Team Bradley is made up of family and friends who won't stop believing in Bradley! Bradley is 3 year old boy who was born with a brain abnormality called Lobar Holoprosencephaly. Studies show that only 3% of fetuses with this diagnosis make it to birth and only 1% make it to six months of age. There is no treatment or cure for this diagnosis, but Bradley is tremendously strong and beating the odds everyday. We couldn't be more proud!
Please, join us on Team Bradley to support The Little Miss Hannah Foundation. Bradley is the proud recipient of a floor chair from this amazing organization. Our hearts have been touched by the love and generosity of the LMHF. Please either join us on the walk, or if you are unable to attend, please consider a donation. Your donation will help kids just like Bradley receive special equipment to better enhance their lives. Thank you!!