Anybody here being treated in North Wales? - MPN Voice

MPN Voice

10,342 members14,253 posts

Anybody here being treated in North Wales?

jointpain profile image
1 Reply

Would like to ask about the treatment one can expect here in North Wales. Though my wife is getting treatment for her Myelofibrosis, we are not sure how good or upto date it is. Probably contact via messaging would be best.

Written by
jointpain profile image
jointpain
To view profiles and participate in discussions please or .
1 Reply
Rachelthepotter profile image
Rachelthepotter

Hi. A month or so ago I posted some links on this forum to good practice in Dx and treating MPNs. They might help to provide a standard to assess your wife's treatment against And her locsl haem might find them useful too. All the best

Rachel

You may also like...

Molecular remission of MF which is being treated with PEG

If this is the case, I’m wondering what that would mean for my illness and symptoms? I have...

Anybody here on methotrexate?

Saw this article about methotrexate giving symptom relief to MPN patients. Just wondering if anybody

Anybody here with ET and hearing impairment?

diagnosed with ET in my 20s but like many people here I often wonder how long I actually had the...

Would any one being treated for an MPN at the Churchill Hospital, Oxford like get in touch?

there too, and would like to get in touch, do please do send me message, or make contact via this...

Is there an MPN Support Group in the Teesside or North East area?

the North East? Posted my request for a buddy yesterday so eagerly awaiting a response but would...