Our son archer is that 1:20. He has a rare genetic condition which affects his adrenal function. After a challenging first few months of life with a NICU stay and sepsis at 4 months, he was finally diagnosed at 7 months old when he reacted unusually to a vaccine. We were very lucky that doctors at the WCH noticed a pattern of illness and unusual bloods and pushed for answers.
Since diagnosis with Primary adrenal insufficiency we have found out this has been caused by a very rare gene mutation carried by both parents. He will require medication for the rest of his life and will always have to live with the risk of adrenal crisis with any illness or injury.
We are forever grateful to the researchers and people that have come before us that allow him to live a very normal life most of the time and the incredible treatment he receives when needed.
There are many children with other genetic illnesses that are not as lucky and that is why this August, I’m taking on the Ks for Kids challenge - walking or running to raise funds for Children’s Medical Research Institute, supporting scientists who are working today to find cures for tomorrow.
Your donation will help keep labs running, research advancing, and hope alive for kids who need it most.
Every step I take is for them. Your donation will help me go the distance and fund vital research!
Your donation will help keep labs running, research advancing, and hope alive for kids who need it most.
Every step I take is for them. Your donation will help me go the distance and fund vital research!
