My Personal Fundraising Page
POWERLESS
This word resonates with me in such a profound way. It describes exactly how I felt about my mother’s death. My mother had developed a neurological disease that had no other mission but to destroy my mother’s brain. There is no cure, there was no slowing down the process, there was nothing. We had no idea of the time we had before it finished its course. It was ravenous, it was demanding, it was unquenchable, unforgivable, and it would stop at nothing until it took her life.
The disease was awakened and from that moment on, it worked all day and night. Like a thief in the night, it worked overtime to take control of every function of my mom’s body. Before I realized it, my mother was no longer capable of using the part of her brain that makes you able to hold a loving and caring conversation with your child. As I look back, ninety-five percent of the time was in caretaking mode, trying to understand what was happening to my mother. The last five percent was trying to spend as much time with her, hoping to get even a glimpse of the mom we once knew a few months earlier. I sat next to her bed, telling her not to be afraid and that it was okay for her to leave and be with God, that we would be okay. But deep down inside I wanted to scream and drop down to my knees and beg and plead with her, to not go! I yelled at that stupid prion, yelled – why her! I asked God for a miracle, I asked for him to make her new but even as I asked, I heard a small still voice inside me, tell me, that this was His way and His will. I knew then that this is the way it had to be, so I didn’t ask again. Instead, I dug deep down in the comfort of God’s promise that He will be with me, beside me, through this extremely difficult next chapter.
It still hurts. I never realized it before but there are so many things around me that remind me of her. She is gone, but I miss her in a way that I have never missed anyone before.
We do not know why this sporadically happen to her and we need more research to find this out. Please join me in raising money for this cause to help further research for answers and a cure.
Text to Give
To donate to my personal fundraising page, text STRIDES2023 to 50155.
About Fundraising
Donations of $250 and above are considered sponsorships.
Sponsorship Levels:
- Premier: $20,000
- Diamond: $10,000
- Platinum: $5,000
- Gold: $1,000
- Silver: $500
- Bronze: $250
Premier, Diamond, and Platinum Sponsors will have their name or logo displayed on participant t-shirts, the Strides for CJD website, and signage. Gold Sponsors will have their name or logo displayed on the Strides for CJD website, and will have their name (not their logo) listed on participant T-shirts and signage. Silver and Bronze Sponsors will have their name listed on the Strides for CJD website only.
$493.60
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How to Register
My Supporters
- Jennifer Gonzalez October 2023 $37.10
- Gracie Castillo I'm praying for a breakthrough, praying for a cure. October 2023 $106.00
- Clemente Saucedo Jr. GOD BLESS YOU. August 2023 $53.00
- Delia Mendoza Miss you comadre. Love, Delia. August 2023 $53.00
- Anonymous August 2023
- Stefanie Mendoza July 2023 $112.00
- Gracie Castillo I'm praying for a breakthrough, praying for a cure. October 2023 $106.00
- Clemente Saucedo Jr. GOD BLESS YOU. August 2023 $53.00
- Delia Mendoza Miss you comadre. Love, Delia. August 2023 $53.00
- Jennifer Gonzalez October 2023 $37.10
My Badges
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My Teammates
- Nanette Sigala Team Captain $837.60
- Stefanie Mendoza $493.60
- Angelina Gil
- Alyssa Gil
- Amber Diaz $0.00
- Anna Degollado
- Keith Ferguson
- Frankie Mendoza
- Princeton Mendoza
- Emma Mendoza
- Kenneth Avila $0.00
- Karen Sanchez $0.00
- Estella Avila $0.00
- David Vasquez $0.00
About Strides for CJD
Strides for CJD is an annual walk/run to raise awareness of Creutzfeldt-Jakob Disease (CJD), a rare neurodegenerative disease that has no treatment or cure. Through this event, anyone -- anywhere -- can pay tribute to their loved ones and raise funds for the CJD Foundation, a 501(c)(3) organization.
Funds raised support our programs including:
- Our 24/7 helpline, support groups, conference, and other family programs throughout the year.
- Research grants to help scientists make important discoveries and bring us closer to a cure.
- Medical education to help raise awareness and understanding of prion disease.