Hey everyone....It's Nancy,Mallory's mom.
It's that time of year again and I want to update you all on how Mallory is doing since Great Strides 2021.
Mallory was in the hospital several times for her DIOS-Distal Intestnal Obstruction Syndrome and had to have "clean outs". She also had her 7th sinus surgery in September 2021 for nasal polyps and infection.
Mallory was able too start 8th grade at her new school for children with learning disabilities,she was diagnosed with intellectual disability, ADHD,anxiety and dyscalculia a math disability. Mallory also has POTS which causes her to have a very high heart rate, dizziness and fatigue. So with all these new diagnoses along with her Cystic Fibrosis makes the daily life of a 14 1/2 year old scary.
Due to her lung function her Cf dr's have her doing Homebound school and I must say her new school has been amazing about it! She works so hard everyday and we care so proud of her!
I'm not going to beat around the bush...I'll come right to the point!
WE NEED DONATIONS....there is STILL so much work to be done to find new,better medications for Cystic Fibrosis patients. The ones we currently have are NOT ENOUGH and DO NOT WORK for all CF patients like my Mallory.
So I ask you to make a donation today of any amount, Our goal is $1,000 and since Graet Strides is not till May I want to make an early start and pray we make our goal!
Please your family and friends to make a donation in honor of Mallory and all CF patients, We really would appreciate it.
Thank you and remember....That breathe you just took...it's a gift!