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Post by Linda51 on Jul 24, 2008 14:18:57 GMT -6
Okay you guys that were at the conference help me out with this question that was sent to the SCTA email address. I was at the conference but I was working behind the scenes so please help us out. Also Jennifer you may want to advise as well since you did speak on this. Thanks in advance. ~Linda
I am a 10 yr survivor of an intramedullary ependymoma, and am having problems with muscle spasticity and pain. I noticed that the recent conference had a number of sessions on spasticity, and wondered what treatment options were suggested for this particular issue. I would really appreciate any information you could share with me. thank you. Janet
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Post by Scott on Jul 26, 2008 11:18:50 GMT -6
Janet, I have suffered from severe spasticity in my feet since my first of four SCT surgeries ( T7-9 ependymoma ) back in 2001. I've tried a lot of treatments and currently have baclofen in my pain pump as it got so bad a few years back. Please email if you have any questions. I'll let you know what I have experienced and maybe that might help some. My email is Gatorshime_2000@yahoo.com.
Scott
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Post by otjenn on Jul 27, 2008 19:06:36 GMT -6
Hi Janet. After my first surgery, I had a lot of spasticity and went through a lot of different treatments. There are medications, which I found to be very sedating, tried Botox shots and then got a Bacolofen pump which has been the best - less fatigue etc - in combination with therapy including aquatics (in a warm therapy pool). Also myofascial release (www.myofascialrelease.com for more info) is great if the pain is musculoskeletal vs. nerve. any further questions, just let me know...jdwot01@hotmail.com. Good luck! Jenn
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