Well, dang it I had a whole entire post almost ready to go and it disappeared on me so let's try this again.
I want to thank each of you for your kind and great responses. You all have given me so much over the last year that I have been on this site that I can't begin to tell each of you enough. You are all my inspiration and my rocks in the tides of a torrent sea. That comes from the heart!
Okay, so I have spoken with my husband about this and he is concerned that the SCS will not work, especially with my track record as of the last few years. This has given me more reason to fight for a "REAL" solution to each of our CP. I think that with all of the technology that is out there, after all they have cures for many diseases that were horrible and final in their end, there has to be something more that those smart and brillant scientist can do right?
I believe that there has to be something that each of us with CP can do to make these people believe that we are worth saving. I'm taking the first steps by emailing my Senators in Wyoming about WC. Then after that I will be speaking with my doctor to see what my next steps are in the goal of improving my health.
Anyway, I want to thank each of you. I hope that your pain is lessoned today and that you are able to do what you desire to do.
Hugs and kisses,