My ALS Page
Hi friends and family,
Since my diagnosis in March 2023 I?ve lost my legs, hands, arms, independence and my voice. Even though I?ve lost my ability to speak, cook, do my gardening, hold a book, use the remote control, brush my hair and all the other things that are to numerous to name, the one thing I did not lose is my ability to fight.
That?s why we are on this rolling stroll and this journey to raise money that the government took away from cutting edge medical research on numerous diseases including ALS.
The good news is that I am now a grandma to a beautiful baby boy by the name Solomon; he?s given me more strength to fight for the future generations.
Unfortunately its too late for mine, there is no cure on the horizon and we need the cutting edge research to fight to show that we care about neurological diseases.
Please show your support in any way that you can by joining us on this walk on October 18th 2025 to raise awareness or by giving any amount that you can. Every dollar matters in this fight! Just follow the link below to get all the information that you need.
Thank you in advance for your support,

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