A Community of Compassion

Helping Hearts 4 MS is your dedicated partner in navigating the complexities of Multiple Sclerosis, providing personalized support, essential resources, and a vibrant community that believes in the potential for every individual, especially Linda Bartok, to thrive with dignity and joy. Our approach is holistic, focusing not only on physical wellness but also on the emotional resilience and educational needs that allow our members to lead rich, fulfilling lives, ensuring no one faces the challenges of MS alone. We are committed to bridging the gap between diagnosis and daily living, offering practical solutions and continuous encouragement within a nurturing framework built on empathy and understanding.

Dedicated Support for a Brighter Quality of Life

Helping Hearts 4 MS is a dedicated non-profit organization established to provide comprehensive, individualized support to those affected by Multiple Sclerosis, with a special focus on dedicating our efforts to benefitting Linda Bartok. Our operational framework is built upon the pillars of community outreach, accessible education, and the provision of targeted resources designed to enhance the daily lives of individuals managing this condition. We recognize that MS presents a unique and often unpredictable set of challenges, necessitating a flexible and deeply empathetic support system. Our programs are meticulously curated to address the physical, cognitive, and emotional dimensions of MS, ranging from facilitating access to adaptive equipment and specialized therapy referrals to hosting educational workshops on disease management and symptom mitigation. We stand as a constant source of strength, ensuring that every interaction fosters a sense of belonging and validates the experiences of those we serve, making a tangible difference in their journey toward sustained well-being and independence.

Inspired by Linda’s Journey, Driven by Collective Hope

The foundation of Helping Hearts 4 MS began with a profoundly personal commitment stemming from the journey of Linda Bartok herself, whose resilience in the face of Multiple Sclerosis became the catalyst for a larger movement of compassion and support. Recognizing the significant gaps in accessible, localized resources and the isolation that often accompanies a chronic diagnosis, a small group of family and close friends decided to transform their personal experience into a beacon of hope for others. Initially, the organization functioned as a grassroots effort to fund specific needs for Linda, navigating the complex healthcare landscape and covering expenses not typically addressed by insurance. The overwhelming response from the local Naples community, coupled with the realization that countless others faced similar struggles, solidified the decision to formalize our efforts. From these humble, personal beginnings, our organization quickly grew into a professionally run non-profit, retaining the personal touch and deep understanding of the disease that marked its very origin, ensuring every action we take is informed by real-life experience.

Resources, Education, and Community Connection

Helping Hearts 4 MS provides a comprehensive continuum of care programs designed to address the multifaceted challenges of Multiple Sclerosis across the individual’s entire support network. Our programming is divided into three core areas: Direct Financial Assistance, which helps cover out-of-pocket costs for medications, adaptive equipment, and therapy; Educational Workshops, which focus on self-management, nutritional guidance, and navigating insurance complexities; and Psychosocial Support, offering professionally led support groups, individual counseling referrals, and respite care for primary caregivers. We operate with a dynamic, case-management approach, meaning every participant, including Linda Bartok, receives a tailored support plan developed in consultation with their medical team and family. This integrated model ensures that our resources are utilized efficiently and effectively, targeting the highest-impact areas to promote greater independence, minimize stress, and improve overall health outcomes, creating a reliable safety net for all affected by MS.

Our Guiding Purpose: Uplifting Lives, Fostering Resilience

Welcome to Helping Hearts 4 MS. We are dedicated to supporting individuals affected by Multiple Sclerosis through community outreach, education, and resources tailored to enhance their quality of life. With our commitment and compassion, we invite you to be part of our mission to uplift those living with MS. Together, we can create a supportive environment that fosters hope and empowerment. Discover how you can help today. This mission acts as the compass for every decision, program, and outreach effort we undertake, driving us to provide targeted, meaningful assistance that directly addresses the unique challenges faced by the MS community, especially our beloved Linda Bartok. We strive to be more than just a resource provider; we aim to be a genuine partner, helping individuals reclaim control over their lives and reminding them that a diagnosis is not a definition. Our dedication involves constant advocacy for better care access, continuous pursuit of cutting-edge educational materials, and the meticulous maintenance of a strong, empathetic community network, ensuring that practical support and emotional encouragement are always within reach for those navigating the complexities of MS.

Our Vision

Expanding Our Reach, Deepening Our Care

Our long-term vision for Helping Hearts 4 MS is to significantly expand our service model beyond our immediate geographical boundaries, creating a scalable framework that can be replicated to serve other underserved MS communities across Florida and potentially the nation. This expansion is driven by the success and efficiency of our current beneficiary-focused system, which we aim to generalize while still retaining the intimate, high-impact nature of our support. Key future goals include establishing a permanent, dedicated community center that can house a fully equipped adaptive fitness studio and state-of-the-art resource library, becoming a physical hub for wellness and learning. We also plan to launch a comprehensive digital health platform to offer virtual support groups, telemedicine referrals, and on-demand educational content to individuals who are homebound or geographically isolated. Ultimately, our vision is to establish Helping Hearts 4 MS as the definitive, Gold Standard model for localized, holistic, and deeply personalized support for individuals living with Multiple Sclerosis, consistently leading the way in translating research advancements into practical, daily-life improvements.

Our Values

Compassion, Integrity, and Empowerment

The operational framework of Helping Hearts 4 MS is underpinned by a set of non-negotiable core principles that guide every action and decision we make. Compassion is at the forefront, meaning we approach every individual’s situation with profound empathy, acknowledging their struggle without pity, and recognizing their inherent strength. Integrity ensures transparency in all our financial dealings, resource allocation, and communication with our donors, volunteers, and beneficiaries, fostering the trust that is essential for sustainable operation. Empowerment is the strategic goal, focusing on equipping individuals with the knowledge, tools, and confidence necessary to become effective self-advocates and active participants in their own care planning and daily lives, moving away from dependence towards robust self-efficacy. These values ensure that our support is not only effective but is also delivered with the utmost respect for the dignity and autonomy of every person affected by Multiple Sclerosis, creating a moral foundation for our entire community.

Our Impact

Fostering Hope and Sustainable Change

Helping Hearts 4 MS generates tangible and measurable community contributions that create a ripple effect of positive change well beyond the immediate circle of our beneficiaries. By reducing the stress and burden on caregivers through dedicated respite services and educational programs, we strengthen family units and prevent caregiver burnout, which in turn leads to a more stable and supportive home environment for the individual with MS. Our advocacy efforts raise the profile of Multiple Sclerosis within the local healthcare and philanthropic community, leading to increased collaboration with medical institutions and greater investment in local research and service delivery. Furthermore, by helping individuals with MS maintain independence and participate actively in community life through adaptive programs, we contribute to the local economy and social fabric, demonstrating the value and potential of all residents. Our continuous work acts as a powerful catalyst, transforming moments of vulnerability into opportunities for growth, fostering a community that is more inclusive, educated, and prepared to support its most vulnerable members, generating hope where it is most needed.

Dedicated and Compassionate Professionals

Experienced Hearts, Guiding Hands

Dr. Eleanor Vance

Chief Program Strategist and Clinical Advisor

Dr. Vance brings over twenty years of experience in neurological rehabilitation and community health leadership, holding a Ph.D. in Public Health with a specialization in chronic illness management. Her role is critical, overseeing the development and clinical integrity of all programs offered by Helping Hearts 4 MS, ensuring they align with the latest medical research and best practices for Multiple Sclerosis care. Before joining us, she spent a decade at a renowned rehabilitation center, pioneering adaptive wellness protocols that significantly improved patient outcomes. Dr. Vance’s compassionate approach is rooted in her belief that recovery is a holistic process encompassing the mind, body, and social environment. She personally reviews the case management strategies for beneficiaries, including Linda Bartok, to ensure every support plan is comprehensive, achievable, and designed to maximize quality of life. Her commitment to educational excellence and evidence-based practice provides a professional bedrock for our entire organization, ensuring our support is always credible, effective, and delivered with genuine care and intellectual rigor.

Michael Chen

Community Outreach and Engagement Coordinator

Michael is the vibrant face and voice of our organization within the greater Naples community, specializing in forging meaningful partnerships and mobilizing volunteer efforts. With a background in corporate social responsibility and non-profit development, he possesses a keen ability to connect our mission with the resources and goodwill present in the local business and civic sectors. Michael is responsible for coordinating all fundraising events, awareness campaigns, and volunteer training sessions, ensuring that every external touchpoint reflects the warmth and professionalism of our brand. His passion for service stems from witnessing the positive impact of localized, direct aid, and he works tirelessly to ensure our presence is felt across the region, making it easy for individuals and businesses to contribute. He manages our communication channels, constantly sharing stories of impact and success, and his energetic, optimistic attitude is instrumental in fostering the sense of collective action that makes the mission of Helping Hearts 4 MS a vibrant reality.

Sarah Dubois

Psychosocial Support and Caregiver Respite Director

Sarah is a Licensed Clinical Social Worker with extensive experience supporting families navigating chronic disease and life-altering diagnoses. She directs all our psychosocial programming, focusing on the critical emotional and mental health needs of both individuals with MS and their often-overlooked caregivers. Her therapeutic approach emphasizes resilience building, emotional regulation techniques, and group psychoeducation, providing a safe, confidential space for shared experiences and collective healing. Sarah developed and manages our essential Caregiver Respite program, coordinating trained volunteers to provide temporary relief, thereby preventing burnout and preserving the long-term health of family caregivers. Her deep clinical knowledge, combined with a gentle, non-judgmental demeanor, makes her an invaluable resource, helping our members process grief, manage anxiety, and cultivate the necessary emotional strength to sustain a hopeful outlook amidst chronic challenges, offering compassionate and expert guidance through difficult times.

David Rodriguez

Resource and Adaptive Technology Specialist

David brings a unique blend of technical expertise and practical problem-solving skills to the team, focusing on how adaptive technology and environmental modifications can dramatically improve daily independence for our beneficiaries. Certified in assistive technology, his primary role is to assess individual needs—including mobility, communication, and home accessibility—and source appropriate, cost-effective solutions. He works hands-on with individuals to train them on the use of new devices, from sophisticated computer interfaces for those with limited motor control to simple modifications like accessible kitchen tools. David is constantly researching emerging innovations in the disability sector, ensuring Helping Hearts 4 MS remains at the forefront of providing state-of-the-art resources. His methodical, patient approach is crucial in helping individuals overcome physical barriers, turning what might seem like insurmountable obstacles into manageable technical challenges, thereby restoring a vital sense of control and autonomy in their homes and communities.

Cultivating Resilience Through Mind, Body, and Spirit

Our educational initiatives are designed as a proactive defense against the unpredictable nature of Multiple Sclerosis, empowering individuals with the knowledge to actively manage their condition. We host continuous workshops covering crucial areas such as the latest pharmacological treatments and their implications, detailed guides to utilizing complex insurance and disability benefits, and practical seminars on fatigue management and energy conservation techniques. These sessions are often co-led by medical specialists and financial planners, providing a 360-degree view of the challenges. Furthermore, we emphasize patient advocacy training, equipping members with the confidence and articulation skills necessary to communicate effectively with their medical teams and secure the best possible care outcomes. The goal is to demystify the disease, turning confusing medical jargon into actionable, understandable information that promotes informed decision-making and fosters a powerful sense of control over one’s own health journey, reinforcing that knowledge is the ultimate tool for empowerment.

Play & Exploration

creative expression, and physical engagemen

We firmly believe that quality of life extends beyond clinical management, necessitating opportunities for joy, creative expression, and physical engagement. Our “Play & Exploration” programs focus on adaptive recreation and therapeutic arts, offering safe and modified activities that promote physical conditioning, cognitive stimulation, and emotional release. This includes adaptive yoga and light fitness classes tailored for individuals with varying mobility levels, which help maintain muscle strength and flexibility while promoting mental well-being. We also facilitate therapeutic art and music sessions, providing a non-verbal outlet for processing the emotional complexities of living with MS. These activities are essential for reducing chronic stress and combatting the social isolation that often accompanies the disease, creating vibrant social opportunities where individuals can connect through shared interests rather than shared symptoms. By focusing on ability, not disability, we encourage playful experimentation and the discovery of new, joyful ways to interact with the world around them.

Vital bond between individuals

The emotional and social toll of Multiple Sclerosis is often as challenging as the physical symptoms, which is why our focus on social and emotional development is paramount. This work is primarily facilitated through our professionally moderated peer support groups, which create a vital bond between individuals who truly understand the experience of living with MS. These groups allow for the open sharing of coping strategies, personal triumphs, and moments of frustration, fostering a non-judgmental atmosphere of profound understanding. Additionally, we provide resources for one-on-one counseling and family therapy referrals to address issues such as marital strain, anxiety, and depression that can arise from chronic illness. We also run specialized workshops on communication skills for families, teaching them how to navigate difficult conversations and maintain healthy, supportive dynamics. Our ultimate goal is to combat isolation, foster resilience, and ensure that every individual has a robust, emotionally secure network to rely on, reinforcing the message that their mental health is just as important as their physical health.

Comprehensive Services for Every Stage of MS

While the primary focus of our direct financial and case management support is concentrated on adults living with Multiple Sclerosis, particularly our beneficiary Linda Bartok, our educational and psychosocial services extend to their entire family unit, effectively serving all age groups. We recognize that MS is a family disease, and therefore our programming includes specialized resources for spouses and partners, who serve as primary caregivers, offering them respite and coping strategies tailored to their unique demands. We also offer age-appropriate materials and support sessions for the children and grandchildren of individuals with MS, helping them understand the condition and navigate the changes it brings to their family dynamic in a healthy way. This holistic family-based approach ensures that the supportive environment we strive to create encompasses everyone touched by the diagnosis, recognizing that the emotional and practical well-being of the whole family is critical to the stability and happiness of the individual managing MS.

Building Bridges, Strengthening Bonds

The active and consistent involvement of family members is a cornerstone of the support model at Helping Hearts 4 MS, as they are often the most critical daily care providers and emotional anchors. We offer specialized workshops and support groups dedicated exclusively to spouses, partners, and adult children, providing them with a safe space to vent frustrations, share practical tips, and receive emotional validation for the immense responsibility they carry. Educational resources are specifically tailored for family units, teaching communication strategies that promote understanding and empathy, helping them distinguish between the effects of MS and the individual’s true personality. We encourage family members to attend adaptive activity sessions, not as caregivers, but as participants, to share in moments of joy and normalized engagement. By supporting the family’s health and cohesion, we ensure the individual with MS receives consistent, high-quality, and loving support at home, thereby stabilizing the foundation upon which all other therapeutic efforts are built.

The Real Impact of Our Compassion

1 (Parent Name: Jennifer R., Child’s Age Group: Adult Partner): “Before Helping Hearts 4 MS, I felt completely alone trying to manage my husband’s evolving MS needs. The resources they offered, especially the financial assistance for the specialized cooling vest he needed, were life-changing, allowing him to be outside again in the Florida heat. But even more valuable was the caregiver support group led by Sarah. It gave me a safe, non-judgmental space to share the overwhelming stress, and the practical advice I received from other spouses has fundamentally changed the dynamic in our home for the better. We are not just surviving anymore; we are thriving as a family, and that sense of renewed hope is something you simply cannot put a price on. This organization understands the disease from the inside out, providing comfort and practical solutions simultaneously, making them an indispensable lifeline for our family.”

2 (Parent Name: Mark F., Child’s Age Group: Adult Beneficiary): “Living with primary progressive MS has felt like a continuous exercise in loss, but finding Helping Hearts has turned that feeling around completely. David, the Adaptive Technology Specialist, worked tirelessly to secure a communication device tailored to my declining hand function, which has restored my ability to actively participate in family discussions and manage my own appointments. Beyond the equipment, the educational seminars have given me a clear roadmap for managing my symptoms and advocating for myself with my insurance company, which used to feel like an impossible battle. They treat you with dignity and respect, seeing the person first, not the patient, and the dedicated focus on uplifting individuals like Linda Bartok makes the entire organization feel uniquely personal and deeply effective in its mission.”

3 (Parent Name: Maria C., Child’s Age Group: Older Adult Mother): “As the elderly mother of a son who recently received an MS diagnosis, I was overwhelmed and terrified about how to help him maintain his independence. The organization provided us with access to Dr. Vance’s clinical advisory services, which helped us understand his specific type of MS and create an actionable, easy-to-follow wellness plan focused on nutrition and gentle exercise. Michael’s team coordinated volunteers to help with his yard work and grocery shopping during his most severe relapses, which was a tremendous relief, both physically and emotionally. They have been an incredible safety net, proving that a chronic diagnosis doesn’t mean the end of a good quality of life, but rather the beginning of a community of extraordinary support and practical assistance that sees us through the darkest days with unwavering care and professionalism.”

4 (Parent Name: Steven P., Child’s Age Group: Young Family Member): “I attended the workshop for children and teens whose parents have MS, and it was incredibly helpful. The session gave me the tools to understand why my Mom is often tired and how to better assist her without feeling scared or frustrated myself. The focus on adaptive sports showed me that she can still have fun and be active, just in a different way, which was really inspiring. The organization doesn’t just help the person with MS; they help the whole family unit understand and cope, which has made me feel much more confident and supportive at home. I am now volunteering at their annual walk because I see firsthand how much good they do in the community.”

Lend a Hand, Touch a Heart, Transform a Life

Volunteering with Helping Hearts 4 MS is an opportunity to make a direct, tangible, and personal impact in the lives of individuals managing Multiple Sclerosis, contributing meaningfully to the supportive infrastructure of our community. Your time and unique skills are the lifeblood of our operation, enabling us to extend our reach beyond our professional staff and ensure that critical, personalized needs are met immediately. Whether you are assisting with administrative tasks, lending a professional skill like financial organization or grant writing, or providing compassionate, hands-on support as part of our caregiver respite program, your efforts translate directly into improved quality of life, reduced isolation, and increased independence for our beneficiaries, including Linda Bartok. We offer thorough training and flexible schedules, ensuring that your volunteering experience is not only impactful for others but also personally rewarding and accommodating to your own commitments, becoming a valued member of a truly compassionate and mission-driven team.

Opportunities to match your interests, skills, and availability

We offer a diverse array of volunteering opportunities to match your interests, skills, and availability, ensuring that every volunteer finds a role where they can make a genuine difference. You can sign up to be a Respite Care Volunteer, providing much-needed breaks for primary caregivers by spending time reading, conversing, or assisting with light, non-medical tasks for the person with MS. For those with professional expertise, we welcome volunteers to lead or assist with educational workshops on topics like technology, insurance navigation, or adaptive exercise. Our Outreach Support team needs assistance with event planning, fundraising coordination, and community awareness campaigns, helping us secure the necessary resources for our mission. Alternatively, administrative support roles in our office, such as data entry, mailings, and general organization, are critical for maintaining our operational efficiency, ensuring that all efforts contribute directly to the ongoing success and vital work of the organization.

investment in the sustained hope and dignity

The impact of your volunteering hours extends far beyond the time you dedicate; it is an essential investment in the sustained hope and dignity of the MS community. By providing respite care, you are actively preventing caregiver burnout and preserving the health and emotional stability of entire family units. By assisting with educational outreach, you are empowering individuals with the critical knowledge needed to manage a complex chronic illness and advocate effectively for their own care. Your presence combats the profound sense of isolation that often accompanies MS, fostering a welcoming, connected community that reminds individuals they are seen, valued, and not alone in their struggle. Every phone call you make, every event you staff, and every hour of support you provide contributes directly to the comprehensive and compassionate network that is the hallmark of Helping Hearts 4 MS, making you an indispensable partner in our commitment to empowering lives and transforming the narrative of living with Multiple Sclerosis.

Lend a Hand, Touch a Heart, Transform a Life

Q: How do individuals enroll in programs and what are the eligibility requirements?

A: Enrollment in the programs at Helping Hearts 4 MS begins with a simple application process that can be completed online or over the phone, though the primary focus of our most dedicated financial resources is aimed at benefiting Linda Bartok. Eligibility for broader services is centered on a verified diagnosis of Multiple Sclerosis by a licensed neurologist, and residency within our defined geographical service area, currently focused on the Naples, Florida region. Upon application, a Program Strategist conducts an initial needs assessment interview with the individual and their family to collaboratively determine which educational workshops, support groups, and resources are most relevant and impactful for their unique situation, ensuring a tailored approach from the very beginning.

Q: What safety protocols are in place for the protection of individuals with MS during activities and volunteer interactions?

A: The safety and well-being of our beneficiaries are the highest priority in all our programs and interactions, necessitating rigorous protocols for all activities and volunteer engagements. All volunteers undergo a comprehensive background check and are provided with mandatory training that covers confidentiality, safe transfer techniques, basic emergency response, and detailed awareness of MS-related symptoms like fatigue and heat sensitivity. All group activities and events are held in fully accessible venues, and we maintain an appropriate staff-to-participant ratio, often including a trained medical professional or a volunteer certified in first aid, to ensure immediate and knowledgeable support is always available in case of an unforeseen health event or mobility issue.

Q: Can you describe the educational curriculum for family members and caregivers?

A: The specialized educational curriculum for family members and caregivers is structured to address the specific challenges of supporting an individual with a variable chronic illness like Multiple Sclerosis, moving beyond general caregiving tips. Topics covered include advanced techniques for energy conservation, non-verbal communication and recognition of subtle cognitive changes related to MS, and strategies for navigating complex legal and financial planning related to long-term care and disability benefits. A significant component of the curriculum focuses on caregiver self-care and stress management, providing tools to prevent burnout and ensure the caregiver remains healthy and emotionally stable, recognizing their essential role as the backbone of the entire support system.

Q: Does the organization provide direct financial aid for medical expenses or adaptive equipment?

A: Yes, a core component of our mission is the provision of direct financial assistance, though this is primarily concentrated on supporting the needs of our designated beneficiary, Linda Bartok, while also allocating a portion of general funds to the wider MS community when possible. This assistance helps cover out-of-pocket costs for essential items not fully covered by insurance, which can include co-pays for disease-modifying therapies, specialized adaptive equipment like stair lifts or modified vehicle controls, and funding for necessary home accessibility modifications. Requests for financial aid are reviewed by the Program Strategy team against predetermined need-based criteria, prioritizing items that directly impact independence and quality of life.

Q: What is the typical scheduling commitment for group support sessions and educational workshops?

A: Our scheduling is designed to be as flexible and accessible as possible, recognizing the unpredictable nature of MS-related fatigue and symptoms, offering a variety of formats to accommodate different needs. Group support sessions are typically held once a week in the evenings or on weekends to accommodate working family members and caregivers, with some available virtually via secure teleconferencing platforms. Educational workshops are scheduled monthly, often broken down into shorter segments to prevent fatigue and allow for better retention of complex information, and are consistently varied between daytime and evening hours, ensuring maximum participation regardless of an individual’s daily energy levels or mobility constraints.

Q: What are the expectations for parent or family involvement in the organization’s events?

A: We highly encourage, but do not mandate, the active involvement of family and loved ones in our community and educational events, as their participation is a tremendous source of encouragement for the individual with MS and reinforces the sense of a supportive network. Family members are strongly encouraged to attend educational workshops to gain a deeper understanding of the disease, and their attendance at social and fundraising events is vital to the success of our mission and the sense of shared community. The expectation is simple: to participate as an active, positive member of the Helping Hearts community, supporting the individual with MS while also utilizing the resources we offer for their own well-being and growth.

We’re Here to Connect, Support, and Serve

We are committed to being accessible to our community, whether you are seeking support, looking to volunteer, or inquiring about our mission. You can reach our dedicated staff directly by telephone during standard business hours, Monday through Friday, from 9:00 AM to 5:00 PM Eastern Time. For general inquiries, or to submit a request for information or assistance, our primary email address is monitored continuously throughout the day, ensuring a prompt and thoughtful response to all correspondence received. We encourage you to reach out via whichever method is most convenient for your specific needs, knowing that a compassionate member of our team is ready to assist you with personalized guidance and information.

Full Contact Details: Organization Name: HELPING HEARTS 4 MS BENEFITTING LINDA BARTOK Address: 998 JARDIN DRIVE, NAPLES, FL 34104-6660 Email: info@hhmsnl.site

Invest Your Talent in a Mission of Meaning

Working at Helping Hearts 4 MS means joining a small, highly dedicated team of professionals who are deeply committed to making a tangible difference in the lives of those affected by Multiple Sclerosis. Our career opportunities span various fields, including program management, clinical advisory roles, development and fundraising, and community outreach coordination. We seek driven, compassionate individuals with verifiable experience in the non-profit or healthcare sector who are looking for more than just a job; they are looking for a calling where their daily efforts directly contribute to human empowerment and dignity. We offer competitive salaries, comprehensive benefits, and a supportive, collaborative environment where professional growth and personal well-being are prioritized, ensuring our team is equipped to deliver the highest quality of support to our community.If you are inspired by our mission and possess the skills and dedication to contribute meaningfully to our team, we encourage you to initiate the application process by submitting a formal cover letter and your professional resume to the Human Resources department via the email address listed on our contact page.