Strength Made Perfect In Weakness

After two months of fighting one respiratory virus after another Joey is finally doing better. Every time he gets sick we buckle up for another roller coaster ride of uncertainty and sleepless nights. Degenerative neurological disorders bring so much uncertainty. They are the perfect nightmarish combination of definitive and unpredictable. At least that’s our experience. … More Strength Made Perfect In Weakness

Goodbyes Along the Way

Saying goodbye is a natural part of life often marking the end of one season and the beginning of another. We transition out of the old and into the new, many times bidding adieu to the familiar and reluctantly accepting the unknown. Sometimes joyfully leaving the past behind and expectantly entering a promising future. Goodbyes … More Goodbyes Along the Way

Three Months Later

It’s been three months since we found out Joey has a lysosomal storage disorder, two since the official diagnosis.  My concept of time has changed completely.  In some ways it’s been three very long months – many, many sleepless nights, a gazillion doctor appointments, meetings upon meetings with various agencies including two with Hospice of … More Three Months Later

Joey Bear

This is a blog about Josiah, our youngest son, and his journey as he battles GM1 (infantile gangliosidosis). A baby with Infantile GM1 gangliosidosis usually appears normal until onset (usually by 6 months of age), but developmental regression eventually occurs.  Signs and symptoms may include neurodegeneration, seizures, liver and spleen enlargement, skeletal irregularities, joint stiffness, distended … More Joey Bear