Greg Sheldon

First post: Sep 16, 2019 Latest post: Jun 3, 2020

         Greg has been having what he thougth were concussion symptoms for the past few years. He has been having increased illness over time and recently his symptoms were worsening. He was hospitalized and many tests were performed . They are waiting for an exact diagnosis and plan for Greg. He is at home and unable to work.  Jenny is taking care of him, her kids, and helping her parents out a great deal. We created this page to help Greg , Jenny, and the kids Zoie and Hayden. 
         Feel free to send cards, gift cards, or leave Well wishes on this site. Greg loves Cap city, Bob Evans, Scramblers, Panera, First watch,&  Napa kitchen. Grocery store gift cards , fast food and pizza for the kids would be helpful as well.  Rob Carlisle started a Go fund me at :

         Meals are set up at this time for Sunday thru  Wed  delivered to a cooler on the Sheldon's Porch.   Please go to Supported links  to sign up for the Meals. We changed the link to a Meal train due to the planner was not as user friendly for meals.  They would love a protein , veggie, and or fruit for some meals.   Over time we will  be adding to the ways to help in the planner . 
Thank you for all your help, thoughts and prayers for Greg and his family.  Any questions please reach out to Monica 740-815-7605 (tel:740-815-7605) about meals or Jenny 614-425-7561 (tel:614-425-7561). 

Jenny has released  this statement recently:   On August 29, 2019 our world changed. Greg, my husband, was diagnosed with CJD. Creutzfeldt-Jakob disease (CJD) is a rare, degenerative, fatal brain disorder. It affects about one person in every one million per year worldwide; in the United States there are about 350 cases per year. CJD usually appears in later life and runs a rapid course. As you can imagine, we are devastated as a family. We have been asked many questions about this disease because it is so rare. We have not been able to contact many of our friends to pass along this information. For more information about CJD, please go to the CJD Foundation at ( We ask for prayers for Greg. Thank you from the bottom of our hearts, Jennie, Zoie and Hayden

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