Welcome to Mountain Trifecta Alliance
Where Zebras Thrive! 🦓
Living with EDS, POTS, and MCAS can feel tough, but you’re not alone. We’re building a vibrant community for patients, caregivers, and providers to spark real change. Chronic illness isn’t just about doctor visits; it’s about finding support and understanding. Our mission? To lighten the load, break barriers, and empower every zebra to live fully.
What We Do:
🦓 Financial Assistance – Easing the costs of living with EDS.
🦓 Provider Support & Education – Helping providers better assist patients.
🦓 Community & Advocacy – Uplifting through support groups, campaigns, and resources.
Joining us means being part of a dazzle of zebras working to revolutionize Trifecta care. Whether seeking guidance or a fierce community, you're in the right spot. Together, we don’t just survive—we thrive. 🦓
Join the movement. Embrace the dazzle. Let’s reshape Trifecta care!
#MountainTrifectaAlliance #ZebraStrong #EDS #POTS #MCAS
Support services
Support Group
At Mountain Trifecta Alliance, we understand the unique challenges that come with living with chronic conditions like Ehlers-Danlos Syndrome(EDS), Postural Orthostatic Tachycardia Syndrome(POTS),and Mast Cell Activation Syndrome(MCAS). Our support group meets on the second Monday of every month,providing a safe and compassionate space for individuals to connect with others who truly understand their experiences. Whether you're seeking emotional support,practical advice, or simply a sense of community,we welcome you to join us. Together, we share stories, offer encouragement, and empower each other to navigate the complexities of these conditions. If you're looking for a place to belong and feel supported, we invite you to be apart of our group.Reach out today to learn more and take the first step toward joining our community of care.
Outings and Get Togethers
We believe that building a strong community goes beyond virtual connections—it’s about coming together in person to create lasting friendships and support. That’s why we organize group outings and get-togethers where individuals living with the trifecta can share experiences, laughter, and meaningful moments. Whether it’s a casual meet-up or a fun outing,these events are designed to help us bond, form deeper connections, and create a tight-knit community of people who truly understand one another. In this space, you’ll find not only new friends but also a sense of camaraderie, as we navigate life with the trifecta together, with compassion,mutual support, and shared strength.
Connection to Resources
We know that access to the right resources can change lives. That’s why we work tirelessly to connect our group members with the tools, support, and guidance they need to navigate life with Ehlers-Danlos Syndrome (EDS), POTS, and MCAS. Whether it’s finding knowledgeable healthcare providers, accessing financial assistance programs, securing mobility aids, or understanding insurance options, we’re here to help every step of the way. Our team curates educational materials, expert referrals, and personalized support plans to ensure that no one is left struggling to find answers. Through our monthly support groups, advocacy efforts, and direct patient assistance, we empower zebras to take control of their health and well-being—because no one should have to fight this battle alone.
Coming Soon
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Merchandise- COMING SOON
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Outings, hikes, bowling, yoga, mind body medicine, podcasts, newsletter, gym time, swimming, weekend retreat, auction, different fundraisers that aren’t overdone in our area, and so many more fun things coming to you.
Provider Program- coming soon
The **Pay-As-You-Go Provider Program** allows healthcare providers to access **Mountain Trifecta Alliance’s** services on a flexible, per-need basis. Instead of committing to a monthly subscription, providers can opt for **one-time, in-office support sessions** for **newly diagnosed patients** (up to 2 per week). Each session costs **$200**, giving providers the option to connect their patients with **resources, care, and support groups** without the ongoing commitment of a subscription. This
The monthly fee for the Provider Program is $1,500. This subscription provides healthcare providers with comprehensive support for their patients, including ongoing access to resources, care coordination, and support groups for individuals with EDS, POTS, and MCAS. The program is designed to help alleviate the workload of providers’ offices by connecting patients with essential services that improve care and outcomes.
The yearly membership for the Provider Program is $18,000, offering the same comprehensive support as the monthly plan, but with the added benefit of annual savings. The $18,000 yearly membership offers a cost-effective option for providers who want consistent, long-term support and resources for their patients with chronic illnesses, while also benefiting from annual savings.
Events Coming Soon!!!!!!
Join the Herd: Events with MTA!
At Mountain Trifecta Alliance, we believe in the power of community, education, and a little bit of fun! 🎉 Whether it's a support group meeting, an educational webinar, a fundraising event, or an awareness campaign, our events are designed to connect, empower, and support those affected by EDS, POTS, and MCAS. From expert-led discussions to local gatherings, we create spaces where patients, caregivers, and medical professionals can learn, share, and grow together. Keep an eye on our calendar—because at MTA, there’s always something exciting happening! 🦓💜✨
Newsletter and Pod Cast Coming Soon
Mountain Trifecta Alliance is excited to launch its official newsletter! This monthly update will keep our community informed about upcoming events, support group meetings, educational resources, and the latest developments in chronic illness advocacy. Subscribers will gain access to expert insights, patient stories, fundraising opportunities, and ways to get involved in our mission. Whether you're a healthcare provider, a patient, or a supporter, our newsletter will help you stay connected and engaged with the MTA community. Sign up today to stay informed and be a part of the change!
Mountain Trifecta Alliance is launching a podcast dedicated to shedding light on the realities of living with chronic illnesses like Ehlers-Danlos Syndrome, POTS, and MCAS. Through candid conversations, expert interviews, and firsthand experiences, we’ll explore the challenges, breakthroughs, and resources that shape our community. Whether you’re looking for medical insights, emotional support, or just a reminder that you’re not alone, this podcast is here to inform and uplift. Join us as we amplify voices, share knowledge, and advocate for a better future—one episode at a time!
Contact Us
Interested in working together? Fill out some info and we will be in touch shortly. We can’t wait to hear from you!