Jak 2 and Waldenstrom's Macroglobulinemia
Hi to all on this group. I was diagnosed with jak 2 and mgus in 2016 and then Waldromstrom Macroglobulinemia(WM) in august 2019. The hematology/oncology doc didn't test for the WM until 2109. I have many symptoms of both cancers and have had for many years. I am trying to get care via the mayo clinic; however, the scottsdale mayo clinic (15 miles away) doesn't take medicaid and the rochester clinic only takes patients with Medicaid who reside in States that border Minnesota.
Dilemma:
Given the fact that I have two different categories of blood cancers, would the Mayo Clinic in Minnesota make exceptions to their policy so I can be seen by the experts under my az medicaid?
I have the ability to be in rochester for all appointments. My son lives in minn.
Thank you for any help anyone can offer.
Interested in more discussions like this? Go to the Blood Cancers & Disorders Support Group.
I had NHL 15 years ago. I don't know if there are many forms of it. I had a radio-immuno-therapy with 2 different Zevalin. One to target the blood cancer cells and one to destroy them. I had rituximab also. Chemo with Rituxan in the morning and Zevalin in the afternoon. Only one day treatment for 2 weeks. I never heard about this treatment since. I hope it can help.
Thank you ginpene. That's what I thought too, as well as for waldromstrom Macroglobulinemia. Again, thanks.
Thank you. It sounds like you are doing very well. So far, I'm just on hydroxyurea 1000/day, oral chemo.
I think my bottom line question to myself and to those who are knowledgeable and /or experienced, should I request a different doc? I'm thinking, yes.
If anyone else has suggestions or answers on staging, I'm interested.
I will say yes. My first oncologist told me you are in stage 4, even the chemo cannot help you. Go and live your life. My daughters ask for the head of oncology in the hospital for a second opinion. I happened to know about this treatment in Germany. By chance they had the product and never use it because not recognized by the FDA. I assumed the responsibility and sign all the papers. Good luck.
Thank you Ginette 55.
Hi justin. Are there any words of wisdom from your net worth of doctors but from your experience and knowledge?
I meant to say any word from mayo clinic network or from your experience regarding my questions?
Hello @janemichele. Here is some additional information:
From a Mayo Clinic Hematologist,
"A provider could apply the same staging system (Ann Arbor Staging for lymphoma) to WM, which goes from 1 to 4 (like the TNM staging system for solid cancers that also goes from 1-4). However, in particular for WM, the Ann Arbor staging system is not helpful as all WM patients would be classified as stage 4, therefore, not giving us any information regarding prognosis. More commonly used is the IPSS-WM (international prognostic scoring system for WM) score, which is designed for WM and actually carries some meaningful prognostic information."
Here is a link to the original IPSS-WM publication: https://www.ncbi.nlm.nih.gov/pubmed/19196866.
@janemichele, were any of these tests discussed with you?
Hi Justin. Thank you so much! And thanks to the hematologist/oncologist for the information.
This was very helpful for me. I sent it to my hematologist. No. she hasn't discussed any of this with me. When I asked via medical portal, she said there isn't any staging because it's in the blood. I have also asked for clarification as to the number of cancers I have but I haven't heard from her. ( MPN, ET, JAK2, WM, NHL).
Again, thank you for your help.
Anyone have experience with recurring waldenstroms? And treatment?