CCSVI in other parts of body & MS!
Hey Alby, how are you?alby wrote:Mutley,
any progress in your MS improvement? and any other MRV or doppler for your other veins? i think a full body MRV WOULD BE A GOOD IDEA FOR EVERYONE AND THAT INCLUDES ME.
Sadly, my liberation improvements all vanished within a few weeks of coming home. I was supposed to fly back tomorrow for them to take another look at me, and maybe try a stent, but my appointment has been shifted because of all this Volcano business. Now scheduled to head over at the beginning of May. I hope to report good news real soon
I think a whole body MRV is the least that should be done for PWMS, let’s face it, the professions haven’t exactly gone out of their way to investigate many symptoms so far have they. Once you get labelled with MS, they just stop looking for anything else since any/all new symptoms can be explained aways as just being 'MS'
Mutley goes to Poland 1st symptom was Optic Neuritis in 1998, DX RRMS Jan 2001, DX SPMS 2007. Last EDSS by doctor 7.5
this thread just started (connective tissue disorders, collagen and CCSVI), and would apply to this one:
http://www.thisisms.com/ftopict-11311.html
http://www.thisisms.com/ftopict-11311.html
-
- Similar Topics
- Replies
- Views
- Last post
-
- 1 Replies
- 5551 Views
-
Last post by NHE
-
- 1 Replies
- 1710 Views
-
Last post by NHE
-
- 6 Replies
- 2459 Views
-
Last post by vesta
-
- 0 Replies
- 1611 Views
-
Last post by Anonymoose