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<div>Help Support Mel in His Fight Against Splenic Angiosarcoma

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<div>Our dear friend and coworker Mel was given news no one ever expects to hear—he was diagnosed with splenic angiosarcoma, one of the rarest and most aggressive cancers known, affecting only 2 out of every 10 million people.

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<div>At the time, doctors told him he had only four months to live. In fact, he was minutes away from losing his life when his spleen ruptured. Thanks to the incredible team at Brigham and Women’s Hospital, surgeons were able to remove his spleen and give us more time with him. But because the rupture allowed cancer cells to spill into his abdomen, the risk of the disease returning was always there.

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<div>Since then, Mel has faced this battle with unbelievable courage. The cancer has returned three times and is now considered stage four and non-curable. Yet Mel has continued to fight, beating the odds every single day—now standing strong and longer than his original prognosis.

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<div>Mel is a man who has dedicated his life to service. He spent four years in the United States Marine Corps, where he worked in logistics and military police. After his time in the military, he continued his commitment to protecting others by serving as a police officer for the town of Ashland. His strength, discipline, and devotion to others are the same qualities he brings to his fight against cancer.

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<div>While his doctors continue treatment to give him more time, the reality is that the chemo he is on may one day stop working, and stronger, more expensive medications may be needed. Every treatment, every doctor’s visit, every round of chemo is a chance to extend the precious time he has with his family, friends, and loved ones.

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<div>Mel is more than a patient—he is a husband, father, coworker, and friend. His wife Mary and children, Darwin Jr. (22), Deja (22), Taliya (18), Kiyra (18), Daniel (18), and little Kayleigh (7), are his whole world. He continues to fight not only for himself, but for them.

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<div>We are asking for your support to help ease the financial burden of ongoing treatments, medical expenses, and the day-to-day challenges that come with a battle like this. Every donation—no matter the size—makes a difference and gives Mel more time to share laughs, hugs, and memories with the people who love him most.

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<div>If you are unable to give, please consider sharing this page so we can reach as many people as possible.

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<div>Thank you for standing with Mel in this fight. His strength is inspiring, and your kindness will help carry him forward.

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Support Mel in His Fight Against Splenic Angiosarcoma

<div>Hi, I want to raise money to help Queens subway attack victim Elizabeth Gomes who can lose vision in her right eye. As a New Yorker and woman, what happened to Elizabeth is unfathomable. She will be scarred for life and have severe PTSD about ever riding the subway or being anywhere alone again. She will need help with her medical bills and deserves restitution and justice. Anybody that can help, it's appreciated more than you know. She's deeply overwhelmed by the love and support the public is showing her. Every little bit counts. 
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<div>For everyone messaging and asking if I'm in contact with Elizabeth, the answer is yes, and they have requested that I keep this account going for them; all proceeds are set up to go directly to Elizabeth Gomes. 
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<div>Thank you all again. Olga
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Help Queens subway-attack victim Elizabeth Gomes

A Holiday Inn employee was harassed and filmed by a customer having a mental breakdown &amp; is now receiving death threats &amp; having thoughts of self-harm. It turns out this employee has BPD with schizo-active tendencies.  According To Him.  "While I’ve now quit this position (my management supported me, and told me I’m welcome back. The guest was ejected from the hotel for escalating issues with staff and the owners.) I do have mental disorders. I suffer from BPD and schizo-affective disorders. What this fine, gentleman behind the camera DIDN’T record was the fact that he called me a F**GOT for an associates mistake. He was aggressive, and fishing for a reaction. He sure got it; and I’m glad this was a wake up call for me to stop slaving away for corporations who do not care about you at all, or the guests." Let's give him enough of a head start on finding a job where people don't treat him terrible &amp; he can take a nice little vacation

Help Harassed Holiday Inn Employee

Recuperação Doença Rara Syndrome Lyell (NET)

Friends and family, we need your help.  After experiencing a series of temporal lobe seizures, Marcy has been diagnosed with a glioma (brain tumor) and her doctors have determined surgery is the best course of action. The goal of the surgery, scheduled for the week of July 27th, at the Albany Medical Center, is to remove approximately 75-80% of the tumor, and treat what remains with radiation.  After Marcy is released, she will recover at home under the care of her mom, Jan, and son, Adrian.  The neurologists (and the cards) estimate it will take a minimum of three months for brain and body to heal.   During the recovery period, Marcy, Jan and Adrian will be out of work.   You won’t be surprised to hear that Marcy is handling all of this with a positive attitude, her trademark curiosity, and a realistic outlook as she faces the unknown.   We will continue to send good vibes, prayers, affirmations and visualizations for Marcy's recovery; we also know that the road ahead presents some distinct practical challenges.  With all of us on Marcy’s side, we will be able to make things easier on her immediate caregivers, and ensure she has the resources she needs to make a full recovery. Our hope is to provide financial support to: ·      allow Jan and Adrian to focus on Marcy's recovery ·      pay for recommended procedures or devices not covered by health insurance ·      replace lost income to cover Marcy’s living expenses ·      cover additions or changes to the home to better support Marcy during recovery   Marcy as family, friend, colleague, performer, artist, and reader has touched so many from all walks of life. She has been dedicated in life and work to helping others find their truth, heal, and live in happiness. She is smart, kind, determined and strong. All of which will come in handy in the days, weeks and months ahead.  We love and support Marcy and her family. Please donate whatever you can as we all come together to help Marcy through this most challenging time. One last thing… a note directly from Marcy (which you’ll find is SO Marcy): “The main thing I’m asking of you is for you to hold a picture of me in your mind, brilliant, vibrant, vital, strong— whatever combination of your favorite things about me that you like— and beam it my way.”   This fundraiser is being organized by a team of loving friends and family members including Jan, Becca, Katie, Jacquetta, Dale, David, and Skye. TESTIMONIALS: From Dale Mott: Marcy is a gift whose light and wisdom has guided me to my best me. I’m happy to do a bit of re-gifting here:  My dear Marcy, sending you the light, love, and healing power you’ve so generously have shared with me over 8 years. Hey everyone out there, let’s please help our dear Marcy kick this tumor’s $&amp;%#!!!   From Becca DeWitt: Marcy has become like family to me over the six years I've known her. Her intuitive prowess, hilarious wit, playful spirit, creative brilliance, sharp intellect, and big loving heart (the list could go on!) are some of the qualities that make Marcy one of the most admired role models in my life. I don't think I could adequately describe how much she has changed my life for the better. Marcy has gotten to the foundation of my psyche and helped reorganize it piece by piece. She has been there for me through so many twists and turns. Every trouble I bring to her she turns into a gold nugget of truth. Getting to know her as a mother, business owner, kundalini yogi, healer, and artist has been such a gift to me, and I know that she is a gift to countless others. In short, Marcy rules! From David Eaton: Marcy has been one of the key pieces in my support system for over a decade now.  Her wisdom and insights have steered me towards love and truth.  Besides the many gifts she shares with the world, I've witnessed her as one of the strongest people I've ever met.  As a self-employed, single mother I've known Marcy to handle the hardships of life with grace, trust, and curiosity without ever abandoning her passion.  Part of this strength (and sometimes stubbornness) is that she rarely asks for help. Though the circumstances are harrowing, I'm grateful for the opportunity to show up for her the way she has showed up for so many people over the years.  Marcy Currier is a treasure, and let's rally together and support her family and that beautiful brain of hers. From Gabe Pacheco: I've known Marcy for over a decade and she has profoundly changed my life.  She's one of the most empathetic and vibrant people I know.  She's helped me gain greater insight into myself and has been a great cheerleader for my journey as I pursued my passions.  I've witnessed her help dozens of people gain insight into their lives, relationships, and the world.  So right now I'm asking you for money to help Marcy recover from brain surgery.  I'm asking this both as a way to help repay her for all of her contributions to humanity in the past, and also to help her regain her health so that she can continue serving the world in the years to come.   From Joey Cummings: I have worked with Marcy for over twelve years across a myriad of challenges, both personal and professional.  Marcy offers immense passion, love and focus for my soul through this Covid time and other life events.  What she does is real and big, life saving and life changing. I consider myself a very lucky person to have met her and I am so grateful to have a someone (like Marcy) to watch over and under and around me. From Zabrina Aleguire: Working with Marcy has changed my life.  I know that's a cliche thing to say, and it's not something I say.  Ever.  Marcy truly has the gift of sight, and her ability to see and understand what is happening in an instant -- in my case, across the country from her -- is magical.  What makes her work transformative, though, is Marcy's deep wisdom.  When I have felt lost, hopeless, or despairing, Marcy's insights give me faith in life and humanity and the Universe again.      From Mom (Jan Roberta): As her mom, I can say that Marcy is one of the strongest people I know, and I have witnessed her lifelong commitment to understanding herself and others.  She has spent years fearlessly working on herself, all while using her knowledge, energy and love to heal others and the world.  We need your financial support right now to get her through this “bump in the road “, and back to her healing life work. I love her and want her to make the best possible recovery with all her artistic and healing abilities intact!

Support Marcy Currier's Brain Surgery Recovery

There is a saying that goes “The hard times that you go through build character, making you a much stronger person!” If this is true, then Dave Paczosa’s character must be damn near flawless! Just when we think that this man can’t possibly take much more heartache and stress....BAM! He is slammed with another profound life changing event! As many of you know, Dave has been battling with a very rare form of cancer that is almost unheard of in adults, Ewing Sarcoma wrapped around his spinal cord. After months of chemo and numerous complications, he received disheartening news this week at Mayo that there has been no change in the tumor making surgery impossible due to the extensive risks. True to Dave’s optimistic attitude and his sheer strength and determination, he is continuing this fight full force. Unfortunately, further treatment must be done at Mayo in Rochester. They will try a new Proton radiation therapy along with chemo starting August 1st lasting 33 cycles for 6 1/2 weeks. Only a couple places in US have this technology, so it has to be done there. As you can imagine the expense of this is weighing very heavily on Dave’s mind, which is only magnified by the expenses he has already sustained! Anyone who has met Dave knows there is nothing he wouldn’t do for someone in need. You also know that he would never himself ask for help no matter what the situation. For this reason, as his family we ask if there is anyway you can help, whether it is monetarily or a few moments in prayer for Dave and his medical team, we would be eternally grateful.

Stronger than Cancer

Meet Isabelle Ceron, about a month after her first birthday( feb21,2019)Isabelle started getting fevers almost constantly, rashes would come and go, she would just want to lay on her mother’s chest  and infections were a normal that had no explanation.  On April 8 2019 Isabelle was extremely lethargic and we feared the worst and rushed to an emergency room where Isabelle was admitted and a sonogram of her concluded she had fluid build up around her heart; a tap was scheduled to remove the fluid build up but due to constant Advil dosing by the hospital the day of the surgery the fluid had disappeared. We were sent home without any explanation. For over a year our life changed from caring for Isabelle to countless doctors visits with multiple specialists who told us that there was no need for genetic testing but couldn’t give a diagnosis. On March 27, 2020 everything changed after a grueling year of us fighting with specialists for a diagnosis. Isabelle unfortunately was diagnosed with juvenile myelomonocytic leukemia (jmml), which is a rare and serious form of childhood leukemia. Jmml occurs in children usually under two years of age, jmml occurs when too many blood stem cells become white blood cells(monocytes and myelocytes). Jmml is thought to be a 1 in 1,000,000 genetic mutation and is more common in males under two years of age. If left untreated there’s a slim chance(5%) any child makes it to 5 years of age. Once treatment is complete and she goes into remission there is a 50% chance of jmml reappearing and having to undergo a second treatment plan. This has been a long journey for Isabelle and her parents. May 2, 2020 Isabelle had a double broviac lumen line surgically placed in her chest so she could receive her first round of conditioning chemotherapy, all which were outpatient.  June 9, 2020 Isabelle was admitted to Wolfsons children hospital in Jacksonville, FL. The only curative treatment for jmml is allogeneic hematopoietic stem cell transplantation(HSCT). leukemia recurrence is the main cause of treatment failure because jmml progresses so rapidly. We’ve watched our sweet, sassy, caring daughter go from bad to worse. Due to the covid 19 pandemic Isabelle is limited to one visitor in the room during her &gt;90 days treatment plan which makes matters worse on top of that COVID has caused her dad to become unemployed with no means of income we are at one hardest times of our life’s. We don’t have reliable transportation and our financial position makes it impossible. On top of everything we are 3 hours from home and have to stay in the Jacksonville area for 2 months after isabelle is cured so they can monitor any serious complications. We hate to ask for charity but this is our last resort. This fundraiser has been established to ease the financial, transportation, food, medical, and any other burdens that we are not prepared for. Any unused funds will be donated to children cancer funds to help children and families in need. No donation is too small, if you are unable to donate PLEASE continue to share her story any way you can.Anything  helps we just want our daughter to be able to live a normal life after all that she’s gone though. We are beyond thankful to any help we receive <img src="https://d2g8igdw686xgo.cloudfront.net/48876942_1592335278636766_r.jpeg" width="100%" media_type="3" alt="48876942_1592335278636766_r.jpeg" /><img src="https://d2g8igdw686xgo.cloudfront.net/48876942_159233530454254_r.jpeg" width="100%" media_type="3" alt="48876942_159233530454254_r.jpeg" /><img src="https://d2g8igdw686xgo.cloudfront.net/48876942_1592335343735060_r.jpeg" width="100%" media_type="3" alt="48876942_1592335343735060_r.jpeg" /><img src="https://d2g8igdw686xgo.cloudfront.net/48876942_159233536671961_r.jpeg" width="100%" media_type="3" alt="48876942_159233536671961_r.jpeg" /><img src="https://d2g8igdw686xgo.cloudfront.net/48876942_1592335394828268_r.jpeg" width="100%" media_type="3" alt="48876942_1592335394828268_r.jpeg" />

Isabelle Ceron family jmml cancer fund

As many of you know, our family friend Cora Showers received the shocking news of her recent cancer diagnosis- a rare form of leukemia called Acute Promyelocytic Leukaemia ( APML ).   Cora is a 22 year old smart, beautiful young woman inside and out, no matter the situation she always has a smile on her face. She recently graduated from UMASS Dartmouth, and was eager to start her life in this world as a college graduate, with her new career. On the morning of July 3rd, 2020- Cora woke up with intensifying bruises all over her body, and bleeding from her mouth- her mom, who is an RN at children’s hospital, took her to be evaluated at the ED- from that moment on things began to get serious, after drawing labs they rushed Cora to BID Boston- where she later received her cancer diagnosis.  Cora has a long road ahead of her, she will be in patient at Boston hospital for 5-6 weeks, and then she will be continuing out patient care for the next 4-6 months. If you would like to donate to help Cora through this medical rollercoaster it would be greatly appreciated- we also have an address where she can receive cards to hang on her hospital wall for the time being. Thank you all for your love and support! #CoralynneStrong

CoralynneStrong

Dear Friends and Family Members,  On June 24, 2020, Julia was involved in a boating accident which required her to be Med-Flighted to the nearest Trauma Center. She suffered multiple fractures in her back and a completely severed spinal-cord. Over the coming months and years, Julia will have needs that will not be covered by insurance. We are here to support Julia in her long road to recovery and rehabilitation. Our first objective is to have her begin this rehabilitation in her hometown of Boston. This week she is being transferred to Spaulding Rehabilitation Hospital in Charlestown, MA to begin this work.  Many of you know Julia Carr Gangemi as your classmate, teammate, neighborhood tutor, or gymnastics coach. If not, you definitely know her as the star cheerleader being hoisted gracefully into the air at every Boston Latin football and Northeastern basketball game. Julia is the main attraction in every aspect of her life. Born and raised in the West Roxbury/Roslindale area, Julia is just shy of her 21st birthday. She is a BLS graduate, currently studying Computer Engineering at Northeastern University. She is a best friend and role model to her younger brother Sebastian, as well as a loving and devoted daughter to Beth (née Walsh) and John. Julia is in no way limited to the previous description. She is driven. She is fearless. She is unstoppable. She is a leader, attaining the title of “captain” on both her high school and college teams. She is a selfless and generous friend, never failing to make time for those in her life. Julia brightens every room with her bubbly and electric energy. She excels at everything she does, so we have no doubt she will overcome every obstacle she faces. Julia has met this unfathomably life altering experience with grace, grit and wit. Her inner spirit is evident and gives those around her the strength to meet each day's challenges. Julia’s determination is evident as she impresses the TICU staff with attempting all that is asked of her. And she has been able to laugh...even though it hurts. Julia, her friends, and family believe that she can regain enough mobility and learn the adaptive skills to live a full, productive, and meaningful life. Many people have reached out looking for ways to help and support the Gangemi family at this time. For those of you who wish to follow Julia’s journey and progress, we will be creating a Facebook page to keep you all updated. Thank you all for your care and generosity. Additionally, we are eternally grateful for the outreach and offers of assistance of the many communities in which Julia is a part: · Northeastern University, College of Engineering · Boston Latin School, Class of 2017 · Cheerleading (Northeastern, Boston Latin School) · Softball (Boston Latin School, Parkway Softball) · Ohrenberger Community Center (gymnastics)

Help Support Julia's Recovery and Rehabilitation

Ian Youngblood is a 29-year-old Arizona based Registered Nurse who has a big heart for others. When COVID-19 cases rose in New York City, Ian responded to our nation's call by leaving his home in Arizona (where he worked and studied for his CPN license) and brought his emergency room experience to what was the epicenter of the pandemic at that time. Towards the end of Ian's deployment, he started experiencing excruciating pain and nausea. Ian was admitted to the ICU at White Plains Hospital, where tests and scans identified a large mass in his brain; he was quickly scheduled for emergency surgery to remove a large percentage of the tumor. A few days later, Ian was told he has a Grade IV Glioblastoma (GBM), a rare and aggressive brain cancer, an especially shocking diagnosis for someone Ian's age. The path for treatment will require chemo, radiation, clinical trials, and professional expertise to slow the progression of this terrible disease. At the time the brain tumor was discovered, Ian was not insured and is now reliant on all available aid to face both cancer and the many hospital bills that accompany it. Ian has opened his heart and hands, gaining new loved ones and families as he worked to help others fight their battles, and now he needs our help to fight for him. We believe in Ian, and choose to believe that he will be the exception against this cancer, just as he has been the exception in so many other things throughout his life. Please consider donating to remove the financial worries that come with extensive cancer treatments, and give our Nurse, Youngblood, the chance he deserves. These funds will help Ian  with previous and future treatments, therapies, and quality of life costs. --- For media inquiries, contact Lindsey Carnett, CEO &amp; President of Marketing Maven at [email redacted] or (310) [phone redacted]. No GoFundMe donations have been used for publicity. She is a friend of the family and has offered her services pro bono as her donation to help tell Ian’s touching story.

Beat down brain cancer for NYC COVID Nurse Ian

Kevin Clements: A Husband, Father of 3, Son, Brother, Uncle, Friend, Neighbor, Coach, Olympic-Trained Swimmer... and so much more. On October 30, 2019, after just a few weeks of not feeling well and unexplainable symptoms, Kevin was diagnosed with T-Cell Acute Lymphoblastic Lymphoma &amp; Leukemia, a rare and aggressive form of cancer. The very next day on October 31, 2019, Kevin began an intense regimen of induction chemotherapy and will continue several rounds until a "remission" state is achieved. At that point, he will most likely need to receive a Bone Marrow Transplant, followed by additional chemotherapy and treatment. As you can imagine, this has taken a huge toll on the family emotionally, physically and financially. Together with the love and support of his family, friends, and the community we will fight alongside him as KEVIN is CRUSHING CANCER! 100% of your donations are assisting the family with medical bills and the cost of ongoing treatment which is keeping him from being able to work at this time. The needs are immediate and indefinite. Please share this link and let's do our part to help this sweet family. On behalf of the Clements Family, THANK YOU for your generosity, thoughts, prayers, and support. "PAIN IS TEMPORARY, PRIDE IS FOREVER" #KEVINCRUSHINGCANCER With Gratitude, The Kevin Crushing Cancer Committee

Kevin Crushing Cancer

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Investigations and Reporting

Funeral expenses for Faith and charitable donation in Faith’s name to Eve’s Place in Youngtown.

Funeral for Faith

What if I told you that Congressmen settled over 250 sexual harassment lawsuits using taxpayer money, and there was no way to find out who these Congressmen were? Would you believe me? The truth is that the situation is as described in the question. For decades members of Congress would use your taxpayer dollars to buy their way out of bad publicity. (Read, <a href="https://www.buzzfeednews.com/article/paulmcleod/she-complained-that-a-powerful-congressman-harassed-her">She Said A Powerful Congressman Harassed Her. Here’s Why You Didn’t Hear Her Story</a> ) When a member of Congress was accused of sexual harassment, the case went to a secret court known as the Office of Compliance. Hidden from public view, Congress's Office of Compliance paid out over $17 million for 264 settlements involving misconduct and sexual harassment.  (Read, <a href="https://www.washingtonpost.com/news/politics/wp/2017/11/17/over-the-past-20-years-congress-has-paid-17-2-million-in-settlements/">Over the past 20 Years, Congress has paid out $17.2 million in settlements</a> ) It is time to Unseal the Deals! Who are these members of Congress? Right now it's impossible to know, because the law demands that the settlements remained hidden in a vault, although I have been able to obtain one confidential sexual harassment settlement. Congressman John Conyers was forced to resign when I obtained documents showing that he had settled a sexual harassment lawsuit with taxpayer dollars. I would have broken the same story if it had involved a Republican. (Read, <a href="https://www.cjr.org/analysis/buzzfeed-conyers-cernovich-sexual-harassment.php">Buzzfeed receives scoop from controversial source</a> ) 100% of the Funds will Go to Legal Support and Investigations. I've been investigating sexual harassment in Congress, and there are all sorts of hard costs associated with investigative journalism. All funds will go to legal support, private investigators, and whistle blowers. Every dollar is matched through Sunday July 14th, up to $10,000 in total. Double your impact! Jeff Giesea has offered to match donations up to $10,000.  UPDATE: Thank you! This campaign was a major success and has reached the milestone of $10,000. UPDATE 2: Go Fund Me has asked me to post the following information: Who you are and where you’re from I'm Mike Cernovich, journalist, author, and filmmaker. Congressman John Conyers resigned because of my reporting. Your relationship or contact to the parties you're raising funds for I'm raising the funds for Cerno Media. Cerno Media was a prevailing party in a lawsuit seeking to unseal confidential records in a lawsuit involving Jeffrey Epstein. How the funds will be spent (be specific as possible) Legal support, research using Lexis and other databases, whistle blowers will also require support. Your withdrawal plan to get the funds from the campaign to the ultimate beneficiary/ies. Cerno Media is the "beneficiary," although all funds will be spend on hard costs like legal and investigative fees.

Unseal the Deals!

Mark Seely, age 51, in the early morning hours of his birthday, on Saturday, April 20, 2019 died in Phoenix, AZ, his home for over 30 years.  He was involved in a tragic motorcycle accident on his way to work. From his birth in Warwick, NY on April 20, 1968 to his death, he lived to serve with the biggest heart for others, always putting his faith, family, friends and co-workers before himself. Mark attended Warwick Valley High School in Warwick, NY and Glendale Community College, Glendale, AZ and worked as an airline painter/mechanic for America West, USAir and American Airlines for over 30 years in Phoenix, AZ.  He married the love of his life, Alyson Burger Seely on Sept 5, 2018 reuniting their union from their Warwick High School days and lovingly worked to plan for their future together.  Mark is a child of Christ and was proud of who he became in his recent years. He was active in supporting several non-profit entities in which he believed and could aide others. Mark is survived by his beloved wife, Alyson Burger Seely of Dallas, TX, his five children, Joseph Sombrovich (28), Janethe (22), Ashley (17), Mary Kate (14) and Mark Jr. (12) and his bonus (step) children, Jack (18) and Tess (16). His family has established this GoFundMe page to receive donations (in lieu of flowers), and contributions to assist his minor children with their future education.  He was so very proud of Janethe, being the first to go to college in his family and she will be graduating May 9th from Arizona State University, which Mark will miss but her family will be there in support.  He leaves his three minor children and so desperately wanted to see them love education and learning and hoped they would explore topics that intrigued them.  He wanted each to find a passion and embrace it.  With his early departure from our earth, these needs continue to exist for his children and fall to their mother, Sandra, and Aunt Kate and Uncle Boyd to continue to nurture, demonstrate ethical and moral behaviors while sharing the possibilities ahead of them. With much appreciation for your gift, know it will be well managed and distributed as these children progress through their young lives.  Your generosity and messages are very meaningful and heartfelt.  Thank you from the bottom of our hearts. May your heart be full with happy memories of Mark, ones that can keep you laughing and smiling for years to come.

Mark Seely Children – Education Fund

AMTV GoFundMe Campaign 2017

<a href="https://www.facebook.com/ruth.alvarez.9210" target="_blank" rel="noreferrer noopener">Ruth Alvarez, a young mother of three killed by a drunk driver in front of her home in Northridge while taking out her daughter from their car.  Please help us in supporting the family she leaves behind, a new born baby boy, a teenage son and a one-year-old currently hospitalized. </a> <a href="https://www.facebook.com/ruth.alvarez.9210" target="_blank" rel="noreferrer noopener">Ruth was the brightest of stars, warm and giving, always lighting the day with her contagious smile. She welcomed you into her home whole-heartedly and gave her love unconditionally. Her three-month-old baby will not ever know his mother, but her legacy of honesty and absolute love will live in our hearts and in the stories we will share. </a> <a href="https://www.facebook.com/ruth.alvarez.9210" target="_blank" rel="noreferrer noopener">Any donations will help in alleviating the stress of this horrific situation. Thank you in advance for your support.</a> <a href="https://www.facebook.com/ruth.alvarez.9210" target="_blank" rel="noreferrer noopener">-Angelica Cordero</a> <a href="https://www.facebook.com/ruth.alvarez.9210" target="_blank" rel="noreferrer noopener">All proceeds will go directly to the direct family, if you have any questions please call me at [phone redacted].</a> <a href="https://www.facebook.com/ruth.alvarez.9210" target="_blank" rel="noreferrer noopener"><a href="https://www.facebook.com/ruth.alvarez.9210" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.facebook.com/ruth.alvarez.9210</a></a> <img class="not-resizeable" src="https://d2g8igdw686xgo.cloudfront.net/25692006_1511817542.7089_funddescription.png" alt="" width="100%" />￼

Joseph Wells

Joseph Wells

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