Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)


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Old 02-18-2016, 09:20 PM #1
swimtime swimtime is offline
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Default Magnesium for CRPS

For those of you taking magnesium for CRPS, what have you found to be the most effective form? Dose? Also, has anyone heard of magnesium infusions being used to treat CRPS?

Since ketamine isn't an option, I'm looking for alternatives for our teen son to help him regain his mobility.
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Old 02-19-2016, 04:54 AM #2
BioBased BioBased is offline
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Before I was diagnosed with RSD and I had few pain control options, I took a combination of magnesium glycinate and malic acid. This particular combo was mentioned as being helpful on a fibro support site.
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Old 02-22-2016, 11:58 AM #3
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Swimtime,
Sorry I saw this so late. I take magnesium supplements daily as recommended by Chopra and my doctor. Chelated magnesium is suppose to be the most highly absorbable by the body. You can purchase it on Amazon for about $10.00 a bottle. Here is an article that might interest you http://www.drugs.com/. It is a supplement not easily absorbed by the body. I also try to get it from food sources.
II have also had 4 magnesium infusions. My doctor uses it with ketamine. He also says the infusions are more readily absorbed.
All of this having been said, I don't know if it is helping. It's hard to say what it would be like if I hadn't started last September. A lot has been tried since that time and nothing is working very well. I figure with supplements it won't hurt and OTC pills are not expensive. Also, with supplements they work slowly and build over a long period of time. For what it's worth, that is my experience thus far. ~mac
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