Robbie Wright

Aubree is turning 3 in July and in almost 3 years medicines and treatments have changed but the battle is still there.  There are many times, Aubree is offered cookies, Cupcakes or snacks and we have not planned for or forgotten her enzymes, spoon, applesauce and we have to tell her she can’t have these things because we don’t have her meds. The times my son is offered these snacks in front of Aubree and because we don’t have her meds he has to understand he can’t have the snacks either.  We leave birthday parties and events early because Aubree has to get back home to receive her breathing treatment, but this is CF way of life. She has labs drawn quarterly to make sure her liver is functioning adequately because of the meds.  The CF Foundation has come a long way with their research and strides to find a cure or at least maintain this awful disease. Why should you donate? Because the more research and studies they can do, the more this can eliminate some of the meds and treatments.  I want Aubree to have a long healthy life and the only thing this can happen is to put it into the hands of professionals like researchers and doctors to find a cure. 

 Please become a part of the Aubree Angels and/or donate to Cystic Fibrosis Foundation, anything can and will help.  The CF walk is May 18, at Wannamaker Park in North Charleston,  come and be a part of the team and walk for a cure.  Please Share the post.  If you can make the walk form a team under Aubree’s Angels and help Raise money.  If you form a team, you will receive a shirt and some other CF Gear but you have to make it to the walk. If you are unable to make it, please donate.