
I am proud to announce I have founded a new organization for families affected by ALS (Lou Gehrig’s Disease), called Forward Focus.
My cousin Kenny, a father of 6, was diagnosed with ALS in the Spring of 2006. He passed away on July 10, 2008.
This disease has no mercy. It is 100% fatal, claiming most lives within 2-5 years of diagnoses.
For this reason, I am passionate about these families having the opportunity to have professional family portraits taken at no cost to them.
Currently, we are offering free sessions to ALS affected families in North Carolina only. At any given time, there are 350-400 ALS persons in touch with the ALS Association in North Carolina. ALSA will spread the word about Forward Focus to the families, and the families will be put in touch with me. For now, there are two photographers in our volunteer effort, and we are seeking others.
Each photographer agrees to donate their time, talent and 20 free prints from the session to the family. There is no obligation to purchase any additional purchases, but if some are desired, a discount will be available.
If you know anyone in North Carolina currently living with ALS, please give them my email address. We will be happy to provide portraits to them! (sheri@sheriallison.com)