3W4DW – prompts: chronic/invisible illness; sexual abuse
Here we are again back where we’ve been before. The landscape looks a bit different with less fog. Clarity would only be helpful if it created momentum yet here I am back where I was years before.
With the recent resurgence of the neck issues via the discs that have shifted over Gods knows how many years it appears I do have to consider the idea that surgery may be in my future. This saddens and terrifies me.
Physical therapy did wonders for it. The continuation at home has kept my back fairly consistently at the better level than it was when I began. Except when something untoward happens in my neck. When that occurs it sets everything a bit off down my back, through my left hip and oddly my right knee. ( I seem to recall that my right knee was jacked anyway.) But still, the back fares far better than it did and the stretching undos whatever goes off. *is very pleased*
Though I am grateful to be one of the chosen lucky enough to have health care coverage, the details of it right piss me off when it comes to PT. I understand the mindset of insurance companies that dictates more $$$s for them than for the medical field, thus a restriction on benefits. It is the way they restrict. My insurance is 60 days for "X" condition per calendar year. Got it. However, it is "60 days from first day of PT for ‘X’ condition" regardless of how many times you go. So theoretically you could go a gazillion times, or once, in the 60 days.
My opinion, which granted fits into the "best for me, not for the insurance company" category is that the benefit should be "60 days/sessions per condition per calendar year distributed any damn way just do not exceed 60". This is one reason I am not running insurance companies. Our old insurance did it that way, but I didn’t need the benefit. <insert laughter here> If such were the case for my current insurance I could do one visit per week and not even exhaust the benefit and when combined with the stretches I do at home live virtually pain free Every. Single. Day. That would be deliciously awesome, yes?
So that’s where I am at. Without the manual therapy I have a few choices when the neck returns to its previous state:
1) Sit in a chair and wave at life as it goes by (tried this briefly in early Fall and decided I’d rather eat a bullet)
2) Just continue on doing what I’m doing AKA living my life and hurt like hell some days
3) Go back and consult with the neurosurgeon with the idea of being open minded to surgery at some point
Number 3 is the one that feels like volunteering to die. If the dying felt merely like it would physical death (and there is that chance and fear considering my prior experience with surgery) I might be able to get on board with that. But the death is more than physical ~ emotional, psychological ~ pieces that if they die will change everything and it feels like not for the better.
First let us address the rational fears. Well now that builds confidence. Feel free to Google it yourself. There are many testimonials for the wonders of neck surgery. They are on the surgeons’ web sites. *cough*
The reason this has reared its head again is because I’ve been doing my stretches, I’ve been mindful of my body and its limitations in spite of the "ugh" factor such a mindset invokes and somehow I still saw the return of the ouch in my neck and the knife stabbity pain down my upper back. *scowl*. I’ve been tending the other parts of me by eating properly, resting appropriately, minding my spirit and utilizing laughter daily. I’ve played "we are dreaming". I cannot pinpoint what particular activity triggered the renewed onset of symptoms. I can semi-pinpoint 3 separate incidents that occurred over a number of days that collectively may have contributed yet none of them were OTT for my health. What I cannot do is point and blame. It would be better if I could like when I lifted the organ, or the treadmill, or painted a bunch of ceilings. Because when you can point and blame you can then avoid the activity or movement that caused the pain.
Addressing the (called by others) irrational fears is decidedly difficult. I do not consider them irrational. I consider them safe and sane. I attempted to talk to my husband about these fears surrounding the recurrence of pain, the recurrence of the pins-and-needles bother running down my arm and through my hand (since subsided) and my wondering out loud about surgery.
I mentioned needing a pass until after the wedding in October because it would suck to be paralyzed for it, or dead. I mentioned that I didn’t want to spoil their day that way. (I really really really do not want to spoil mine that way, either.) *imagine look of horror on husband’s face* People who know me will think I was merely deflecting with sarcasm. Nope, not this time. He said, "Well, we don’t want to think way!" I replied, "Yeah, because the last surgery went so well." He responded, "True, but ….." Me: "But…… what is there to make me think this time would be different, except maybe ‘different’ equals dead?"
The backstory it is long, it explains much