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<div><a href="https://allseniors.org" target="_blank" rel="noreferrer noopener">All Seniors Foundation</a> is dedicated to uplifting the lives of our senior citizens by connecting them with the resources, support, and companionship they need to thrive in their golden years. Founded on the belief that every senior deserves dignity, care, and love, we strive to create a community where the elderly are not forgotten but celebrated and supported.
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<div>As a nonprofit organization, our mission is to bridge the gap between seniors and the essential services they require. From providing free supplies and medical equipment to offering emotional support and companionship, we aim to ensure that no senior faces their challenges alone.
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<div>Our Mission
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<div>At All Seniors Foundation, our mission is clear: to enrich the lives of seniors by addressing their most pressing needs. Whether it's helping with daily necessities, connecting them with healthcare services, or simply offering a listening ear, we are committed to making a meaningful impact in the lives of those who have given so much to society.
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<div>Why We Need Your Help
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<div>Our work relies on the generosity of individuals like you. Your support enables us to continue offering these vital services to seniors who need them the most. With your donations, we can expand our reach, provide more resources, and ensure that every senior in our community feels valued and cared for.
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<div>Every dollar you contribute goes directly to enhancing the lives of our seniors, whether through providing essential supplies, facilitating social activities, or expanding our support networks. By donating to All Seniors Foundation, you are not just giving money; you are giving hope, love, and a sense of belonging to the elderly.
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<div>Join Us
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<div>We invite you to join us in our mission to make a difference. Whether through donations, volunteering, or spreading the word, your involvement can help us reach more seniors and make a greater impact.
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<div>Together, we can ensure that our seniors live with dignity, surrounded by a community that cares.
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<div>Thank you for your support.
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<div>AllSeniors.org
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Join Us in Caring for Our Seniors

<div>Marie Begley, know to many as Toodles, started her working career as a hairdresser. As a young mother, she balanced her job with raising her two sons.
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<div>After a divorce, she took extra jobs to supplement her income as a single
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<div>mother. She sometimes discounted her services to help others who couldn’t afford the going rate, sometimes doing it for free.
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<div>Family genetics discovered not only cancer but cardiomyopathy in her genes. Twenty years ago this heart condition worsened, but Marie stayed positive and pushed forward. She eventually had to go on disability and it was a constant struggle to make ends meet.
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<div>Her heart reached its lowest level of function at 18 percent, with fluid retention requiring many hospital stays to relieve it. She is at UCLA Hospital and on May 4th, 2023, after a lengthy hospital stay, received a heart transplant. We are hopeful for a full recovery and many more years for her to enjoy watching her two young grandchildren play baseball.
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<div>Aftercare, which includes 24/7 help for months, will be a struggle and her family will be grateful for any help with these expenses.
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<div>My brother, James Icenogle, will be taking a leave from work for a few months to ensure my mom has 24/7 care, and will be making sure all monies received will go toward her recovery care/expenses. Thank you all.
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Marie (Toodles) Begley’s Heart Transplant Recovery

Our brother Keith Mineo was present at the Route 91 Festival in Las Vegas during the shooting on October 1st. He sustained a serious gunshot wound and is currently hospitalized in stable condition. Keith is a self-employed contractor and any ongoing medical costs will be out-of-pocket. We are looking to raise funds to help Keith with living expenses while he goes through recovery.  We appreciate any contribution. Please feel free to share this link. Please keep Keith and his fiance Jessie and baby Beckham in your thoughts and prayers at this time. We will continue to update on his condition as we receive more information.

Keith Mineo Care Fund

Sweet, smart, adorable, Cameron Combes, 3 years young, recently received a confirmed diagnosis of Childhood Apraxia of Speech (CAS).  Anyone who has met Cameron, can see an incredibly smart, funny, little boy who can understand everything you say, but can not reply or communicate his thoughts back to you. This is not because he doesn't want to, it is because he CAN'T. The reason has now been confirmed...Childhood Apraxia!  Although the cause is not known exactly, Cameron is unable to move his mouth, jaw, tongue and lips to speak when his brain tells it to. There is essentially a disconnect between what his brain is thinking, and the motor planning that takes place in order for his mouth to express it.  The only way of improving this, is to work with a Speech Language Pathologist as often as possible.  Research shows that therapy, 5 days a week, with a SLP specifically trained in Apraxia is the only effective way for a child to resolve Apraxia.  <br />Cameron's therapy is extraordinarily costly, and Chris and Lindsey have been paying out of pocket for nearly a year, in order to have Cameron with the best Speech Therapists in Los Angeles, who are Apraxia trained. Sadly, many insurance companies specifically deny coverage of Apraxia, because they know it is a LONG, insensive and expensive endeavor to take on.  However, with the proper therapy, it is entirely possible to overcome the challenges of Apraxia!  Unfortunately, many  therapists do NOT understand how to properly treat Apraxia, and because it requires specialized training and additional education, many therapists can not afford to gain the additional knowledge needed to help these children overcome their speech challenges. <br /><br />On June 21, 2016, the Combes Family received the phone call of a lifetime! Out of hundreds of children who have applied, Cameron has been choosen to participate in the Summer Speaks program, with Nancy Kauffman, in Detroit Michigan.  He will be one of ONLY 12 children who have been accepted to participate in this 2 week long, intensive therapy program with the GURU of Apraxia!  This is a once in a lifetime opportunity for Cameron to receive therapy from a highly skilled, highly trained staff of therapists, who truly understand his diagnoses and needs.  Nancy Kauffman has been the angel to help MANY young children find their voice!  <br /> <br />Due to the fact that Cameron has just been granted a spot in the program from the waitlist, the Combes family has been presented with the challenging task of raising a very large sum of money in order to fund this much needed therapy, in a very short amount of time.  Many friends and family have expressed a strong desire to help in any way they can, and have urged Chris and Lindsey to start this Gofundme campaign, but they have been apprehensive to do so.  I'm taking it upon myself to help rally their village! Let's show them we are behind them, and support their amazing efforts to seek out THE BEST, most effective help, for Cameron to succeed today, and in all his future endeavours! <br />I know we ALL want to help Cameron do something that we all take for granted, and that is to help him speak!  So please think about the life changing benefits this sweet boy, his family and his friends will reap, from your generosity and kindness.  Any amount you are able to give, will be greatly appreciated!  Let's get Cameron to Michigan for this life changing therapy opportunity!<br />Thank you all for your love, prayers and support of the  Combes Family!

Help Cameron Conquer Apraxia

<p dir="ltr">This is Alexander.&#160; He is one amazing kid born with cerebral palsy.&#160; Alex is going on 12 years.&#160; He loves swimming, Jiu Jitsu, acting, dancing, cars and video games!&#160; He has the kindest heart and has never met a stranger.&#160; He teaches us what the true meaning of strength and perseverance really is.&#160; He is a loving son, grandson, big brother and friend.
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<p dir="ltr">Around six months old our suspicions became a reality. His development was significantly delayed.&#160; He was very "floppy" due to low muscle tone and as he grew he was not hitting the typical milestones.&#160; By age three, an MRI confirmed his cerebellum was affected due to a lack of oxygen at birth and he was diagnosed with CP.&#160; 
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<p dir="ltr">A few years ago, Alex was fortunate to receive stem cell therapy and we were blown away by the amazing improvement we saw over night!&#160; His balance improved tremendously, bathroom accidents stopped completely and his overall strength improved.
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<p dir="ltr">Over the last year, Alex has had tremendous growth and a lot of changes. He is more and more independent with each passing day and he has even taken steps on his own without the assistance of a walker!&#160; Now is the best time to go back for more stem cell therapy. Unfortunately, this wonderful therapy is considered alternative for someone like Alex.&#160; Insurance does not cover stem cell treatments and the cost adds up quickly.
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<p dir="ltr">We need your help!&#160; All funds raised will go to Alexander's stem cell therapy.&#160; With your help we can hopefully start this therapy in September.&#160; Alex is ready and excited for another opportunity to help make everyday life a little easier!
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<p dir="ltr">Thank you for taking a moment to read about Alex, sharing his story and helping us hit our goal!
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<p dir="ltr">Forever grateful,<br>
Melissa, Christopher, Eleni and Jason<br>
Alexander's Family
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Alexander's Stem Cell Therapy

<span style="font-family:'Thread-00002010-Id-00000011';">" PLEASE ..HELP MY DAUGHTER SHANNON" <br />          WITH LARGE BRAIN TUMOR REMOVAL<br /><br />MEDICAL EXPENSES / TRAVEL EXPENSES <br />          NEEDS SURGERY OUT OF STATE.               <br />           <br />        3 MONTHS OF HELP WITH LIVING <br />     EXPENSES WHILE SHANNON RECOVERS<br /><br />Hello... my name is Gail, Shannon‘s mother. I am reaching out to family, friends, and anyone who can help us please.<br /><br />My daughter Shannon has suffered for the last 12 years in chronic pain with many autoimmune disorders; Rheumatoid Arthritis, Fibromyalgia, Chronic Fatigue, Reynaud’s Disease &amp; Lupus.  Shannon’s life is hard enough to manage as it is with all these medical conditions. She has tried everything from weekly shots to chemotherapy. Unfortunately, an MRI has diagnosed on January 29, 2015. Shannon with a large brain tumor; its 3.23cm x 6cm x 3cm.1cm and located behind her left ear and its pushing on her brain stem. As the brain tumor grows it’s causing the tumor to press on the facial nerves and currently pressing on the Trigeminal Nerve causing Shannon to not be able to sleep. She screams in her sleep all hours of the night because of the pressure &amp; electric shock &amp; the stabbing pain she feels just under her jaw and around the back of her head.    <br /><br /> The Trigeminal Nerve pain has been described as the most excruciating pain known to humanity. Shannon is extremely exhausted 24/7 everyday she gets weaker and weaker.  During the day Shannon experiences extreme vertigo and alarming blood pressure issues.  She can’t take it anymore, if her brain tumor isn’t removed soon, Shannon will experience irreversible facial paralysis.<br /><br />Shannon is my daughter and I love her with all my heart, but I wish I could do something to make it all go away, but, all I can do is pray. Please pray for my daughter, Shannon she needs all the prayers she can get and then some.<br /><br />Shannon lives in northern Nevada with me and I am her caregiver. This couldn’t have come at a worse time for us. I just went thru domestic violence and was just divorced January 26, 2015. My ex-husband decided it would be funny to close our joint account without my knowledge only leaving us with .18 cents, leaving us totally impoverished. In my divorce he was to pay the lease out until June 1, 2015, and because my advocate couldn’t get me an attorney, he didn’t have to pay for the remainder of the lease to our landlords.  I have sold whatever I could to keep Shannon, and I from being out on the streets. The lease is up May 31st and we are struggling. We have to move out of the house as we can’t afford the rent and at the same time Shannon needs this Urgent surgery it can’t wait anymore… So I decided to put everything in storage and figure out how to get Shannon, her daughter Ashley and myself to Los Angeles for her surgery at USC on May 26th. I am sincerely reaching out for help to everyone we know to please help. We have a lot of family and friends and if everyone does just a little we are hoping to get through this and we are so grateful for any amount without putting anyone in any hardship situation. Shannon cannot work and has no income and still waiting on disability benefits for 1 ½ years now.  Shannon and I need flights to Los Angeles for Pre-Op and Post-Op appointments, she will need a hearing aid that is several thousand dollars.  I am so overwhelmed and don’t know what’s going to happen.  I have never been in this kind of situation but Shannon can’t suffer anymore.  We have less than 20 days. We are praying we don’t have to reschedule again due to finances. Seriously Shannon is growing so weak and so tired I don’t think she can last much longer, it’s been 4 more months since the MRI and looking at her, I think her condition is deteriorating to the point of exhaustion she just isn’t herself, at her age she should be strong but she is very weak. <br /><br />Dear family, friends, and all who read this sad existence of a beautiful young lady, we can’t make it without you, I ask for whatever help anyone is able to do. Thank you for taking the time to read my letter about my daughter.  I have never asked anyone for anything like this but it’s for my daughter who I would do anything for and Shannon has a daughter, Ashley, who she would very much like to be around to see her daughter grow up. Please help me make this Miracle happen, to help Shannon through these trying times.<br /><br />God Bless,<br />Gail Cribbins<br /><br /> <br /><br /> <br /><br /></span>

"Team Shannon" 

Brandon Begley

Brandon Begley

Brandon Begley

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