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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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07-22-2013, 03:58 AM | #1 | ||
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Dear friends - I have been taking ALAmax CR from Xymogen as recommended by Dr. Sajben. Could other RSD sufferers please share their thoughts on what they have found to be the best alpha-lipoic acid for us? Maybe there is a thread on this you could point me to? I am now looking at some other options. Tx!
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"Thanks for this!" says: | AZ-Di (07-22-2013) |
07-22-2013, 02:44 PM | #2 | |||
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I've heard of ALA but not for CRPS. I'm anxious to hear about how it may help. I take magnesium (helps nerves and muscles) and vitamin C (supposed to help prevent spread) along with some usual RX meds.
Thanks for sharing! |
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"Thanks for this!" says: | CRPStweet (07-22-2013) |
07-24-2013, 04:06 AM | #3 | ||
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I have also heard doctors sometimes recommend Acetyl-L Carnitine ALA for RSD. I would greatly appreciate hearing from other RSD patients reading this. What form of ALA have you found to be the best recommended option for RSD? Thx for sharing!
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07-24-2013, 05:00 AM | #4 | ||
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Interesting related link:
http://www.healthyvim.org/Neuropathy...lor_Slides.pdf |
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"Thanks for this!" says: | Djhasty (07-29-2013) |
07-24-2013, 11:27 PM | #5 | ||
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Quote:
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07-29-2013, 03:50 PM | #6 | ||
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I have gone through many procedures and meds over the years and have decided to go with natural means also. I am currently taking *admin edit* essential oils. I have been taking the *admin edit* for three months now. I feel better mood wise and have improved my range of motion. They have other oils and creams as well. *admin edit* for info. Let me know if you have any questions. Prayers and soft hugs.
Last edited by Chemar; 07-30-2013 at 06:04 AM. Reason: No MLM marketing allowed here |
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