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Is Anyone Living With Bertolotti Syndrom Or Sacralization?
i got diagnosed with this syndrome after 10 years of having pain and surgery. its very funny i met dozens of doctors in my country and dozens in Germany and no one could identify the extra bone stick to my L5 vertebrae. i had to find it myself, search it myself and spoon food the idiot doctor to finally admit it
i was born with it and i tried almost everything too much time adn money are wasted. it requires another surgery but i dont wanna. i just can't have another 50/50 surgery and the pain⦠read more
First time ruptured disc. Second take out bone and clean up. Third was narrowing of the spine. Next was going to be a fusion but I stopped there. Able to get around with a cane and that is fine by me.
Same thing happened to me. After first surgery that didn't work is when they said I had an abnormal bone growth they didn't see before. Pain was horrible. Yes have the surgery. Not pain free but much better.π
sorry to hear that
what kinda surgery did you have? resection or fusion?
Me!!! I was diagnosed last year with type 4.
Does Anyone Else Have Bertolotti Syndrome On Here?
Is Anyone With Ehlers-Danlos Syndrome Willing To Talk With Me?
Hi Has Anyone Done The Qutenza (capsaicin) Treatment To The Feet For Neuropathy, I Am Going To Be Doing The Patches. 4 My Feet
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