Anyone living with Essential Thrombocythemia with JAK2?
Has anyone been living with,ET, jac2 mutation
Interested in more discussions like this? Go to the Blood Cancers & Disorders Support Group.
Has anyone been living with,ET, jac2 mutation
Interested in more discussions like this? Go to the Blood Cancers & Disorders Support Group.
@esperanzam
Forgot to say that the PA told me that day that the way they treat those with LOW platelets is to give them steroids ... to increase their platelets! I still take them on occasion if I really need them. I would not be terribly afraid of another steroid injection but I just have to work with my PA on my chemo (Hydroxyurea) dosage. Right now I am having shoulder problems which I have had before. In the past (about 7 or 8 years ago) it was a calcium deposit and the treatment was a steroid injection with dissolves it, hopefully. Well, it took two steroid injections about 4 months apart but it did dissolve it and took care of the problem. I am not sure if I have the same problem but possibly will have to do the injections again.
@esperanzam thank you for your information. Hips, shoulders, backs…it would be nice if our bodies would give us a break now that we are dealing with ET! I am waiting for an appointment for my hips so more to come. I hope your husband can get his levels down, carpal tunnel can be so painful.
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Thanks! Let's stay in touch. It can only help to learn from each other.
Sandy
I was diagnosed 10 years ago and began taking hydroxyurea daily to reduce the platelets from 1600 to the 600 range. My count is still above the 400 normal range. I take 9 hydroxyurea caps weekly as higher doses cause my tongue to swell and restrict breathing and eating. I am blessed with a balance that works for this day.
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