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Fetal Hope Foundation
June 3, 2011

After being diagnosed and given poor odds for my twins to survive I came to Fetal Hope's site and asked tons of questions. I had an overflow of compassion and answers. After many of my bi weekly Perinatologist visits, Fetal Hope gave me more clarification, personal experiences...and quickly. In one of my first visits, I saw the TTTS specialized Peri wearing his FetalHope support bracelet and it confirmed how tight knit these highly specialized doctors and Fetal Hope were. At one point we were given less than a day to get to another doctor (a flight away), Fetal Hope was there to offer help in getting us there. I still to this day (my twins will be 4 in Aug) can't speak highly enough of what they do. I direct everyone I come in contact, that is pregnant with multiples, to them. Heaven forbid they have a diagnosis that would need Fetal Hope, but if so, there is no group I feel that stays on top of research, educates (both dr and mom), is quick help, and has compassion for those that come looking.

Years later I made another flight to Seattle to attend a Fetal Hope event and again thank them and the Peri that helped me.

The Great!

I've personally experienced the results of this organization in...

my pregnancy. Without their assistance I fear I would not have the knowledge I needed to make life saving decisions I needed to make for my boys.

Ways to make it better...

If I had to make changes to this organization, I would...

Nothing.

MY ROLE:
Client Served & Needed their help after a Twin to Twin Transfusion Syndrome pregnancy.