Hi all,
I was diagnosed ET JAK2+ last month and joined this forum a few days ago.
I just want to wish everyone a Merry Christmas.
I’m looking forward to getting to know you all as we go through our journeys together.
Have a wonderful day ☺️
Hi all,
I was diagnosed ET JAK2+ last month and joined this forum a few days ago.
I just want to wish everyone a Merry Christmas.
I’m looking forward to getting to know you all as we go through our journeys together.
Have a wonderful day ☺️
Hi. Welcome. I’ve been a member for nearly 3 years, and value this group: we are an amazingly diverse bunch, and have every variety of MPN, and every variety of doctor and healthcare system to deal with.
I have myelofibrosis, ( MF) and live in England. Three years post MPN diagnosis. Living as full a life as I can. All the best.
Rachel
Welcome and Merry Christmas to you too. I joined this year, very helpful and friendly group. All the best.
Hey! And merry Christmas! I love this place! I've got ET, three months since diagnosis and still trying to figure out what it means.
From what I can see there’s lots of helpful information which is great. My haematologist pretty much gave me my diagnosis and then called in the next patient, so I’ve had a lot to learn about by myself. Let me know if you do figure it out as I’m trying to do the same 🙂
The same happened to me as well, I had no idea what ET was. I googled it at work later the same day and I realized I had cancer(!). However, it is starting to sink in now and I have a game plan I think. The positive side for me is that a lot of my weird health issues finally has an explanation and Im not a hypocondriac😄
Hi Rae 25
Merry Christmas 🎄
Welcome to this friendly and supportive group. I was diagnosed with ET Jak2+ about 18 months ago.
I hope you had a great day yesterday.
Welcome, this is a great group that is always here to help answer questions and for support! ET Jak2+. Happy Holidays!
Merry Christmas Rae25,
Welcome to our wonderful circle of support, info and love. We are all happy to share our experiences, lives and insight as well as our friendship.
Anag🙂
Hi Rae,
I was diagnosed with ET over Christmas/New year 3 years ago, and it was a lot to take in! Very pleased that you have found this forum as you will find a lot of support here and help with understanding your medical condition.
Kind Thoughts and all the best for Christmas and the new year!
Peter
Welcome! You will get a lot of support and good advice here. I had ET for 11 years and I just found this site last year when I started feeling worse and people encouraged me to get a second opinion. In September I found out I had myelofibrosis but now I have a really great doctor who is treating me correctly for the first time in a long time.
I wish you all the best on your MPN journey.
Welcome Rae. I have ET JAK2 diagnosed 18 months ago. This is a lovely friendly group to chat with and bring your worries to. We are all going through it together and it's good to share any worries. Wishing you all the best in 2020. Just seen your post and glad you had a nice quiet Christmas. Fran
Hello. Glad you had a lovely Christmas Day. Also jak2 + diagnosed October 2018. This forum is a godsend. Jx
Thank you all for your welcomes and kind wishes. It’s reassuring to know how knowledgeable and supportive everyone here is.
Welcome to the group. I was diagnosed in January & joined soon after having spent last Christmas waiting for results. I don't post often but regularly look in as there is always lots of good advise. Glad you had a good Christmas x