Paris Hilton

Jimmy  Darts

Flavor Flav

SB Mowing

Kalina Silverman / @makebigtalk on Instagram

The Dogist

Patriotic Kenny Foundation

Pattie Gonia

Little Miss Flint

Carlos Eduardo Espina

Samuel Weidenhofer

Ben Saunders - Flawless Cleaning

Peter Bond

That Good News Girl

Ask Uncle Jack

Amy Jandrisevits

FowlMouthFarmer

Tess Bohne

Latonja and Taylor Richardson

Officer Richard Craig

Heather is raising this fundraiser for her sister Danielle and Danielle’s family during an overwhelming crisis. A few weeks ago, Danielle was crossing in a crosswalk on an e-scooter with the walk sign on when she was hit by a car. In a terrible turn of events, the driver then mistook the gas pedal for the brake and hit Danielle again. Danielle suffered a broken tibia and fibula in her leg and had to undergo surgery to have a rod and screws placed. Since then, Danielle has been unable to work. As if that were not enough, Danielle is now back in the hospital battling DKA and blood clots in the lungs while the family is also facing the loss of their home. 
 
 
 Danielle has three children and a husband, Geoff, who has been unable to work because he has been caring for the kids through all of this. Right now, Danielle and the family are doing everything they can just to make it through each day. The funds raised will go toward helping keep them off the streets and making sure they have food during this incredibly difficult time. Please consider helping in any way you can. Thank you to everyone willing to give a helping hand, whether it is a share or even $1. Anything truly helps, and every bit of support means so much to Danielle and the family.

Help Danielle and Family

I have known Amanda for 13-plus years. She has put herself through school to be a pharmacy technician and then continued her education to obtain her Master's in Special Education. During this time she had a miracle daughter Larissa as she was told she would never be able to have children. Larissa is now 12 years old and was recently diagnosed with Paroxysmal nocturnal Hemoglobinuria (PNH Clone) which is a rare and complex blood disease that involves the destruction of red blood cells and causes patients a variety of symptoms such as anemia, blood clots, and/or bone marrow failure all of which can lead to life-threatening complications. Larissa’s condition is not curable but is treatable through monoclonal antibody therapy which she will have to receive every 8 weeks for the remainder of her life. Larissa and her mom have been at Stanford’s Children’s Hospital since September 22, 2023. Amanda is the sole provider of her family and has not been able to go back to work as she has been at the bedside with Larissa. This has put a huge financial burden on the family and caused a tremendous amount of stress on Amanda, trying to figure out how she will be able to pay bills, utilities, and rent that are overdue. Larissa is a genuinely happy young lady with a heart of gold and has kept a positive attitude through everything she has been going through. The family is currently staying two blocks from the hospital at a Ronald McDonald House so they can be close to the hospital where Larissa is starting her treatment and receiving blood transfusions bi-weekly.   We are asking for any financial assistance to support the family so they can continue to support themselves during their hospital stay as well as their utilities and rent back at home. I am so very proud of both Larissa and Amanda for keeping positive attitudes and supporting one another through this difficult time. If we can please help Larissa and Amanda to be able to come back from the hospital and still have their home. We are trying to raise at least 20,000 for rent, utilities, transportation, and basic necessities so the family has what they need now during their hospital stay and a home to come back to. Please help my dear friend and her family in any way possible during this challenging time. Anything will be greatly appreciated prayers included.

Help Larissa diagnosed with a rare blood disease

<div>As many of you know, Tim Tucker, passed away on January 18, 2023, after a year and a half long battle with leukemia. Tim was loved by all who knew him. His sobriety and family were the most important things to him. He made everyone laugh, including his doctors who worked so hard to treat his leukemia. He was a lover of life through and through, and had the biggest heart and the best spirit. In the last year of his life, Tim lived with Anna, his modern wife, and two of her sons whom Tim called “Nicky” and “Al,” and who he lovingly regarded as his stepchildren. During this time, Tim described himself to one of his cousins as, “the happiest Ive ever been in my whole life.” 
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<div>Despite Tim’s illness, his passing was sudden and unexpected. As a result, Tim’s family is humbly asking for financial assistance to help offset the costs of funeral expenses. Please know that any donations are so appreciated. Tim’s family is so grateful for their community who has rallied around them since his passing.
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Funeral Expenses for Tim Tucker

<img src="https://d2g8igdw686xgo.cloudfront.net/51095530_1599688359457057_r.jpeg" alt="51095530_1599688359457057_r.jpeg" width="100%" media_type="3" /><img src="https://d2g8igdw686xgo.cloudfront.net/51095530_1599688374424366_r.jpeg" alt="51095530_1599688374424366_r.jpeg" width="100%" media_type="3" /><img src="https://d2g8igdw686xgo.cloudfront.net/51095530_1599688412979981_r.jpeg" alt="51095530_1599688412979981_r.jpeg" width="100%" media_type="3" />Monica and Mark lost their home in the Creek Fire Sept. 2020.  Their family through the loss of their son Josh in 2013 started a non-profit to help our Mountain Community. Over the past 7 years we have watch this family give so much of themselves in Josh's memory.  They helped those in need with monetary donations raised by the JHF for children and families in our community and beyond. Today with a heavy heart  the Hansen Family suffered yet another loss, their home.  I am asking you to give to help them rebuild their lives during this tragic time. The Hansen Family would never ask for help, they are endlessly a giving family.  The phrase they lost it all. you will never hear them say.  They have each other. They are so humble and a God loving family who has given so much for those in need in the past. Now it is our turn to help them. Give what you can any amount will add up.   God Bless you Monica, Mark, Sarah Mae and Joseph Hansen you are in our hearts and in our prayers .

Hansen Family Home Lost in Creek Fire

The SCU fire has burned my good friend's home and his father's and brother's too. Dylan, Todd, and Robert Clary all lost their homes. They have built completely off the grid homes on the back side of Mt.Hamilton called the Skyranch. All three homes and everything in them, burned to the  ground.  Their solar fields have damage,  their water containment systems are destroyed. Sadly, even with  insurance, their coverage will only pay a portion of the massive damages. Please help with whatever you can.  They have worked hard to build and harness the land around their homes, and are good people. They need your help to rebuild.  Three families have been displaced, and whatever you can spare will be used with gratitude! Thank you and God bless.  For transparency, my name is Bert Lankins, and I've been friends with Dylan for over 30 years.

Dylan's family fire rescue

Many of you know that Kristen Frost was diagnosed with Lyme’s disease as well as two co-infectors which add even more complications. After four months of treatment, her health is still deteriorating with no improvement. She has lost 25 pounds, has many neurological issues and is bed-ridden much of the time. Her body is unable to tolerate antibiotics, many natural herbs or even detox the parasites. Her doctors here have recommended she seek alternative care at a facility in Franklin, Tennessee. This facility is NOT covered by insurance. Her care there will be daily, outpatient for three weeks. Their success stories are great. We pray that we can raise funds for the total cost of treatment, travel , lodging and follow-up visits. Thank you for blessing our mom, family and dear friend.

URGENT  Lyme & Babesia treatment

This campaign is for my dear friend Merry Mayes Francom who was diagnosed with Stage 3 "triple negative" breast cancer in September 2017, just 5 weeks after receiving a clean mammogram. This type of cancer is not fed by hormones, and she tested negative for all 28 cancer genes. This cancer is so unique. Just like Merry. She had phase 1 of chemo, and developed a toxic side effect to phase 2 and had to stop, then a double-mastectomy in March 2018, and radiation (May-June 2018), and was declared cancer-free in August. That moment was beautiful, full of gratitude, and victorious! Just like Merry. Just 3 months later, she had a biopsy on a lump under her arm and it was cancerous. The cancer had spread to her bones, specifically, in  the tops of her femurs, hips, pelvis, spine, right shoulder, left underarm, and a spot on her skull. This cancer is persistent. Just like Merry. The pain is such that she needs a walker or a cane. Because it has metastasized to her bones, they are weak and have resulted in hairline fractures in her hips that cannot be treated. Typically, breast cancer that metastasizes to bone leaves the patient with an 18 to 48 month lifespan. The survival rate beyond 5 years is roughly 20%.  This past week Merry received another blow. She was given 1 to 12 months to live. Like the cancer that is fighting to be present and survive, so is Merry. Even in the midst of her diminishing physical health, she remains persistent, beautiful, full of gratitude, and she is victorious for continuing to fight.  Some of the many things that make her so unique. If this is her last year on earth, I want nothing more than to make come true, all of those birthday wishes that would have surely been. Her wishes in her own words: 1)     Seeing the Grand Canyon again 2)     I want to visit my father's grave in North Carolina, and my mother's          grave in Wisconsin 3)     I want to go to the beach - a real beach, from the ocean, with Jim                (my husband) and watch the sunset (or sunrise, depending on             which coast we are on) 4)     I want to visit Yellowstone 5)     See the group Boston perform 6)     I want to meet Steve Young (former NFL player) 7)     Make a trip to the Diamond Park in Arkansas 8)     Go to Snake River to spread my brother's ashes as he requested 9)     I want to have a nice dinner in a nice restaurant on the East Coast              -- Boston, NY, RI, wherever 10)  I want to meet the President, Clint Eastwood, and Robert Redford. 11)  I want to go to church at Shelter Cove Community Church           again, with Pastor Seifert presenting the sermon. 12)  Lastly, and most important, I want a family reunion here in Utah. I  want my family to come see me -- all at once. Sheryl (Oregon),            Diane (Arizona), Heather, David and kids (San Jose, CA), Kathleen, Octavio and kids (Escalon), Naomi (California), Chris and Jazmine           (Utah), Lorena, Ana and Christopher (Manteca, CA), and Meagan,           Noah and family (Modesto, CA). Merry and her husband Jim have good medical insurance, but have substantial out-of-pocket costs that have been a significant financial burden. This campaign fund is not only to help make those wishes come true, but to relieve some of that financial burden while Merry is no longer working full-time.  Please help give her the memories to last an eternity if this is her last year of making wishes come true. Your donations are greatly appreciated. Please share this campaign with at least 10 of your Facebook friends and ask them to share with 10 of their friends to help us reach her goal. Thank you for your love and support of Merry!

Make the wishes of a lifetime come true for Merry

My wife, Kaye, moved to California from Nashville many years ago to escape an abusive marriage.  She packed up her two girls and drove as far as she could - to the Pacific Ocean.  There, she built a life, raised her daughters, and many years later, met and married me. Now, the daughters are grown and live in Arkansas and Tennessee.  Kaye is 70.  Her last surviving brother died a couple weeks ago, and it hit her hard that she couldn't attend the funeral.  Kaye has sisters, cousins and children she hasn't seen in over 20 years.  She has great-grandchildren she has never seen.  Her greatest wish is to make a trip back to see her family. I want to raise $2,000 for her to take that trip.  Kaye is disabled and will need special care on her flights.  I want her to have her hair and nails done and to have a few new outfits.  I want her to be able to cover expenses and not to have to worry about money while she's on what will probably be her last trip back to where she grew up.  If any money is left over, it'll be used to catch up on our bills.  We need this money by the end of August, 2017. We are elderly and live on Social Security.  There's no way we can afford for her to make this trip - but it would mean so much to her!  And it would mean so much to me to be able to give her this. Kaye's health is failing.  She won't be able to contemplate a trip like this for much longer.  Kaye has spent her life helping others.  She was once an aide to the governor of Tennessee.  She was friends with Roy Orbison and was riding motorcycles with him and his wife on the day she was killed.  She knew people like Dolly Parton and Porter Waggoner.  Now, we are just a couple of old folks living in a trailer park in Modesto, California.  Help me send her back for this last trip to her roots!  Help me help her hold her great-granchildren.  If I could give my wife this one thing, I'd be happy for the rest of my life.  I don't want anything for myself.  I just want to give my sweet wife the one thing that would mean more than anything else in these last years of our lives.  I'm saving too, because I want her to have the memory of it.  But with car repairs, medical expenses, soaring utilities and groceries, it's pretty hard to save at all.  It's hard for me to put this out there - I'm always the one who's saying, "I got this."   But I need some help with this one. Thank you for taking the time to read this, and please share what you can!

Help Kaye Reunite With Her Family!

Hello, My name is Gina Shoars and I am one of Raschel's best friends. On Saturday 5/13/17 we lost a wonderful, bright, lady. Our world is a bit dimmer as we remember the light of our dearest friend, Stanislaus County Sheriff's CSO Raschel Johnson. As a daughter, sister, wife, mother of three, grandmother of two, and a friend to more people than she could count, she lived her life to the absolute fullest. She was passionate in everything she did, and loved without reservation. Her love for her community was shown in her commitment to her career as a CSO. As we celebrate her life we would appreciate you joining us in supporting her family during this time. Any money received will go directly to Michael Johnson to be used for funeral expenses along with any and all needs for the family.

Memorial fund for CSO Johnson

As many of you know, Jenn is in the ICU battling a severe infection that is still affecting her kidneys, blood sugar, and calcium levels, which in tern, is affecting her heart. All of this started with a high fever, vomiting, lack of oxygen and eventually, blood clots.  She has made some progress but is still in a very serious state. She will be in the hospital for quite awhile longer. She and Greg are amazing parents to 4 little ones who need childcare and babysitters more than ever now. As we all know, these can be hefty bills and any amount of donation you can give will help make this expense lighter for them as they are both off of work.

Jenn's childcare & medical expenses

On October 16, 2016, Karen learned that her daughter Kasaundra and boyfriend Tony were tragically killed as they were crossing the street and hit by a car.  They resided in Georgia and they leave behind a 2 year old daughter Lailanee.  The funds will assist Karen with travel and funeral expenses. "They were together when God took them back to his loving arms.  Going to plan on a joint Celebration of Life." Karen Muldrow

Support Karen Muldrow

Please help us raise money for a Marty’s difficult road ahead. Marty is a single Mom of a 20 year old who is in college, she is a sister, a loving daughter and loyal friend to many. A week ago, Marty was diagnosed with a neuroendocrine tumor on her pancreas. This is the same disease that Steve Job was diagnosed with too. Marty already suffers from auto-immune disease in her liver and has been fighting it for 10 +years. On an average day, Marty already suffers from chronic pain, fatigue and insomnia. She struggles to make it through a day’s work but she keeps pushing. Over the last 2 months, she started dealing with a new pains that she was getting in her side, back, as well as constant stomach issues. Her doctor ran tests and a CT scan. The scan revealed a dark spot on her pancreas. Last Monday, March 16, the biopsy confirmed it was a cancerous tumor that had to be removed. They also found a suspicious lymph node that they took a biopsy. On Monday, March 23, she will have the tumor removed and we are hoping they are able to get all of it and the treatments after will be minimal. No matter what, we know that the cost of these procedures, treatments and time off of work is more than Marty can afford. We are asking for any help you can give so that she can worry only about recovery, beating this battle with cancer and not about the bills that will inevitably come. Marty is an amazingly giving and generous person and I don’t mean with money but her time. She is always willing to help anyone she can. During the time her daughter was in track at Mt. Pleasant she not only helped raised money, but took over running the snack shack selling, cooking and doing anything she could to help. Marty’s daytime job is as a visual manager which comes in handy when people want to help decorate for the holidays. She is amazing and always willing to come to family and extended families houses to help. She doesn’t do it for money but because she loves to make people’s holidays special. She is just talented and puts so much love into anything she does. I have seen her design custom block letters for high school letterman’s jackets, make flower and ribbon leis for friend’s kid’s graduations, and there is so much that she does that makes her special and loved by so many. And when it comes to family, Marty would give anything she had to support a family member in need. She is the same with friends who have become family.   Marty would never ask this for herself so we are asking it for her. Prayers and healing thoughts are always requested and are welcome. Thank you! The Munoz Family

Marty Munoz Medical Expense Fund

This is my son Christopher with his mom,  He dreamed of becoming a Ear Nose And Throat Doctor at a very  age. He had many problems with his ears at a very young age due to allergies we did not know about. His doctor for many years was Dr. Venterini which he just loved. Dr. Venterini was the one that inspired Chris to go into the medical field.  Chris always loved school, baseball, mountain climbing, extreme bike riding, motorcycles, skate boarding, and every other sport he could get involved in. We all climbed half dome in yosemite right before this happened to him. I can remember going to hundreds of baseball  games throughout his younger years. When Chris started High School he was planning on going out for the high school baseball team, but plans changed when he broke his arm snowboarding. So he went out for water polo after the healing was over. Was not quite the same but he loved this also and it sure got him in shape.  We have changed our entire life style to help Chris with this medical issues. This money will be used to receive treatment for my son Chris.                      He was diagnosed with Hashimotos Encepalopathy About two years ago. He has had this disorder for over 8 years and we have been dealing with doctors for all these years trying to get one of them to figure out what was causing his issues, and not just giving him medication to treat the symptoms they were seeing. Chris has not talked in over 4 years due to this condition. We have spent all of our life savings, we have even borrowed and been given money from family in the past to help. Chris was a full time student and was planing on becoming a doctor before this all happened. He has been to multiple hospitals and we have paid for every test imaginable to try to help him. I decided to retire from my job early to become his care taker in 2008. This disorder affects about 2 people in every 100,000. Doctors do not know exactly how to treat it or what causes it and so we are hoping to take him to a facility out of state for some other kind of treatment. The Doctors at the facility we go to now want to try immune suppressant drugs which are very dangerous and have very serious side effects. If Chris could talk and wanted to try this avenue we would stand behind his decision, but without him having a say in this potentially deadly treatment we will not do this treatment and put his life in danger. Chris had insurance a few years ago to cover most of his treatments but the insurance company decided to cancel his policy saying it was a pre existing condition to which our doctor said it was not. $98,000 in hospital bills later we had no health coverage for him, which left him with a ton of bills. Chris is now 29 years old and i take care of him full time while my wife works a few more years, we have run out of money to help him and just use the income from retirement and my wifes job to help him and pay the massive bills we are left with.  I could go on for days on all the doctors and misdiagnosis we have seen and been given over the years by the so called experts, I have had to threaten to sue, get an attorney, even call the Citizens Commision on Human Rights, (CCHR) to get him out of hospitals and for them to stop giving him medications that were causing more problems for him. We are never going to give up on him and hope we can find a soulution to this horrible disorder he has been inflicted with, Doctors say ther is no cure but  he can get lead a normal healthy life if we can get it under control.

David Swanson