At 16 years old, Daniel is getting taller and heavier. When my lift needs repair (which is often) I am left with NO way to get him to the hospital or doctor. So we started researching a light weight, foldable special needs stroller. As with everything else related to the disabled, the price was shockingly high. ($2000 +) Since Daniel also needs a new regular wheelchair, the insurance would not cover it.
That's when a friend I met on my Polymicrogyria Support page on facebook, contacted me. The Lindsay Foundation, started after a young lady name Lindsay with the same condition passed away. They offered to buy Daniel the stroller.
Simply making ends meet is virtually impossible. However, we face life with a spirit of faith, and a positive attitude. It gets really hard. Julie has an MBA but stays home to care for Daniel. And financially, the battle gets worse better than easier. So this stroller was a WONDERFUL gift we would not have been able to have.
This is our journey. Medical issues, pain, laughter, and love. PLEASE SUBSCRIBE and join our journey.
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Please watch: "HANGING BEACHBALL"
• HANGING BEACHBALL
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4 окт 2024