Thank you for supporting Cameron's Crew!
A message from Cameron's mother, Danielle:
Daniel and I are parents to our sweet baby boy, Cameron. He was diagnosed with cystic fibrosis when he was 2 weeks old. We will never forget how our world stopped when we received the phone call. However, as parents, we are his foundation. We picked ourselves up and accepted our new path. CF will be in our daily lives but it will never define Cameron.
This past few years we have watched Cameron grow into the happiest and most curious toddler. We have also seen how truly tough he is.
Many ask how Cameron's health is and we are thankful to say that he is currently doing well and "healthy". What goes into keeping him healthy are a tremendous amount of medications, treatments, doctors visits and tests. Cameron currently takes about 35 digestive enzymes a day to digest any fats or protein. He has chest physiotherapy performed twice daily (or more if he is sick). That is started with albuterol, followed with hypertonic saline in a nebulizer, and then 20 minutes of his special vest to shake any mucus from his lungs. The less mucus in his lungs means less germs who call his lungs home. He takes an antacid to help his enzymes breakdown in the correct spot in his digestive tract. Since Cameron's body cannot absorb fat on its own, that also means he is not absorbing fat soluble vitamins. He takes these vitamins supplementally in a form his body is able to absorb. He is currenlty on a modulator called Orkambi but we are hopeful that Cameron will start Trikafta this year!
Trikafta was approved in 2019 for those 12 and older with specific gene mutation requirements. It is currently approved for 6 years and older and we are (not so) patiently waiting for Trikafta to be approved for the 2-5 year old range. This drug has been funded by the Cystic Fibrosis Foundation because of donors like you. This drug is NOT a cure but it's a fantasitc tool we can use until Cameron can be cured. Unfortunally, 10% of the CF population are not eligible for this medication. Their only hope is a cure. This is another reason we need to raise funds so we can get to the finish line ASAP.
We are so very hopeful for all that is coming down the pipeline. The Cystic Fibrosis Foundation is dedicated to find a cure for ALL those with CF. We are beyond thankful for The Foundation and all of their work to get us to that end goal.
We are continuing on this journey with Cameron and we hope to have you by our sides for the ride.
“The CF Foundation continues to lead the way in innovative research and drug development, promoting high-quality, individualized care, and helping people with CF live better today. Nearly every CF drug was made possible by the Foundation and because of funds raised from Great Strides, people with CF are living longer, healthier lives and pursuing their dreams.”