Hyatt entities were negligent in that they failed to use reasonable care to keep the Hyatt Ziva Puerto Vallarta in a safe condition, which would have prevented Nico’s tragic death, the complaint alleges.
According to the complaint (Case number: ’23CV1838 BAS AHG), “On the morning of October 11, 2021, James Carter and his almost two-year-old son Nico walked from their hotel room to the elevator bay area. James watched as Nico walked up to what appeared to be a balcony area with safety glass panels near the elevators. Then suddenly, Nico vanished. James quickly realized to his horror that the area was not protected by safety glass panels. On that day, at that moment, Nico fell nine stories to his death.”
The complaint further alleges the “defendant claimed it is the perfect spot for ‘family fun,’ and that the Hyatt Ziva puts ‘safety first.’ The Carters believed the defendants’ representations.” Furthermore, the complaint alleges, “the Hyatt Ziva website reassured them stating “safety first, well-being always.”
Francavilla added, “Instead, the Carters lost their only child – the most tragic and painful loss a parent can endure. The pain is even more severe when the death is so easily preventable as it was here.”
The child’s parents, Duboshina and Carter, say their goal is to seek justice for their son Nico and prevent future tragedies.
“I remember how happy we were to plan a family trip to such a beautiful and family-oriented resort,” Duboshina said. “Nico was almost two years old, and we had also been planning his birthday celebration for when we returned from our trip. Instead, we had to plan his funeral. They shouldn’t have to make coffins so small, and no parent should have to bury a child. I don’t know how I survived, but I know I buried a part of myself alongside my son.”
In a joint statement, Nico Carter’s parents said “Nico’s death was senseless and completely avoidable. We want justice for our son. We relied upon Hyatt for its safety and want Hyatt to take responsibility for its conduct. We hope that through this lawsuit nothing like this ever happens again at any resort or hotel, and that the hospitality industry feels the gravity of what senseless mistakes and carelessness can cause.”
Case number: ’23CV1838 BAS AHG
San Diego Federal Court
All claims are alleged in the complaint.
About CaseyGerry
Headquartered at 110 Laurel St. in the Banker’s Hill neighborhood of San Diego, CaseyGerry was established in 1947 and is the oldest plaintiffs’ law firm in San Diego. The firm’s attorneys practice in numerous areas, including serious personal injury, automobile, maritime, trucking, aviation, product liability, sexual abuse and class actions. For more information, visit www.caseygerry.com.
“I am immensely grateful to the community and our dedicated supporters who have stood by us for 35 years,” said Zammeah Bivins-Gibson, executive director of Isaiah House. “The expansion of our 14th Street facility will continue our mission and create a safe environment for those transitioning back to work and the community after incarceration. I am thrilled to celebrate this program and the many others initiated by Isiah House at the upcoming Gala of Gratitude, which will be a testament to the resilience of those we serve and a reminder that together, we can create lasting change.”
The event will take place on Oct. 27 from 7 p.m. to 11 p.m. at the Orange Lawn Tennis Club, 305 N. Ridgewood Road in South Orange. It will include casino games, hors d’oeuvres and dinner, an open bar, music, a silent auction, and tributes to past supporters and esteemed honorees who have played vital roles in the organization’s efforts to reduce homelessness across Essex County over the last 35 years.
This year’s honorees include Alan Pasternak, Co-Owner of BAMCO Inc., Pastor Terry L Richardson of First Baptist Church South Orange, and Jason Cejour, a former Isaiah House resident whose journey is a testament to the transformative power of support and opportunity. As well as two Isaiah House staff members, Nancy Hicks-Saleem, deputy director and Stacy Rodgers, program director.
Attendees may dress in the night’s theme of the 1920’s. Tickets are $250 per person, with all proceeds considered a tax-deductible donation to the organization. More information can be found at https://isaiahhouse.org/gala. Additionally, event sponsorships are still available, with more information on sponsorship tiers available online.
ABOUT ISAIAH HOUSE Isaiah House is a community fixture established in 1988 with a mission to reduce the prevalence of homelessness, hunger and unemployment throughout Essex County, focusing on the Oranges and Newark. It provides temporary and permanent lodging, food, social and financial services, comfort and hope for families and individuals every year. The organization’s unique approach is based on the firm belief that individual progress and development are enhanced and augmented by the assistance of loved ones. To learn more about Isaiah House, visit: https://www.isaiahhouse.org/
Collaborative fundraising is organized in partnership with Community Foundation of South Jersey (CFSJ). CFSJ’s work includes building permanent, component funds established by many donors to carry out shared charitable interests, such as this home repair work in Ocean County.
Andy Fraizer, CFSJ Executive Director said, “When donors pool resources to create change through community foundations, they realize greater impact and economies of scale. I congratulate the forethought of the team at Causeway CARes and the other Ocean county funders who have come together in this work.” The first projects supported by Project Home Repair are the following:
Northern Ocean Habitat for Humanity is undertaking a crucial project involving roof and gutter repairs, along with subfloor renovations for a residence located in Manchester Township. The investment for this project amounts to $14,943.
Northern Habitat is also partnering with Project Home Repair to provide a roof replacement for a home in Lakewood. The estimated investment for this project is $13,047.
Starve Poverty International is dedicated to ensuring accessibility and safety, and they are taking on a ramp construction project for a property in Ocean Township, with an investment of $10,000.
Homes for All is actively involved in three essential projects. They are overseeing roof replacement projects for residences in both Lacey Township and Manchester Township, with investments of $10,484.00 and $6,517.00, respectively. Additionally, they are conducting a roof repair project for a property in Toms River, which requires an investment of $2,960.00.
Under the experienced leadership of the coalition, the team aims to enhance the health and safety of individuals residing in vulnerable homes. The recent launch of Project Home Repair’s first projects marks a significant milestone in fulfilling the coallition’s mission.
“We are committed to making a difference in the lives of vulnerable populations in our community,” said Dave C. Wintrode, President of the Causeway Family of Dealerships and Causeway CARes. “The launch of these first projects is just the beginning of our efforts to address critical home repairs and positively impact the lives of those in need within Ocean County.”
Project Home Repair will continue to identify and undertake essential home repairs, ensuring that individuals and families can live safely and comfortably in their homes. The coalition’s collective efforts and partnerships will play a pivotal role in fostering a stronger and more resilient community in Ocean County.
About Project Home Repair Project Home Repair is a collaborative effort between Homes for All, Habitat for Humanity of Southern Ocean County, Northern Ocean Habitat for Humanity and Starve Poverty International. The coalition aims to enhance the quality of life for the aging, disabled, and vulnerable populations of Ocean County by providing critical home repair services. Through collaboration, compassion, and community involvement, Project Home Repair seeks to make a lasting impact on the community.
About Homes for All Homes for All, Inc. is fully dedicated to providing affordable housing and support services for low and moderate-income families in local communities. They strive to ensure that everyone has access to safe and affordable housing.
About Habitat for Humanity of Southern Ocean County Habitat for Humanity of Southern Ocean County works to develop communities with individuals in need by building and renovating houses. They believe that all people deserve a clean and decent place to live.
About Northern Ocean Habitat for Humanity Northern Ocean Habitat for Humanity puts God’s love into action by bringing people together to build homes, communities and hope. They work to improve the living conditions in need in the local community.
About Starve Poverty International Starve Poverty International is a nonprofit organization dedicated to breaking the chains of poverty.
About Community Foundation of South Jersey Community Foundation of South Jersey (CFSJ) helps South Jersey residents harness the power of philanthropy to transform their community and the issues they care about most. CFSJ envisions an eight-county region thriving where all neighbors aspire, succeed, participate, and give. The vision is realized as CFSJ inspires generosity, manages and deploys permanent charitable assets, and exercises collaborative leadership to create a more equitable region. communityfoundationsj.org
Media Contact
Allison Brown, Project Home Repair, 732-292-2400, [email protected], projecthomerepair.org
Road Rally fundraiser, a picturesque fall foliage tour of scenic Frederick County, will take place on October 21, 2023
FREDERICK, Md., Oct. 11, 2023 /PRNewswire-PRWeb/ — Second Chances Garage, a nonprofit organization dedicated to providing individuals and families with a fresh start on their journey to independent living through assistance with personal transportation needs, is proud to announce its 10th Annual Road Rally fundraiser. Located in Frederick County, Maryland, Second Chances Garage collaborates with Partner Agencies to identify and assist low-income families needing reliable transportation. Through community and business support, Second Chances Garage has successfully placed more than 325 cars since its inception in April 2010.
The Road Rally fundraiser, a picturesque fall foliage tour of scenic Frederick County, will take place on October 21, 2023, with registration beginning at 8:30 AM at Adventure Park USA, 11113 W Baldwin Road, Monrovia, MD 21770. Participants follow a specific route and search for scavenger hunt clues along the way. It is not a test of speed or knowledge of cars, but of teamwork and awareness of your surroundings. It is a great event for families.
During the rally, participants will make stops at three unique attractions, where they can explore the attractions at their own pace. The event also features a car show, allowing attendees to vote for their favorite car and compete for the Hi-Lo Auto Sales People’s Choice Award. Additional games of chance and raffles will offer opportunities to win exciting prizes.
Ticket options include $35 per person or $100 for a car with up to four occupants. To learn more about this engaging and supportive fundraiser, please contact Second Chances Garage at 240-SCG-1919 (240-724-1919) or visit their website at https://secondchancesgarage.org/road-rally-annual-fundraiser/. You can also connect with Second Chances Garage on Facebook, Instagram, LinkedIn, and YouTube to stay updated on their inspiring work in the community.
About Second Chances Garage Second Chances Garage’s mission is to make a difference in the community of Frederick County, Maryland, by “creating second chances” for individuals and families on their journey to independent living by providing assistance with their personal transportation needs.
In August 2022, the U.S. Congress passed the Inflation Reduction Act (IRA) to reduce the cost of prescription drugs borne by patients. While many individuals certainly benefited from the legislation, the 30 million Americans suffering from rare diseases seem to have been left on the wayside.3
Due to the act’s provision that allows certain FDA-approved drugs, including those targeting multiple diseases and small molecule medicines, to be eligible for price negotiation after just seven years, one can anticipate a sustained slowdown in drug development and innovation. This stagnation is expected to be especially acute in rare disease research, as the field relies extensively on experimentation with repurposed drugs and small-molecule medicine to achieve medical advancements.
Alnylam Pharmaceuticals Inc., for example, halted its research on Stargadt treatment in October 2022, explicitly attributing the pause to the IRA.4 As Alnylam was basing its treatment on a drug that was approved to treat a different condition, the resulting cure would have been subject to price renegotiation.
Since its enactment, the IRA has sent shockwaves across the world. Given that the U.S. plays a prominent role in biopharmaceutical research, the abrupt restrictions imposed by the IRA present a major setback to the global battle against rare diseases.
New hurdles on the horizon for India and the Indian Diaspora
One country that is likely to bear the brunt of the deceleration in rare disease research is India, a long-standing partner of the U.S. in this field. With 70 to 96 millions living with rare diseases,5 many of which are unique to the Indian subcontinent, India has its hands full managing these conditions.
The Indian government has a great start in 2021 with the Ministry of Health and Family Welfare formulating and adopting a National Policy for Rare Diseases (NPRD) that includes a one-time treatment subsidy of USD 61,000 per patient. The program initially promises to be accessible to 40% of the population and has since established over 11 diagnostic and treatment centers of excellence across the country.6
However, this program needs significant expansion to cover all 10,867 (and growing) known rare diseases and not just those small number of currently treatable rare diseases. The policy currently only covers persons afflicted by a subset of the 450 recognized rare diseases. The implementation of NPRD will also need to at least triple the number of centers of excellence to meet the needs of the entire rare disease population of India and provide more accessibility across the country including the rural population. As for the diagnostic and treatment centers, their impact is currently hampered by the absence of formal referral channels established between primary care, secondary care, and tertiary care centers, which hinders patient access.
“A national policy with funding is a great start but is insufficient to cover the treatment of many rare diseases as orphan drugs have to be imported into India,” says Dr. Harsha Rajasimha, founder and executive chairperson of IndoUSrare, a nonprofit centered on combating rare diseases through cross-border collaborations. “Furthermore, many known rare conditions in the U.S. such as ALS (also known as Lou Gehrig’s disease or motor neuron disease (MND)), ultra rare indications caused by single gene mutations such as ADSSL1, DLG4, MNGIE, VCP, and SYNGAP, are not officially recognized by NPRD, thus leaving over 90% of the rare diseases on the fence. Thousands of rare diseases fall under the realm of genomics, precision medicine, patient registries, and clinical research. This is where IndoUSrare seeks to collaborate with the GoI, patient groups, and industry stakeholders to foster cross-border collaborations to accelerate research and clinical trials.” Says Dr. Rajasimha who has also pioneered an intelligent technology platform for efficient implementation of patient registries and clinical trials.
The call for more inclusive research and clinical trials
Considering the rare disease research slowdown in the U.S. and the growing concerns about these disorders in India, increased Indo-US collaboration, particularly in the context of clinical trials, can help mitigate consequences.
The U.S. conducts nearly half of the global clinical trials for rare diseases. However, these trials are not representative of the country’s ethnic makeup, underrepresenting many diasporas, Indian included. For example, despite India having one-third of all rare disease cases worldwide, only nine of the 202 trials registered in the U.S. were conducted there. Participation of the Indian diaspora in these trials is hardly better; in the 193 trials that did not take place in India, only 1% of participants were of Indian origin.7
This lack of representation in clinical trials is problematic because it raises questions about the applicability of the findings; different patient groups may respond differently to identical treatments. This is relevant for specific Indian demographics, as their long history of genetic isolation and unique cultural practices may shape the way they respond to treatments.
By failing to capture the ethnic diversity within the U.S., these non-representative clinical trials may not only lead to a misinterpretation of treatment effects on American rare disease patients but also impede India’s efforts due to the absence of Indian participants. Indeed, considering the additional costs associated with conducting clinical trials in India, Indian regulators have in the past waived the requirement for representative trials if the orphan treatment has already been approved by the U.S. Food and Drug Administration. Consequently, Indian patients may at times receive treatments may be ineffective for them.
“Without a diverse base of study participants, researchers lack representative data on disease progression and research efficacy,” says Frank Sasinowski, MS, MPH, JD, Director at Hyman Phelps McNamara P.C., and Founding Board Member of IndoUSrare.
The need for more inclusive clinical trials is timely because it provides both the U.S. and India with an opportunity to deepen their understanding of the rare diseases affecting both countries — even under the clamping effect of the IRA. Cross-border initiatives, such as those focused on research digitization, data sharing, and the creation of patient registries, can increase the participation of Indian patients as well as those from other groups in these trials.
Coming to a head in the Bridging RARE Summit 2023
Though the U.S. deserves to be congratulated on the 40th anniversary of the Orphan Drug Act of 1983, recent policy changes such as the IRA have stifled biopharmaceutical innovation in the field of rare diseases. This shift is poised to exacerbate India’s struggles in addressing these disorders as it endeavors to improve access to orphan drugs and advance rare disease research and treatment.
One way for both countries to alleviate the fallout resulting from the IRA is to invoke their trusted biopharmaceutical partnership. Collaborative research efforts can expedite the development of treatments, expand their accessibility to regions in pressing need, and pave the way for more inclusive clinical trials.
The intricacies of managing rare diseases, including challenges and potential solutions, will be explored in greater depth during the two-day Bridging RARE Summit 2023. Join the host, IndoUSrare, alongside representatives from the rare disease community, on October 29-30 in this culminating event.
The Summit planning committee has selected two legendary leaders to honor this year with the Abbey Meyers Khushi Bridging RARE Award in recognition of their dedicated lifetime of achievements to foster cross-border collaborations in the field of rare genetic and undiagnosed diseases. The two honorees this year are Dr. William A. Gahl, Senior Investigator at the National Human Genome Research Institute, National Institutes of Health, and Padmashri Dr. Ishwar Chander Verma, Senior Advisor at the Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, Delhi. “The U.S. and India possess complementary skillsets and resources in the context of researching and treating rare diseases,” says Dr. Verma upon accepting the award. “Collaboration is the way forward.”
“Dr. Abbey Meyers is a living legend who was instrumental in the enactment of the U.S. FDA Orphan Drug Act of 1983 which has had immense impact in the U.S. and kicked off a global crusade. By honoring these legends who have advanced research in rare and undiagnosed diseases, the Indo US Organization for Rare Diseases together with the Bridging RARE planning committee seeks their vast wisdom and guidance to carry forward the mission of catalyzing cross-border collaborations for patient-focused research and the next generation of affordable orphan drug development.” Says Rajasimha.
About the Bridging RARE Summit: The Bridging RARE Summit 2023 is organized by the Indo US Organization for Rare Diseases, a non-profit organization based in the Biohealth capital region and a platinum member of the National Organization for Rare Diseases (NORD). The main collaborating U.S. and Indian organizations for the 2023 Summit include George Mason University, Virginia BIO, BioHealth Capital Region Forum, All India Institute of Medical Sciences (AIIMS) New Delhi, Centre for DNA Fingerprinting and Diagnostics (CDFD) India, Global Genes, EveryLife Foundation for Rare Diseases, other collaborators and sponsors. For the full agenda, keynote speakers, Gala, Registration, and Sponsorship opportunities, visit https://bridgingrare.org.
About Indo US organization for rare diseases: IndoUSrare is a humanitarian nonprofit 501(c)(3) tax-exempt public charity organization based in the United States. Founder and Executive Chairman Dr. Harsha Rajasimha, who lost a child to a rare disease in 2012, has been a rare disease advocate for more than 10 years. To address the unmet needs of diverse patients with rare diseases globally, the leadership team comprised of experienced professionals from research, advocacy, regulatory, and drug development seeks to build cross-border collaborations connecting stakeholders of rare diseases in low- and middle-income regions such as India, with their counterparts and clinical researchers in the United States to improve the diversity of clinical trial participants, accelerate research and development, and improve equitable access to life-saving therapies to diverse populations of rare disease patients. Visit https://indousrare.org.
References:
Ministry of Health and Family Welfare. “National Policy for Rare Diseases, 2021.” Ministry of Health and Family Welfare, rarediseases.mohfw.gov.in/uploads/Content/1624967837_Final-NPRD-2021.pdf. Accessed 16 Sep. 2023.
Roberts, Alexis-Danielle, Roopma Wadhwa. “Orphan Drug Approval Laws.” National Library of Medicine, ncbi.nlm.nih.gov/books/NBK572052/. Accessed 16 Sep. 2023.
Saltonstall, R.K., Peter L. (2023). The IRA needs changes to better support patients with rare diseases. [online] STAT. Available at: Accessed 9 Oct. 2023.
Scott, R. (2022). Alnylam Opts Against Phase III Trial for Vutrisiran in Stargardt Disease – Updated. [online] BioSpace. Available at: Accessed 9 Oct. 2023.
Salian, Priti. “What price a child’s life? India’s quest to make rare disease drugs affordable.” The Guardian, theguardian.com/global-development/2021/mar/15/what-price-a-childs-life-indias-quest-to-make-rare-disease-drugs-affordable. Accessed 16 Sep. 2023.
Ministry of Health and Family Welfare. “National Policy for Rare Diseases, 2021.” Ministry of Health and Family Welfare, rarediseases.mohfw.gov.in/uploads/Content/1624967837_Final-NPRD-2021.pdf. Accessed 16 Sep. 2023.
Chakraborty, Monoswi et al. “Rare disease patients in India are rarely involved in international orphan drug trials.” PLOS Global Public Health, journals.plos.org/globalpublichealth/article?id=10.1371/journal.pgph.0000890. Accessed 16 Sep. 2023.
Media Contact
Karla Jo Helms, JOTO PR™, 727-777-4619, [email protected], jotopr.com
The whitepaper emphasizes the power of personalization, data-driven insights, and seamless integration between text messaging and mobile apps to empower nonprofits.
RALEIGH, N.C., Oct. 10, 2023 /PRNewswire-PRWeb/ — Tatango, the leading text message platform in the nonprofit sector, has partnered with Nuclavis, a digital marketing and mobile software company focused on nonprofits, in the creation and publication of a whitepaper entitled, “Winning Mobile-First Peer-to-Peer Strategy to Engage Participants and Maximize Fundraising.”
The COVID-19 pandemic caused a 34 percent decline in revenue for the top 30 peer-to-peer programs. The proposed strategy in this whitepaper aims to bridge the $220 million gap that continues to exist today by providing cost-effective alternatives to traditional outreach methods, ensuring real-time engagement with participants and the rise of smartphone usage.
Tatango and Nuclavis aim to advance peer-to-peer fundraising strategies and provide guidance for nonprofits adapting to the post-COVID landscape. The whitepaper emphasizes the significance of utilizing text messaging and mobile applications for participant engagement and fundraising optimization. This approach integrates real-time engagement, cost-effectiveness, and personalized interactions to enhance participant involvement and fundraising efforts.
“We are excited to collaborate with Nuclavis and present insights showing nonprofits that when adding a mobile app and text messaging, the digital fundraising toolkit is ready to deliver big results. By meeting participants on their phones, we can ensure urgent communications are noticed and acted upon, in turn helping nonprofits meet their fundraising goals,” said Geoff Alexander, Tatango’s Chief Marketing Officer.
“With a mobile-first strategy, nonprofits can meet their constituents where they are. With a comprehensive mobile combination of texting and a mobile app, nonprofits can optimize user engagement, improve communication, and maximize fundraising.” said Kathy Kempff Nuclavis Founder and Chief Executive Officer, “We’re thrilled to partner with Tatango, bringing leading-edge mobile technology to the nonprofit sector.”
This whitepaper is anticipated to have a significant impact on the peer-to-peer fundraising landscape, providing nonprofits with valuable insights to navigate and excel in an evolving digital environment.
On October 18, 2023, at 11 AM CST/12 PM ET, Tatango and Nuclavis are hosting a webinar to share the contents of the whitepaper in a session called “Unlocking the Power of Mobile“.
SBTi is a collaboration among the United Nations Global Compact (UNGC), World Resources Institute (WRI), the CDP, a nonprofit helping entities disclosing environmental impact, the World Wide Fund for Nature, (WWF) and one of the We Mean Business Coalition commitments. SBTi defines and promotes best practice in science-based target setting, offers resources and guidance to reduce barriers to adoption, and independently assesses and approves companies’ targets.
“As a company that has long been committed to a healthier planet, we take our role as a leader in reducing emissions in the supply chain as profoundly important for our economic and environmental well-being,” added Hannah Kain, President and CEO of ALOM. “Given that close to 90% of GHG emissions result from supply chains serving companies that produce and ship physical goods, we believe our industry has an opportunity – and a responsibility – to act decisively with SBTi targets in mind.”
In line with SBTi criteria to limit the global temperature rise, ALOM is prioritizing direct emissions reductions and neutralizing all residual emissions. This verification is one of ALOM’s science-based milestones of rigorous certifications, best-in-class partnerships, and innovative programs to monitor and report GHG reduction.
For example, ALOM’s ISO 14064-1 certification ensures transparency in tracking and reporting all direct and indirect scope 1, 2, and 3 GHG emissions. As a Green Power Partner with the U.S. Environmental Protection Agency (EPA), ALOM must verify its ongoing use and GHG reduction impact of clean energy use.
Further initiatives enacted by ALOM to achieve its SBTi verified GHG reduction targets include:
Nearsource its supply base to reduce freight transport distance
Execute meaningful sustainable procurement and packaging strategies
Support aggressive recycling and reuse programs
Implement energy-saving technology
ALOM works collaboratively with customers and suppliers to extend the scale of its GHG emission reduction initiatives. The company can provide GHG data specific to the delivery of customer programs to quantify its contribution to achieving customers’ own GHG reduction goals. Across its supply base, ALOM partners with suppliers that support its environmental values and have enacted greenhouse gas reduction and measurement initiatives – or are in the process of doing so.
SBTi target verification is an important milestone for ALOM in meeting its GHG emission reduction goals. Read about the company’s ESG commitment and download its 2023 ESG report: https://alom.com/esg-centric-values/
About ALOM ALOM is a global supply chain management services and solutions provider, serving as a strategic partner to its Fortune 500 clients in the technology, automotive, life sciences, and highly regulated industry sectors. Headquartered in Fremont, CA, USA, its teams of technology engineers and supply chain specialists operate globally from 19 locations.
Committed to environmental and social responsibility, ALOM manages the physical supply chain from procurement, inventory management, contract assembly, digital media and print, to omni-channel fulfillment and returns. ALOM seamlessly integrates digital and financial streams into the physical supply chain, deploying e-commerce and payment solutions, visibility tools, digital delivery tools, data management, and strong back-end systems, all while producing and fulfilling goods worldwide.
ALOM is proud to deliver its clients’ products and services impeccably, enrich the end-user experience, and uphold their brand reputations. https://alom.com/
Williams also announced the launch of the Arise And Shine Foundation, a 501(c)(3) that aims to advance the professional development of underserved and underrepresented women and girls. The E.S.T.E.A.M Project will be the pilot program under the new nonprofit.
LOS ANGELES, Oct. 6, 2023 /PRNewswire-PRWeb/ — On Sunday, October 1, 2023, Actress, Author, and Entrepreneur Malinda Williams celebrated her 5th year of elevating, empowering, and uniting women of color at the Arise And Shine Women’s Empowerment Brunch. This year’s milestone celebration took place at the Sheraton Universal in Los Angeles, California, and included the announcement of her new philanthropic endeavor, The Arise And Shine Foundation Inc., a 501(c)(3) with a mission to serve as a conduit of information, inspiration, and empowerment of women in all walks of life.
Malinda Williams, founder of the Arise and Shine empowerment events series, embarked on this journey five years ago to offer a supportive hub to connect accomplished women. From exchanging ideas to fostering relationships, the Arise and Shine brunch serves as a bridge in the opportunity gap for Black women. “My whole life and career, I have been uplifted by and stood on the shoulders of many powerful women. These past few years have illuminated that connection to community is more important now than ever,” said Malinda Williams. “I am honored to collaborate with so many brilliant minds who understand the value of community, sisterhood, and using our resources to empower and give back to others.”
As guests arrived at this year’s event, they strolled down a beautiful pathway adorned with stunning rose blossoms and inspirational messages. Soon after, the room filled with love, laughter, and a gathering of like-minded women. Before diving into the main topic of discussion, Malinda took a moment to acknowledge and honor her “village” – her husband, son, mother, father, and two sisters, all of whom were present. To their surprise, she presented each of them with a bouquet of flowers and offered a flower to every guest in the room. Malinda and special guest, media executive Amy Dubois Barnett, engaged in a fireside chat, followed by an open discussion on AI, Algorithms, and the Impact of Technology On Our Culture. The discussion highlighted the importance of promoting more Black women in technology and STEAM fields and explored ways Black Culture can fearlessly leverage technology for community advancement.
Malinda also proudly announced the establishment of The Arise And Shine Foundation, the non-profit arm of Arise And Shine, co-founded with her sisters Leslie Williams-Dunn and Lisa Williams-Sorensen.
The foundation’s pilot program, The E.S.T.E.A.M Project, slated to run in Summer 2024, is an HBCU development and coding camp designed around three pillars: upskilling core competencies in technology, fine-tuning soft skills for business success, and facilitating connections for industry mentorships. Students will learn to code using Apple’s Everyone Can Code curriculum.
In addition to coding, The E.S.T.E.A.M Project will further prepare and empower young women to be future leaders through lessons in cultivating wellness, creative thinking, esteem building, and problem-solving.
The program will begin accepting applications in the Spring of 2024.
Hallmark Mahogany will return as the Premiere Partner and Sponsor under the leadership of Alexis Kerr. “Mahogany is immensely proud to sponsor the Arise and Shine event, which uplifts Black women and celebrates the power of amazing creatives like Malinda Williams,” said Alexis Kerr, Vice President – Mahogany Brand Leader Hallmark Cards, Inc. “Our commitment to telling our own stories and affirming the soul-strengthening narratives of our sisters remains steadfast, and we are proud to celebrate her 5th anniversary.”
About Arise and Shine Foundation
Founded in 2023 by actress, author, and entrepreneur Malinda Williams, the Arise And Shine Foundation is a 501(c)3 non-profit organization that helps fulfill Malinda’s vision to be a conduit of information, inspiration, and empowerment to women in all walks of life. The foundation partners with educational institutions, corporations, and the community to implement and support programs that advance the personal and professional development of underserved and underrepresented women and girls. The work is led by Malinda along with founding members and sisters Lisa Sorensen, a communications specialist and wellness advocate, and Leslie Williams-Dunn, retired Senior Director of Technology for Johnson & Johnson. Additionally, a team of highly accomplished, passionate women from varying professions are aligned in support of the cause. This dynamic group collaborates to bring a wealth of experience, expertise, and excellence to achieve the goals and mission of the organization. To learn more, visit The Arise and Shine Foundation.
About Hallmark Mahogany
For nearly 40 years, Hallmark Mahogany has built a relationship of trust with the Black community by honoring, celebrating, and supporting emotional connections among Black families, friends, and other loved ones. In December 2021, Mahogany introduced Mahogany.com, a lifestyle destination where Black women can trust that their unique stories will be told, their truths will be heard and honored, and their collective culture celebrated through the vibrant spectrum of their individual experiences and launched its e-commerce site in September 2022.
Dewberry Foundation, Midtown Alliance, and Museum of Design Atlanta (MODA) are pleased to announce the Heart of the Arts Studio Residency Bus Tour, taking place during Atlanta Art Week on Wednesday, October 4th, 2023. The Heart of the Arts Studio Residency Bus Tour will take place from 6:30 PM to 9:00 PM.
ATLANTA, Oct. 6, 2023 /PRNewswire-PRWeb/ — Dewberry Foundation, Midtown Alliance, and Museum of Design Atlanta (MODA) are pleased to announce the Heart of the Arts Studio Residency Bus Tour, taking place during Atlanta Art Week on Wednesday, October 4th, 2023. The bus tour will offer participants a behind-the-scenes look at the studios of seven artists participating in the Heart of the Arts Residency Program, a new initiative that provides artists with space and opportunities to work in Midtown Atlanta.
The Heart of the Arts Residency Program is a collaborative effort between Midtown Alliance and its partners to create a more vibrant and inclusive arts community in Midtown. The program provides artists with studio space, mentorship, and other resources to support their creative practice. The Heart of the Arts Studio Residency Bus Tour is an opportunity for the public to meet the artists in the program and learn more about their work.
“We are thrilled to partner with Midtown Alliance and MODA – all powerhouses in our beloved Midtown community – to present the Heart of the Arts Studio Residency Bus Tour during the second annual Atlanta Art Week,” said Jaimie Dewberry, Director of the Dewberry Foundation. “This is a unique opportunity for the public to meet the artists in the program and learn about their work in a more intimate setting. We hope that this event will help to raise awareness of the Heart of the Arts Residency Program and its important role in supporting Atlanta’s arts community.
“MODA is so excited to join forces with Dewberry Foundation and Midtown Alliance to connect art lovers from near and far to Midtown’s incredible artists in residence, whose work demonstrates the power of art and design to enrich our communities and make Atlanta a more vibrant place,” said Mary Catherine Kelly, MODA’s Programs Manager.
The Heart of the Arts Studio Residency Bus Tour will take place on Wednesday, October 4th, 2023 from 6:30 PM to 9:00 PM. The bus will depart from Peachtree Pointe, 1545 Peachtree St NE, and visit the studios of the following artists:
About Atlanta Art Week – Atlanta Art Week is a new initiative that celebrates the visual arts in one of the fastest growing art hubs in the United States. Founded by Art Advisor Kendra Walker, AAW aims to create a dynamic environment that brings together galleries, artists, collectors, and art enthusiasts to promote cultural exchange, education, economic development, and appreciation of the arts. Our goal is to highlight contemporary art, provide opportunities for growth and recognition, and promote Atlanta on a national level.
About Dewberry Foundation – Established in 2002 by John Dewberry, the Dewberry Foundation is dedicated to supporting youth, art, and community. We believe that all young people deserve the opportunity to reach their magnanimitas, greatness in spirit and that arts and culture play a vital role in building vibrant communities. The Dewberry Foundation is now under the leadership of Jaimie Brown Dewberry.
About Midtown Alliance – Midtown Alliance is a non-profit membership organization and a coalition of leading business and community leaders – united in our commitment to Midtown as a premier destination for commerce, culture, education and living. Guided by a visionary master plan – Blueprint Midtown – and in partnership with the Midtown Improvement District, our mission is to improve and sustain the quality of life for those who live, work and play here. Midtown Alliance accomplishes this goal through a comprehensive approach to planning and development that includes initiatives to enhance public safety, improve the physical environment, and strengthen the urban amenities which give the area its unique character.
About MODA – Museum of Design Atlanta (MODA) is the only museum in the Southeast dedicated exclusively to the study and celebration of all things design. It seeks to address contemporary interests and issues through its exhibitions and programming, empowering visitors to think like designers as they face current and future challenges. As one of the city’s most important arts organizations, MODA’s exhibits focus on all areas of design, including architecture, graphic design, and more. Its current exhibition, Level Up: Pixels, Play, & Progress, provides a lens into how video games can help to strengthen players’ empathy, ultimately making the world a better place.
Media Contact
Jaimie Brown Dewberry, Dewberry Foundation, 1 706-217-8462, [email protected]
“NAIFA is pleased to welcome Roger Moore to our Government Relations team,” said NAIFA Senior Vice President for Government Relations Diane Boyle. “Roger brings a wealth of experience and connections in policy areas of great interest to NAIFA and our members. His work at federal, interstate, and state levels meshes nicely with NAIFA’s role as the leading advocacy association of insurance and financial professionals in the United States. We are the only association of agents and advisors with strong advocacy influence in Washington, D.C., and every state capital, and adding Roger to our team will help us grow that influence to new heights.”
Moore holds an M.A. in political science from Georgia State University and a B.A. in history from New York University. He currently resides in the New York City metro area.
ABOUT NAIFA: The National Association of Insurance and Financial Advisors is the preeminent membership association for the multigenerational community of financial professionals in the United States. NAIFA members subscribe to a strong Code of Ethics and represent a full spectrum of financial services practice specialties. They work with families and businesses to help Americans improve financial literacy and achieve financial security. NAIFA provides producers a national community for advocacy, education, and networking along with awards, publications, and leadership opportunities to allow NAIFA members to differentiate themselves in the marketplace. NAIFA connects with members in 267 different local areas between State Chapters, Local Chapters, and Local Affiliates. NAIFA members in every congressional district advocate on behalf of producers and consumers at the state, interstate, and federal levels.
