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>It is with heavy hearts that we share the devastating news that on February 20th, <strong>Beth and Ralph O'Sullivan experienced a devastating house fire</strong>. The fire and water damage destroyed a significant portion of their living space along with many personal belongings and memorabilia. Assessments are still happening to determine what items can be saved within their home. Thankfully, they are all safe, but the emotional and financial toll is overwhelming.

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<div>As you can imagine, the road to recovery after such a tragedy will not be easy. Beth and Ralph will need assistance to rebuild their lives from the ground up. They are starting from scratch, needing everything from clothing and food to household items, furniture, and rebuilding costs. In addition to the immediate needs, they will also face the financial burden of possible temporary housing and other unexpected expenses.

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<div><strong>We’re asking for your support to help them through this difficult time.</strong> Any contribution, no matter how big or small, will make a huge difference in helping them recover and begin to rebuild their lives. If you can’t donate, we ask that you please share this campaign with your network so that we can reach as many people as possible. In addition, the O'Sullivans would deeply appreciate your thoughts and prayers during this difficult time. They continue leaning into their trust and faith in the Lord and the power of prayer.

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<div>Here’s how your donations will help:

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<div>Emergency supplies: Clothing, toiletries, food, and other basic needs

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<div>Possible temporary housing in the future: Assistance with rent and housing-related expenses if needed (they are currently staying with family)

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<div>Rebuilding their home: Donations will help with repairs and replacing lost belongings

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<div>Emotional support: Helping them focus on healing without the added burden of financial stress

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<div>If any friends and family are able to help with physical labor when the time comes (clean up, moving items, etc.), please reach out to Mollie or Chelsea to be added to a list. We will reach out with requests when needed. 

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<div>We’re grateful for any support you can provide. Please keep the O'Sullivans in your thoughts and prayers as they navigate this challenging time. Together, we can help them heal and rebuild.

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<div>Thank you for your kindness and generosity.

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<div>With love and gratitude,

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<div>Beth and Ralph O'Sullivan

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<div>Mollie and Brian Morris

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<div>Chelsea and Ryan Cox

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Help Beth and Ralph O'Sullivan Rebuild After House Fire

<div>On January 26, 2024, Wallace (Wally) Reed Anderson (at just 10 days old) was taken to OSF St. Francis Medical Center to be admitted for what they thought was jaundice. When they arrived at the hospital they discovered he was in multiple organ failure due to an undetected congenital heart defect, called a Coarctation of the Aorta. That night Wally coded twice, starting the scariest 48hrs Jessica and Kyle could possibly endure.
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<div>As of now, it is unclear if it's a genetic disorder, but it is a fairly rare condition that happened when his ductus arteriosus closed and also started to close his aorta. Wallace is scheduled for his first heart surgery this Tuesday, 2/6. Currently, he has two other heart defects they aren't going to treat at the moment. After this one is fixed, it is possible he will have to have a balloon catheter inserted to fix his bicuspid valve.
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<div>The surgery itself has a pretty high success rate and low risk. However, since the aortic valve was already pretty much closed when they arrived at the hospital and caused organ failure, he has a long, unknown road of recovery ahead of him. Wallace has proven to be a fighter and we are very hopeful, but the unknown of the extent of damage his body has gone through has not been fully accessed yet.
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<div>Jessica and Kyle have been at the hospital by his side since last Friday while the wonderful team in the Neonatal Critical Care unit gets his little body back to stable so he can withstand surgery. Every doctor at the hospital has told them they are the only reason Wallace is still alive and they saved his life. And just how lucky he is... If it weren't for their persistence of getting him seen when they knew something was wrong, he might not be here today fighting. Most kids who aren't diagnosed at birth with this condition, don't make it back to the hospital in time.
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<div>I have started this goFund me on behalf of my family to offset a small percentage of the medical cost they will incur caring and fighting for Wally over the next month, and beyond.
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<div>Jessica (mom), Kyle (dad), and big sister Alexis appreciate all of the love and support they have received through this difficult time. If you are not able to financially support this amazing family, please share this GoFund Me and continue with your healing thoughts and prayers.
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Wallace's Medical Expenses

<div>Brooklin was born march 18th, 2020. She spent 12 days in the NICU at Methodist hospital due to feeding issues, poor weight gain and Jaundice. Brooklin has always been a noisy breather but it wasn't until multiple trips to the pediatrician and 3 ER trips that she was finally diagnosed with her condition. Brooklin spent about a week in OSF NICU where she was diagnosed with Laryngomalacia at 2 1/2months old. At 3 months old brooklin was referred to ENT and she underwent surgery to correct her defect. Prior to the surgery Brooklin suffered with lots of feeding, breathing and choking issues. She was also seeing physical therapy and speech therapy for feeding therapy on a weekly basis. When she ate she would choke and gag on every single bottle to the point where she was starving and needed to eat but just couldn't..she started to lose weight and fall off her growth chart. She would cry constantly because she was so hungry but wasn't able to maintain nutrition properly due to her condition . During these choking episodes she would struggle to breathe to the point where she would often gasp for air and turn blue or pale. Brooklin had recurrant Stridor and has always sounds congested due to this condition. They say typically kids will outgrow laryngomalacia on their own but as weeks passed it was clear that her symptoms were only getting worse and that she was not improving. On June 18th 2020 Brooklin underwent a Bronchoscopy, Laryngoscopy and a supraglottoplasty. The surgery was to officially diagnose the severity of the laryngomalacia and to repair the floppy tissue above her vocal cords in hopes to open up her airway so that she would be able to not only eat better but breathe better as well. She had an extensive 4 day stay in OSF PICU after her surgery due to increased pain and swelling in her throat. The swelling in her throat started to cause her oxygen to drop down so they had to start her on a steroid to help keep her airway open. Brooklin was discharged home with medication... 3 days after she was discharged Brooklin stopped breathing. I frantically picked her up and started patting her back while we waited for 911 to come. Brooklin was transferred by ambulance to OSF where she has spent 5 days in ICU and intermediate care. She was having recurrent apnea episodes and after many tests she was diagnosed with survere acid reflux. Her reflux is so survere that it is causing her to stop breathing. She is also aspirating on her acid reflux. Brooklin has since been started on numerous medications to attempt to control the reflux and also medications to help with the inflammation in her throat. So far the medications seem to be helping. But if they stop helping her next step would ve stomach surgery to correct her reflux. The surgery needed is very high risk with many bad side effects. Currently brooklin is admitted at OSF children's Hospital in peoria IL where her mother has been staying with her 24/7. Due to her condition brooklin will need lomg term physical therapy, speech therapy and ongoing care. Her mother hasn't been able to truly work her business due ti multpile hospitalizations with brooklin and her father has missed lots of work due to her being sick as well. They are now behind on multiple bills and are asking for help. If you are unable to donate please just pray for them as They get through this difficult time.
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<div>UPDATE 9-5-20
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<div>Unfortunately Brooklin was MISDIAGNOSED and does not have laryngomalacia but has a terminal illness called Spinal Muscular Atrophy type 1. We are now fighting for her life daily ❤️ she was dosed with Zolgensma (gene replacement therapy) a few weeks ago. She currently ramains inpatient in Chicago where we do daily breathing treatments/physical therapy/occupational therapy/speech as we try to perfect her daily routines. She also had a NJ tube placed as we await gtube/nissen surgery for her survere reflux. She also has since started bipap treatments. PLEASE keep her in your prayers. 
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<div>I have been posting frequent updates following the 9-5-20 update above so make sure you scroll through the entire updates section to get 100% up to date on this storyNatalie Bomke from FOX news Chicago has done several news stories on our sweet baby as well❤ you can view those just by searching her name: Brooklin Konczak on google.
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<div>On August 14 2020 Brooklin was one of the FIRST BABIES IN THE NATION to recieve a revolutionary treatment called Zolgensma aka GENE REPLACEMENT THERAPY. It saved her life. And while there is still NO CURE for her disease... She is doing things today that we were told she would never do! We were told she wouldnt live past 6 months of age, she just celebrated her 1st birthday in March 2021. We were also told she would never eat by mouth, roll over, talk, crawl or walk.... While mostly tube fed... She CAN NOW EAT 2 OZ A DAY ORALLY!!!! SHE TALKS SO MUCH!!! &amp; HER LAUGH WILL WIN YOUR HEART❤ SHE IS SERIOUSLY ALWAYS SO HAPPY. SHE ALSO JUST STARTED ROLLING OVER FULLY LAST WEEK. we are so incredibly thankful to god and her care team at luries childrens hospital in Chicago as well as her primary care team here in peoria. I will continue to post updates on this go fund me in the updates section for anyone who wants to follow her journey. Every single day she is here is a blessing. We live life one day at a time with so much gratitude. 
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<div>I have also reached out to the ellen show in hopes to get Brooklin on her show and spread awareness for her disease to get all 50 states to add SMA to the newborn screen. I pray my daughters story helps get babies tested at birth globally and that her story saves lives. I dont want any other baby misdiagnosed and being treated late like brooklin was. She lost so much function in those 5 months
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<div>We are also still trying to desperately raise funds for a handicap accessible vehicle with A wheelchair ramp. Our vehicle is no longer fesiable the bigger she gets. She is getting very hard to physically transfer and transport. Any donations on this page to help us with that are so appreciated. My husband (brooklins daddy) was also just diagnosed with renal cell carcinoma, kidney cancer at age 31. He just had surgery to remove it and is out of work for a while...donations will also help us financially during this time to help us pay our bills such as (rent, water, electric) if you are unable to donate and help us please just share this go fund me so that more people see it. Thank you everyone and god bless each and every follower/supporter we have. 
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<div>UPDATE: 10/3/22
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<div>I have been continually updating the updates section on My daughter and her condition but I forgot to update here as well. Brooklin is currently admitted at OSF children's hospital on Peoria where she has been on life support for 28 days. She was admitted for Respriatory failure following Rhinovirus and Parainfluenza type 4. It has been a down hill battle since she was admitted. We attempted to extubate her last week and she collapsed her lungs requiring emergency re intubation. Brooklin isn't getting any better and hospice was consulted on over the weekend. The Drs here feel stuck and do not think they can successfully extubate her off of the life support. They want a second opinion on her care from somewhere who is more specialized in her disease. We wanted to transfer her to Luries in Chicago because that is where all of her specialists are and we see them every 3 months at MDA clinic however Luries hasn't had any beds available in the PICU. At this time our only option is Luries doesn't open a bed is to transfer her to either Wisconsin or st Louis where they are more familiar with her disease. Currently all donations received will go towards our immediate family traveling with her life flight wherever we have her transferred. We are currently in need of help with gas expenses, lodging expenses for her dad and sister (I will be staying in her hospital room but sister can not) , food expenses and whatever else may come with us making this transfer. Brooklin is in critical condition and she will be a high risk transfer so she will be life flighted and we will have to drive seperately. I have received tons of messages and so many prayers and I just want to say that we are so greatful for all of the support we have received. I will continue to post updates in the "updates section" on her condition. I also post frequent updates on my personal Facebook page for anyone who is wanting to follow there as well. (Angela Konczak on Facebook). 
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<div>Angela Brooklins mommy 
</div><img alt="49140526_1599336972545807_r.jpeg" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/49140526_1599336972545807_r.jpeg" width="100%" /><img alt="49140526_1599337006386221_r.jpeg" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/49140526_1599337006386221_r.jpeg" width="100%" /><img alt="49140526_159933703032298_r.jpeg" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/49140526_159933703032298_r.jpeg" width="100%" /><img alt="49140526_1599337089698917_r.jpeg" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/49140526_1599337089698917_r.jpeg" width="100%" /><img alt="49140526_1599337137909196_r.jpeg" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/49140526_1599337137909196_r.jpeg" width="100%" /><img alt="49140526_1599337175695308_r.jpeg" media_type="3" src="https://d2g8igdw686xgo.cloudfront.net/49140526_1599337175695308_r.jpeg" width="100%" /><img alt="49140526_1599337189934801_r.jpeg" media_type="3" 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Brooklin Konczak care and family expenses

Mollie Morris

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New funds eligible - Video Sharing (PROD)

NPO email opt-in candidates

GB Donation Upsell audience 

Auto Thanks V3 Rollout Audience

Thank you V3 testing whitelist

Excluded funds - Video Sharing

Fundraiser Without Instagram Deep Link (amp15)

NPO upsell animals category

NPO upsell disaster relief category

Logged In Users

CH Donation Upsell audience

Android v10.6.0 and above

NPO upsell essential needs category

NPO upsell medical category

userCurrencyCode

Localized Currency

NPO upsell cancer category

v11.5.0 and above

testAudience

pathname

Survicate

appVersion is at or above 12.8.0

Non-charity fund

isChallengeFundraiser

challenge-fundraisers

Payment Identity Launch Verification - Production

New funds eligible - Posters v2

CAD Donation Upsell Audience

iOS App Version

hasKnownDonors

PYMK has donors

iOS v12.3.0 and above

Mollie Morris

Mollie’s featured causes

Help Beth and Ralph O'Sullivan Rebuild After House Fire

Wallace's Medical Expenses

Brooklin Konczak care and family expenses