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1 reviews

Review for Gastroparesis Patient Association for Cures and Treatments, Inc., Etters, PA, USA

Rating: 5 stars  

I was diagnosed in March 2012 with Gastroparesis. This changed my life as well as my family's living/eating habits. I hit the computer to find help, as my GI Dr at that time (I now have a new one) did nothing for me, education/reassurance/nothing! In all of my on-line search for help to understand GP, I found G-PACT to be the most informative. I ordered a Restaurant Card from them so when I was out 'eating' with family, I could order a small portion or off the kid's menu without a problem. They have links for credible doctors and other helpful info. G-PACT has several campaigns going as well. Such as the one asking the Federal Government for funding for research. This doc is so close to being passed, I can almost taste it and it is much needed for all of us! Just picture having the flu 24-7 and you are only partially in our daily shoes! G-PACT is involved with so much and they provide up-to-date information (check Facebook too), that I asked what I could do for them in return. That is how I became a volunteer and have just now assisted with the launch of our “Please, Pass The Puree” on-line fundraiser. We wanted to honor all of us that are unable to eat a Thanksgiving Meal! This is currently going on, so check it out. I can't picture not being part of this great non-profit organization. It is my dream one day to be able to eat food again and enjoy life the way I did before GP hit me. It is my belief that with G-PACT we can make this happen!

Would you volunteer for this group again?


For the time you spent, how much of an impact did you feel your work or activity had?

A lot

Did the organization use your time wisely?

Very Well

Would you recommend this group to a friend?


When was your last experience with this nonprofit?


Role:  Volunteer