This is a bad decision. You make yourself a judge and jury of all recommendations Made on this formn. What qualifies you to make These decisions.? You acknowledge that you’re not a doctor And even if you were information contained here in this forumn Is so varied and Can envilve such complexity That no doctor could effectively advise. We are all big boys and girls here and realize clearly that it is reader beware This is the very nature of forum
Your decision has reduce the value of this forUmn
Sorry couldn't understand what you want to say. sorry for low IQ
Have I missed something
Sorry I posted where I should have responded to the post regarding removing Dr. Costantini b1 be info. So much for using a smart phone 
Pat man 60,
We are all saddened by his decision and I can see some of us are hurt and maybe even angered, but we need to be careful not to condemn him for his choice.
Actually, if I remember correctly, Easilly was not affected by Parkinson’s disease. I didn’t understand his passion for the B1 protocol and this surprising post using a new assumed identity doesn’t pass the smell test.
I do NOT have PD or any other neurological disease. My son for almost 3 years was under a dx of PD....later it was changed to PSP. While under the belief of PD, as his caretaker, I was an avid reader of this site.
Perhaps I have not interpreted Easilly's (safetyfirst) recent post correctly. My interpretation was an announcement to us that he was taking down a site, HE HAD ORIGINATED and his reasons. I believe/understand we each are entitled to do that.
Each of us can still use Vit B1hcl, we can each read shares and posts by others on Vit B. We can each do research. What we CANNOT DO is access the site where Easilly did all the work for us.
I think my husband may be misdiagnosed with PD, can you tell more about your son's experience? Thanks
Hi, at the beginning of a brain nuerological disease, almost always the DX is parkinSONISM. What happens is that we hear Parkinson's. My son's nuero dx Parkinson's and told him it was a very liveable disease. Since the symptoms of almost all neuro diseases are usually the same (but not always in the same order of appearance) it is given the label of ParkinSONISM.
My son's nuero skipped the "sonism" and went direct to "son's"
My son's symptoms continued to progress and multiply. At the end of the 3rd year it was changed (re-dx) by a different neuro to Progressive Supranuclear Palsy (PSP).
I would encourage you to watch on youtube Jim Bower of the Mayo Clinic, "MAKING A DIAGNOSIS OF PSP, CBD, OR MSA". It's well worth the watch.
No diagnosis can be proved/confirmed until death with a brain autopsy.
I hope I was helpful.
Los Angeles, CA, USA
Thank you, yes very helpful.
The good news is that the posts themselves are still on this forum. They can still be obtained through the search function...
That will not last long, Jim. Somebody big is after him and finds a commercial threat to his work. Think chess, the first move is the first in a long, thought out strategy. His influence will be systematically erased. You never read 1984 and "unhistory?"
Also I suspect that we will not see or hear from Dr. Costantini again.
😂
Synaptic misfire?
This has all gone far enough. Why don’t you put in the work that Art did? You are an ungrateful lot.
Decision Time
New to this site 
The joy of being a bad drummer
Oh why is this disease......................
