Meet Jake.
Jake is an energetic year old who certainly kept me on my toes during his photo session! I had the honour of meeting Jake and his mom through the Tiny Light Foundation. You see, Jake has Cystic Fibrosis which affect the lungs and digestive system. In the email that his mother sent to TLF, she writes:
“My Son Jake was born March 23, 2009 and on April 23, 2009 he was diagnosed with Cystic Fibrosis, which affect the lungs and digestive system. Jake must take pancreatic enzymes before each meal and snack to be able to digest his food properly. He also has to endure breathing treatments and chest physiotherapy twice a day to keep his lungs free of mucous and to try and prevent infections.
He’s a vibrant two year old with a great personality!”
Yes, he certainly is and he certainly does! You can tell by these pictures!
It was an honour to meet you Jake, and your mom and Nana too! God bless you, sweet child.
Amelia - Wow Jen. He is a tiny light himself… so cute and what a smile!!