Jimmy  Darts

SB Mowing

Pattie Gonia

Little Miss Flint

Kalina Silverman / @makebigtalk on Instagram

The Dogist

Patriotic Kenny Foundation

Samuel Weidenhofer

Peter Bond

That Good News Girl

Ben Saunders - Flawless Cleaning

Flavor Flav

Ask Uncle Jack

Amy Jandrisevits

FowlMouthFarmer

Tess Bohne

Latonja and Taylor Richardson

Officer Richard Craig

John Wolfe

Khloe

<strong>Dominic Sigler</strong> is a local high school football player and FCA chapter leader who is facing an incredibly difficult and unexpected medical emergency. During football practice, Dominic suffered a heat stroke and had to be life flighted for emergency treatment before being admitted to the ICU for care. This has been a frightening time for Dominic and for everyone who knows and cares about him, and his family is now walking through the emotional and financial weight that comes with such a serious situation. 
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 The funds raised will go directly to Dominic and his family to help with medical bills, meals, and everyday needs as they focus on his care and recovery. Any support can help ease some of the pressure they are carrying right now and allow them to put their energy where it is needed most. Please consider donating if you are able, and please share and spread Dom's story so he can get as much help as he needs. Thank you for keeping Dominic in your thoughts and for showing up with kindness, prayer, and support. <br /><br />Dominic is my fellow FCA leader, classmate and friend whom I care for deeply. A check for the amount raised will be personally handed to Dominic by both me and the Head Football coach. Mrs Cassevah the sga sponsor and head will write the check out as Pace High School will not allow us to write it in their name. The funds will then be added to her bank account to cancel out the cost of the donation.

Support Dominic Sigler

<div>Friends and family, we are asking for your support for a beloved family in our community. On April 9th, <strong>Kyle suffered a serious fall and was airlifted to a Level 1 trauma center</strong>. He is currently being treated for a spinal cord injury along with several other significant injuries.
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<div>As medical expenses continue to grow and Kyle’s return to work remains uncertain, <strong>we are asking for a wave of healing prayers to rush heaven’s gates. And if you’re able, financial support to help ease the burden during this difficult time.</strong> Any contribution or share means so much to the Duponts and is greatly appreciated.
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Support the Duponts through Kyle’s healing journey 

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<div>Nick and Kristin have closed donations. They have so far reached their fundraising needs to their knowledge. If anything changes I will add another update for them. 
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<div>Our family greatly appreciate everyone’s support.  Thank you so much. 
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<div> -Liz 
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<div>Kristin and Nick are facing the unimaginable loss of their beloved 6-year-old daughter, Aviana, who passed away on Thursday. Aviana was the happiest girl, always dancing and bringing joy to everyone around her. Her bright spirit touched the lives of all who knew her, and her absence leaves a profound emptiness in the hearts of her family and friends. 
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<div> This tragedy has brought not only overwhelming grief but also unexpected financial burdens. The family is now facing significant expenses, including funeral costs and medical bills from Aviana's emergency airlift to the hospital. During a time when they should be able to focus on grieving and remembering Aviana, the weight of these costs is an added hardship. 
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<div> Your support can help ease their financial stress, allowing them to give Aviana the beautiful memorial she deserves and to begin healing as a family. Any contribution, no matter the size, will make a meaningful difference. Please consider donating or sharing this fundraiser to help Kristin, Nick, and their family during this incredibly difficult time.
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Support for Aviana's Family

<div>Our daughter is 8 years old and was diagnosed with an eating disorder approximately 2 months ago. We really did not know what to expect and how to help her through this journey. My wife and I have done everything we can do at home and are going to have to send our daughter to a facility for adolescent eating disorders. <strong>One of us will be going with our daughter because we do not want to just let her go by herself.</strong> Talking with multiple places that help children with eating disorders, it is very expensive, but it is something that she needs, and I'm going to do everything I can to get our daughter the help she needs! <strong>We do have two older children at home that one of us is going to have to stay with.</strong> I have checked with the VA, and there is no help through them, plus our insurance doesn’t cover eating disorders. <strong>Anything you can help with would be greatly appreciated!</strong> Thank you for your time!
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Support Our Daughter's Journey to Recovery

<div>This wonderful family needs your help.
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<div>After almost 10 years of marriage, 4 beautiful children, and what seemed to be a life full of possibilities... horror struck.
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<div>The reliable, sole wage earner these children trusted became a monster. Arrested for molesting his 8-year-old daughter, he is facing a life of incarceration.
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<div>The stay-at-home mother, who also homeschooled 2 of the children, has found her world upside down. The trust and love she once had for the father is forever changed.
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<div>There is one autistic and handicapped child in the household (familial hemimelia). The other 3 children are artistic, smart, and very lovable.
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<div>At this time, <strong>an attorney is needed for the family to figure out how to make sure they don’t lose the assets that have been acquired in 10 years.</strong> The mother is going to have to get steady employment, but it’s not happening at this moment. So many other things are barriers to normalizing their lives.
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<div>Just the emotional upheaval has become an everyday obstacle for these wonderful people.
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<div>The damage one person can do to a whole family, and more, is just overwhelming. Hopefully, this horrible person will never be a part of this family’s life again.
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<div>In lieu of all this, life has to go on, including paying the bills. This is where a huge problem lies. This family is young and had very little savings. They always paid their bills on time and managed to keep afloat off one income. Now that has changed.
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<div><strong>This family needs your help.</strong> They do not want this person in their lives again. They want to be independent, and that will take time. They just need folks to pitch in till the mother can get a job and child care. The main thing is to keep the children safe and happy, to keep the mother with some peace of mind to deal with this trauma.
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Support a Family in Crisis: Help Them Heal

<div>You have cancer... No one likes to talk about the big "c" word until it hits home. It is always unexpected. Something no one ever plans for, especially when you have a young family. Savannah is a beautiful young wife and mother, who was recently struck with the news of Ewing Sarcoma. 
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<div>Savannah is a beautiful young soul who aims to love her family each day. She spends most of her time with her husband and her kids. Savannah is a "making sure they are taken care of first", type of wife and mother. Honestly, they are what drives her to fight every day just to keep going. 
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<div>Savannah will find joy in the smallest of things and make light of any situation. Who likes awkwardness? Savannah does! She thrives on being awkward. But that's what makes her shine and be different. Savannah has such a unique light to her that you can't help but gravitate to it. Her laugh and her smile will brighten any room. She truly is a special person inside and out. What makes her more special is how great of a wife and mother she is. Each night she will love on her kids by making sure bath time is a little entertaining with bath toys and then wind the night down with snuggles and rocking her two beautiful kids to sleep. She is a diamond in today's world. 
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<div>Savannah was recently diagnosed with Ewing Sarcoma which is generally found in pediatric patients. It is rare to be found in adults. Savannah has had a couple of biopsies done however they have only been informative to conclude the doctor's findings in what type of cancer. The treatment is extensive and per the doctor's words, "This will be a long rough year for you". 
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<div><strong>Savannah and her family need our help by helping with all expenses while she is undergoing her treatment and surgeries. Every bit counts towards, gas, food, medications, along with other necessities. So, join us by donating to Savannah today and helping her in her fight against cancer!</strong>
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Help Savannah's Fight Against Cancer!

<div>Hi, my name is Maggie Wadkins and I am Selina Foster’s cousin. Let me explain a little of her history as to why this GoFundMe has been created.  She has an ileostomy bag and has had it for the past 12 years. She has no large intestines at all and so that puts a lot of pressure on her small intestines. Over the last 12 years she has had 8 major surgeries and 66 hospitalizations. There were times when it was very touch and go to say the least. 
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<div>Selina is currently in the hospital. She recently went via ambulance because her stomach was expanded, she couldn’t stop vomiting, she was shaking in pain, and was already starting to become septic. 
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<div>This is what the hospital discovered: 
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<div>She has hernias that need to be removed and her small intestines were obstructed. Her hernias were trying to rupture because her small intestines had wrapped around a hernia. She has had blood in her ileostomy bag, has no appetite, and has had to receive nausea medication around the clock or else she stays sick. Her abdomen wall needs to be totally reconstructed along with several other things. Baptist wanted to transfer her, but she was too weak. 
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<div>At this point she needs to go to a hospital that specializes in this area. It has been recommended that she go to a specific hospital in North Carolina for treatment. Even if she doesn’t go to North Carolina, she would, at the very least, have to go to the Ochsner Medical Center in Louisiana because she is an established patient at that hospital, and then go from there. 
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<div>Selina has two boys and is also currently in the middle of a divorce. She needs our help to secure funds for a plane ticket, possible lodging for family, and most importantly - the insane amount of medical bills that she is going to accrue from this. 
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<div>Thank you for taking the time to read this and I ask that if you are not able to donate, please share. 
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Medical fundraiser for Selina Foster

<div>Landry Logan Lasseter was born on June 28, 2021 at 28 weeks and 2 lbs 4 oz in Tallahassee, FL.  Landry was born with Bronchial Pulmonary Dysplasia - a critical lung disease.  He was transferred from the Tallahassee NICU at two days old to the Shands Children's Hospital in Gainesville, FL where he stayed for nine months in the NICU.  Landry was airlifted to Nationwide Children's Hospital in Columbus, Ohio, where they specialize in this lung disease.
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<div>Kami - his mom - has never left his side through the last 16 months, so she has been unable to keep her job in Tallahassee.  As you can imagine, this journey has taken a substantial financial and emotional toll on this sweet young family.  Jared - his dad - has remained in Tallahassee to work to try and take care of the monthly basic living expenses.  Due to his work and the cost of plane flights, Jared only sees Landry and Kami every 6-8 weeks.
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<div>Kami and Jared need and would surely appreciate any financial assistance to help them pay the $2400 health insurance premium each month to keep Landry at this excellent hospital and allow Kami to stay with Landry every day.
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<div>This journey is far from over; any help you might give them would be treasured and much appreciated.
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<div>Thank you for keeping this family in your prayers - the Lord has been with them every minute, hour and day of Landry's young life. We know in our hearts that Landry will come home one day!
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Love4Landry

<div>Meet Mike Luker, a dedicated 70-year-old dishwasher at The Dog House.
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<div> Mike has been working with us at the restaurant for the past year. Mike at 70 is still fun to work with, a little grumpy at times but an all around good old man who has overcome a lot of battles in his life.
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<div> Recently, he achieved a milestone by purchasing his own electric bicycle, thanks to his improved credit and savings from avoiding Uber expenses. However, his joy was short-lived when the bike was stolen outside of his home on Scenic hwy the same night, despite being securely locked.  
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<div>This infuriated us and we wanted to do something about it. 
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<div>So while we are searching for the bike and the criminal who stole it we are asking you for help to get Mike back on wheels again and to clear his loan
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<div>Thank you Pensacola for the support!
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Mike Luker - 70 - Stolen Electric Bike

<div>A soul taken too soonI went into the hospital on 5/3/2023 with such excitement to have baby Amelia via vbac but little did we know the next few days would have been a never ending nightmare for us all. Everything was going good until pitocin was bumped up to 5. At that point, my contractions had gotten closer &amp; stronger. I felt a pop which was my baby breaking out of the placenta due to my uterus rupturing. At that point, they had just given me the epidural. All I remember is doctors saying “prep the OR” and that my baby’s heartbeat was dropping. Amelia was born on 5/4/2023 through an emergency c-section with no heartbeat due to lack of oxygen for several minutes before doctors could pull her out. They rushed her to the NICU where she continued to have issues. She suffered a severe brain injury from lack of oxygen which caused her to have soo many issues. We finally had to make the hardest decision that no parent should have to make which was to let her go and be free. She is the most beautiful little girl that we have ever met but god had other plans for her. She was just too good for this world. Amelia passed away on 5/6/2023. She’s looking down on us now as beautiful as ever with no more pain. Until we meet again my sweet little ray of sunshine ☀️
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Rest easy angel baby

<div>For those of us who are parents, we all remember having our baby put into our arms for the first time and having our hearts burst with pure and unconditional love for that child. It is at that moment that, all of us parents know, we will do anything for our child. We will move heaven and earth if we have to.
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<div>Thankfully, most parents don’t have to. But some of us - we actually do.
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<div>Our family has spent the last four years in the battle of our lives. Every minute of every day we are faced with the horrific reality of the disease that is slowly killing our daughter and suffocating our family. This disease is known as Alternating Hemiplegia of Childhood, or AHC for short.
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<div>For our daughter, AHC causes episodes of paralysis, dystonia, and nystagmus. These episodes come on without warning and take her from a happy, playing, dancing four year old to a helpless, paralyzed, dystonic child screaming in pain. During these AHC episodes, Estella loses her ability to walk, crawl, swallow, and even hold her head up. Her hands become clenched from dystonia, and this same dystonia eventually travels throughout her entire body, causing levels of pain I’ve never experienced in my lifetime. Eventually, she loses consciousness because the pain is so great. These episodes last from minutes to hours to days at a time, but we never know how long it will last until it is over. Estella is completely aware of what is happening during these episodes, but she’s a prisoner inside her own body, and has absolutely no control over what is happening to it. As her parents, there is literally nothing we can do. We hold her as her body writhes in pain, we try to massage dystonic muscles, we monitor for breathing, maintain her airway, see the look of fear in her eyes…and we again feel our hearts shatter inside of our chests.
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<div>Every AHC episode has the risk of skill regression, permanent brain damage, and sudden death. When an AHC episode starts, we don’t know if we will get our little girl back on the other side of the episode.
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<div>There is no treatment.
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<div>There is no cure.
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<div>Yet.
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<div>This is where we need your help. We had the honor of meeting some of the leading doctors, researchers, and scientists studying AHC earlier this year, and they have identified three different avenues to create a gene therapy to cure AHC. All three projects are happening right now, and all three are showing great promise. We now realize the problem is not whether or not AHC can be cured; the problem is getting the funding to do it. Our disease only affects about 300 people in the United States, so there is no funding for the disease outside of what parents can raise themselves.
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<div>We will do anything for our daughter, just as you would for yours. With the humblest of hearts, we ask for your help in raising money to develop a gene therapy treatment for Estella. All funds will be used for the costs associated with the development and administration of an AHC gene therapy cure for Estella and for her needs as they pertain to this disease.  Any remaining funds will be donated to an AHC organization of our choice. With your help, Estella and other families in our position can hold on to hope that there is a future for our children.
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<div>The science is there. The money is not. Let’s change that.
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<div>With deepest gratitude,
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<div>Estella's parents -- Stephen &amp; Lacey Henderson
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Estella's Wish to End AHC

<font color="#333333">Hey everyone, we started this go fund me for Sabrina and the kids so they have one less thing to worry about while Pete is missing. Search efforts are full swing all around the Pensacola Pass where his boat was found, one of the men made it safely to shore on NAS Pensacola. Every dollar counts, Pete is a good man and a stellar outdoorsman and he would do the same for you.</font>

Pete Griffin and Family

Hi, I am asking for help for my sister Chelsey Brackin and her husband Willie Brackin and their 3 kids . They are dealing with a scary health battle for Willie . He has been dealing with some health issues for a couple of years and the drs kept blowing them off , so Monday he went to the hospital to find out that he had brain swelling , fluid on his brain , and a mass on his frontal lobe . He has been transferred to two hospitals now because the surgeons did not want to touch it . But from what they are saying it does not look like they have an easy road ahead of them . They own their own business so they can’t get sick leave or paid time off , and my sister is spending as much time with him at the hospital as possible because both of his parents are deceased and they are both so scared . I would really appreciate if people could help donate to help them through the financial struggles that will come with this . They are the kind of couple who are always Helping others , they always watch several different kids as favors to people who need the help and never ask for a dime , they often donate to go fund me for others in need , he coaches ball in Baker , and they genuinely care to help others . So please help me in helping them , even if it’s only $5 , it will add up and they will appreciate anything . Their 3 boys are miracles who have an amazing daddy and I hope we can pull together to help relieve any stress that we can .

Hope for Willie and paying for his treatment

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<div><span>I’m Julia Cole, country artist and family friend of the Durand’s. Through virtual benefit concert’s to be planned and this GoFundMe we want to help Jacqueline as much as we can. Barreca, Jacqueline’s sister, and I are hosting this page.</span><span>  </span>


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<div>Jacqueline Durand, 22 year-old from Coppell, Texas, was planning to graduate from the University of Texas at Dallas in May 2023. While in school, she started her own pet sitting business, Paw Paradise. As a lifelong dog lover, this entrepreneurial venture was a dream come true for her. 



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<div>Devastatingly, during her last assignment, on December 23, 2021, she was viciously attacked and mauled by 2 dogs and remains hospitalized. Jacqueline has hundreds of bites all over her body, however the most severe damage was done to her face. While being mauled, she lost both ears, her nose, her upper lip, her cheeks and lost essentially all jaw muscles along with the capability to chew food. Jacqueline will have a very difficult and long road ahead through surgeries, various therapies, and the everlasting trauma of this attack. 



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<div>To date, Jacqueline has undergone 8 surgeries with more planned soon. Initially, her surgeries were lifesaving in nature. Her subsequent surgeries have been and will be reconstruction of her face over the next several months including:



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<div>• Formation of a new nose



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<div>• Multiple procedures to ensure her ability to hear sound



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<div>• Replacement of her lost ears with prosthetic ears



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<div>• Skin grafting of the interior of her face 



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<div>• Installation of lower eyelids to ensure that her vision and eyes can function properly



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<div>• Reconstruction of upper lip 



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<div>Should these efforts prove unsuccessful, a full facial transplant may be her only option, but that cannot even be considered until several months from now.



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<div>Donations to Jacqueline will be necessary for each of the following expenses that will last from the date of the attack, 12/23/21, throughout potentially her lifetime. 



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<div>• Medical care expenses incurred due to this violent tragedy



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<div>• Physical, occupational, and emotional therapy 



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<div>• Loss of earning capacity sustained 



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<div>• Costs to cover physical impairment and disability sustained



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<div>As you can see, Jacqueline can truly use all the support she can get. Her many friends are asking for your financial assistance in the amount of $2 million to offset the considerable financial burden of this traumatic attack. Even if you are unable to donate now, please pray and share with friends and family to circulate her miraculous story of survival, strength, and courage.



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Jacqueline Durand Nearly Killed in Dog Mauling

<strong>If you know Karissa and Trent Stewart then you know that they are the first to offer help to anyone in need and the last ones to ask for help for themselves. However, our dear friends need our help at this time. <br />Last Thursday, July 20, 2017, Karissa underwent surgery to have her left kidney and ureter removed. This was her third surgery in less than a year. Since this surgery was going to be removing a kidney and ureter, we were prepared to help Karissa recover from surgery and adjust to life with one kidney. It would be an adjustment, but many people go on to live long productive lives with one kidney. She will too! Not to mention, this surgery was removing the source of the pain she had been experiencing for so many months. <br />The day after her surgery I went to the hospital to visit with Karissa and Trent. Karissa was back to her happy smiling self. She was alert, talkative, and patiently answering every question her youngest son, Sam, (4) had about the machines and tubes surrounding her. Seth (9) stood quietly waiting his turn to see his mom. She was delighted to have her boys there because she had been missing them so. It was wonderful to be able to see my friend doing so well after her surgery and surrounded by so many people who love her. <br />I wish this was the end and those surgeries were all this loving family needs help with. Sadly, this is just the end of one journey, but the beginning of a much longer one.<br />A few hours after I left the hospital feeling so positive and optimistic, I received a text message that knocked the breath out of me. My best friend, your loving friend, family member, teacher, coworker, classmate has Stage 3 Transitional Cell Cancer.  <br />This is an extremely rare form of cancer for someone Karissa's age to have and usually removing the kidney and ureter is enough action to remove the cancer from the patient's body.  However, that is not the case with Karissa. She will need to undergo radiation and chemotherapy treatments. Karissa is going to be sent to M.D. Anderson, in Houston, Texas so they can develop her plan of action.  Trent will be traveling with her. Hopefully, they will be able to develop her plan with the panel of doctors at M.D. Anderson and then receive treatments close to home  in Pensacola, FL. <br />The Stewarts have a long road ahead of them, but Karissa is a strong woman with a strong, loving, and supportive family. I know that she can do this, but they need our help.<br />As I said earlier, medical bills have been piling up. With this recent diagnosis travel expenses are now going to be added to that pile. I am asking for prayers, positive vibes, and any assistance you can give to help this family in their greatest time of need. If you can't donate money at this time, please share this post on your facebook page, so that maybe someone else will feel lead to help. I have witnessed this family helping so many people throughout their lives, my family included. It is our turn to help them. Your thoughts and prayers are very much appreciated. Thank you for taking the time to read all of this. <br /><br /></strong>

Taylor Dover Bryan

Taylor Dover Bryan

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