This is the first movie of a long term project, and my thesis work, on EB epidermolysis Bullosa.
Please take a look and tell me what you think.
You can view the full photo essay by visiting my web site: http://www.andrehermannphoto.com/#a=0&at=0&mi=2&pt=1π=10000&s=0&p=0
wow. that was so incredibly moving and absolutely heartbreaking. you did a really wonderful job editing the video so people could be educated about this horrible disease.
Andre, Great body of work! After seeing your piece you can almost feel the pain and joy within the family. Love the presentation, music, B&W to color effect. I smell some awards in your near future.Frederic Larson
Lorraine sent me a link to your blog.As a mom of a child with EB i am deeply grateful for your work here.I am once again powerfully moved- many tears- by precious Garrett and his extraordinary family.Thank you Andre! I pray this reaches a verrry wide audience!
For those who are not aware of Epidermolysis bullosa….Garrett’s form of the disease- is indeed the MOST painful disease out there!! Please research more about it and consider donating to the fight for a cure! Thank you!!!
This was absolutley beautiful and heartbreaking at the same time. This horrible disease took two of my babies from me. I am so grateful that this was done. I pray everyday for a cure. The more awareness out there the more of a chance these poor children have!Sue Ostrander
Wow! You have captured Garrett and his day to day pains. He is great kid and Lorraine is the best of the best and you are amazing. Thank you for sharing your work with us.