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Living with Neuropathy - Welcome to the group

Neuropathy | Last Active: 10 hours ago | Replies (6021)

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@artscaping

Good afternoon @carlyschneider. I'm @artscaping or just Chris. John Bishop has asked me to introduce my experience with MFR, Myofascial Release therapy. If you have seen the video in this section then you have a pretty good idea of how fascia connects everything in our bodies. When it becomes restricted or tight, it hurts. A therapist has to have very sensitive hands to be able to find the restrictions. If you have accepted your diagnosis then you understand that there is no cure for SFN.,,,,,,and that it progresses in different ways and on different time schedules for different individuals.

Five years ago, I started with MFR sessions every other week and that was enough to mitigate the symptoms of SFN so that quality of life was maintained. Now, I have two MFR sessions a week plus at-home treatments I can manage by myself or with props. I actually moved here lock, stock, and barrel in part because the MFR therapist is excellent. The other reason was that I could not handle the wildfires on my mountain.

Two realities: 1. sometimes when an area in the body needs a great deal of work, you may not feel results for 24 hours. 2. sometimes when a restriction is super tight, it does not release without some discomfort/pain. You just have to let your MFR therapist know your tolerance level and when the source of the pain has been reached. It is such a relief.

May you be free of suffering and the causes of suffering.
Chris

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Replies to "Good afternoon @carlyschneider. I'm @artscaping or just Chris. John Bishop has asked me to introduce my..."

Thank you Chris @artscaping for your insight and for reaching out. Honestly, I don’t think I’ve accepted this yet. I’m sure many on here share my story of feeling like the rug was ripped out from under them. Last year, I was a healthy, active 42 year old woman chasing my 5 year old son around, exercising regularly, enjoying hikes and my new treadmill and bam, within a year, all of that stopped. I’m still in shock. I’m still figuring out the cause and looking into treatments.

Can you tell me how you got started on MFR? Had you tried other treatments? I haven’t seen the video so I will look for it. I’m interested in hearing about everything that is out there! IVIG was recommended to me. Medications were also recommend which is a path I don’t want to go down if possible, at least not yet. Thank you again for your time and I look forward to learning more about MFR.
Carly