Specific ALA Recommendations Needed

Posted by cecelia19 @cecelia19, 1 day ago

I’ve been taking ALA 600 mg since August after my PN exploded to the next stage. No neurologist I’ve seen, even at a major medical center will answer me
1) R form, S form, or combination (their answer is always it doesn’t matter, just make sure you take 600mg).
2) Brand
3) Does it matter if you take it with or without food?
4) Time of day
5) Is there any benefit to taking more than 600mg?

I take two 300mg (total 600mg) of a timed release “S” form but I will gladly change to anything that will be the most beneficial. As I understand it, ALA treats the underlying nerve condition rather than just mask the pain. My goal is to stop or slow the progression of my SFN. Since no neurologist has been able to give me answers to any one of these questions, does it truly not matter which one I use?

Interested in more discussions like this? Go to the Neuropathy Support Group.

My neurologist recommended (1) 600 mg ALA per day... not sure if time of day is important or with?without food. My symptoms are so severe in my feet Im not sure if I could feel any benefit. My best OTC product is CBD/THC cream to settle the nerve agitation. Hope this helps.

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Thank you for your help. I have a topical from Mary’s Medicinals but it is more of a balm than a cream and hard to spread. Could you tell me what brand of cream this is?

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@groverb24

My neurologist recommended (1) 600 mg ALA per day... not sure if time of day is important or with?without food. My symptoms are so severe in my feet Im not sure if I could feel any benefit. My best OTC product is CBD/THC cream to settle the nerve agitation. Hope this helps.

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I also have severe neuropathy like you in both my feet.
Can’t even stand on them at times without wobbling, and they hurt me every day.
Please let us know if the ALA helps you if you take it.
Thanks!

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I have heard the R form is better and have been taking ALA of all forms for almost 8 years. It has helped me. I take mine at night to help minimize symptoms while sleeping. Capsaicin neuropathy creams have helped but can’t recall the brand names. There are lidocaine creams and Rollins that can help temporarily, too. I like the Salonpas brand. I also take Acetyl L Carnitine supplements which are known to help neuropathy, too.

Here are the creams I just ordered on Amazon.
https://a.co/d/fcZrbNH
Here is the brand of combined alpha Lipoic acid and Acetyl l carnitine supplements I also recently bought.
https://a.co/d/6bk913I

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I have been taking two pills and a foot cream that have helped me significantly. They are: Nervive, which has besides B12 complex 300 mg S-ALA; 300mg Immunovite R-ALA and Mama Bear Oasis cream, which has magnesium in it. It sounds crazy but it seems to really work for me. Give it a try. In any event my understanding is that S-ALA is “synthetic “ and not as effective as R-ALA which is a natural ingredient!

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@dlydailyhope

I have heard the R form is better and have been taking ALA of all forms for almost 8 years. It has helped me. I take mine at night to help minimize symptoms while sleeping. Capsaicin neuropathy creams have helped but can’t recall the brand names. There are lidocaine creams and Rollins that can help temporarily, too. I like the Salonpas brand. I also take Acetyl L Carnitine supplements which are known to help neuropathy, too.

Here are the creams I just ordered on Amazon.
https://a.co/d/fcZrbNH
Here is the brand of combined alpha Lipoic acid and Acetyl l carnitine supplements I also recently bought.
https://a.co/d/6bk913I

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Thank you for sharing the information.

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