Penny’s Pals, a Nonprofit 501(c)(3) organization formed by the parents of Penelope Rose Winsman, in her memory. Through our personal experience, we have become passionate about supporting medically fragile/complex children and their families. Providing Financial Aid, Quality of Life and Burial Assistance. Funding obtained through private donations, fundraising activities, and sponsorships. Through life, Over the Rainbow and Beyond.
When a parent finds out their child has a terminal or complex diagnosis, their world stops. The outside world does not. Living day to day, not knowing when it will be the last with their child and hearing only time will tell is the reality for many families in this case.
Penny’s Pals hopes to support these families in being together from beginning to end. Creating more time for bonding and being their parents. Also creating opportunities for these families to learn about their child’s medical cares and needs. When there are so many unknowns, we want to help these families celebrate their child’s life! Cherishing every moment! Sharing love, finding joy, hugs, kisses, birthdays, music, art, and creating memories that will last forever.
These things can never substitute for proper medical care but can enrich their lives. As your child transitions, Over the Rainbow and Beyond. Penny’s Pals will be here for your family with applications for burial assistance and bereavement resources. Final arrangements can be costly and is the last thing a family should worry about when experiencing the loss of their precious child.
Apply for support for the following programs:
- Burial Assistance
- Financial Relief Expenses, Grocery Cards, Ext.
- Quality of Life Music, Art, Birthday Box, Clothing, Other Areas of Support.
Penelope Rose Winsman (Penny), arrived Oct 31, 2019, at 31 weeks, weighing 2lbs 15.9oz after a vehicle failed to yield causing an auto collision. Penny and Mom were rushed to the hospital where an urgent emergency C-section was performed to save Penny’s life. Penny battled prematurity and an irreversible severe Traumatic Brain Injury, sparing her brainstem and cerebellum. Medical Professionals said, “Only time would tell until Penny passed.” She was given a life expectancy of six months or less. Penny’s medical conditions were complex and unpredictable. Throughout Penny’s journey she experienced many events and conditions relating to the neurological impairment and others relating to prematurity. Eventually, she grew out of some conditions and others were lifelong. Just to name a few: (Sleep Apnea, Central Apnea, Respiratory distress/ Respiratory failure, Neuro-irritability, Microcephaly, eating difficulties/G-Tube dependent, Spasms, Spasticity.)
Penny kept fighting! She kept amazing us with her strong will to live! Showing everyone what she was capable of. We loved her single every day and always told her how proud we were. She overcame prematurity after 3 months in the NICU and was finally able to experience life at home with Mom and Dad on Hospice. We cherished every moment and created a beautiful life full of love and happy experiences for Penny. We danced, listened to music, made a healing garden for Penny, celebrated monthly birthdays, played shows on Penny’s Porch, Photoshoots, starred into each other’s eyes, talked and hugged day and night.
Throughout Penny’s journey, she faced many challenges, but was also very accomplished. She did a lot more than what was expected from her MRI and CT and EEG Results. She knew who Momma and Dada were! She could hear us and she could see us. She loved to hit her toy fish and every time we said, “You did it Penny!” The BEST day ever was when she learned how to SMILE! It was so beautiful. Penny loved affection and responded to encouragement. She often told us in baby talk and through the expression of her pretty eyes.
As Penny grew, her brain couldn’t keep up with her body’s demands and the conditions worsened. After 8 courageous months, Penny decided it was time. She peacefully passed away in Mom and Dad’s arms from respiratory failure on June 28, 2020. She finally gained her glitter wings she requested and rode her unicorn Hope, onto a rainbow into the sky. We always told her she could do and be anything she ever imagined and could visit us anytime.
During our journey with Penny, we received an outpouring of support from our family, friends and community, who we now call PALS! We are beyond grateful and hope to provide that kind of love and care for our medically fragile/complex pals and their families.
Every Penny to Penny’s Pals will go towards the betterment of medically fragile children and their families. Each donation will go to fund Financial Relief, Quality of Life Support, and Funeral Funding. You can allow families with medically fragile, complex, and terminally ill children to be together when time is limited.
There can be no price put upon the beautiful time these families have. All Penny’s Pals initiatives and program support our little warriors and their families, as they navigate Through Life, Over the Rainbow, and Beyond. Thank You for your donation. Thank You for being a Pal!
Do you want to share Penny’s Pals with your Family & Friends on Social Media? Use the link above and head to Penny’s Pals Facebook page. Follow the instructions below and Start Your Own Fundraiser in support of Penny’s Pals! You can also Donate Directly with the donate link on our Facebook page.
- Click Fundraisers in the left menu of your News Feed
- Click + Raise Money
- Select Nonprofit or Charity
- Select a charitable organization, fill in the fundraiser details and choose a cover photo
- Click Create
Copyright © Penny’s Pals Inc. 2020. All rights reserved. No portion of this website may be reused without prior consent from Penny’s Pals Nonprofit. All content is for Quality of Life, Family Support, and Funeral Funding for medically fragile children. All requests for help will need social worker verification. **Full services not offered until announced in 2021.** No portion of this website should substitute for proper medical care from your child’s medical team and providers.