Our Story
Elena is a sweet determined little girl, who brings a ray of sunshine everywhere she goes. Despite navigating ongoing medical challenges she lives each day with joy, curiosity, and celebration. Recently, we received a confirming diagnosis through the Undiagnosed Disease Program at the National Institutes of Health (NIH) that she has a rare genetic form of mitochondrial disease, for which she is the only documented patient. This affects Elena’s growth, metabolism, development, energy and also causes many secondary conditions which affect her health.
Thanks to advanced diagnostics, modern medicine, and a massive team of clinical specialists Elena has created her own “normal” despite her complex medical needs. Her diagnosis has provided critical information to tailor medications, supplements, interventions and target areas of her health that need monitoring. She will continue to “write her own story” and with each new step we will continue to do our best to keep her as healthy as possible and prepare for any health challenges ahead.
As Elena’s disease continues to progress, the most immediate needs are a new kidney and potentially a new liver. We hope this kidney transplant will help ease some of the difficulties she has experienced since birth as well as improve her overall health. Elena is resilient to say the least, her courage through hundreds of doctor visits, blood draws, tests, hospitalizations, surgeries and daily interventions at home are extraordinary. No doubt she’s a real-life super-hero!
Her medical journey has been an intense constant evolution and we are thankful for the support from family and friends during this time. We know many of you would like to be kept updated, you can follow her Facebook/Instagram accounts as well as updates on this website. If able, please consider donating to COTA in honor of Elena. 100% of your donation goes towards transplant-related expenses. The Willardson family is immensely grateful to their army of family and friends for the outpouring of love and continuous support!
The Children’s Organ Transplant Association (COTA) helps children and young adults who need a life-saving transplant by providing fundraising assistance and family support. COTA is the nation’s only fundraising organization solely dedicated to raising life-saving dollars in honor of transplant-needy children and young adults. 100% of each contribution made to COTA in honor of our patients helps meet transplant-related expenses. COTA’s services are free to our families, and gifts to COTA are tax deductible to the fullest extent of the law.
Elena Willardson
Walton, KY
Transplant Type: Kidney
Transplant Status: Waiting for Transplant
Goal: $100,000.00
Raised: $59,510 of $100,000 goal
Raised by 153 contributors
Updates
Elena Adventures This Past Year
Posted
It has officially been a year since our family began fundraising for COTA (Children’s Organ Transplant Association) to assist with transplant-related expenses. This last year has been quite challenging... Continue Reading »
Adventures of Elena’s Doctor Visits
Posted
We recently had an appointment with Elena’s nephrologist and wanted to share a little bit of Elena’s medical world with you. Elena is typically very excited to go... Continue Reading »
Music and Dance With Elena
Posted
The moment you met Elena, she immediately pulls you in and wants to play with you, within 10-20 minutes you most likely will be doing a combination of... Continue Reading »
Seasons of Elena
Posted
Elena is a curious little girl who loves being outside no matter what the season is, every season is her favorite season in different ways. Her appreciation of... Continue Reading »
WELCOME TO TEAM ELENA
Posted
For those of you that are new to “Team Elena”, we wanted to share a little more detail about her medical journey thus far. If you have had... Continue Reading »
Elena
Posted
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Our Story
Elena is a sweet determined little girl, who brings a ray of sunshine everywhere she goes. Despite navigating ongoing medical challenges she lives each day with joy, curiosity, and celebration. Recently, we received a confirming diagnosis through the Undiagnosed Disease Program at the National Institutes of Health (NIH) that she has a rare genetic form of mitochondrial disease, for which she is the only documented patient. This affects Elena’s growth,...
Continue Reading »Elena Willardson
Walton, KY
Transplant Type: Kidney
Transplant Status: Waiting for Transplant
Goal: $100,000.00
Raised: $59,510 of $100,000 goal
Raised by 153 contributors
Updates
Elena Adventures This Past Year
Posted
It has officially been a year since our family began fundraising for COTA (Children’s Organ Transplant Association) to assist with transplant-related expenses. This last year has been quite challenging... Continue Reading »
Adventures of Elena’s Doctor Visits
Posted
We recently had an appointment with Elena’s nephrologist and wanted to share a little bit of Elena’s medical world with you. Elena is typically very excited to go... Continue Reading »
Music and Dance With Elena
Posted
The moment you met Elena, she immediately pulls you in and wants to play with you, within 10-20 minutes you most likely will be doing a combination of... Continue Reading »
Seasons of Elena
Posted
Elena is a curious little girl who loves being outside no matter what the season is, every season is her favorite season in different ways. Her appreciation of... Continue Reading »
WELCOME TO TEAM ELENA
Posted
For those of you that are new to “Team Elena”, we wanted to share a little more detail about her medical journey thus far. If you have had... Continue Reading »
Elena
Posted