← Return to Parsonage turner syndrome *
Discussion
Brain & Nervous System | Last Active: Aug 4 7:56am | Replies (239)
Comment receiving replies
Replies to "Hello good people. I have been diagnosed wit pts for about 4 months now. Im a..."
Hello! It’s funny that I was reading online this morning about surgery for PTS. It’s the first time I’ve ever seen surgery for it. It was always take your pain meds, wait it out, and hope for the best. This is from the Hospital for Special Surgery (HSS) website:
With exciting new MRI and ultrasound imaging protocols, we have identified tiny twists or 'hourglass' constrictions inside nerves that were previously healthy, allowing us to diagnose patients more quickly and predict those who may not recover," said Dr. Scott Wolfe, chief emeritus of Hand and Upper Extremity Service at HSS. "In order to save the affected muscle, we’ve identified surgical techniques that release the nerve and restore function in a matter of months."
You can read more at hss.edu and then search for Parsonage Turner Syndrome. I hope this helps you and others. It’s always best to check with your doctor first. Good luck!