Open offer to all on CD forum

[e13 boy]

Hi all,

To hopefully show you all that i am 100% genuine.

My website went on the web approx 7-8 weeks ago.

If anybody would like me to forward a few e mails i have received from CD patients taking AMP please feel free to send me your e mail address & i will forward them to you.

My only aim is to hopefully stop people going through the hell & agony i did.

Best Wishes

 

[handle]

I bought it after reading your posts, but it only made things worse for me. Glad you found it a great help - remember we are all different. I think until a randomized double blind trial is done you might want to hold your horses. Your evidence is anecdotal only. It's a lot of money to chuck away - and as a lot of us will try almost anything, it is always annoying to feel let down, though I understand your enthusiasm.
All the best.

 

[e13 boy]

Handle,

I'm sorry to read that AMP didn't work out for you.
I totally agree with you about doing some trials,as is done with all pharma' drugs.All CD/UC patients would then have a far better understanding of what percentage of people it will help.At the moment the AMP companies all say 98%.Trials would give a far clearer picture.
Quite a few people have PM'd me re AMP & i always say to them i don't think their is a 'sure fire bullet' for every CD/UC sufferer whether it be pharmac',natural,worm therapy etc.If only their was!
After the hell i went through i just wanted to tell people how i finally found remission.
I wish you every success in finding treatment that works for you.

Best Wishes

 

[Miss Underestimated]

I doubt there will be any trials done, if no drug company manufactures it - that is a long, expensive process. I've read the posts with interest, though.