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#1
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![]() The other week the gang at Shift.MS (https://shift.ms/) interviewed me on my stem cell transplant experience. I tried to be honest, and maybe I was a bit too honest. Worth a listen if you are interested in pursuing this treatment.
The interview was broken up into several parts. The first Q: How did you make the decision to have HSCT? They will post them all gradually on their MS Reporters "experts" page on their site: https://shift.ms/msreporters-expert/dave-bexfield Enjoy! I'll get better at this interview thing and try to arrange better audio. And I said it a few times during the conservations, that I am going to get flamed. Ah, such is life when news that is not perfectly rosy is presented and there are patients for which anything not rosy is unacceptable. ![]()
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Dave Bexfield ActiveMSers |
#2
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![]() They've released video #2.
Can you tell us about your experience with HSCT? https://shift.ms/msreporters-video/c...xperience-hsct
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Dave Bexfield ActiveMSers |
#3
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![]() Videos 3 and 4 are up.
Now you’ve had HSCT, what are your symptoms like? https://shift.ms/msreporters-video/n...-symptoms-like What was the criteria you had to meet for HSCT? https://shift.ms/msreporters-video/criteria-meet-hsct
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Dave Bexfield ActiveMSers |
#4
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![]() Video #5
Would you consider another treatment over HSCT? https://shift.ms/msreporters-video/c...treatment-hsct
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Dave Bexfield ActiveMSers |
#5
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![]() Part 6
Under what circumstances would you recommend HSCT to other MSers? https://shift.ms/msreporters-video/c...end-hsct-msers
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Dave Bexfield ActiveMSers |
#6
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![]() Part 7 (final)
Do you have any advice for people considering HSCT treatment? https://shift.ms/msreporters-video/a...hsct-treatment
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Dave Bexfield ActiveMSers |
#7
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![]() Bumping this thread to the top, as UK's Shift.ms members might be discovering this site with my recent post on Barts MS blog. Hi gang!
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Dave Bexfield ActiveMSers |
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