Saturday, February 22, 2014


Please watch the trailer for this important work. Donate if you can. Then share it with everyone, everywhere.

I started this blog because I wanted answers but did not have them. I hoped to find them. Thought they had to be just on the horizon. Days passed. Weeks. Months. And years. Today I am still there at the beginning.

We still don't know.

I started this blog because I felt so alone. I hoped to find others who could relate. Thought they had to be searching, too. That maybe we would find each other then find our answers together.

Today I still hope for answers, and though we still don't know I have found that there are good people who are using their amazing talent, giving their time, and even sacrificing their own resources to bring the undiagnosed from the darkness. To bring to light the challenges of searching for answers. Creating a film to "make a difference... in how medicine is practiced now and in the future."

My thanks goes out to Dr. Katia Moritz, Nicholas Miller, Crystal Shearman, and Dr. Jonathan H. Hoffman for such amazing work! Please consider contributing to help complete this film. I know their efforts have already blessed many lives, and I just can't wait to see how far this film will go in making all the difference for families like ours.

1 comment:

  1. As a sign of gratitude for how my son was saved from Alpers' Disease , i decided to reach out to those still suffering from this.
    My son was diagnosed of Alpers' Disease in 2013 and it was really tough and heartbreaking for me because he was my all and the symptoms were terrible, he always have seizure , and he always complain of loss of cognitive ability . we tried various therapies prescribed by our neurologist but none could cure him. I searched for a cure and i saw a testimony by someone who was cured and so many other with similar body problem, and he left the contact of the doctor who had the cure to Alpers' Disease . I never imagined Alpers' Disease has a natural cure not until i contacted him and he assured me my son will be fine. I got the herbal medication he recommended and my son used it and in one months he was fully okay even up till this moment he is so full of life. Alpers' Disease has a cure and it is a herbal cure contact the doctor for more info on on how to get the medication. Thanks admin for such an informative blog.