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>Dear Family, Friends, Charger Fans, and All Fans,
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<div>With humble hearts we come before you to ask for your support in a cause that holds immense significance to us all. Our beloved Claudia, fondly known as Mama Bear, has endured a series of medical challenges, and most recently, a stroke. Her unwavering strength, coupled with her selfless nature, has always been an inspiration to those around her. Now, in this time of need, it is our turn to rally together and offer our unwavering support.
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<div>Claudia has always been the embodiment of compassion, readily offering help to strangers without expecting anything in return. Her radiant energy and kindness have touched countless lives within the Charger family and the wider community. She has become a cherished pillar among her friends and family, bringing joy and love wherever she goes. Words cannot fully capture the essence of her beautiful spirit, but today, Claudia needs us more than ever.
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<div>We have established this GoFundMe campaign to provide another opportunity for those who feel led to contribute, no matter how big or small the donation may be. Every dollar received will go a long way in assisting Claudia's journey towards recovery and easing the burdens that she and her family face during this challenging time.
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<div>By coming together as a united front, we can make a significant impact on Claudia's life, allowing her to focus on healing and regaining her strength. With your generosity, we can help alleviate the financial strains that often accompany medical crises, enabling Claudia to access the best possible care, therapies, and resources needed for her recovery.
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<div>We kindly request that you not only consider making a contribution but also share and spread this campaign within our family, friends, and the broader NFL community. Together, we can create a ripple effect of compassion, touching hearts and inspiring others to extend their support.
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<div>Let us rally behind Claudia, showing her the same love and kindness she has selflessly given to others. As we join forces to uplift her during this challenging chapter, let us prove that a collective outpouring of compassion has the power to transform lives.
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<div>We express our heartfelt gratitude for any contribution, as each act of kindness will contribute to Claudia's journey of healing. Together, let us be the difference she needs, affirming that no one walks alone in their time of need.
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<div>Every dollar, thought, prayer and positive thought is greatly appreciated!
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Claudia's Journey to Recovery

Skylar’s Fight for sight<br /><br />The money donated well go to Skylars medical bills which is well over 100k alone . Also to her family's bills, housing, food, care for Skylar and anything that the family needs to support her as bills have tripled. <br /><br />Hi my name is Jessicah Sullivan I am married to an amazing veteran Lucas Sullivan and we have a beautiful four year old Daughter named Skylar. Skylar was a healthy and happy baby up until just about two years old when my husband and I noticed that our daughter was not the same happy and healthy little girl anymore. We started to notice her Left eye was red, puffy, lazy and her pupil was not round but star shaped. Trying not to panic as new parents we thought allergies of course. But after days even weeks of her health progressively getting worse we realized this was not just allergies it was time to see an eye doctor. That day would be filled with more questions than answers and the start to a very long journey for our family.<br />All the doctor could tell us was that Skylar had developed a cataract in her left eye, her vision was nearly gone, and the next steps would be crucial if we wanted to save her sight. Being in a small town in Steamboat, Denver was the only option for pediatric care. Soon after we called our jobs packed our bags and headed to Denver so that Skylar could undergo her first of many surgeries to come. After the first few surgeries, doctors still had no clue what was going on, test after test, her eye was still not functioning she was coming in and out of remission when her optic nerve would become inflamed. We made the roughly 4 hour trip to Denver, nearly 6 times a month for days at a time the first year. Finally we had some idea to what was going on, Uveitis. Uveitis is inflammation of the part of the eye called the uveal tract: the iris, ciliary body and choroid, for Skylar this was caused by an Autoimmune and inflammatory diseases. Our immune system normally makes small proteins (antibodies) to attack bacteria, viruses, and other 'germs'. In people with autoimmune diseases, their immune system makes antibodies against the tissues of their body, causing damage and inflammation. In Skylar’s case, something triggers her immune system to attack the body's own tissues. The 'trigger' is not known. Any parents worst fear is being told you have a very sick child.<br />Soon our tiny 2 year old was on steroid drops, dilation drops, methotrexate, remicade infusions, pain medication, and countless other drops and gels just to keep her condition stable. She now wears a contact in just that one eye, while her right eye is patched every day and her sight is 20/400. We are heartbroken to see our little girl struggling to see her toys, struggling to see us. Two years now and the weight of all the bills and traveling expenses have put an incredible hardship on our family, living paycheck to paycheck not even getting by, trying to make the best out of birthdays and holidays with not much to give, and on top of money my now four year old has missed out on going to preschool because of surgeries, appointments and just being sick, she’s missed out on playing with other kids, she has missed out on 2 years of her young life, years that she should have been learning, exploring, and making her first real memories.<br />We travel to Denver still to meet with her two specialist and to get her infusion at the children’s hospital. We patch her eye everyday hoping and praying her sight will be renewed, and that she can experience being a “normal Child”. It has not been easy explaining to her on those tough days why she can’t jump and play as the other kids do, or why she must patch her good eye in order to make her weak eye stronger, or explaining to her why she can’t go to school yet. Skylar is living with uveitis and every day is a new challenge that she makes the best out of. With a very long road ahead of her she will still need more surgeries in the future, her infusions won’t stop for years, and the fight to get her sight back will be costly and will not happen overnight. She will struggle, she will have to deal with more children pointing, not understanding her patch, and will have to explain to her one day why she is “different”. But one thing we are sure of, she will always remember all of the amazing people that are helping her and our family along the way. Thank you for taking the time to hear about Skylar’s fight for sight.<br /><img class="not-resizeable" src="https://2dbdd5116ffa30a49aa8-c03f075f8191fb4e60e74b907071aee8.ssl.cf1.rackcdn.com/7546263_1449810544.9894_funddescription.jpg" width="100%" alt="7546263_1449810544.9894_funddescription." /><br /><a href="https://m.facebook.com/Skylars-Fight-For-Sight-1665496923667298/?ref=bookmarks" target="_blank"><a href="https://m.facebook.com/Skylars-Fight-For-Sight-1665496923667298/?ref=bookmarks" target="_blank" class="" rel="nofollow noopener noreferrer">https://m.facebook.com/Skylars-Fight-For-Sight-1665496923667298/?ref=bookmarks</a></a>

Skylar's Fight For Sight 

Bree'Aunna Turman

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<div>As some of you have heard I was recently diagnosed with Heart Failure. On the morning of April 10th, I woke up with an intense migraine and no feeling on the left side of my body, and a heavy feeling on my chest, it was hard to breathe. Geoff quickly rushed me to the hospital. They told me that they believe I was having a “Waking Stroke”, but something else more serious was going on with my heart. 
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<div>After numerous test, cat scans, MRIs, blood work, and a heart Echos, they found that my heart was only working at a merely 15%. My cardiologist said it was one of the craziest cases he’s seen and he was surprised I was alert. Even scarier was when he said the words “heart transplant”. Thankfully we are taking a different path first and I’ll be wearing a device called the Zoll. It’s vest I wear that is constantly monitoring my heart, it will also shock my heart if my heart stops or has an irregular rhythm (a defibrillator). I have to wear this wearable defibrillator 24/7. It’s been a hard adjustment but I’m thankful for this device that watches over me day and night. After being in the hospital for a week, I was finally able to go home with plethora of new medication keeping my ticker ticking. I’m so glad to be home with my babies. They are so incredibly strong.

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<div>As of today I had heart surgery on Dec 3rd to receive a pacemaker/defibrillator implant. I have been slowly recovering as the surgery was intense and was more aggressive then expected. Every day has been a struggle to find strength to get up and do daily activities. Although I’m healing I’m still unable to work. 
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<div>Due to my condition I have not been able to work or contribute financially and has set us back drastically. We have fallen behind in lot rent and now risk losing our home we have raised our kids in. 
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<div>I’m a very humble person and asking for help has never been something that I have been good at. But unfortunately I’m not able to work and financially, this is a hit for our family. If you feel inclined to you can donate via Zelle, Venmo, cash app. Anything you can donate is greatly appreciated and will go to keeping us afloat until I’m better. Im planning on doing some fundraising soon.

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<div>As our family gets use to this hopefully temporary “new normal”, I will be taking things pretty slow . All I ask is you be gentle with us. Love on my babies, invite them out so they are not stuck inside. If you see us out and about, don’t be afraid to say hello, and Please, please do not bring up my weight (it just makes me sad). lastly add us to your prayers

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<div>I will fight like hell to get better, it will be a long journey but I’m not giving up.

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Bree’Aunna’s Heart Failure Journey

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Bree'Aunna Turman

Bree'Aunna’s featured causes

Bree’Aunna’s Heart Failure Journey

Claudia's Journey to Recovery

Skylar's Fight For Sight