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Sacroiliitis
mandy macrae
Wednesday, January 28, 2009 at 01:26 PMre: Sacroiliitis
Anonymous
Wednesday, June 24, 2009 at 04:40 PMI would not recommend an SI joint fusion, all the patients that I have seen that have had this performed have increased pain, I have not seen any patients whom this has helped. Cortisone injections under a fluroscope, Radiofrequency lesioning of the SI joint, or Prolotherapy have better outcomes than surgery.
re: re: Sacroiliitis
Mandy
Thursday, June 25, 2009 at 06:23 AMre: Sacroiliitis
Raven Star
Thursday, June 25, 2009 at 09:33 AMI've also had; fluroscopic Radiofrequency lesioning/ablasion in my Lumbar. It's supposed to work 6 Mos. to a Yr. or so. I've had this proceedure done approx. 4 times. Each time it seems it doesn't last as long as the previous. I would like to try the pain pump but the pain Dr. thinks thats a last resort option. I have a TENs Unit & it seems to help me some, as well as medications. Yet I am still in pain daily.
re: re: Sacroiliitis
Anonymous
Friday, September 04, 2009 at 07:30 AMI agree with this statememnt. I had the SI Joint infusion last Aug 0f 2008 and I am worse off now. I went for the fluroscope injections again yesterday. I was having these injections in 2007 then my Orthopedic thought the surgery may help me, but the pain is now worse after surgery and I am in constant pain.
re: Sacroiliitis
Stan
Monday, August 03, 2009 at 01:15 AMI had a total hip replace, rt side, in March do to a motorcycle accident I had in 1972.
I have also been diagnosed with a degenerative disc at L5 and buldging disc at L4, nerve damage at L5 S1 with no nerve root compression. I have sinced been diagnosed with sacroillitis, can't sit or stand very long. I had a SI Facet injection on July 28th and so far it hasn't done a thing. Percocet 3 times a day takes the edge off but not enough. Not sure what the next step is going to be. Getting tired of this as I have been on disability since April 2007.
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You can also have a sacroiliac fusion which i have had but unfortunately it didn't work for me.
I was diagnosed 6 yrs ago but due to the severity i can not be cured and i have been left permanently disabled and requiring a wheelchair to move.