It’s Jay aka CrohnsBoy from CrohnsBoy.com writing you an important email, asking for your help with the utmost sincerity coming from my heart. I ask you to please finish reading this email and hear me out.
I’m helping a stand up guy named Reid Kimball spread the word about a documentary he is producing called WANTED: Crohn’s End and PLEASE view the awesome recently released 3 minute trailer here:
The purpose of this documentary is to show the IBD community (IBS, COLITIS, CROHN’s etc) and newly diagnosed patients that many people are trying alternative protocols and have been very successful with overcoming their diseases (cured), maintaining long lasting remission, etc you choose the terminology. Most IBD’s patients are typically only educated on the medical systems solutions. BUT, do we not deserve to know all of our options…? I believe in my heart that every person deserves to know the options that are out there so they can research them, verify their validity, make an educated, objective, and diligent decision which is ultimately their own. It is our body and we deserve the right to decide what is best for us.
I can remember being diagnosed with severe Crohn’s Colitis and I was told my disease was incurable, diet and lifestyle had nothing to do with it, and I would be lucky enough to take meds for the rest of my life, live with pain & inconvenience, have multiple operations, and a good chance of getting colon cancer in the future. Wow! This sure made me happy NOT. I can only imagine how hopeful I would have felt if I was told that I needed to make various lifestyle changes as many other people who made these changes were now med free and living Awesome lives.
Reid has started creating this documentary using his own funds, traveling across the US & Canada, speaking with med free people using various protocols. But his cash for the project has quickly diminished. Reid has decided to start fund-raising in order to raise enough cash to see this project through. I have met Reid and spent time with him in my home and I will personally back up his character. See my Blog Post talking about Reid and my time spent with him this summer for 1 week.
**THE FAVOR**: We're looking to find about 5 people to help us between 2-4 hours or less per person helping promoting this project around the net. To help spread the word by guiding people to the trailer and where to donate etc using: , Blog, Facebook account, You Tube channel, Twitter, Forums, CCFA meetings, and anywhere else you can spread the word about this documentary.You may be thinking I do not know anything about this but I can tell you the tasks we need help with are very easy just too much for Reid to complete by himself which is why I have volunteered to help out. **I am sending this to people that I have spoke with or helped in the past etc. Anyone that knows me will usually indicate that I have spent time working on a game plan with them or have offered to do so.... Now, I am asking for your help to kick in and help us show other IBD suffers the other options that are out there and working etc. If you have any advice or input in regards to how we can effectively make this video trailer go wild we would love to hear from you.
Please drop me a line because ASAP ,we urgently need help as Reid's deadline of DEC 8th is quickly approaching.
If you have the ability to donate financially that would also be greatly appreciated. The truth is that every dollar counts so do not think a 5.00 donation will not make a difference.
The purpose of this request is to help the video trailer go VIRAL through the IBD community and beyond so we can raise enough funds so Reid can complete this documentary which will indeed help so many people. We need to meet the goal of $10,550 by Dec 8th so please help us get there. I know many of the people I am sending this email to have used various protocols to overcome their IBD’s and all have their own opinions in regards to what is the best way etc. But I think one thing that all of us have in common is that we know how good it feels to get our lives back from these “crappy” diseases regardless of what protocol we used. This is a time where we need to come together so we can make larger impact in educating more people on the options available besides surgery and pharmaceutical products.
Please get back to me with your feedback and comments. I’m more than willing to talk with anyone on the phone or through Skype about this project and to answer any questions you may have. Also if you are interested in being part of the documentary (sharing your story, what protocol you used, etc. drop Reid Kimball a line anytime.
If you have any suggestions on how we can spread this message faster or more efficiently I urge you to be blunt and open so we can make this documentary a smash hit in the IBD community.
I look forward to your responses and want to sincerely thank you for your time and consideration.
**Also it would be greatly appreciated if you could forward this info to whomever you think may be interested in helping out the cause etc**
