My Personal Fundraising Page
Welcome to TeamNattie
Natalie was officially diagnosed with CJD in February of 2021, but by that time, she had already declined from a witty, funny 22 year old college student. As the pandemic caused every student to come home in March of 2020, we started noticing some behavior changes. We struggled to understand what was happening and all her vitals came back 'normal'. We were told that she was suffering from anxiety and depression and needed some medication.
Her condition kept getting more and more out of character; sudden OCD, repeating comments, struggling with words, failing to remember common things and directions, incoherent thoughts, and hallucinations. We knew this was more than 'anxiety and depression'.
We were told that Natalie's MRI from September 2020 was "normal". Then in December 2020 during Natalie's CT-Scan, the same radiologist noticed a drastic change in just 3 months. They amended the MRI from September and that was the first time we heard of CJD. At first, we were happy that there was finally a name for what was happening to our daughter, but then our hearts completely sank when the doctor said there is no cure and the lifespan of a CJD patient averages around 6 months.
Due to Natalie being young, a female, and symptoms started cognitively (rather than physically), we were told her duration would be longer. She declined so fast and was at the last stage, completely bedridden and unable to communicate for her last 18 months. Her duration was about 3 years.
During that time, we heavily relied on the CJD Foundation. Early on, we found a Facebook group and many people recommended getting hold of the Foundation. We called and left a message late one night and surprisingly, Debbie Yobs from the CJD Foundation called us right back. She was a calming influence and helped us get on track with what would be coming down the road.
The CJD Foundation is instrumental in finding a cure as well as providing care for both caregivers and patients. Help us continue the fight for a cure by sharing this fundraiser and contributing if possible.
Thank you!
Natalie’s Graduation Speech (2017)
Text to Give
To donate to my personal fundraising page, text STRIDES2024 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.
$459.00
achieved
$1,000.00
goal
of your goal reached
0
days
0
hours
0
mins
0
secs
How to Register
My Supporters
- Helen Tacon 3 weeks ago
- Judy Rosenbaum Natalie's light will always shine. Love to all her family and friends. September 2024 $53.00
- Debra Beck June 2024 $106.00
- Frank Myers June 2024 $100.00
- Debra Beck June 2024 $106.00
- Frank Myers June 2024 $100.00
- Judy Rosenbaum Natalie's light will always shine. Love to all her family and friends. September 2024 $53.00
My Badges
This user hasn't earned any badges yet.
My Teammates
- Rosemary Vaswani $1,557.50
- Frank Myers Team Captain $459.00
- Tracie Funk $100.00
- Lindsay Stollman
- Madison Harman
- Mateo Beckman
- Rosalee Beckman
- Sue Yaller
- Maralisa Ortiz
- Andrea Ortiz
- Ann Sobel
- Kim Hutton
- John Strege
- George Vincent
- Catalina Briones
- David Briones
- Teresa Myers
- Jake Myers
- Josh Myers
- Hannah Strege
- Marlene Strege
- Wendy Jimenez
- Tierney Anderson
- Kyle Brooks
- Holly Werner-Thomas
- Debbie Beck
- Evan Smith
- Emmie Wordin
- Rhiannon Madison
- unknown unknown
- unknown unknown
- Rhiannon Madison
- Sofie Werner
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.