deuce
I can offer you a bit of a story around why I have stalled on GcMAF- for what it is worth.
I have my MAF 878 from Dr Enlander sitting in my fridge. I was hoping on giviing it a 'go' as I thought it may cause a less inflammatory response.
The reason I haven't trialled it yet is because I am still SO inflamed!
I have tried in vain over the last 6 months to get the inflammation down, but have had no luck on any of the supplements- in fact they all make me feel worse.
I am currently taking some bile acids that my dr suggesed due to some bad bugs in my gut- and guess what - more inflammation!
Also, my big and surprising news is that I have had a recent ( last week) diagnosis of lyme - borrelia, and I live in Australia, like you. Who would believe? But there is no mistaking it as it is a positive result from a PCR test.
In fact the lyme and possible co infections (I have some more test results that are still pending) may help to explain my impossible reactions to tiny doses of GcMAF.
So for now, I am waiting to see if I need to treat the lyme and co infections - get the pathogen load down a bit and then try the GcMAF again.
Like everyone else, this is turning into a long, painful and hideous process. I hope that a treatment pathway emerges soon, that I can stick with. The treatment options are going to be had to decide on, but I am researching that now.
I think until you have been on the MAF for 3 months it will be difficult to see the results. Perhaps just hang in there, if you can.
