I have known this little girl for years and I have witnessed how GM1 changed her life. I’ve seen her cry and I’ve seen her struggle to walk but couldn’t.
Today is her 5th birthday and until now, no cure has been found for GM1 – Gangliosidosis. Let’s all offer a prayer that a cure will be found soon. They have various ways to generate funds not just for Kate but for all those who are suffering from GM1.
The link below is for your donations, any amount will do. 5 cents, $5 – it will surely help not just Kate but all those fighting to survive GM1 every day. If you are still unaware what GM1 is, feel free to watch the video.