Our Services
Our nonprofit was born out of personal experience and a profound understanding of the challenges faced by individuals with chronic, often invisible illnesses such as Ehlers-Danlos Syndrome (EDS), Postural Orthostatic Tachycardia Syndrome (POTS),and Mast Cell Activation Syndrome (MCAS). These conditions can be debilitating,isolating, and misunderstood. Recognizing the gaps in resources, financial support,and comprehensive care available to people affected by these illnesses, we saw a need for an organization that could bridge these divides and provide the support that is often missing.The idea began with a few simple but powerful goals: to build a community,provide reliable resources,and educate both patients and healthcare providers. As we shared our vision with others, it quickly became evident that there was a strong demand for a supportive network specifically tailored to these conditions. With the dedication of our founders and the backing of early supporters, we began the groundwork for establishing an official nonprofit structure to bring these goals to life. While we are in the early stages of our journey, we are focused on building a foundation that will allow us to serve our community effectively for years to come.Our journey is just beginning but our commitment is unwavering. We look forward to growing alongside our community, increasing our reach, and making a meaningful impact in the lives of those who need it most.
Financial Assistance
Many people living with Ehlers Danlos (EDS) face financial hardship due to the high costs associated with medications, specialized medical treatments, and daily necessities. By providing financial assistance, we aim to alleviate some of these burdens, ensuring that these individuals receive the treatment and support they need without financial distress.No one should have to decide between paying bills or buying medication.
Education and Training
We recognize the importance of improving healthcare providers' understanding of complex chronic illnesses. By offering specialized training, we will help providers offer more empathetic and effective care, thereby enhancing patient outcomes and fostering a greater understanding of these often-misunderstood conditions.
Community Support
Ehlers Danlos can be isolating. Through support groups, online communities, and events,we aim to create a safe space for individuals to connect, share experiences, and build emotional resilience. This network will be a source of strength and understanding, promoting mental and emotional well-being.
Contact us today—we’re in this together! ✨
Need Resources or Support? We’ve Got You! 💜🦓
Whether you’re looking for guidance, support groups, or educational resources for EDS, POTS, or MCAS, Mountain Trifecta Alliance is here to help. Reach out to us, and let’s find the right support for you!