Intro first... I'm 41 (tomorrow!) and my CP problems began (officially) six years ago. I have DDD with very "messy" C5-6 & C6-7. My second MRI, just done in June used the word "obliterates" in reference to C6-7, among other descript
ors... This one is actually herniated, C5-6 is still hanging on, I reckon, although it doesn't look much better.
Anyway, the short version is that I have been with my (first!) PM doc since '06 trying the myriad of 'tools' he has to offer in an attempt to learn to live with this pain. Currently, I am on Fentanyl patches w/ Oxycodone, Neurontin, Robaxin, Topomax (weaning off); I use a topical cream w/ ketamine, ketoprofin (sp) and some others in it, can't remember at the moment, I have a TENS but I mostle feel more sore when I use it. In the six years, I have tried ESIs, facet joint injections, trigger point injections... My doc is wonderful with always suggesting options and working with me, I consider myself lucky, especially since he was the first, and only, PM doc I've been to.
I've been lurking here for a couple of months and decided to take the plunge! I must apologize for typos... I'm using an on-screen keyboard and I find it makes me appear much more illiterate than I really am, so I ask for forgiveness in advance!
The disability question... I am a teacher. This is sort of my second career, after being fortunate enough to stay home for a couple of years when I had my third child (I have three kids - ages 13, 11 & 9). Since the CP issues have gotten worse, my days, naturally, get worse. Last year was particularly awful. I had to come home every day, during the day, to have my husband put the topical on my back (we only had one car then and still, financial reasons). I don't get *that* much relief from the topical, but enough to take the edge off for a few minutes!
Well, this year has started back and it is even worse! To sum it up, I spend my day consumed with the pain! How effective can I be in the classroom when I am in that state? This leads to me coming home, going straight to bed on the heating pad (the Robaxin makes me too sleepy to take during work), which leaves absolutely nothing of me left for my own kids! I find myself becoming resentful in many ways and I just don't like it!
My PM doc has referred me to a neuro surgeon. He made the referral early summer, as the pain is simpky getting worse and radiating. However, after getting the MRI report, he felt that he could address the pain with injections (it didn't work). He still wants me to get the surgeon's opinion... I want to talk more with my PM doc before I see the surgeon (I have PM appt on the 10th), since I haven't gotten to talk with him since the results of the MRI (I saw him, but it was for injections).
Anyway, I do have disibility insurance that I have purchased thru my work, but I don't know how it all works. Do I look into short term disability now (some days, I struggle to get out of bed, thinking that I JUST CAN NOT do this right now!). Do I ask my doc if he will "disable" me? Do I just stop working, then submit the papers and hope? I am the only income right now. My husband is currently out of work and trying to find something.
Sorry this turned into a long novel! It is just all so scary!! Oh, and thank you all for being so supportive to each other! I offer the same 'feel good, light pain' thoughts