Dwayne - What have you read or been told that makes you think fetal stem cells would be an advantage over other types of stem cells for you?
Barbara - I think it is the marketing and maybe hopeful thinking. It makes sense that they will not have an ID to a certain age and that they are more potant than using your own or umbillical. The cost is about a wash either way, I am just looking for the best chance of me getting better or at least not getting any worse. MS has already taken my selfesteem and vitality, I can only believe it gets worse. I have stopped Copaxone and am doing the PK Protocal. The very first treatment, within hours I would have sworn that I was cured, no more limping, no more numbness, within a week I was back to where I had been. $7K and 6 months gone.
I would like to know if there is a reason that it isn't as good or better.
Dwayne, have you ever been tested for Lyme Disease?
I've recently been treated at a hospital in the UK, having been diagnosed with Lyme. I met some people there who were misdiagnosed as having MS. A lot of the symptoms overlap, so I would urge you to get tested. As you live in the US, you should ask to be tested at Igenex labs.
Believe me I've no vested interest in that lab, wasn't even tested there.
FAO of others who know me from previous posts, my stem cell experience didn't do me any good. In fact it made me a hundred times worse, because the Lyme was still active, so autologous stem cells was not a good idea to say the least!!
Anne
Anne - I have not been tested for Lyme disease, but I will get tested. Thanks for the heads up. I guess the reason I never questioned it was because of the slow nature in which it happened, I see it now but, did not at the time. I love two sports that show your abilities, Slalom waterskiing and snowboarding. Slalom skiing is done in a standard course at set speed the only variable is the length of the rope, the better you are the shorter the rope. I have skied and competed all over the world. Each year from 2003 I got progressively worse each summer, same with snowboarding each winter.
On my birthday in 2007 I woke up with my left foot asleep, it has been asleep since then except for the one week when I started the PK now it has added my left hand and I have a pronounced limp - drag.
I guess those and the fact that my sister was diagnosed with MS in 1995 are the reasons I trusted what they told me.
Sorry about the long reply.
Dwayne