Two weeks ago, we were still in Washington state enjoying our time with my family and friends. Ronan resembled nothing short of his loving, active, happy, playful self. As I was taking the boys’ Christmas card picture, I noticed Ronan’s left eye looked a little off. It was so minor that no-one else except my neurotic picture taking eye would have noticed. The days went by, and nothing changed. His behavior, activity levels, appetite, etc. remained unchanged. Still happy Ronan.
About a week ago, right after we got home, Woody noticed. We thought perhaps some dust, a leaf, bug bite, infection . . . could have been the culprit? Here is how the rest of our week unraveled:
Monday (8/9) Saw Dr. Campbell (Pediatrician) – she was not concerned and thought it was a chalazion; got referred to a Pediatric Opthamologist.
Tuesday (8/10) Saw Pediatric Opthamologist – walked out due to MOTHER’S INTUITION (horrible experience).
Wednesdsay (8/11- early afternoon) Saw Pediatric Opthamolgist #2, Dr. Brendan Cassidy. Mother’s intuition was positive with him and his team. Sent us to Phoenix Childrens Hospital immediately for an MRI.
and so our journey begins . . . . .
Ronan has been diagnosed with Stage 4 Neuroblastoma, a rare, but most common, childhood cancer. Findings from an MRI and CT Scan show two masses. One in his abdomen (adrenal gland) which is the primary source, the other on his left orbital bone (causing his eye to push forward). Neuroblastoma is very treatable and even curable. We have our plan in place, and the Thompson Family Combat Boots are on!
We are so blessed to be surrounded by the most amazing family and friends on this planet. We know that Ronan is a fighter and the strongest little boy out there, and we know we are going to beat this. Please continue to pray and keep our family in your thoughts at this time. Love, Maya