We are participating in the Million Mile fundraiser in an effort to raise money for Rhabdoid Tumor research. Our beautiful firstborn son, Juno Augustus Wolff,  was born October 11, 2022. He was diagnosed with Malignant Rhabdoid Tumor at only 9 weeks old and passed away on February 2, 2023 at almost 4 months old. Juno was such a happy, curious, and loving little guy.  His vast and enduring spirit made such an impact on countless people.  We are so blessed to have known the greatest joy of our lives through the beautiful blue eyes and laughter of our beloved son. He deserved a full and healthy life alongside us. 

Rhabdoid tumor is very rare and very aggressive.  There are only about 20 kids that are diagnosed each year with it, and there is no standard protocol because there has not been enough research to establish one. The reality is that pharmaceutical companies are not incentivized to search for effective treatment because it is so rare that it would not be considered profitable. As it stands, only about 8% of the national budget for cancer research goes towards all childhood cancers in general, so funding is severely lacking for the cancers that are more uncommon. 

 We want to help create a world where children are given a chance to live despite these unjust barriers. A world where no other parent has to endure the pain we endure every day. Please help us go gold for childhood cancer in the month of September. Every mile matters and every dollar gets us closer to a cure.

This team was created in memory of Juno and these precious children who passed away from Rhabdoid Tumor or Atypical Teratoid/Rhabdoid Tumor:

Eleanor Luckenbill, 5 weeks old

Claire Marie Ferguson, 6 weeks

Magnus Watkins, 6.5 months

Weston, 7 months

Logan Ford, 9 months

Luna Claire, 9 months

Aslan Yildirim, 2 years 1 month

Daniel Peter Sangregorio, 3 years

Forever in our hearts.