Jimmy  Darts

SB Mowing

Pattie Gonia

Little Miss Flint

Kalina Silverman / @makebigtalk on Instagram

Samuel Weidenhofer

Patriotic Kenny Foundation

Ben Saunders - Flawless Cleaning

The Dogist

Peter Bond

Amy Jandrisevits

Ask Uncle Jack

That Good News Girl

Tess Bohne

FowlMouthFarmer

Latonja and Taylor Richardson

Officer Richard Craig

Flavor Flav

John Wolfe

Khloe

<div>Archer Rowland was unexpectedly born 9 weeks early. After delivery, he was immediately taken to the Neonatal Intensive Care Unit, where he spent his first 56 days of life. Going home from the hospital without your child is truly every parent's worst nightmare. Throughout Archie's stay in the NICU, Charles and I received unparalleled support from the NICU staff as they worked tirelessly to achieve the best possible outcome for our son. Not only did our Archie receive excellent medical care, but the NICU staff made sure to address our needs as well. The amount of support we received as preemie parents made such a difference as we navigated the hardest time of our lives.
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<div>As Archie's birthday approaches, we couldn't think of a better way to celebrate his first year of life than to give back to the place that made such a difference in all three of our lives. In lieu of birthday gifts, we are asking for donations that will be made directly to <strong>Good Samaritan Hospital NICU</strong>. Our hope is that with these donations we can help to continue to support the NICU staff and other families with children in their care.
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<div>We have chosen not to share photos of Archie publicly, but if you would like an update/pictures, please message Ali or Charles privately and we are happy to share!
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Archie's 1st Birthday Wish: Support NICU Families

<p>Olivia has been fighting a chronic disease for awhile now, she was diagnosed with Mast Cell Activation Syndrome a few years ago. Due to this disorder her mast cells don’t work properly, making her more susceptible to randomly frequent anaphylaxis. Olivia has been working with a great MCAS team of doctors to try and find the right therapy for her body. She has become allergic to multiple lines of therapy in the past, making it difficult to manage her symptoms. Xolair is a common MCAS medication given once a month to manage chronic anaphylaxis and asthma. She was hopeful this would be the medication to help stabilize her mast cells. Over a month ago, Olivia was receiving her 3rd dose of Xolair and within 10 mins suffered from severe anaphylaxis and ended up in the ICU for nearly 2 weeks. Though she is home now, she is still running her own infusion center in her home daily. She receives IV therapy 24/7. To reduce cost, she has been trying to manage her care at home rather than going back to the hospital. She is unable to work and the road ahead is unclear. Weekly testing and labs are being done in addition to many doctors visits. Though it’s been two months since her Xolair admission, Olivia’s mast cells have continued to cause her ongoing issues. She is still trying to gain strength and slowly eliminate all IV medications, electrolyte replacement and parental nutrition. As this is a chronic illness, it will always be a problem from Olivia but her goal is to try every route available to help heal her inside &amp; out. This is going to be a slow process to recovering, as this was one of her worst flares to date. As a result of this recent severe mast cell crisis, she has become extremely weak and unable to do her daily activities alone. She is working with a whole mast cell team of doctors including immunology, allergy, neurology, rheumatology, gastroenterology, cardiology, pulmonology, dermatology, psychology, genetics, dietary, occupational therapy and physical therapy. She has a great team who work closely together in order to create the most optimal, ongoing plan for Olivia’s healing. She is working with them weekly to help her regain her strength and get back to the things she loves. Olivia has been extremely positive despite not knowing what her future holds. As she continues to get treatment, there’s no doubt that her medical bills are getting expensive. Finances have become a stressor as she can not work and isn’t sure when she will be able to return to work at this time. Every little bit will help, if not financially - every prayer is appreciated. All funds raised exceeding her medical bills will be donated to Mast Cell Activation, funding research in this disease. 
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Olivia’s Mast Cell Medical Bills

Hello Pawpurr's friends and family,<br /><br />Unfortunately, there is an issue with Fleet's life insurance and his family is facing a heavy financial burden to host his viewing and funeral this weekend (<a href="https://www.legacy.com/obituaries/athensmessenger/obituary.aspx?n=steve-vanfleet&amp;pid=197958247&amp;fhid=16379"><a href="https://www.legacy.com/obituaries/athensmessenger/obituary.aspx?n=steve-vanfleet&amp;pid=197958247&amp;fhid=16379" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.legacy.com/obituaries/athensmessenger/obituary.aspx?n=steve-vanfleet&amp;pid=197958247&amp;fhid=16379</a></a>). There are other financial factors as well - Covid has had a major negative impact on profits over the last year and the joint ownership of the business has added complexity to the current situation.<br /><br />For these reasons, I've created a new GoFundMe and am asking for your help again. Any donation you can provide to help Spencer, Wendy and the family with funeral costs would be greatly appreciated. My hope is that helping with some of the funeral costs will give them some relief to properly celebrate Fleet's life and give us all some hope for what lies ahead. <br /><br />Steven VanFleet “Fleet” was many things to many people: a father, Vietnam Veteran, friend, boss, brother, role model, Buckeye Fan. He was kind, loving, hardworking, the life of the party, but above all he was selfless. Whether you were a friend, employee, family or bar patron, he always went out of his way to make sure you were taken care of, never asking for anything in return. His legacy will live on forever and we are all struggling with the loss of this great man. Many of you are familiar with his son, Spencer, and his mom, Wendy. I can say they are doing the best that they can right now. We all know the Pawpurr's family can have a big impact and I hope we can pull together again now. Let’s give Fleet the celebration he deserves, he would do the same for us.  <br /><br /> For those who I have not met, my father, Steve Meadows, was Fleet's best friend and the handyman at Pawpurr's for many years. I worked at Pawpurr's from 2014 – 2018 and grew up with Spencer. As a boy I remember how cool it felt to go to Fleet’s with my dad for his staff parties or come into Pawpurr’s Happy Hour and watch Dad and Fleet run the table. I am sure we all have memories that we will cherish forever. Fleet will truly be missed and Court Street will never be the same.<br /><br /><br />Thank you so much,<br /><br /> <br />Wesley Meadows

Funeral Fundraiser for Steven "Fleet" VanFleet

Ali Rowland

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Ali Rowland

Ali Rowland

What they care about

Featured causes

Archie's 1st Birthday Wish: Support NICU Families

Olivia’s Mast Cell Medical Bills

Funeral Fundraiser for Steven "Fleet" VanFleet

About me