol! I'm female. That's a picture of me and my husband Wessley.

That really gives me hope for my son who went full AU in a month at 11 1/2 years old.  He is now turning 14.   He had patchy eyebrows and some missing hair spots for the year or two prior to the AU condition.  Thanks for sharing and continued success.  God Bless.

Thank you for sharing. I believe this is the one drug that has made a difference and will help your son.
The Doctors have tried everything under the sun to treat me, many very painful. This is the first one where I am
Not have injections in my head and serious repercussions.
33 YEARS without a single hair and now thousands to come! Blessing, where do you live? I would love to meet you and help you celebrate! PARTY!!! No more painful injections! XELJANZERS UNITE! We need to start planning our first annual Convention, lol! Who wants to come to California this summer? I'm serious.

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