Hi All,
I just wanted to introduce myself and say hello. I was diagnosed with ET in April and have been lurking on the site for a bit. I really appreciate all of the information! It's very reassuring to know that I'm not alone and that my symptoms aren't just in my head. Thank you for sharing your experiences!
Welcome we are a friendly lot really and it's helpful to just read other posts sometimes.
When you do ask something you get lots of advice, to help you through. Once again welcome.
Hello and welcome to our forum, glad to hear that you have found our forum to be helpful. Best wishes, Maz
Welcome from a fellow ET sufferer and well done for 'lurking'! You have found the most friendly and helpful site that any of us could possibly imagine. Very best wishes, Tinkerbell13
Hello fellow ET sufferer! Isn't it a relief when you find this site and realise by reading the posts you're not alone and that most of the things you've read about ET on the internet aren't true. 😳😄
Best wishes
Lizzie
Welcome to the forum. I too have ET and have found it incredibly helpful.
Hi Jason - welcome to the site - feel free to ask any questions - it's great how much information and experience we have to share between us..!
Best regards
Andy
Hi Jason, welcome to the forum. 
Hi just wanted to say welcome to this forum. I was diagnosed with ET in 2001 and really wish I had this forum to help me at that time. I was very fearful then but after all these years accept this and get on with my life to the best I can. Just relax and know that there are lots of folks who can and will help you. All the best.
Welcome, I have found even though I am from the US this is best site out there! Mickey
I'm in the US (Texas) also and agree!
Welcome, welcome, welcome
Welcome to our forum - I am sure you will gain useful information and help from everyone.
May you find many pearls of wisdom from friends who really do 'understand'. Welcome .
We
Welc
Welcome, et jak2 + here in CO. Diagnosed 8 mos ago. Are you on medication? Platelets under control and doing fine.
Thank you! I'm only on aspirin at this point. I'll go back in a month or two and see how it's working. Hopefully it's doing the trick. I feel better on it than off.
Good luck, if they do suggest Hu it's not that bad.
Thank you! What exactly is HU? I see it posted a lot, but don't know what it is.
Hydroxyurea, one brand name here in the states is Hydrea.
Few years back in UK changed drug name to Hydroxycarbamide. You're right Kerrial most folk tolerate it quite well. I was taking it for 10 yrs and some been taking it 20+. , , Chris
Glad you found our Forum as everybody is so supportive and helpful. The folks on here have helped me through some challenging times with their unwavering support. . Cheers Chris
Welcome to the group. It is a wonderful feeling to know your not alone the information on this site is amazing. I am also new diagnosed in jan and feel so much better knowing that you can interact with peoplethat have the same diseases as you
Welcome Tracey from australia
Newly diagnosed
New to the site and diagnosed with PV in February 2018
Newly diagnosed
Newly Diagnosed PV
