article on Clare for human SM association
I came across this on the web today -- an interesting article on Clare Rusbridge's research on SM for a website for human sufferers of SM:
Likewise people might find this link useful, as it explains what SM is in humans and what humans feel when they have it. Interestingly symptoms most frequently show in humans between 25-40 -- so it isn;t generally something people realise they have early on.
CKCS & ASAP working together
Hi Karlin, thank you for the warm welcome! I have to say a joint fund-raiser sounds like a wonderful idea. I believe the key to finding a cure for syringomyelia is to work together. I will keep an eye on your sight for future postings. Thank you again!
Sparky (7/8ths Irish...almost there :) )