Can you tell me what dosage you are on and what type of pain it help you with?

That is what ketamine was supposed to help with the brain and reseting it so to speak.
I have tried many meds like neurontin and though I thought they were not helping they may have but it just seemed not enough. Sometimes it is hard to know. I have never heard Namenda I am going to look that up. Glad it is helping

Namenda has had a colorful past. It was used in Europe for nerve pain, but when it got to OUR FDA, it was only approved for Alzheimer's treatment.

We used to discuss it back when at our old home at BT.

I believe some posters on RSD forum here use it, or have used it.
So do a search there for the posts.

I get 37 posts with that keyword Namenda:
example:
http://neurotalk.psychcentral.com/sh...hlight=Namenda

I cannot post the search string, as it expires on the boards. You have to do that yourself, I'm afraid.

The generic name is memantine... searches are fewer for that version here. But if you decide to search Google or PubMed especially use memantine. You get better hits on PubMed using the generic names for drugs.

I have done research on it and its a mixed bag. Some get good response and some not. You can say that for any drug and since everyone symptoms and causes are different the only thing you can do is try it for yourself.

The only thing I have noticed with Namenda is that I've seen people go up to 55mg which the normal most docs give is 20mg.

haha - I should have typed "it has helped with my Allodynia pain!" But of course I forgot - I guess they need to up my dose! I am only on 10mg 2x a day. But before I started taking the Alladynia once the pain started it would not back down and I would be miserable and hit 9/10 pain levels every night for hours. Now if I become active and my pain begins to rise if I sit down and rest the Allodynia pain levels will recede and I can begin again. All of it cannot be just contributed to just the Namenda because I had had some Ketamine before the Namenda - But the largest part is due to the Namenda by far.

thank you for the update. One last question. How long were you on the med to notice a difference?

About 3 weeks I‘d say. Maybe a bit more or less . It’s really hard to remember but I do know it was a couple of weeks or so. But once it started to really work it was recognizable at once. I could feel a difference quite readily.

I still got/get Allodynia, but I was amazed at how much the Namenda took away. I also still have many other types of "pain" and PN symptoms. Unfortunately there has not been any medicine to help all of my symptoms a lot. Instead, I have a lot of medicines that help a little, and Namenda that does a decent job on the Allodynia - especially for recovery. That was the most beneficial to me. Because like said before, it used to be that when my pain got high it stayed high until I fell asleep, now if it will recede.

I never read up on it once I got the presciption; I didn't want to bias myself in any way. I just waited for the results and since they were positive I never looked into it. So you have found out that others did not have a very positive experience? I am so sorry about that ... It has really helped me for this sort of pain. Well good luck

Yes, two drugs are Nuedexta and Namenda that people are getting benifit from.

Some say it does nothing while others like you say it works well.

What sort of symptoms do these drugs help? Just allodynia?

They can also help with pain in general since they work on the NMDA receptors.

There is one other drug that works on Allodynia.

Called Neurotropiin. It's been out in Japan over 30 years and testing in NIH for 10 years.

I spoke to someone who has CRPS and she said it reduced allodinya by 40 percent.

http://clinicaltrials.gov/ct2/show/N...otropin&rank=2

I tried to apply for trial but you need to have CRPS.