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

<div>Flooding Crisis on the Rio Gregório — Help Us Rebuild
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<div>The Rio Gregório has flooded, devastating villages across our territory. Families have lost their crops, their homes, their boats, and their tools — the very things that sustain life deep in the Amazon.
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<div>Right now, our most urgent needs are:
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<div><br />
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<ul>
<li>Food for families who lost their crops and can no longer reach their fields
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<li>⛽ Fuel to travel by boat between villages and deliver aid
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<li>Reconstruction materials to repair homes and community structures
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<li>Replacement of lost boats, motors, and basic tools
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<li>Small animals (like chickens) to help families begin recovering
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<li>Seedlings to replant what was lost and restore food security for months ahead
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</ul>
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<div>Every dollar goes directly to the affected families. With USD 50,000 we can cover immediate relief and begin a dignified recovery — reaching every village, leaving no family behind.
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<div>This support is not only about surviving the flood. It is about helping our communities heal, rebuild, and continue protecting our territory and the Amazon forest.
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16 Yawanawá Villages Devastated by Flooding, Help Us Rebuild

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<div>Dear Suya Joint Family,
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<div><br />
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<div>We are writing to you today with a heavy heart to share that we are facing an incredibly difficult moment at Suya Joint and in the Lizotte family.
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<div><br />
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<div>A husband, brother, uncle, and our beloved manager, Paul, was recently detained by ICE while on his way to church. This sudden and painful event has shaken our family to the core, and we are currently navigating both emotional and legal challenges surrounding his detention.
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<div><br />
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<div>Because of this, we are taking time to reflect and reassess what comes next for Suya Joint. While we are not closing at this time, we are seriously considering what’s best for our team, our mission, and our family. This is not an easy decision, and we want to be transparent with you all—our loyal supporters—every step of the way.
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<div>Suya Joint has always been rooted in love, culture, and community. Every dish we serve is more than food—it’s a story, a connection, a piece of our heritage. Paul has been a vital part of the restaurant, serving in both Boston and Providence whenever and wherever he is needed. His work ethic, calm nature, and strong moral compass help define the culture of our business. Your continued support means the world to us and has carried us through many highs and lows.
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<div><br />
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<div>This sudden separation has been incredibly traumatic for our family, and we are doing our best to hold things together without the person who has always been an anchor in our lives. Paul is a peaceful, faithful, and hardworking man who gives everything he can to those around him. His absence is deeply felt, not just by his family, but by our Suya Joint team and the communities he serves. Therefore, we are seeking these donations in hopes that they can begin to help us cover the cost of an immigration attorney, Paul’s bond, and the proceedings after Paul reapplies for his asylum visa. As of June 26th, Paul attended his first hearing in front of an immigration judge and will have his bond hearing on July 3rd. Thank you in advance for your time, compassion, and any support you can give to us in this time of need.
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<div>Sincerely,
</div>
<div>The Lizotte and Suya Joint Family
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<div><br />
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<div>Testimonials to Paul:
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<div><br />
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<div>“Paul has shown an exceptional capacity to navigate the roles he plays with intelligence, warmth, and commitment. He has become the Program Director’s “right hand man”, taking leadership in Evan’s absence during a serious flood in the house that required evacuation and relocation of the men, as well as managing the major construction work necessary to repair the home.
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<div>Paul treats the men he serves with full respect and dignity. He offers patience and kindness when he needs to assist in personal care and activities of daily living, but he also engages the men around their preferences in all aspects of life and is instrumental in ensuring their participation in the social/recreational activities of their choosing.”
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<ul>
<li>Catherine Conrade MEd LMHC — Paul’s Boss
</li>
</ul>
<div><br />
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<div>“Paul is not an illegal alien.  His one misdemeanor offense does not merit detainment and deportation in my view.  He is proud to be a contributing member to our society.  He is college educated, speaks and writes fluent English, and is an actively practicing Catholic.  He tries his best every day to build a better future for himself and is a positive influence to everyone he knows.  If he were to be deported it would be a devastating blow to our family and to the greater local Nigerian community as a whole.  He has done his proper due diligence in the process of trying to become a US citizen.”
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<ul>
<li>Jeffery Lizotte — Paul’s Brother-in-Law
</li>
</ul>
<div><br />
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<div>”His sudden absence has left a void that cannot be overstated. It has shaken those closest to him, disrupted a family-owned business that serves as a gathering place for so many, and sent ripples of fear through a community already under heightened
</div>
<div>scrutiny. We are living in a time where the criminalization of immigrants, particularly African immigrants, is intensifying — and where good people like Paul, who contribute positively to society, are being removed without justification.”
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<ul>
<li>Chioma Nnanji, MPH, MEd — Paul’s friend
</li>
</ul>
<div><br />
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<div><br />
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Stand with Paul: Legal Fees for His Release

<div><strong>Hi everyone,</strong>
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<div><br />
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<div>Hi, I am the daughter of two parents who were refugees from the war in Bosnia and Herzegovina in 1991. Growing up, war was something I always understood, it shaped my family’s history and deeply connected me to the struggles of displaced people.
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<div><br />
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<div><strong>Nearly a year ago</strong>, Sameh, a 19-year-old from Gaza, found me through Instagram. He reached out in desperation, sending me videos of what he and his family were going through. We later spoke on a video call, and his reality became painfully clear, his family had lost everything.
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<div><br />
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<div><strong>Sameh’s Story</strong>
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<div>Sameh is not just fighting to survive; he is fighting to keep his family safe. He is the backbone of his household, caring for his <strong>mother, father, two brothers, sister, and young niece</strong> in the midst of war and devastation. They lost their home and, for a time, had nowhere to go but a <strong>tent</strong>.
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<div><br />
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<div>Thanks to your generosity, Sameh was able to secure a small home for his family. It’s not perfect, but it’s a step up from living in a tent. However, even this progress has come with heartbreaking setbacks, <strong>landlords in Gaza are price gouging</strong>, raising rents as more and more families are left homeless. The first home they secured was suddenly made unaffordable when the landlord found someone willing to pay more.
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<div><br />
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<div>Sameh managed to find another place, but at <strong>$340 per month</strong>, it’s a massive burden for a family with nothing. They are doing their best to clean and organize, but the reality is that they need ongoing support to stay housed and fed.
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<div><br />
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<div><strong>How Your Donation Helps</strong>
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<div><strong>$10-$50</strong> provides food for the family.
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<div><strong>$200</strong> buys just 1 kilo of flour—due to extreme shortages, food costs are unimaginably high.
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<div><strong>$340</strong> covers one month of rent, ensuring they stay sheltered.
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<div><strong>$5,000</strong> per person is required to secure refugee status if they ever get the chance to leave.
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<div><br />
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<div>With war still raging, the cost of <strong>rent, food, and basic necessities continues to rise</strong>. Every single dollar makes a difference in keeping this family safe.
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<div>If you can, <strong>please donate</strong>. If you've already given, <strong>THANK YOU</strong>, your generosity has given this family a home. Even if you can’t contribute, sharing this fundraiser can help reach someone who can.
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<div>Sameh and his family are incredibly grateful for this community. Let’s keep showing up for them.
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<div><strong>Thank you for your love and support. Free Palestine.</strong>
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Help a 19-Year-Old Keep His Family Safe in Gaza

<p dir="ltr"><img src="https://d2g8igdw686xgo.cloudfront.net/24408708_1507221768.5585_funddescription.jpg" alt="24408708_1507221768.5585_funddescription.jpg" /><br />
Aloha friends, family, and kind strangers I have never met before. My heart is saddened to share this news, but my future brother in law, Codee, has been in a terrible accident; A head on collision on the highway. I am relieved to say that he is going to live through this traumatic incident, but he has a very long road to recovery ahead of him. 
</p>

<p dir="ltr">Codee is a young 26 year old father-to-be. He is caring, open-minded, has the best sense of humour, one of the most outgoing people I have ever met. He has this ability to start a conversation with just about anyone and become their best friend by the end of it. Most of all he loves my sister, and he is so excited to become a father. He is having his first son, Riley James, with my younger sister Katelyn. Their baby is due on the 22nd of October, which is this month. 
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<p dir="ltr">He currently remains in the hospital, his doctor anticipates he will have to stay there for another 2 - 3 weeks. Which means whether or not he will be available when my sister delivers the baby is in question. 
</p>

<p dir="ltr">His injuries are immense. The seatbelt he was wearing at the time of the collision cut into his gut, rupturing his intestines, his colon, and severing his abdominal muscles. He also shattered his hip and broke his hand. He immediately went into a surgery that lasted a few hours where the doctors found that they were unable to repair the damage in his abdomen at this time. They removed a portion of his intestines and, as a temporary solution, has to wear a colostomy bag for the next 3 to 6 months until the inflammation of his organs subsides. He will then undergo another surgery to see if they can then repair his intestines, and if he will regain function of his colon. Which they are still unsure of how bad the damage is. (For those who are unaware of what a colostomy bag is, it is a bag that basically replaces the function of your colon. Rather than moving through the digestive tract, bodily waste goes straight into the bag, which rests outside of the abdomen, and you have to empty it out when it gets full. Not something you want, or should, be dealing with at 26 years old. Or at any time in life for that matter.) 
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<p dir="ltr">He suffered no head injuries, which we are extremely grateful for, but he is still left temporarily disabled. Which is going to put a lot of stress on this family's lives for a short time. 
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<p dir="ltr">His recovery could be as short as 4 months to as long as a year, and in the worst case scenario he could be living the rest of his life wearing a colostomy bag. Which, is manageable, but will put limitations on what he can do and how he can live. 
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<p dir="ltr">Although most of his medical bills will be covered by insurance, it will not cover any of their living expenses as neither of them will be in any shape to work for at least the next few months; my sister will have to take on the reponsibility of taking care of their newborn along with Codee. 
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<p dir="ltr">We are asking out of the kindness of your hearts to make any donation to help with the basic expenses of rent, utilities, food, baby supplies, transportation funds, and any other expenses that come with day to day life. Here is a link of the baby registry.  <a href="https://www.target.com/gift-registry/gift/Riley1017">Katelyn and Codee's Baby Registry</a> ‌We feel that 6 months should be enough time for my sister to return to work, and we can only hope that by then that Codee is steadily recovering. 
</p>

<p dir="ltr">Thank you so much for your time and support. Little Riley needs all the love and stability he can get coming into this world. 
</p>

Support This Small Family

Erin Duddy

<div>Our names are Ashley (Tim’s partner), Robbie, Breanne, and Erin (longtime friends), and we are fundraising for Tim’s medical treatment and associated costs.
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<div><br />
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<div>In 2022, Tim was diagnosed with Myalgic Encephalomyelitis (ME), a serious and debilitating, complex condition that was triggered by a COVID infection. His health has progressively worsened since, and we're reaching out to our community as he has reached a new, critical condition in this tortuous disease.
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<div><strong>Today, Tim is fully disabled and confined to his bed in extreme sensory deprivation (virtually no light, sound, or company). We are urgently seeking financial assistance to allow him to access necessary and potentially life-saving treatments before his disease surpasses a threshold he cannot recover from.</strong>
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<div><br />
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<div>We are committed to honoring Tim’s autonomy and dignity, uplifting his voice, and following Tim’s commitment to disability justice and collective liberation. Below is Tim’s story, along with information about ME and Long COVID.
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<div><br />
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<div><strong>Tim’s Story:</strong>
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<div><br />
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<div>For those who haven’t had the privilege of knowing Tim, <strong>Tim spent his entire career defending low income clients for free— first as a public defender, then as a legal aid civil rights attorney. </strong>He was an attorney for the people in the truest way. He fearlessly stood up to systems for the benefit of his clients. His success could easily be measured in the high percentage of trials and cases he won, but the most beautiful reflection of his work was how attentive he was with every client, taking the time to hear their needs, truly listen to them, and ensuring their dignity was protected in a system that so often degrades people. Tim is the attorney, friend, and partner you want by your side.
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<div><br />
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<div>Outside of work, he loved hiking, doing advocacy work, listening to live music, bird-watching, spending time with family and friends, reading, and writing poetry. Life as he knew it took a sudden halt after a COVID infection in July 2022. <strong>Now, at age 33, Tim is fully disabled, no longer able to tolerate standing or walking, and can only talk for brief periods.</strong> He spends nearly 24 hours a day lying horizontally in a dark room in immense pain and requires full-time care from his partner. He lives in near total isolation, unable to socialize or even see friends and family.
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<div><br />
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<div>Following his COVID infection, Tim developed autoimmune autonomic neuropathy, a type of autonomic nervous system dysfunction thought to be caused by an overactive immune system. Experts now know that a COVID-19 infection can directly trigger autoimmune and autoinflammatory diseases. This can be one presentation of Long-COVID. Tim’s autonomic nervous system can no longer maintain stable blood pressure or supply his brain with sufficient blood, resulting in a racing heart rate, lightheadedness, brain fog, and blood pooling.
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<div><br />
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<div>In addition, Tim was subsequently diagnosed with myalgic encephalomyelitis (ME), a chronic and systemic disease associated with neurological, immunological, autonomic, and energy metabolism dysfunction. <strong>Even minor physical, cognitive, or sensory exertions triggers debilitating headaches, brain fog, and exhaustion, all of which cannot be helped with rest or sleep.</strong>
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<div><br />
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<div>With ME, every time you over-exert yourself, you experience post-exertional malaise (PEM). PEM is a debilitating state, in which you feel dazed, disoriented, having trouble tracking information, cannot move or speak. Every PEM crash reduces your baseline. Not only is it days or weeks of suffering, but with each one, your baseline reduction risks becoming permanent. This is what happened to Tim.
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<div><br />
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<div>It’s hard to articulate how fundamentally disabled Tim is. Dr. Ron Davis, a researcher and ME expert at Stanford University, put it this way: “ME patients are similar to a critically ill patient 24 hours before they die, except they live like that for years and years.” Here are some examples to illustrate the profound level of debilitation he experiences:
</div>
<div><br />
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<ul>
<li>Tim has to budget energy to even pet his dog Boris and is only able to pet him once or twice, before becoming too fatigued.
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</ul>
<div><br />
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<ul>
<li>Tim, even on good days, can only listen to 2-3 minutes of an audiobook, and cannot read a book without triggering severe symptoms.
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<li>Tim cannot listen to music or watch TV, as his light and sound sensitivity is too severe.
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<div><br />
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<ul>
<li>Even walking across a room can trigger weeks of suffering and severe symptoms.
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<div><strong>ME has no cure. </strong>Even under the care of top experts, Tim has only made marginal improvements in the last year. The few treatments that do exist are limited and Tim has exhausted all FDA approved treatments in the US. He is now trying experimental treatments, all of which are incredibly expensive and require significant planning.
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<div><br />
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<div>Donations from this fundraiser will go towards treatments including:
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<div><br />
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<ul>
<li>Invasive Cervical Traction (ICT) surgery. Tim was diagnosed with craniocervical instability (CCI) after his COVID infection deteriorated the collagen in his neck. His ICT surgery will be performed by a New York-based neurosurgeon who specializes in spinal surgery for patients with ME. Some post-viral illnesses like Tim’s are a result of abnormalities in and compression of the brainstem. It’s very likely that Tim has gotten as sick as he has because he has compression on his brainstem. ICT surgery in New York will determine if he's a candidate for CCI surgery, which could provide him with lasting remission.
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</ul>
<div><br />
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<ul>
<li><strong>In Tim’s fragile state, he is required to travel by private jet to ensure he arrives safely to ICT surgery. Navigating an airport and boarding a commercial flight would be so physically and neurologically taxing that it would risk irreversible harm to his health. Private jets, providing door-to-door transport from Oregon to NY, are estimated to cost upwards of $50,000 in each direction. </strong>
</li>
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<ul>
<li>Plasmapheresis. A treatment where blood is removed from the body and filtered, removing harmful antibodies and widespread blood clots, both of which Tim has. His plasma is disposed of and replaced with substitute plasma from donors. It costs $5,000 per session and is not covered by insurance. Tim needs at least 6 sessions, amounting to $30,000.
</li>
</ul>
<div><br />
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<ul>
<li>Intravenous immunoglobulin (IVIG). This is a pooled antibody, and a biological agent used to manage various immunodeficiency states. This treatment costs tens of thousands of dollars and is not covered by his insurance.
</li>
</ul>
<div><br />
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<ul>
<li>Phosphodiesterase inhibitors with anti-inflammatory effects have been repurposed to treat ALS, multiple sclerosis, and ME. These drugs are very inaccessible in the U.S. and must be ordered directly from Japan at a premium rate.
</li>
</ul>
<div><br />
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<div>COVID-19 robbed Tim of the life that he knew and loved. Living in complete isolation and in near total sensory deprivation, cut off from the natural world, and away from family and friends, is a cruel, unsustainable existence. Tim deserves his life back.
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<div><br />
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<div>As his partner of ten years, it has been the most heartbreaking experience of my life to watch these diseases render Tim an entirely different person. I know him better than anyone. And the level of debilitation is readily apparent, striking, and profound. Tim is so ill that he is unable to meaningfully participate in his own life.
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<div><br />
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<div>Tim’s disease is not new, unknown, or rare; it is simply underfunded and effective treatments are under-researched. The ME patient cohort is often too sick to participate in studies and too sick to make it to doctor’s appointments, so we are left to our own devices in seeking appropriate medical care. The number of people who have ME has more than quadrupled in the pandemic. And studies show that the quality of life for severe ME is comparable to late stage cancer patients. Yet the vast majority of doctors won’t treat the condition, as only 6% of medical schools even teach about this common disease.
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<div><br />
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<div>As his partner and as his friends, we are obligated to explore all avenues to improve Tim’s quality of life. This is a dire circumstance, and we are raising funds to go towards getting Tim the treatments he needs as soon as possible.
</div>
<div><br />
</div>
<div><strong>Thank you for reading Tim’s story. We appreciate anyone who’s able to contribute or share this fundraiser.</strong>
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<div><br />
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<div>The Realities of Living With ME and Long COVID:
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<div><br />
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<div>“ME/CFS is one of the worst conditions one can have. Most people know little to nothing about it, but make no mistake, if you get it, your life, as you know it, is over. It’s worse than that. The very essence of life is gone. The severity of symptoms coupled with lack of a single effective treatment against a backdrop of decades of gaslighting, obstruction of biomedical research, total lack of research funding and thus lack of hope, means many patients commit suicide. Suicide is the most common cause of death in M.E.
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<div><br />
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<div>M.E. is one of the most disabling conditions on earth. Contrary to false beliefs, M.E. is not “tiredness”, you cannot push through it and soldier on just like you cannot walk through walls and it does not respond to lifestyle interventions. M.E. is a paralyzing lack of cellular energy no amount of mental willpower can overcome.
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<div><br />
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<div>At the “mild” level, patients lose 50% of their function (hardly “mild”). At the most severe levels, patients are bedbound, tube fed, cannot move at all, cannot tolerate light, sound, seeing words, images or even tolerate human presence. People exist in this state for decades and it is not rare. You don’t hear about it because for so long, nobody wanted to know. Studies show that severe ME patients have a quality of life comparable to late stage cancer patients.
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<div><br />
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<div>The hallmark of the disease, post-exertional malaise or PEM is that anything you do beyond your personal, inhumanely small energy envelope, you will be punished for days, weeks, months or permanently. This could be trying to hold onto a job, an outing, a short walk, having visitors, a phone call, reading, making food, or even trying to sit up in bed or being around noise or sunlight. Yes, the very pathophysiology of the disease can permanently deteriorate because you did a “thing”. Imagine living with that axe hanging over your head in perpetuity.
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<div><br />
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<div>Contrary to another false belief, the disease is not mysterious. We have thousands of studies elucidating pathophysiology. We know this is an extremely complex, neuro-immuno-metabolic disease involving multiple organ systems. The only reason we can’t make progress is because the research funding compared to diseases with similar burdens is so incredibly low, it’s insulting. Science doesn’t take time, it takes money.”
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<div><br />
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<div>–Open Medicine Foundation
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<div><br />
</div>
<div>Additional information on ME:
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<div><br />
</div>
<ul>
<li>Video: Diagnosis and Management of ME/CFS <a href="https://www.youtube.com/watch?app=desktop&amp;v=XOpyLTyVxco" target="_blank" rel="noreferrer noopener"><a href="https://www.youtube.com/watch?app=desktop&amp;v=XOpyLTyVxco" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.youtube.com/watch?app=desktop&amp;v=XOpyLTyVxco</a></a>
</li>
<li>Video: Unrest, a documentary about the experience of living with ME/CFS
</li>
<li><a href="https://www.youtube.com/watch?v=RC9TjgE_PlU" target="_blank" rel="noreferrer noopener"><a href="https://www.youtube.com/watch?v=RC9TjgE_PlU" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.youtube.com/watch?v=RC9TjgE_PlU</a></a>
</li>
<li>Article: Fatigue Can Shatter a Person: <a href="https://www.theatlantic.com/health/archive/2023/07/chronic-fatigue-long-covid-symptoms/674834/" target="_blank" rel="noreferrer noopener"><a href="https://www.theatlantic.com/health/archive/2023/07/chronic-fatigue-long-covid-symptoms/674834/" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.theatlantic.com/health/archive/2023/07/chronic-fatigue-long-covid-symptoms/674834/</a></a>
</li>
<li>Various articles: What is ME/CFS: <a href="https://www.omf.ngo/what-is-mecfs/" target="_blank" rel="noreferrer noopener"><a href="https://www.omf.ngo/what-is-mecfs/" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.omf.ngo/what-is-mecfs/</a></a>
</li>
</ul>
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Help Tim Access Potentially Life Saving Treatment

Erin Duddy

Erin Duddy

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