The state of Amy
Jun. 21st, 2007 09:59 pmI am going to the doctor in the morning, to see if I can't pinpoint the cause of my pain. I suspect it is MS related, but I think it would be easier to check for arthritis or whatever first, before we go for the MRIs and stuff. I can't wait for treatment any longer, since I can barely move my left arm without searing pain, and a lot of my other joints are aching.
To be honest, I can't even remember the name of the neurologist I was seeing before, and didn't feel any big connection with her. I have done some research online to find a neuro covered by my plan, and will ask my doctor about my choice while I am there tomorrow. I need someone I have some sort of rapport with, and looked for the ones most recommended by my plan (meaning that they have actually been checked out). I won't go to Dr. Killian again, since he is the one who completely botched my spinal tap when I was first presenting symptoms. (He did it in his office exam room and had the wrong sized needle, and tool THIRTEEN tries to get a sample that he said he was not happy with because there was blood in it.) After the last time I saw him, I was so traumatized, that I didn't go to another neuro until I had another major episode.
Anyway, I am not sure whether to hope it is arthritis or MS or something else all together. Either one would suck, and I don't know how they would treat either one.
Also, my fatigue is out of control, even with the Adderall that I've been taking. I have extreme trouble staying awake during the day, no matter how well I sleep the night before. I often nap for two or three hours and feel drugged all the time. Another unfortunate symptom of MS that gets worse with the heat. I got excited today, because this is the third day in a row that I didn't take a nap at all, then felt depressed, because it's sad that that is a major accomplishment for me.
After my appointment, I may be sitting around waiting for x-rays or something...I don't know. I am hoping it's a simple fix, and that I don't have to have a huge dose of Solumedrol and course of Prednisone to try and get it under control...steroids have the worst effect on me.
Anyway, that is enough whining.
To be honest, I can't even remember the name of the neurologist I was seeing before, and didn't feel any big connection with her. I have done some research online to find a neuro covered by my plan, and will ask my doctor about my choice while I am there tomorrow. I need someone I have some sort of rapport with, and looked for the ones most recommended by my plan (meaning that they have actually been checked out). I won't go to Dr. Killian again, since he is the one who completely botched my spinal tap when I was first presenting symptoms. (He did it in his office exam room and had the wrong sized needle, and tool THIRTEEN tries to get a sample that he said he was not happy with because there was blood in it.) After the last time I saw him, I was so traumatized, that I didn't go to another neuro until I had another major episode.
Anyway, I am not sure whether to hope it is arthritis or MS or something else all together. Either one would suck, and I don't know how they would treat either one.
Also, my fatigue is out of control, even with the Adderall that I've been taking. I have extreme trouble staying awake during the day, no matter how well I sleep the night before. I often nap for two or three hours and feel drugged all the time. Another unfortunate symptom of MS that gets worse with the heat. I got excited today, because this is the third day in a row that I didn't take a nap at all, then felt depressed, because it's sad that that is a major accomplishment for me.
After my appointment, I may be sitting around waiting for x-rays or something...I don't know. I am hoping it's a simple fix, and that I don't have to have a huge dose of Solumedrol and course of Prednisone to try and get it under control...steroids have the worst effect on me.
Anyway, that is enough whining.