How does your GP react to your concerns about is... - Fight MPN
How does your GP react to your concerns about issues that could be MPN-related? Tick any boxes that may apply & feel free to add further
My gp, dismisses anything that could be to do with PV & tells me my consultant should deal with it.
I have a new GP that admittedly hasn't had any experience with an MPN.
Thanks for sharing your experience. How do you feel about the GP not knowing about MPNs? Are you seeing a MPN specialist too or someone who knows more about them?
I am seeing a local hemo/onc that hasn't had any experience with MF but is very thorough & I can talk to him because he's been following my case for 3 years. I also go to a larger cancer center in a nearby city to see this doctor's boss, who has had experience with MPNs. He is dismissive of the symptoms I am experiencing, which are many. I have an appt with my local hemo/oncologist tomorrow & I'm going to tell him I'm going to another cancer center in Rochester, NY for a second opinion. I was diagnosed with MF (thrombocytopenia, Hypofibrinogenemia) with enlarged spleen 4 months ago. I'm not on anything for the MF but the 35+ lb weight loss & anemia in 3 months seems significant-of a change.....The local hemo/oncologist ordered an anti emetic to treat n/v, but otherwise I am on no meds yet. I'm not trying to "rush" things I've read that many Dr's are being proactive & prescribing meds early, after diagnosis. I just want symptom relief.