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@esperanzam

Just would like to hear from others out there with this diagnosis. I was diagnosed in early May, 2015. Have been controlled till now with Hydrea but having some changes in blood work and other issues and would like to hear other's experiences.

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Replies to "Just would like to hear from others out there with this diagnosis. I was diagnosed in..."

Hello @esperanzam, welcome to Connect. You may noticed I moved your discussion and combined it with an existing discussion with the same title. I did this so the other members discussing essential thrombocythemia would see your post and have a chance to respond. I also did it so you could read through some of their older posts as well. If you are replying by email, I suggest clicking on VIEW & REPLY so that you will be brought to the new location of your post.

@esperanzam, if you are comfortable sharing, what are some of the changes you are dealing with?

@huronshores
High platelets, no clue until routine blood test. Saw Haematologist, on Hydroxyurea since May/18 and took about 3 months to lower platelets. 78 yrs old, active and reasonably healthy .. Some allergies, well controlled asthma and have had two past surgeries for sinus polyp problem. Polyps are treatable but not curable. Since an infection could affect platelets, I saw a specialist re sinuses. He said I may need another surgery to help with existing polyps but did not seem to think it was cause of high platelets. (However, in doing a bit of reading I have seen some studies that say people with sinus polyps show higher platelets?). Very hard to say what is correct. Also, asked whether diet could lower platelets somewhat. Haematologist said definite no. However, again in doing some reading, there is info that says certain foods can lower platelets. I am not happy to be taking Hydroxyurea, as while it can be used for high platelets, it sounds like it affects pretty well all cells in your body. Certainly have noticed side affects and all seem to match up with the info the drug store provided with the Hydroxyurea. So far the Haematologist has pooh poohed all side affects. I have another appointment coming up soon, so another blood test re platelets. Still thinking and not sure what I am going to do about this but not happy taking Hydroxyurea forever. No one wants to have a possible stroke, thrombosis etc as a result of high platelets .. But at the same time, Hydroxyurea can lead to other problems. Sort of like taking your car to the garage to get get new tires so that you will drive safely but then the wheels fall off! I am speaking only for myself here and not saying you or anyone else should follow my thinking. Part of me is influenced by my age and that makes me wonder if my remaining quality of life is going to be affected too much by the medication. I have a neighbour that told me she has been taking Hydroxyurea for years but I don't know the exact facts involved for her. I have been pretty lucky health wise and have not needed much medical care over the years, as compared to others in my age group. Did have one problem where I exactly listened to a Doctor against my judgment and that turned out to be a disaster. So forever after, I will be questioning and trying to pick up all the information I can on medical issues. Guess I am a doctors nightmare. Don't know if anything here helps but I am just sharing my experience so far.

I have read somewhere that HU may actually increase the risk of leukemia by a slight degree? Possibly because they use it on patients with JAK? I have been on HU since early 2011 (?) and the Dr. several months ago desired to know if my liver was inflaming; before it has just been about my lymph nodes and ease of bruising. How many years of thrombocytosis does it take before they say that one has ET (no underlying infection nor cancer found)?