Originally posted by #LHB#
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Spinal Cord Injury Network USA (SCINetUSA)
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Hey Jim. This is indeed good news! It's been a while since I checked the site but I'm really glad that I did. Congratulations Wise and to everybody who helps him and supports him in any and every way. I have a question. My daughter is pregnant with what will probably be our last grandchild. Is there any benefit to us storing the umbilical cord blood for possibly using it for me? I don't know the science behind what is going on here, but at one time storing umbilical cord blood seem to be an option. My injury is C5/C6 complete. I was injured in late 1993. So, a big hello to everybody on this forum and those who support it in any way! It is all of you that give people like me hope of a brighter future! Looking forward to the results of these upcoming trials. Take care everybody!Here's Hoping!
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Originally posted by DougB View PostHey Jim. This is indeed good news! It's been a while since I checked the site but I'm really glad that I did. Congratulations Wise and to everybody who helps him and supports him in any and every way. I have a question. My daughter is pregnant with what will probably be our last grandchild. Is there any benefit to us storing the umbilical cord blood for possibly using it for me? I don't know the science behind what is going on here, but at one time storing umbilical cord blood seem to be an option. My injury is C5/C6 complete. I was injured in late 1993. So, a big hello to everybody on this forum and those who support it in any way! It is all of you that give people like me hope of a brighter future! Looking forward to the results of these upcoming trials. Take care everybody!
The chances are, the cord blood won't be useful for your grand child's parents, or you. The great thing about umbilical cord blood is that it can be matched just like blood. I would bank it for your grandchild.
Originally posted by Barrington314mx View PostJim, you got anything from the most recent open house that you can share?
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Nice article on a talk Dr. Young gave here: https://norcalsci.org/news/2019/4/21...ming-us-trials
Not so much detail, but nice to know things are moving on.
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"Talk without the support of action means nothing..."
― DaShanne Stokes
***Unite(D) to Fight Paralyses***
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Originally posted by Jim View PostIt was posted here in Jan
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Thank you for responding in Jim's behalf by copy/pasting links of posts that I have already read. I asked because before I had the impression that the FDA was the last obstacle to get the trials going. Learned now that we're waiting for the IRB approval, I asked JIM if there's any other approvals that are left pending or this is it for sure this time.
"Talk without the support of action means nothing..."
― DaShanne Stokes
***Unite(D) to Fight Paralyses***
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Originally posted by niallel View PostNice article on a talk Dr. Young gave here: https://norcalsci.org/news/2019/4/21...ming-us-trials
Not so much detail, but nice to know things are moving on.
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Originally posted by Barrington314mx View PostThere is always that risk in research.
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