45 years post-op spinal fusion w / harrington rod.
Hi I'm new to this site but not to the pain that I know many others go through. A little background I, was fused in January 1976 at 15 years old in Shriners Hospital for Crippled Children in Phila. PA . I have had all kinds of procedures and rx's over the years ,you name it, I have probably tried it. I am now 60 and along with the earlier problems now I have "OLD" problems added to existing and worsening ones. So is there anyone who has found relief with newer treatments? I had an ablation done as my most recent procedure but it took me a year to overcome the pain and numbness and weakness and at times unbearable cementness it felt like . Even my pain center said my condition was" bizarre"!! Not something you want to hear come out of your pm Dr.'s mouth. Needless to say I am very weary of a lot of things , I am open to all info, thanks for letting me ramble. D
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I live alone and have had multilevel fusions, both lumbar and cervical spine, 2011, had them 6 weeks apart. Other than having someone with me that first night I went home, I was ok. I’m pretty used to being alone. I DID need a housekeeper!
Curious, does your insurance pay for that? I can’t afford a massage weekly, doubt I could afford that out of pocket. It’s a sad commentary on healthcare in America. N.B. For me massage is therapeutic, not a luxury.
I find this myofascial release therapy interesting. I also had a spinal fusion down my back for scoliosis in 1975 at Fairview Hospital in Minneapolis, MN when I was 17. In 1978, they did it over again because there were spots down my spine that hadn't fused. I had Dr. Moe, who actually studied under Dr. Harrington, who the rod is named after. My back has been fine, but I have a lot of pain on my tailbone and rectal area and across my buttocks that has been diagnosed as pudendal nerve pain. I've had this for 13 years now . . .I really try to avoid sitting at all! I have recently started on gabapentin but that doesn't seem to be working. I had pudendal nerve entrapment surgery in 2010, but that only took the pain away for 7 months. I guess now I am starting to wonder if this pain could be coming from my scoliosis surgeries because my rod went down to either L-4 or L-5. I either stand or lie on ice. . .the pain can be more than I can handle somedays.
@wisco50 Myofascial release isn't massage. It's considered manual therapy and my PT codes it that way. They write codes for 15 minute increments or units of treatment, and she also does a few other traditional PT things in the session. My insurance does pay for it. I suggest ask your provider what the codes would be and then call your insurance to see if they cover it and check if they are in network. You can also ask your provider for a cash price. Submitting to insurance is complicated because of the "in-network discount" which cuts the payment down a lot to a negotiated rate which is a contract when the provider becomes an in network provider. Sometimes a cash price is about half the retail price which has to be set higher because of the discounts.
@toula Myofascial therapy might be worth looking into. It is so beneficial to a lot of conditions when our bodies get stuck. Other issues that may affect that area could be pelvic alignment. Here is an article that gets pretty technical written for physical therapists that has a section about pundental nerve entrapment that describes the piriformis muscle as a contributing factor. My PT has me stretch my piriformis, but that should be something to ask your therapist about because of your back surgeries. This article describes various issues that cause symptoms similar to back problems that are caused by the pelvis.
Here is an excerpt from https://mskneurology.com/identify-treat-lumbar-plexus-compression-syndrome-lpcs/
"Most of the time, the pudendal nerve will be “double crushed”; first by the piriformis, and then between the falciform process of the STL and the obturator internus."
Aha! Worth trying, having ankle issues from a previous significant injury and thinking I likely have scar tissue in there. It was 6 years ago and betting it’s that and possibly arthritis from injuries sustained.
I equated it with massage because my previous long term WONDERFUL massage therapist did do it, I would be able to feel it sliding, especially on my upper and lower back areas. I’ve actually had another one who did it also. That one moved away and my last one left MT to become an RN. Haven’t found the right person since, sadly.
@wisco50 I think you are on to something. Remember to find an MFR therapist PT in your insurance network, call them and ask about the codes for manual therapy, then call your insurance to ask if those codes are covered. Discuss this with the therapist as they know how to document this for the insurance notes. I hope you can find a good therapist. Here is a provider search. http://mfrtherapists.com/
Come on back and share your progress when you can. There is also a lot you can do to self treat like laying on a couple balls. Put them where the tissue is hot, hard or tender. I sometimes use a foam block against a doorway and I press my body into it and push up to cause a shear. It is the shear that starts the fascia sliding. You can Also have a friend help if yo can give them instructions.
This is not spine related and maybe I should go to a different page, but you seem to know a lot about this myofascial release therapy. I have been having these partial bowel obstructions that are caused by scar tissue on the outside of my small intestines.. I have had surgery to remove this scar tissue, but as soon as 6 weeks after surgery, which includes 2 hours of cutting away scar tissue, the new scar tissue starts to form. Most of these partial bowel obstructions I can handle at home, but I get very dehydrated and I’ve had to go into the hospital several times and have an NG tube put in and go on IV’s for liquid..I can’t usually put anything but popsicles in my stomach at home because of these. Do you think this myofascial release therapy could help with the scar tissue that causes these to occur? I never know when one will hit..just went a year without one and have now had two in the last 6 weeks. They are painful, involve vomiting and diarrhea and land me in bed for 5 days before I can put anything down in my stomach again..going on a liquid then soft diet. Just wonder if this works on breaking up any scar tissue??
@toula Myofascial release does break up surgical scar tissue. It may take a bit more work and more sessions, but it helps. I have had neck spine surgery which makes a tight scar and I and my PT periodically stretch this to release the fascia. I think it may be worth trying. You might want to look for an expert level therapist and discuss this with them. This summer, I spent 3 months not being able to walk because of a broken ankle and spent too much time sitting which caused some issues with overly tight hip flexors and my guts getting adhered to my body wall. My PT was able to treat that and resolve it. It is amazing how everything is so interconnected, and when you stop moving and maintaining good posture, it causes problems. A therapist will be able to feel where the issues are.
Thank you so much, Jennifer Hunter, for your input on this! I am interested in exploring this further!