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If you want to read about people who have undergone the procedure under Dr. Dake's care, check out the “This is MS” site. They are tracking the progress of MSers who are currently being treated.
And here's a link to the Facebook fan club for CCSVI. (Clicking link will open a new window). We're keeping a close eye on the developments
If it sounds like we are hoping that this treatment will work, then you guessed right. We're not doctors, of course, but we still have hope that one day there will be a cure for MS. And if this is the cause of even a small number of people with this disease, then it should be explored.
The studies are continuing in several places. Here are just a few:
~from This is MS
For a more complete list, go to the This is MS Forums. (clicking here will open a new window).
We'd also love it if you use the form below to let us know what you think about this promising study. Sharing your experiences will help others decide if this might be a possible treatment for them, as well.
Here are a few questions you might consider addressing in your submission. You can answer them all - that would be great. Or just the ones you feel comfortable answering - that's okay, too.
I'm sure you can probably think of several more We're excited to see more about this treatment – are you?!
Share your CCSVI story for treating your multiple sclerosis here. How has it helped you or how do you feel it will help you?
Share your story, tips, and advice about CCSVI with other MSers here. Or talk about why you think it should be available for people with MS.
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Cir & Akrista
You are reading original content written by Akrista or Cir L'Bert of Life in Spite of MS. If you enjoyed reading this blog, please consider following us on Facebook, Twitter, Pinterest, and Instagram. See you there!