ShiftMS interviews me on my HSCT experience (warning, may be TMI)

[ActiveMSers]

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.

[ActiveMSers]

They've released video #2.

Can you tell us about your experience with HSCT?
https://shift.ms/msreporters-video/c...xperience-hsct

[ActiveMSers]

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

[ActiveMSers]

Video #5

Would you consider another treatment over HSCT?

https://shift.ms/msreporters-video/c...treatment-hsct

[ActiveMSers]

Part 6

Under what circumstances would you recommend HSCT to other MSers?

https://shift.ms/msreporters-video/c...end-hsct-msers

[ActiveMSers]

Part 7 (final)

Do you have any advice for people considering HSCT treatment?

https://shift.ms/msreporters-video/a...hsct-treatment

[ActiveMSers]

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!