I have several severe illnesses linking from the anthrax vaccines I received while serving over 10 years ago. I'm diagnosed with fibromyalgia, systemic lupus, polyarteritis nodosa, anklosing spondelitis, 6 masses in my brain, large mass in left femur, kidney stones, liver problems, not natural thyroid or testosterone production, and the list goes on. I take hormones, fentynol, oxycodone, lyrica, motrin, was taking cytoxan for over a year but now on a different chemo pill daily. basically im doing chemo so my immune system is compromised so it doesnt do anymore damage to my body. It now thinks everything is foreign. (Thank you uncle sam) Its been so bad from the pain and not being able to get out of the house due to pain and mental problems, I am also seeing a councelor. As well, I am seeing a rhumatologist, neurologist, oncologist, hemotologist, 2 primary care drs (both va and civilian). I am getting state aid, and help from the VA. All the doctors know it is from the anthrax vaccines, but i get no disability anywhere since it is not a real disease? And I'm still waiting for SSI disability since they are backlogged for 3 years? Its been bad, we are putting off xmas with our 2 kids until next year when I hopefully can sell the rest of my tools to buy them presesnts, nice dad huh? they are teens and understand at least.
what I am asking, is that from all this, my pain is so bad that if my family was not here, I'd have been gone a long time ago. The pain is everywhere. The drugs I am taking are maxing out and not working. I already sleep 16 plus hrs per day. I sit 1-2 hrs a day in the hottub and its the only thing that actually takes alot of the pain away.. but that is when it is working and we can afford it.
the pain is everywhere! I can tell when the weather changes since it puts me to sleep and the pain is all over. the feeling is shocking numbness to pain in the back and all extremeties. I already had c2 nerves cut on both side and it took the pain from my chest away. but I have been hearing good things about these spinal stimulators. I am to see a doctor about one, but he is booked for a couple more months. I just want to know if these units can block alot of these pains? anyone out there with lupus and polyarteritis nodosa that have one of these units? any ideas on them and what to expect and ask for. I cant take this much longer. I really dont want to take the easy way out! I want to take care of my family. thanks for your help