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09-22-2022, 02:49 AM | #1 | ||
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Newly Joined
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Had a foot procedure in 2019 which ruined me as I developed peripheral neuropathy along with CRPS.
The surgeons don't seem to know how to treat it which is discouraging. Feel like a cripple especially since I used to walk for miles, and now just 'hanging on' to what's left of my life. Any suggestions would be welcome. |
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09-22-2022, 08:32 AM | #2 | ||
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Grand Magnate
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Welcome Louise54.
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Kitt -------------------------------------------------------------------------------------------------------- "It is what it is." |
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09-22-2022, 09:30 AM | #3 | |||
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Welcome, we have a RSD/CRPS forum and a PN forum - both havet sticky threads with helpful info , or use our site search for finding specific topics.
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Search NT - . |
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09-22-2022, 10:56 AM | #4 | |||
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Welcome, Louise54!
You've really had a radical change in your lifestyle, and that is difficult to put it mildly. I wonder what foot procedure did this to you? Was it surgery of some kind? And that was 3 years ago? I hope that something can be done to help you and wish I could say something more helpful. But as Jomar pointed out, if you look into the resources here, you'll find useful information.
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Repeal the law of gravity! MS diagnosed 1980. Type 2 diabetes, osteoarthritis, osteopenia. Avonex 2002-2005. Copaxone 6/4/07-5/15/10. Currently: Glatopa (generic Copaxone), 40mg 3 times/week, 12/16/20 - 3/16/24 |
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"Thanks for this!" says: | Kitt (09-24-2022) |
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