I have learned a few things that get me through the day. My Vagus Nerve was damaged in the process. Look it up, the funny thing is it controls everything that you do daily, from blinking your eyes to pain! A Neurologist suggested I do exercises to stimulate the Vagus Nerve. Cold Plunges will activate it, but not for long once it has been damaged. You have to be constant in trying to find ways to activate it. Needless to say, I have tried everything. I have researched lots of possible remedies and found that so many of the symptoms are mimicking a lot of different possible conditions. I know when mine started, but my EX Primary Care labeled me on day one after my Surgery on my eye. He did admit the Concussion might have damaged my Vagus Nerve, but instead he put me
on Ativan, the worst thing he could have done, following a Concussion. I took myself off that poison. He did not like me asking questions and we got off to a rocky start. Well, it followed me if I went to the ER in pain, they literally wrote me off. I am sure they read his notes and it was immediately noticeable. I did not give up, I saw Doctor after Doctor, made my own way and that is difficult when it comes to referrals. I have a new Primary Care Doctor, she is listening and trying to help me in any way she can. I have spent thousands of dollars trying to find someone, to at least try to get to the root cause. There are a lot of Docs out there, that promise you help and in the end, you are just another number. I too have been
to numerous pain managements and the last one told me to put a Lidocaine patch on it and she would see me in 8 weeks. Such a frustrated scenario! No one seems to care anymore.
Unless this is happening to them or a member of their family, your pain is just another condition for a Lidocaine Patch. Our Health Care system sucks and I say that literally. I do believe there is a plan to " not" treat chronic pain They don't have the time nor the resources; because mega healthcare systems are dictating what they can and cannot due according to your age. A Spine Stimulator might help me, but according to Insurance( another pothole in Healthcare), I have to be evaluated and approved.( You should ask about a Stimulator for your current pain, might be the answer for you.) I guess the Lidocaine patch will be my Stimulator. I know I have some curvature of the spine, herniated thoracic disc, lower lumbar
osteoarthritis, spurs, sciatic pain and recently had hip replacement with one leg an inch shorter than the other. To tell you the truth, I will never give up. I am going to find out what is wrong, even if it kills me! There is an answer and I know it will be a simple one, because if it were Cancer or some debilitating disease I would be dead by now. I hurt on the right side and it is always there. Stay away from pain meds, they will destroy your Brain and
that will be the end of you. Hang in there! Maybe our future pain Management will be
"AI" ,at least it is not biased in any way shape form or fashion. I have tried everything, but not giving up and neither should you! You are your best Advocate, because you are the one in pain and only you are living it! Take care.