Jimmy  Darts

SB Mowing

Pattie Gonia

Little Miss Flint

Kalina Silverman

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>On August 5, 2022, Kenneth "Kenny" Wells, 17, passed away unexpectedly, leaving his family and friends to mourn his loss. Kenny would have started his senior year at Brandywine Highschool in just a few short weeks.
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<div>The Brandywine Community has always rallied to support its own, and we know this tragedy is no exception. Although nothing can ease the pain of losing Kenny, we encourage all who are able and willing to contribute to this GoFundMe so Kenny may be laid to rest and his family can focus on mourning their loved one rather than worrying over the unexpected expenses that accompany his loss.
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<div>Donations may be made via GoFundMe or dropped off at The Market Place, 2428 S. 11th St. Niles.
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<div>My name is Erin Douglass and Kenny’s mother, Becki Ralston has worked for me for the past 4 years at Antiques on 11th and The Market Place.  She is a valuable part of my business and my life. I am so grateful to all of you for allowing me to organize this fundraiser for her. I will be withdrawing the money to pay the bills related to this tragedy. I will have complete transparency with the withdrawals. Thank you
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Support for the family of Kenny Wells

<div>Hello, my name is Elizabeth and we are fundraising for my Brother David, Sister (in law) Lynnette, and the beautiful Morgan. A little back story here- David and Lynnette have been together for over 10 years, have gotten married, and then tried for over 5 years to be parents. After struggling and not becoming pregnant they ended up deciding that they were just going to be the fun aunt and uncle. Little did they know God stepped in and blessed them with Morgan. Morgan came into the world early causing her extended hospital stay. Now this little fighter is demanding the best care and will have to be transferred to 1 of 3 other hospitals. Miss Morgan is growing faster then her lungs can keep up, she has already spent 4 months in the helpful hands of the Memorial NICU. Now she is getting ready to be transported to a better equipped hospital to help her lungs catch up. They aren’t sure which one yet and due to them not knowing which one is covered under insurance. I can update later with their decision. Thank you for taking the time to read their story and please share. We love all 3 of them very much and we want our little Mo home.<br /><br />******This is what Momma told me:10/25/21: I had a growth ultrasound and doppler, after receiving the RhoGAM shot and a set of steroids to assist Morgan with growth and development. I was admitted into Triage for monitoring of Morgans heart rate. After 2.5 hours, I was informed that I would be admitted into the Special Care Unit for 24-hour monitoring.  <br /><br />10/26/21: I was awoken by my new OB, Dr. B, coming in to inform me that there was an issue with my blood work and that I would not be leaving the hospital until after Morgan was born. Dr. B explained that I had an extreme form of preeclampsia called HELLP syndrome. Being at 25 weeks (about 5 and a half months) along in my pregnancy, this was extremely rare, since I had 0 issues with my blood pressure for the last 22 weeks (we found out we were pregnant at 3 weeks). This means that my RBC was currently sitting at 90 (it was 350+ in June) and my liver enzymes were 8x higher than normal. He informed me that they would be running more blood work to confirm and explained the mother side complications with having a baby this early. Dr. B also let me know that if I would not have been admitted, that within the next few weeks I would have started to have seizures which would have led to a deadly stroke for both of us. <br />A little later Morgans Doctor (Dr. BR) came in and explained the complications baby side. Morgan had a 50-60% survival rate for just the delivery.  <br />2 hours later, Dr. B came in and explained that my RBC had dropped to 87 in the last few hours and that we would be having Morgan now. They had 6 units of blood on standby for both of us in case anything was to happen.  <br />Within minutes, the nurses had arrived, and I began signing paperwork for myself and Morgan. I had called David and he arrived at the hospital only 10 minutes after leaving work. An hour later, at 1:15pm, we had our sweet Morgan, weighing 1lb and being 11in long. <br /><br />Morgan was intubated within 3 hours due to being so tiny and having such a tough time breathing. Morgan remained intubated for the next 3.5 months as every time they tried to remove it, she would stop breathing. <br /><br />Like other micro-preemies, Morgan has had issues over the last 4 months. Issues with feeding, weight gain, edema (swelling), BPD, and her heart. She has a PDA, heart murmur, that has been slowly closing but is causing her issues with blood pressure on the right side of her heart. Unfortunately, if Dr. BR fixes the blood pressure with the PDA there, then it can cause more fluid to press onto her lungs, making it more difficult to breathe. There is no known cause or solution for her edema that is now all in her head. Luckily, there are no and have been no brain bleeds. <br /><br />Morgan currently has a trach to better assist her with breathing as being intubated causes a disruption of the development of her palate. Morgan was initially doing well with the new trach even having a larger one put it as she was growing well. As a result of her prematurity, Morgan has Bronchopulmonary dysplasia (BPD) also known as Chronic Lung Disease. BPD will stunt her lung growth and will give her respiratory issues for the rest of her life. Along with this, Morgan runs the risk of growing faster than her lungs are developed. If this were to happen, Morgan would go into heart failure as she would not be able to pump the oxygenated blood through her body. This is the struggle that we are currently in. Morgan has been struggling with her oxygen levels at various times of the day and the reality is that with her requiring so much oxygen, she is not stable enough to travel. Dr. BR is trying everything that her and the other doctors in the NICU can to help stabilize her. <br /><br />Unfortunately, Memorial Hospital does not have a dedicated team for BPD patients. She will need to be transported to a different hospital with such designated teams. All such hospitals are at a minimum, 3 hours away. When she is transferred, unfortunately, neither of us can take the entire time off due to bills and needing to save the time off for when she is able to come home.  <br /><br />We are already so blown away by everything everyone has done, and we are so grateful as we do not ask for help and will actively not tell people everything so that they do not worry about us, and we are not a burden. <br /><br />Thank you and we cannot wait for Morgan to meet everyone that obviously loves her so much.
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Mo the Great

Let me introduce this young lady to you, my daughter,  Angela Johnson.  This Amazing young women has had a journey that has had a lot of mountains to climb, that represents her strength to get where she is at today.  Her qualities , attributes and perseverance is to be commended.  She just turned 20 on the 4th of July.<br /><br />At age 9, a 3rd grader at Tarkington Elementary School, she had perfect attendance.  Reading at a 6th grade level, you would find her walking around with her books.  Not to mention her strong interest in art.  Very artistic!  There was about 2 weeks left of school, when I received the call from her Girl Scouts leader, a friend that would change Angela’s life as we would know it.   Kristin, who at the time worked at St. Joseph medical,  was with the kids that day, while they were enjoying field day.  Around lunch time, I received a call from her that Angela was having episodes and that we needed to get her into the ER ASAP.  After her explaining what was happening, I realized that Angela was having seizures.  Reaching the hospital, we were taken straight back to an examining room where the nurses and doctor met with us.  They took blood work and then wheeled her off for a CAT Scan.  While she was out of the room, the Dr. came back in asking, “how she was being treated for her diabetes?”.  I relayed to him, “she is not diabetic. “ .   Double Blow!    With not having the pediatric specialist here, we took her straight to the Bronson Hospital in Kalamazoo.  We spent 5 days there, to get her stabilized and learning how to manage both, Type 1 Diabetes and Epilepsy (Focal and petite Mal seizures) .    At first everything seemed in control, but then, Angela started having issues with more seizures and then her high blood sugars.  Her Neurologist referred her to Detroit’s Children Hospital in the summer of 2011, to see if she would be a candidate for  this one surgery.  We received the word that she was, and surgery was set up for Oct. 2nd and Oct. 5th.  First part of the surgery, they went in and placed 124 grids on her brain, to do brain mapping.  Trying to pin point where her seizures was happening.  Then on Oct. 5th, they went back in and pulled 4cm of her left temporal lobe.  After the surgery, the doctor came out to give us an update.  He stated it was much worse then what he even anticipated.  She was having a seizure every second.  All of her left temporal lobe is almost dead, so she has transferred everything to her right side of the brain.  She managed to  be seizure free 2 years then started showing signs again.  <br /><br />Her seizures has come back and now it is not just showing on her left temporal lobe, but her front right lobe.  I asked her neurologist to referee her to Mayo’s clinic.  In June we had taken the trip to Rochester, MN for a week for testing.  With several appointments later, she will now be going under surgery for an en-plant in hope to reduce her seizures.  For right now it is scheduled for Dec. 31st.   We will be returning several trips for check ups and for her to be monitored.  <br /><br />With mounting medical bills and needing funds by the end of Dec. to be able to take her for travel expenses I am reaching out for help.  Anything would be greatly appreciated along with prayers.......

Helping Angel

I am going to be battling a third round of cancer and I am currently not working due to a double hernia.   I am married and have 3 kids and a Grandson living at home. I just need to pay bill cover rent and make up some lost wages.

Please help with medical bills.

Tina Farr

platform

Platform is iOS

Android

Adyen Google Pay Development Audience

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English only

Deprecate Stripe Legacy

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DAF Internal

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PYMK has donors

iOS v12.3.0 and above

Tina Farr

Discover more people

Highlights

Support for the family of Kenny Wells

Mo the Great

Helping Angel

Please help with medical bills.

Activity