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 Vista Grande Community,

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<div>We wanted to update our VG family on <strong>Mr. Frank, our custodian</strong>. As many of you know, Frank was diagnosed with cancer last spring, and he spent the last several months fighting a very difficult treatment battle. While he was successful in completing his treatment, it took a very severe toll on his body, and he came to the unfortunate conclusion that he would not be able to return to VG in his current condition.

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<div>So many of you sent well wishes and donations to the <strong>GoFundMe</strong> that we had set up for Frank at the end of last year, and he is beyond grateful for all of the love and support he received. Frank wants everyone to know that he feels he could not have made it through without the VG community rallying around him.

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<div>Please join us in wishing Frank well on his retirement, and should you feel inclined, <strong>please see the link below for one last opportunity to show Frank our love and appreciation</strong>.

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Falcons for Frank

<div>Our good friend, Anuar Chavez, is currently battling stage 4 cancer. We’re seeking donations to give Anuar a fighting chance to beat cancer. This fundraiser symbolizes love, perseverance, and an unwavering pursuit to beat the odds.
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<div><strong>Anuar’s Story</strong>
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<div>Anuar is a young 42 year old male who lives a very modest life. He works hard, has no car, and lives with his loving mother, Armida, who had him at the young age of 17. He’s overcome many adversities in his life including a lack of educational resources, financial hardships requiring him to work to make ends meet since he was 15, and withstanding emotional abuse from an alcoholic father. He hustled his way to being a renowned bartender, waiter, boxing coach, and most recently climbed his way to management at a high end hotel.
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<div>By nature, Anuar is a very caring and nurturing person who puts everyone before him. He’s been known to accommodate everyone with empathy and compassion whether it’s offering food, drinks, his seat, etc. He’s also known to tip generously (even though he had financial hardships) and would go out of his way to ensure folks at restaurants, hotels, and more were appreciated and seen.
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<div>In December of 2023, Anuar suffered a chronic and debilitating cough that left him bedridden for several months. Finally on March 30, 2024, he turned yellow throughout his skin and eyes leading him to the ER at UCLA Medical center where he was diagnosed with stage 4 colon cancer which had already spread to his lungs, spinal cord, and kidney. He spent nearly 40 days in the hospital before being released in May.
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<div>But given Anuar’s resilience, he’s committed to beating cancer and overcoming the odds. Just like the various obstacles life has thrown his way, Anuar is prepared to fight for his life!
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<div><strong>How does your donation help Anuar beat the odds?</strong>
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<div>As caring family and friends, we’re exploring everything we can to help our dear Anuar and your donation goes a long way. This includes specialists, care, ongoing treatments, and anything to give Anuar a chance. Additionally, there are general expenses we’d be remiss not to mention like rent, food, and transportation.
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<div>Your donation provides more than just financial assistance. It truly means a lot to Anuar and his mother. It offers support, care, and a feeling of unity to battle this dreaded cancer together.
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<div>Follow Anuar’s journey by revisiting this page weekly for updates.
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<div>Thank you for reading this and thank you for supporting Anuar. It means the world.
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<div>-Anuar’s family and friends
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Donate to Anuar’s Cancer Fund: Beat the Odds

<div>It is with great sadness and disbelief that we announce the unexpected passing of our beloved Nicole Roy at only 43 years old.
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<div>Nicole was a loving wife to Brian with whom she shared so many of life’s adventures. She was an amazing mother to her beautiful children, Taliah and Lailani, who made her proud every day.
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<div>Nicole was a beloved daughter, devoted sister, loving Auntie, caring niece, and dedicated cousin. 
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<div>Nicole’s presence would always bring a smile to our faces. She lived a life of true authenticity and had the unique gift of being present to everyone around her. She was a loyal friend to all of us, with such a kind and gentle soul. We are blessed to have known her, and we are forever grateful.
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<div>She spent every day for the past three years homeschooling her daughters. She encouraged her children’s imagination and creativity, and at the early age of 11 Lailani authored a book called Spies in the Museum, which is sold on Amazon.
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<div>While no sum can ever eliminate the trauma and grief that accompanies the tragic loss of a parent, we hope to ease the burdens they now face. In addition, if you wish to encourage a budding writer, attached is the link to Lailani’s book.
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<div><a href="https://a.co/d/0LFELhp" target="_blank" class="" rel="nofollow noopener noreferrer">https://a.co/d/0LFELhp</a>
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<div>Kindness does not cure all, but it helps dry tears and heal hearts.
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<div>Thank you, and may you Rest In Peace, sweet Nicole. You are so very loved and we will miss you dearly.
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Nicole Roy

<div>Hello Falcon Family! 
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<div>At Vista Grande, we pride ourselves on being a strong community that supports one another during the good times and bad.  When one of our own has fallen on difficult circumstances, we pull together to do what we can to support. 
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<div>We are raising funds to help Frank Beasley, our lead custodian, who is currently battling cancer.  Mr. Frank will be undergoing daily treatments 5 days a week, and will not be able to work during this time.  These funds will be used to help him meet any unexpected expenses and costs. 
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<div>Frank is an integral part of our school, and we would love to help support him during his treatment.   
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<div>If you feel inclined, any support will be greatly appreciated.
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Falcons for Frank!

<div>Tim is generous with his time and empathy. He is the kind of person who will go out of his way to be the first person there if you're in trouble or need someone to cry with. He is supportive of others, service driven, and great at building up his friends when they are going through a rough patch or trying to accomplish a goal. Tim is also a lot of fun to be around, and - if you've spent more than a few minutes with him - you'll know he can talk your ear off about fitness, nutrition, history, and video games. He takes a genuine interest in others, and is a once in a lifetime kind of friend. He's the best husband I could have asked for and an amazing cat dad. He's never needed support more than he does right now.
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<div>Tim was unexpectedly diagnosed with Hodgkin's Lymphoma shortly after getting COVID for the first time. One of the lymph nodes in his neck became enormous and never stopped being enormous. He was just starting to get on his feet following a move to NY, and just started a new job that he loves. His job has generously agreed to accommodate him with remote work and days off as he needs them, but we are both about to face some serious medical costs and labor strains on our household. He is going to be at high risk of infection during treatment so we are not cutting any corners on safety.
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<div>The current funding goal is the bare minimum of what we need, and will cover treatment costs, transportation, medication, and other related costs for one cycle of treatment. Tim's oncologist is fairly confident this will be cured in 2-6 months. If he only needs one cycle of treatment, this should nearly cover our costs and we could cover the rest. If he needs more than one cycle of treatment, our funding goal may change.
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<div>If you can't donate but want to help in another way, we will also have a meal train starting soon and could use help with household stuff (maybe).
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Help Tim beat cancer (HL)!

On Monday October 12th, as the Kellso family was loading up to return home from their fall break vacation, there was an accident.  Caleb Kellso (age 5) was severely injured and our gracious Lord saw fit to take him from this world.  We are all grieving deeply but with an unshakable hope in our loving God who cares for us better than we could ever comprehend.  Caleb was full of an infectious joy that spread everywhere he went.  He was sweet, kind, and such an amazing little brother to Kyla, Elijah, &amp; Asher who will miss him dearly.  On behalf of the family, we have set up this GoFundMe campaign to help support the family with potential medical and funeral expenses.  We know that this pain will last a long time and hope to help this dear family financially prepare for those difficult days.<br /><br />There is also a benevolence fund set up through Josh and Julie’s church (<a href="https://www.gbcaz.org/mourning-caleb-kellsos-death-trusting-in-our-good-god/" target="_blank" rel="noreferrer noopener">Grace Bible Church in Tempe AZ</a> ).  If you’d like to send your donation through that fund, <a href="https://gbcaz.ccbchurch.com/goto/giving" target="_blank" rel="noreferrer noopener">click this link</a> and choose the designation “<a href="https://gbcaz.ccbchurch.com/goto/giving" target="_blank" rel="noreferrer noopener">Benevolence Caleb Kellso</a>” and the church will ensure the money is used in the care for this dear family.<br /><br /><strong>Keep reading to see a letter that Josh wrote to his church family:</strong><br /><br />Dear family, friends, and many we have never even met,<br /><br />We want to express our thanks to you all for the overwhelming love and care we have experienced these last few days. Thank you for praying. Thank you for encouraging us with Scripture. Thank you for your practical provisions. Thank you for mourning with us so well. And we especially thank God Who is our Rock and ultimate Comfort. He has used you all as a means of grace to us in our sorrow.<br /><br />For those of you who do not know, on Monday 10/12 our benevolent Lord saw fit to take our precious youngest child Caleb (5) from this world. Our family was vacationing up at our family ranch as we often do. The Lord’s kindness to us was so abundant as we had a wonderful week together as a family. Caleb got to hunt with Asher, Elijah, and me. Caleb got to ride the quad by himself for the first time. He did AMAZING and LOVED it so much. Caleb was the first out of the house to congratulate Asher on his deer, and the whole family enjoyed time processing the deer together. He played many foosball games with everyone in the family. He enjoyed hunting for lizards, spiders, and moths with Kyla. Julie and Caleb got many sweet snuggle times together. There were many hugs, kisses, and “I love you’s” this last week. There were too many joys to mention them all and we continue to treasure each one with thankful hearts.<br /><br />In the afternoon, as we were preparing to come home from our family vacation, we were loading up my truck. The kids were all helping. As usual, Caleb was jumping in to help as well. He was such a sweet servant! I (Josh) was going to move my truck closer to the home to continue loading up. While I had thought the kids dispersed behind me for another activity, our precious Caleb had actually moved in front of me. As I pulled the truck forward, I inadvertently ran over Caleb. The best we can tell, he had possibly dropped something in front of the truck and was attempting to get it. Realizing what might have happened, I quickly jumped from my truck and sought to care for Caleb. It is clear now that Caleb passed very quickly. We thank God for that grace. However, I, with Julie’s help, performed CPR until medical professionals arrived. As they took over, every attempt to revive Caleb was made with no success. We are grateful that the Lord protected Julie and the other children from having to see the tragic accident take place. That was a mercy from the Lord.<br /><br />My cry while performing CPR is our cry today, “WE KNOW GOD IS GOOD!” We dare not ask God to bend His will to ours but rather ask that He bend our will to His, even if that means being broken and crushed. For the tender mending care of our loving Shepherd is precious to us. We will not reject the anguish for in the depths of our anguish are the mountains of His comfort. And we do not fight against our sorrows. For the intensity of each sorrow is a testimony of how precious our Caleb was to us and how intense our love was for him. Both of these are graces from God to us. We thank God for the undeserved blessing it was to be with Caleb for 5 years, 9 months, and 20 days. Each moment with him was an indescribable gift. He brought such joy to our lives and sweet energy to our home.<br /><br />We do not need answers to why beyond what our sovereign God has given us in His Word. For in His Word is every answer we need and His Word is more precious to us than all the riches of the world. Even more than the riches of parenthood. What else would we need, and where else would we go than into the loving arms of our Savior! Our great God has provided for our biggest need in the forgiveness of our sins through the death of His own Son. With that precious truth in mind, we dare not question His love. How could we? Rather, we cling to Him. You all have been a means of God’s loving care for us. And for that, we thank you and worship Him. We know God is sovereign, and there is no better place for us than where He has us today. We TRUST! We YIELD! We mourn! We BLESS His Name! And though our tears fall almost constantly, we fall on our faces and worship! Blessed is the name of our Lord!

Trusting God As We Mourn Caleb Kellso's Death

Four-year-old Ella Simone Newman was diagnosed with leukemia on January 31 at Kaiser Medical Center in Oakland, California. What began with occasional nosebleeds and random bruising was found to be something much more serious.<br /><br />Ella’s treatment going forward will consist of 8 to 9 months of chemotherapy to be administered at home by her parents Rosie and Ari.<br /><br />Ella will not be able to attend school during her treatment since the chemotherapy will likely weaken her immune system. Should she develop a cold or slight fever, she would need to be rushed to be the hospital for immediate care. Sadly, this will also mean that she and her twin brother Desmond will need to be kept apart so that she doesn’t contract anything from him. We have set up this GoFundMe page to help give the family a little breathing room as they adjust to this stressful situation and to allow Rosie and Ari time to focus on Ella’s recovery.<br /><br />Ella’s two favorite things in the world are the movie Frozen and Desmond. They both have a brilliant sense of humor and are full of loving smiles. <br /><br />Anything and everything helps. Please don't hesitate to reach out and offer your support. Thank you!

Ella Simone is fighting Leukemia

Bhavika Taunk

<div><strong>Help Kabir Fight: 3x Leukemia Survivor Facing New Challenges</strong>
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<div>As Bhavika Taunk, both Kabir's mother and his primary caregiver, my relationship with him goes far beyond the anything I imagined for our mother-son journey. It's been shaped by sleepless nights in hospital rooms, a rollercoaster of hope and despair, and witnessing first-hand the extraordinary resilience and of our warrior.
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<div>This fundraiser is more than just a campaign; it's a beacon of hope in our three relentless battles against leukemia and their aftermath—a journey that has stretched our family's strength and highlighted the incredible power of love and resilience. This cause is deeply significant to me. It's about giving Kabir every opportunity to experience a life filled with joy and promise, despite the daunting challenges leukemia has caused. It's a deeply personal fight to ensure a future where Kabir can thrive, fueled by his unbreakable spirit.
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<div>Kabir was just 4 years old when he was diagnosed with a high-risk form of leukemia, known as Philadelphia Chromosome-positive Acute Lymphoblastic Leukemia (PH+ ALL), on April 20, 2017. His initial treatment at Lucile Packard Stanford Children's Hospital involved intensive, high-risk chemotherapy for two years. Following a relapse in July 2019 primarily in his central nervous system, which occurred just weeks after his initial treatment ended, the harsh reality of Kabir's condition became starkly evident, necessitating further, more aggressive treatmehts.
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<div>Our family's journey took a pivotal turn as we sought a CAR-T clinical trial at the Children’s Hospital of Philadelphia (CHOP), motivated by the limitations of insurance coverage in California. Despite our high hopes, Kabir experienced another relapse six months later, and yet again in July 2020 amidst the pandemic, each setback requiring more invasive treatments and introducing new, lifelong challenges.
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<div>In the summer of 2020, amidst considerations for palliative care, our hopes were renewed through a bone marrow transplant from Kabir's younger brother, Ayaan, a testament to their profound sibling bond. Kabir also underwent an orchiectomy requiring future hormone replacement therapy for his entire adult life. The rigors of the bone marrow transplant and its aftermath were daunting, leading to severe side effects and a year-long battle with thrombotic microangiopathy (TMA), which significantly impacted Kabir's kidneys and overall health.
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<div>Now 11 years old and three years post-transplant, Kabir's zest for life is still going strong. His passions for cooking, anime, swimming, and video games, alongside the joy he finds in spending time with Ayaan and our family dogs, Hachi and Mochi, show his enduring spirit. Our return to the East Bay marks a full-circle moment for our family, choosing to re-engage with our community while navigating the complexities of Kabir's recovery.
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<div>Recent challenges have included Kabir grappling with a rare condition affecting his spine's cauda equina region, a consequence of the intensive chemotherapy, which has introduced new neurological hurdles. His educational journey has been significantly disrupted, necessitating a highly individualized approach to learning and daily living, underscored by: chronic migraines, daily debilitating pain, severe nausea managed with chemotherapy-grade medications, neuro-cognitive deficits making learning very difficult, hypertension and neuropathic pain. Additionally, he has experienced intermittent incontinence and limb weakness, necessitating the use of a wheelchair for mobility.
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<div><strong>Supporting Kabir's Journey</strong>
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<div>In facing these multifaceted challenges, we are exploring every possible avenue for Kabir's care, including engaging with specialists from the rare disease networks and the NIH. The support gained through Kabir's GoFundMe page is pivotal, directly contributing to specialized care, ongoing treatments, and potentially life-altering research for other children in the future facing similar fates.
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<div><strong>Detailed Breakdown of Fund Utilization:</strong>
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<ul>
<li><strong>Medical Expenses</strong>: Substantial funds are allocated for Kabir's medical treatments, including those not covered by insurance, seeking second opinions, and maintaining the highest quality insurance through COBRA coverage.
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<li><strong>Travel and Accommodation</strong>: Ensuring Kabir has access to the best possible care, funds will support travel and accommodation near treatment centers.
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<li><strong>Rehabilitation and Therapy</strong>: Essential for Kabir's recovery, covering physical, occupational, and neurological rehabilitation.
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<li><strong>Education Support</strong>: Addressing the educational impact of Kabir's treatments, including specialized programs and the support of a special education attorney to advocate for an appropriate IEP.
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<li><strong>Living and Caregiving Expenses: </strong>Aiding our family in managing the day-to-day care and living expenses, allowing us to focus on Kabir's recovery.
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<div>Your generosity provides more than just financial assistance; it offers hope, a testament to the collective strength and kindness of our community. Join us in supporting Kabir's fight against his three battles of Leukemia. Together, we can make a difference in his journey towards healing and a brighter future.
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<div>Hero Quote: "You mess with one of us, you mess with all of us!" - Kabir Taunk
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<div>Follow Kabir's journey and our family's updates through Mom's Instagram.
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<ul>
<li><strong>IG: @btaunk </strong>
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<li><a href="https://www.instagram.com/btaunk" target="_blank" rel="noreferrer noopener"><strong><a href="https://www.instagram.com/btaunk/" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.instagram.com/btaunk/</a></strong></a>
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</ul>
<div><br />
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<div>Your support means the world to us and to Kabir, as we navigate this challenging journey. Thank you for standing with us.
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<div>-Bhavika &amp; Mandeep Taunk
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<div>YouTube Video:
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<div><a href="https://youtu.be/79T6S01WYmo?si=8_oigwdQ_Zpz-wNY" target="_blank" rel="noreferrer noopener">Roche - Patient Perspectives Blood transfusions</a>
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<div>Kabir and Bhavika are featured here in an internal Roche video to highlight the crucial need for a clean and available blood supply. We share our experience with the first two years of his Leukemia treatment, noting that over two years of chemotherapy, he required 25-30 blood transfusions. These transfusions were vital for his survival and treatment efficacy. Kabir's story raises awareness about the importance of blood donations for cancer treatment.
</div>

Help a Bay Area Boy Keep Fighting - Kabir Needs Medical Care

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Bhavika Taunk

Bhavika Taunk

What Bhavika cares about

Bhavika’s featured causes

Help a Bay Area Boy Keep Fighting - Kabir Needs Medical Care

Falcons for Frank

Donate to Anuar’s Cancer Fund: Beat the Odds

Nicole Roy

Falcons for Frank!