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

Ophelia was the first grandchild, the first niece, and from day one, she had all of us completely wrapped around her tiny finger. We soaked up every single moment watching her grow into the spunkiest, sassiest little soul any of us had ever met. Around her first birthday, things started to shift. Skills she had worked so hard to build began to slip away. After years of searching for answers, she was diagnosed at three years old with Rett Syndrome: a rare genetic disorder that affects brain development and robs girls of their ability to speak, move freely, and control their own bodies. Rett Syndrome doesn't touch who Ophelia is (that diva spirit is alive and well), but it has trapped her inside a body that won't cooperate with her. We have watched this condition steal what should have been a carefree childhood, and it has been one of the hardest things our family has ever faced. 
 
 
 For those of you who have followed Ophelia's journey over the years, who have donated to Rett Syndrome research, who have shared posts and sent prayers - this is the moment we have all been waiting for. Gene therapy has long been on the horizon as a potential breakthrough for Rett Syndrome, and our girl has been chosen as one of the participants in a pioneering clinical trial. Our Opie, a trailblazer, just like we always knew she was. 
 
 
 To make this happen, my sister and her husband Scott will be relocating to North Carolina for three months so Ophelia can receive her treatment. Both of them will be taking leaves of absence from work to be by her side every step of the way. The emotional weight of this journey is already immense, and the last thing I want is for financial stress to add to their burden. If you are able to donate, we are so deeply grateful. But if that's not possible right now, a shared post, a prayer, or simply a good thought sent Ophelia's way means just as much. This little girl deserves every bit of hope, and I truly believe she is about to get some of it back.

Her Fight is Our Fight

<div>Hello, my name is Doug West and I have recently lost a very good friend of mine, Erik Rundle. This was very unexpected and it breaks my heart for all of his family and friends but especially for his beautiful and wonderful daughter Sadie Grace. I know Erik would want everyone to focus on the light of his life right now. Anyone who knew Erik knew he was a very loving guy. He was someone that if you needed him, he would be the first one to put his arms around you and help you anyway he could. I thought I would give an opportunity to everyone who knew Erik and really wanted to do something in his memory to please donate to his Sadie, whom he truly loved and adored. And if you’d like to, please leave positive stories and memories of him for Sadie to see how he impacted others and how loved he was. 
</div>

In memory of Erik Rundle

Not all heroes wear capes! Doctors, nurses, medical professionals, and staff are working around the clock to battle COVID-19 in our community. Mountaineer Chapter of BNI is partnering with Get Fit Juices &amp; Shakes, Crab Shack Caribba, and The Cupcakerie to try and provide meals to feed employees at Mon Health Medical Center &amp; WVU Medicine. Our goal is to provide a meal for all 400+ employees but we need your help!  If you would like to help make this possible, join the Feeding Our Heroes campaign today and donate to provide meals!  Together, we can feed our heroes! Please share this GoFundMe link with your friends, family members and co-workers to help us reach this goal!

Mountaineer BNI Feeding Our Heroes

Simon Lucas Rohaly is the son of Adam and Misty Rohaly and little brother of Rio from Fairmont, West Virginia. He is an amazing two year old with a giant smile that can light up a room. Simon has been diagnosed with Neuroblastoma.  Thousands of people that love him and his incredible family are flooding our God with prayers and offering to help.  Money raised will go directly to the Rohalys to use as they see most helpful during their journey.  Simon's family is so thankful for all of the love and support they have recieved. Please continue to send prayers and lift up Simon!

#SuperSimon

Ryan  Ford

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Ryan Ford

Ryan Ford

Featured causes

Her Fight is Our Fight

In memory of Erik Rundle

Mountaineer BNI Feeding Our Heroes

#SuperSimon

About me