CancerCompass message board discussion started by Robsgrl5600 on 4/28/2007 http://www.cancercompass.com/message-board/message/all,11652,0.htm Mon, 08 Sep 2008 00:00:00 GMT Mon, 08 Sep 2008 00:00:00 GMT http://backend.userland.com/rss RSS.NET: http://www.rssdotnet.com/ Anyone with this myeloproliferative disease that wants to chat, please feel free to message me. I could use the support. THANKS. Robsgrl5600 Sat, 28 Apr 2007 00:00:00 GMT Hi there,  I was just diagnosed with ET a few weeks ago. It's a pretty scary thing to consider. My platelet count was 1.2 million. At the moment, my doc is checking my blood every 2 weeks and I'm on 500mg of hydroxyurea every night. I just started it so I'm not sure how it's going yet. According to my records, my platelets have been on the rise for over a year but they didn't catch it until I went to the Mayo Clinic for something completely different. I've talked at length with my doctor and he feels this medication is the best for me. I'm only 32 and I've read that the angrelide (sp?) can cause fibrosis of the bone marrow in long term use. And as far as ET goes, we will all be on medication for the long term use. I've had it up to my ears with the bruising all over my legs and arms. Plus I will forever be taking baby aspirin every day. My doc also told me that not only is ET dangerous for blood clots, but it can also be dangerous for excessive bleeding due to the fact that since there are so many platelets they can malfunction. Every now and again I freak myself out just thinking about it. I hope some of this info helps and if I can help anymore, just let me know. Good luck and take care. Kellya304 Sat, 09 Jun 2007 00:00:00 GMT Hi, I was diagnosed yesterday with Thrombocytosis.  My platelet count was 1.15 million with my last lab draw yesterday.  They have put me on Hydroxyurea 500mg. (Hydrea)  I have taken 2 doses now, and all seems well. I haven't experienced any side-effects as of yet.  I am not quite sure what all of this means.  I would like to know more about diet.  Limitations and what to expect with this condition.  I understand that this drug has effects on the immune system.  I recently retired as a salesperson in a department store.  I guess just in time since I would be coming in contact with so many people.  One thing I am not too happy about was the fact that my primary physician knew there was something going on with my platelets for 4 years but somehow failed to mention it to me.  I have to say that I would have lived my life a little differently if I would have know that this was going to be my destiny.  I am 68 and really didn't need to work.  Towards the end of my days at the store, just getting there was a real arduous task.  I have to say that I am angry that he dismissed me by not telling me.  I now have an awesome specialist in a big hospital in the big city.  He is very knowledgeable but I am always wanting to find out more. I would like to meet up with other people that are just like me.  People seeking knowledge and tips and new information.  If you feel that you would like to chat with me, drop me a line.Thank you for your time.Camelot R Camelot Rose Thu, 16 Aug 2007 00:00:00 GMT