Each day, several times a day, someone is crying out for help due to being a cp patient. I am so done with all the negative press we get, and until we get out there and start writing to our legislators, this will remain a dark secret that we suffer with.
Its not enough to be in pain 24/7, because lets be real, the meds help with the pain, but it never goes away completely. But we are the people constantly being looked upon in negative ways. Its time to change the pattern. I am going to begin my campain of letter writing tomorrow, (my grandson leaves in the am) so I will be able to get started.
Remember, we are a very large group of human beings, who thru no fault of our own, have been forced to take medicines that give us a quality of life. Without this our lives would be h... So all those who are tired of the very unjust way we have and continue to be victimized by a system supposedly but in place to help us.
So just know, there is power in numbers, and sadly for us we have numbers, I just so tired of it. It is time for a change, a better way to screen out the few that do try to get over on the system. Its just not us, we have had to give up alot in our journey through chronic pain.
Ok thats it, I am now getting off my soapbox,and taken it to the people who can do something about it. This is nation wide at the very least. Please join me in fighting for the right to have the best quality of life we can due to what has happened to us through no fault of our own.
degenerative disc disease, fibromyalgia, osteoarthritis, neuropathy, lumbar laminectomy july 1998 no help, rechargeable neurostimulator unit low right back w/lead wires to left side and right leg unit not working just sitting there.i am 57 years young in may will turn 58. i have 2 grown daughters, 25 and 29. i have 2 grandchildren, 9 year old grandaughter and 5 yr. old grandson