Community NGO for neurological wellness and long-term MS care support.
Connect MS Foundation
We collaborate with clinicians, volunteers, and families to improve mental health, treatment access, and community resilience for people living with MS.
Regional community outreach for early MS symptom awareness and family referral support.
Community Outreach
Our mobile programs link community workers, caregivers, and neurologists so families receive timely guidance and continuity of care.
Regional community outreach for early MS symptom awareness and family referral support.
Events and Training
From caregiver circles to youth volunteer training, Connect MS equips communities with practical skills and trusted information.
Regional community outreach for early MS symptom awareness and family referral support.
We help people take control, feel secure, and live well with MS through practical, compassionate support.
Simple guidance on symptoms, treatment choices, and day-to-day planning.
Find MS informationEveryday support for fatigue, movement, wellbeing, and family routines.
Get everyday helpJoin community events, volunteer groups, and trusted peer support circles.
Start connecting
We promote evidence-led care, practical guidance, and local adaptation of global MS learning.
From navigation calls to family support planning, we help people access the right care path.
We provide tools for symptom tracking, rehab planning, and resilience in daily life.
We advocate for timely diagnosis, specialist referral, and continuity of treatment support.
Learn how MS affects the central nervous system and why symptoms can vary so widely.
Read overviewUnderstand relapsing and progressive MS pathways, and what each may mean for care planning.
Explore MS typesReview treatment goals, monitoring plans, and supportive therapies for better quality of life.
See treatment pathwaysStart with a practical roadmap for your first 90 days after diagnosis.
Get startedLocate care teams, support services, and trusted guidance tools.
Search support optionsLearn how research participation helps improve treatments and quality of life.
Explore opportunitiesJoin community sessions, awareness drives, and learning forums.
View upcoming eventsHonor someone special with a tribute gift that supports MS care services.
Create tribute giftRecommend grants from your donor advised fund to support Connect MS programs.
DAF giving detailsMake a Donation
Your contribution powers helpline support, trusted resources, community groups, and equitable care access programs.
Focused support for women navigating maternal mental health and neurological care.
Remote access to neurologists and support workers for underserved communities.
Emergency continuity plans for medicine, mobility devices, and counseling services.
Inspired by global MS advocacy work, we support equitable pathways to diagnosis, specialist care, and consistent treatment access in lower-resource settings.
We prioritize patient-reported outcomes, practical symptom care, and data-driven programs so local care systems better reflect real community needs.
Training youth volunteers to deliver awareness and counseling referrals in local districts.
Hands-on workshops for early detection pathways and family health communication.
Field engagement connecting rural families with tele-consult and treatment planning.
Profiles will appear here as volunteers are added from the admin panel.
Practical checklists, specialists directory, and support groups.
Open resource libraryCommunication tools, care burnout prevention, and emergency planning support.
Join caregiver supportReceive program updates, new guides, and upcoming event reminders.
The team is preparing practical stories and care guides for this section.
