Here is the list
drive.google.com/open?id=1_...
Interestingly Rasagiline, Selegiline, Naringin (found in the grapefruit ) and ibogaine are among the top GDNF producers
I am already taking ibogaine, considering to add grapefruit extract as well
Here is the list
drive.google.com/open?id=1_...
Interestingly Rasagiline, Selegiline, Naringin (found in the grapefruit ) and ibogaine are among the top GDNF producers
I am already taking ibogaine, considering to add grapefruit extract as well
According to animal studies naringin itself is neuroprotective. It is available as a supplement. I tried it and found it irritating to my stomach.
I read the study iqbaliqbal referenced on Naringin and it was administered by an injection not orally. Grapefruit can enhance or minimize the effect of many drugs. I would be very careful about taking grapefruit extract unless you are sure it will not effect the absorption of your meds
I am a pwp on medication. I have been advised not to touch grapefruit in any form.
My husband has also been told not to touch grapefruit with his medication x
You may be interested in Brant Cortright's book Neurogenisis, diet and lifestyle. He lists foods good for increasing BDNF and GDNF
What is GDNF? Anyone?
Iqbaliqbal, how is your ibogain experiment going? Any symptomatic improvement? Do you still experience the feeling of well being? If so do you sleep better? Thanks.
I was feeling 80 % symptoms free after initial 5 days of use. Then I took 3 days break ( just experimentally) to see the difference. Unfortunately I could not regain the initial improvements even after resuming the dose 8 days ago. The pause broke the momentum and I am lamenting it
This just seems so odd to me. I wonder what causes this. I would have thought that you would be back to where you were after a resumption that is longer than the initial dosing period. Have decided what to try now?
I have started TA today. Will go with it for the next 3 to 4 days and if unsuccessful, will discontinue ibogaine for 1 month to reset my system
Ok. Please keep posting what is going on with you. As far as I go there has been no reoccurrence of toe curling/foot cramping other than the single mild instance that I reported. So I am suspecting it was not the TA but was because of lack of sleep or the excitement around here. Or maybe was just a foot cramp and is unrelated to PD.
Definitely I will post updates. Good to hear that TA is equally effective for you
Hi danfitz
Do you take any PD medications?
Yes. I take sinemet. I have been diagnosed for 10 years and have been on sinemet the whole time.
I should add that I have tried numerous supplements as well. The only one that provided significant relief was marijuana. I decided to try ibogaine when I discovered it stimulates GDNF production in the brain thereby offering the chance of remission. I try not to completely mask the tremor with sinemet because I don’t want to mask the feedback to the brain that dopamine is deficient. If the tremor becomes too annoying I quiet it with medical marijuana. But even when I use sinemet to completely mask the tremor I only have to use approximately 40% of the sinemet I needed to accomplish the same thing just a few months ago.
1 month break sounds like a logical approach. Do people who sell this stuff offer any insight?
They just mislead people. different suppliers advise different approaches. This is the area where the knowledge of people is extremely Limited. I am in touch with some experts on the subject they also don't have any clue. The idea of one month break is based on my own gut feeling, as this phenomenon is common with other drug too.
Plus some of them base their advice based on the use they make of ibogaine. So if they administer “flood” doses they advise based on flood dosing making no adjustment for micro dosing. When I was initially investigating ibogaine for PD one supplier recommended a 200 mg dose to start. That would be right for an initial flood dose but at least an order of magnitude too much for micro dosing. My neurologist got a good laugh out of that.
When do you have next appointment with your Neurologist. Can you ask his opinion about my case
Do you mean about the stop/restart?
My neurologist did not recommend ibogaine to me. I just felt I should disclose my plan to them and was surprised when they were interested and spent some time reading and commenting on some of the information I came up with. And I am certain they would not recommend ibogaine for any purpose given the state of the research. I am just lucky they are interested enough to listen and comment. It simply may be their desire to know what their patient is doing. That is good enough for me.
iqbaliqbal, here is an interesting link that talks about various plants used to treat symptoms of PD:
jarcp.com/614-review-of-nat...
They don't mention iboga but still they offer lots of interesting data