PCD Foundation

October is PCD awareness month! Primary Ciliary Dyskinesia is a rare disorder caused by genetic mutations that affect the tiny hairline cilia in the lungs, nose and ears, impairing their ability to remove germs and pollutants, and allowing mucus buildup and infection.

There have been HUGE advancements in diagnosis and treatment for PCD in the last 20 years thanks to funding for research. AND, even bigger advancements are currently under way. Advancements only possible through generous funding. I'm raising money to benefit PCD Foundation, and any donation will help make an impact.

The PCD (Primary Ciliary Dyskinesia) Foundation seeks to promote research, increase public awareness, and provide information and support services for individuals with inherited ciliary disorders and their caregivers.

Our Mirabelle has PCD. You can help us celebrate our child’s strength and bring awareness to PCD through a donation. Thank you in advance for your contribution- our family appreciates your support!!!

For more information on PCD: https://www.breatheforpcd.com

For PCD Awareness Month, Elliot and Atticus Fox are raising money to benefit the PCD Foundation. PCD (Primary Ciliary Dyskinesia) is a rare disease that Elliot was born with. It is a progressive disease that affects the lungs, ears, sinuses, and more. PCD is a severely under-diagnosed and under-researched disease. The PCD Foundation seeks to promote research, increase public awareness, and provide information and support services for individuals with inherited ciliary disorders and their caregivers. Your support to this lifelong cause of ours MEANS THE WORLD TO US. Thank you. Thank you. Thank you.

For more information on PCD: https://www.breatheforpcd.com

#standforsomething

This Friday, December the 13th, my sister would have turned 45. She had 4 charities that she constantly gave to until she could no longer. One of them was the PCD Foundation, with the hopes of funding research and finding a cure for PCD, a rare lung disease her nephew (my son) was born with. This year I ask that you donate the cost of a beer…or shot of tequila…or bourbon on the rocks (?) and cheers to Melissa Kobe for the beauty and belly laughs she gave us.

For PCD Awareness Month, Elliot and Atticus Fox are raising money to benefit the PCD Foundation. PCD (Primary Ciliary Dyskinesia) is a rare disease that Elliot was born with. It is a progressive disease that affects the lungs, ears, sinuses, and more. PCD is a severely under-diagnosed and under-researched disease. The PCD Foundation seeks to promote research, increase public awareness, and provide information and support services for individuals with inherited ciliary disorders and their caregivers. Your support to this lifelong cause of ours MEANS THE WORLD TO US. Thank you. Thank you. Thank you.

For more information on PCD: https://www.breatheforpcd.com

We are raising money to benefit the PCD Foundation, to raise money to further research and awareness of this rare disorder that Elliot was born with. When he was born, we were told he was 1 of 600 people in the United States. Now he is 1 of 1,500 people that have been diagnosed, though they expect that there are actually 25,000 people living with it. This means that awareness and funding to help find a cure are important to Elliot and everyone else out there living with PCD.

Any donation will help make an impact. Thanks in advance for your contribution to this cause that means so much to us!

More information about PCD Foundation: The PCD (Primary Ciliary Dyskinesia) Foundation seeks to promote research, increase public awareness, and provide information and support services for individuals with inherited ciliary disorders and their caregivers.

#standforsomething

Learn about PCD at: www.pcdfoundation.org and www.breatheforpcd.com