The Sumaira Foundation

Journée patients – Maladies neuroinflammatoires rares et apparentées
2026-06-13 11:00 - 18:00 (America/New_York) | Plaza Centre-Ville, 777 Blvd Robert Bourassa, Montreal, Quebec, H3C3Z7, Canada
À tous les patients et aidants touchés par des maladies neuro-inflammatoires rares à Montréal et dans la province de Québec!
Montréal nous voilà !
Vous ou l’un de vos proches est touché par : la CIDP*, l’IgG4-RD*, la MG*, la MOGAD* ou la NMOSD* ? Vous êtes les bienvenus à notre événement le samedi 13 juin.
Rejoignez-nous pour une journée d’information, de partage et de divertissement pour :

Rencontrer des patients, des aidants et des cliniciens de la région ainsi que nos partenaires
Poser toutes vos questions en direct à des experts sur la gestion des symptômes, les traitements et thérapies, les comorbidités et bien plus encore
Découvrir les dernières avancées en matière de recherche par les spécialistes locaux

Cet événement sera bilingue. La journée se tiendra en anglais avec une traduction simultanée pour les personnes parlant français. L’après-midi, des ateliers et des discussions en français ont été spécifiquement prévus avec des professionnels de santé et des intervenants parlant français. Tous les participants, qu’ils soient anglophones ou francophones, pourront ainsi participer pleinement à la journée.
Cet événement est organisé en collaboration avec le docteur Adil Harroud (Centre universitaire de santé McGill) et en partenariat avec les associations Muscular Dystrophy Canada et IgG4ward.
L’inscription est gratuite et un repas sera servi. Nous avons hâte de vous voir à Montréal !
https://www.eventbrite.com/e/1986690811698?aff=oddtdtcreator
L’équipe de The Sumaira Foundation
—
CIDP : polyneuropathie inflammatoire démyélinisante chronique
IgG4-RD : maladie associée aux IgG4
MG : myasthénie auto-immune
MOGAD : Maladie du spectre des anticorps anti-MOG
NMOSD : neuromyélite optique

TSF HCP Caregivers - Diffusing Family Conflict
2026-06-14 18:00 - 19:00 (Africa/Johannesburg) | Virtual: Global
The Caregivers Human Collective Project (HCP) is a groundbreaking support group hosted by The Sumaira Foundation, created specifically for caregivers of individuals living with rare neuroimmune diseases like NMOSD and MOGAD. This first-of-its-kind session offers a safe, inclusive space for family members, partners, siblings, children, and loved ones to connect, share, and be heard. Led by our dedicated Caregiver Ambassadors, who bring their own lived experience and empathy to the conversation, participants can expect heartfelt conversations, mutual support, and practical insights into the caregiving journey. Whether you’re navigating the emotional, physical, or logistical challenges of caregiving, this group is designed to uplift and empower you through community, compassion, and connection.

CAR-T: What Does This Mean for Rare Neuroimmune Disorders?
2026-06-17 17:00 - 18:00 (America/New_York) | Virtual: Global
You’ve likely heard about CAR-T but do you know what it is and what it means for those living with rare neuroimmune disorders?
Join us on June 17th at 5:00 PM EST for an informative and patient-friendly webinar featuring Dr. Michael Levy and Dr. Marcela Maus, experts from Massachusetts General Hospital/Harvard Medical School, who will break down this complex treatment approach in a way that’s easy to understand. During this time, our expert speakers will educate our live audience about what CAR-T is, how it works and why researchers are hopeful about its potential in conditions like NMOSD, MOGAD, and beyond.
Whether you’re newly diagnosed, living with a condition, or supporting a loved one, this session is designed to empower you with knowledge, clarity and hope for the future of this breakthrough treatment.

Attendees who join live will also have the opportunity to ask questions directly to the experts during the Q&A portion. This webinar will be recorded and made available for replay on TSF’s YouTube channel.
This program was made possible with support from Amgen.

Rochester Patient Day for Rare Neuroinflammatory & Related Disorders
2026-06-20 11:00 - 17:00 (America/Chicago) | Mayo Civic Center, 30 Civic Center Drive Southeast, Rochester, MN, 55904, United States
TSF is inviting patients and caregivers impacted by rare neuroinflammatory & related disorders from Minnesota and the upper Midwest region!

We’re coming to Rochester!
Are you or your loved one impacted by: AE*, CIDP*, MG*, MOGAD*, NMOSD*, or SPS*? You’re invited to our event on Saturday, June 20th.
Join us for a day of education, community and fun to:

Meet local patients, partners, care-partners and clinicians
Ask experts questions in real time about symptom management, treatments and therapies, comorbidities and more
Learn about updates on the latest research and findings from local key opinion leaders

This event is being organized in collaboration with Dr. Eoin Flanigan (Mayo Clinic Rochester) and Dr. John Chen (Mayo Clinic Rochester) and in partnership with Autoimmune Encephalitis Alliance, MG Holistic Society and The Stiff Person Syndrome Research Foundation.
Registration is free and lunch will be served.
Childcare services will be available throughout the duration of the day.
We can’t wait to see you in Rochester!
https://www.eventbrite.com/e/rochester-patient-day-for-rare-neuroinflammatory-related-disorders-tickets-1986578610100
The Sumaira Foundation team
—
AE stands for autoimmune encephalitis
CIDP stands for chronic inflammatory demyelinating polyneuropathy
MG stands for myasthenia gravis
MOGAD stands for myelin oligodendrocyte glycoprotein antibody-associated disorder
NMOSD stands for neuromyelitis optica spectrum disorder
SPS stands for stiff person syndrome

HCP presents Mental Health Mondays
2026-06-22 20:00 - 21:00 (America/New_York) | Virtual: United States, United States
The Mental Health Monday meetings began as a way to address the various mental and emotional concerns that individuals experience when dealing with rare neuroimmune diseases. Patients, caregivers, and loved ones ride the rollercoaster of feelings throughout their daily lives, from the moment of symptom onset. Often, getting the proper diagnosis is a journey of its own, and dealing with life’s difficulties after that can include stressors that only others in your situation may understand. These meetings will offer a safe space for people to come together, share their stories, and highlight how they are coping with everyday challenges. We will discuss a range of mental health topics and have occasional special guest speakers join our meetings. So, whether you are newly diagnosed or a seasoned zebra, we hope to provide a space to help guide personal growth.

Vivir bien con NMOSD: Cómo manejar los desafíos físicos, mentales y sociales
2026-06-24 20:00 - 21:00 (America/New_York) | Virtual: Colombia, Colombia
Vivir con NMOSD puede afectar muchos aspectos de la vida diaria: física, emocional y socialmente.
Únase a TSF LatAm para un importante seminario web, “Vivir bien con NMOSD: Cómo manejar los desafíos físicos, mentales y sociales”, enfocado en ayudar a pacientes y familias a comprender y afrontar mejor estos desafíos.
Este programa contará con la participación de la Dra. Adriana Casallas Vanegas (Colombia) y la Dra. Felisa Leguizamón (Argentina), y será moderado por Lizzy, paciente con NMOSD y Embajadora de TSF en México. Juntas, conversarán sobre estrategias para manejar los síntomas, cuidar el bienestar mental, mejorar la calidad de vida y fortalecer las redes de apoyo mientras se vive con NMOSD.
– 24 de junio de 2026
– 7PM COT / 9PM ART
https://us02web.zoom.us/webinar/register/WN_nsxeD-TRRxaMS_YqbHPIRw
Quienes asistan en vivo tendrán la oportunidad de hacer preguntas directamente a las expertas durante la sesión.

Understanding Step Therapy: How Insurance Decisions Shape Neuroimmune Treatment
2026-06-25 20:00 - 21:00 (America/New_York) | Virtual: Global
Understanding insurance coverage can be overwhelming, especially when treatment decisions are impacted by policies like step therapy. Join us Thursday, June 25 at 5:00 PM PT / 8:00 PM ET for an important conversation with Dr. Rosemarie Walch about how insurance requirements can influence access to care for people living with rare neuroimmune disorders.
In this webinar, Understanding Step Therapy: How Insurance Decisions Shape Neuroimmune Treatment, Dr. Walch will explain what step therapy is, why it exists, and how it can affect treatment timelines, medication access, and patient outcomes. Attendees will also learn practical strategies for navigating insurance barriers, advocating for appropriate care, and working with their healthcare teams throughout the process.
Those who attend live will have the opportunity to ask questions during the session.
Made possible with support from Amgen.

TSF's Human Collective Project Meetings
2026-07-09 20:00 - 21:00, 2026-08-13 20:00 - 21:00, 2026-09-10 20:00 - 21:00, 2026-10-08 20:00 - 21:00 (America/New_York) | Virtual: United States, United States
The Human Collective Project (HCP) is TSF’s support group meeting offered to anyone who has been affected/impacted by NMOSD/MOGAD. The program came into existence during the height of the COVID-19 pandemic in 2020, when most NMOSD/MOGAD felt particularly isolated and vulnerable to the coronavirus as immunosuppressed/immunocompromised members of society. The isolation many of us experienced unveiled a great need and opportunity for us to connect in a meaningful way to offer our support to one another. Since 2020, we have expanded the program to offer more sessions in multiple geographies to ensure that everyone in the NMOSD/MOGAD communities feels welcomed and included. As we always say, HCP is a great way to meet others in similar circumstances in this rare community; it is a safe space to laugh, cry, vent, share wins, etc. This program is driven and led by TSF Patient and Caregiver Ambassadors worldwide.

TSF HCP Caregivers - Fitting in Fitness
2026-07-12 12:00 - 13:00 (America/New_York) | Virtual: Global

Nutrición en Enfermedades Desmielinizantes
2026-07-14 19:00 - 20:00 (America/Bogota) | Virtual: Colombia, Colombia
Nutrir el cuerpo es fundamental cuando se vive con una enfermedad desmielinizante.
Acompáñenos con el Dr. Carlos Navas de Colombia, quien lidera la iniciativa de Inmunonutrición LATAM de LACTRIMS, para conocer las recomendaciones actuales y consejos prácticos sobre nutrición para las personas que viven con enfermedades desmielinizantes.
– 14 de julio de 2026
– 7:00 p. m. (hora de Bogotá, Colombia)
https://us02web.zoom.us/webinar/register/WN_FIj640dVRgmhahBQlgNSNw
Los participantes que se conecten en vivo tendrán la oportunidad de hacer preguntas al Dr. Navas en tiempo real durante una sesión interactiva de preguntas y respuestas. No se pierda esta oportunidad de aprender cómo la nutrición puede apoyar la salud y el bienestar general en el contexto de las enfermedades neuroinmunológicas.

Human Collective Project - United Kingdom
2026-07-20 19:00 - 20:00 (Europe/London) | Virtual: United Kingdom, United Kingdom
The Human Collective Project (HCP) is TSF’s support group meeting offered to anyone who has been affected/impacted by Rare Neuroimmune Diseases. The program came into existence during the height of the COVID-19 pandemic in 2020, when most patients felt particularly isolated and vulnerable to the coronavirus as immunosuppressed/immunocompromised members of society. The isolation many of us experienced unveiled a great need and opportunity for us to connect in a meaningful way to offer our support to one another. Since 2020, we have expanded the program to offer more sessions in multiple geographies to ensure that everyone in the Rare Neuroimmune community feels welcomed and included. As we always say, HCP is a great way to meet others in similar circumstances in this rare community; it is a safe space to laugh, cry, vent, share wins, etc. This program is driven and led by TSF Patient and Caregiver Ambassadors worldwide.

HCP presents Mental Health Mondays
2026-07-27 20:00 - 21:00 (America/New_York) | Virtual: United States, United States
Due to technical difficulties, this event has been cancelled. Please see the TSF Event Calendar for future HCP Mental Health Monday meetings.

Human Collective Project - Africa
2026-07-29 12:00 - 13:00 (Africa/Johannesburg) | Virtual: Global
The Human Collective Project (HCP) is TSF’s support group meeting offered to anyone who has been affected/impacted by rare neuroimmune diseases. The program came into existence during the height of the COVID-19 pandemic in 2020, when most NMOSD/MOGAD patients felt particularly isolated and vulnerable to the coronavirus as immunosuppressed/immunocompromised members of society. The isolation many of us experienced unveiled a great need and opportunity for us to connect in a meaningful way to offer our support to one another. Since 2020, we have expanded the program to offer more sessions in multiple geographies to ensure that everyone in the Rare Neuroimmune community feels welcomed and included. As we always say, HCP is a great way to meet others in similar circumstances in this rare community; it is a safe space to laugh, cry, vent, share wins, etc. This program is driven and led by TSF Patient and Caregiver Ambassadors worldwide.

MOGAD in LatAm
2026-08-05 17:30 - 18:30 (America/New_York) | Virtual: Global
¿Usted o un ser querido vive con MOGAD?
Lo invitamos a acompañarnos el 5 de agosto en un webinar especial con el Dr. Edgar Carnero Contentti, del Hospital Alemán de Argentina, quien compartirá las últimas novedades sobre el tratamiento del MOGAD.
El Dr. Contentti explicará cómo los resultados de un nuevo ensayo clínico podrían ayudar a los pacientes y sus familias a comprender mejor las futuras opciones terapéuticas para el MOGAD en América Latina.
Además, quienes se conecten en vivo tendrán la oportunidad de hacer sus preguntas al Dr. Contentti en tiempo real.
El webinar será moderado por Ernesto, paciente con MOGAD y Embajador de TSF en México.
¡Esperamos contar con su participación en esta conversación informativa e interactiva!

TSF HCP Caregivers - Music Can Improve Quality of Life
2026-08-16 12:00 - 13:00 (America/New_York) | Virtual: Global

When Autoimmune Diseases Overlap: Understanding Multiple Diagnoses
2026-09-01 20:00 - 21:00 (America/New_York)
What happens when one autoimmune or neuroimmune condition isn’t the whole story? For some patients, receiving multiple diagnoses can bring even more questions and uncertainty.
Join Dr. Lilyana Amezcua from USC for an accessible conversation about overlapping autoimmune diseases, why multiple diagnoses can occur, and how clinicians approach symptoms that may not fit neatly into a single diagnosis.
We’ll explore what it means to live with more than one condition, how diagnoses are evaluated, and what patients and caregivers can do to feel more informed and empowered in their care.
Join us live on Tuesday, September 1 at 5 PM PT / 8 PM ET.
https://us02web.zoom.us/webinar/register/WN_-yVXB-6QTsqIMV_NtnpOsg
Those who attend live will have the opportunity to ask Dr. Amezcua their questions during a live Q&A.
Made possible by support from Amgen.

TSF's Human Collective Project - Africa
2026-09-09 12:00 - 13:00 (Africa/Johannesburg) | Virtual: Global

TSF 5K For Rare Neuroimmune Disorders
2026-09-13 09:00 - 12:00 (America/New_York) | Weston Town Hall, 11 Town House Rd, Weston, 02493, United States
Turning Miles into Medical Progress – Join us on September 13th for TSF’s 2nd 5K to raise money for research!
Last year’s inaugural 5K helped fund a groundbreaking AI-powered diagnostic initiative with the potential to transform how rare neuroimmune diseases are identified around the world.
Using only a smartphone image, this technology is being developed to rapidly and accurately analyze diagnostic testing, helping clinicians detect rare neuroimmune conditions earlier – especially in underserved regions where access to specialized care and testing is limited. Earlier diagnosis can lead to faster treatment, better outcomes and a greater chance of preventing permanent disability, vision loss and disease progression.
What started as a community race is now helping drive a global solution that could expand access to life-changing care for patients everywhere. By participating in this year’s 5K, you are not just supporting awareness; you are directly fueling innovation, earlier diagnosis and hope for the rare disease community worldwide.
This is a family-friendly event – all are welcome (including doggos!) https://runsignup.com/Race/MA/Weston/TSF5KForRareNeuroimmuneDisorders

This event is being organized by Terry Clark, NMOSD patient and TSF Ambassador of MA: “As many of you may know, four years ago, May 2022, I was diagnosed with a rare autoimmune disease called NMO. This 5k has been something I’ve wanted to do for awhile so I’m excited to continue organizing this annual race.”

TSF HCP Caregivers - Rewards of Caregiving
2026-09-13 12:00 - 13:00 (America/New_York) | Virtual: Global

Michigan Patient Day for Rare Neuroinflammatory & Related Disorders
2026-09-19 10:00 - 17:00 (America/New_York) | University of Michigan-Dearborn, 4901 Evergreen Rd, Dearborn, MI, 48128, United States
We’re coming to Michigan!
Are you or your loved one impacted by: CIDP*, MG*, MOGAD*, or NMOSD*? You’re invited to our event on Saturday, September 19th.
Join us for a day of education, community and fun to:
+ Meet local patients, partners, care-partners and clinicians+ Ask experts questions in real time about symptom management, treatments and therapies, comorbidities and more+ Learn about updates on the latest research and findings from local key opinion leaders
This event is being organized in collaboration with Dr. Rosemarie Walch (Memorial Healthcare) and Dr. Lisa Stropp (University of Michigan) and in partnership with MG Holistic Society and Myasthenia Gravis Foundation of Michigan (MGMI).
Registration is free and lunch will be served.
We can’t wait to see you in Michigan!
https://www.eventbrite.com/e/michigan-patient-day-for-rare-neuroinflammatory-related-disorders-tickets-1993976685944?aff=oddtdtcreator
The Sumaira Foundation team
—
CIDP stands for chronic inflammatory demyelinating polyneuropathy
MG stands for myasthenia gravis
MOGAD stands for myelin oligodendrocyte glycoprotein antibody-associated disorder
NMOSD stands for neuromyelitis optica spectrum disorder

Little Patients, Big Questions: Understanding Pediatric Neuroimmune Diseases
2026-09-21 20:00 - 21:00 (America/New_York)
When your child is living with a neuroimmune disease, the questions can feel endless. What is happening in their body? What does a diagnosis mean for their future? And how can parents and caregivers feel more confident navigating care?
Join Dr. Kristen Fisher of Texas Children’s for an approachable conversation about pediatric neuroimmune diseases. Together, we’ll explore what makes these conditions unique in children, what families should know about diagnosis and treatment, and how parents and caregivers can become informed and empowered partners in their child’s care.
Whether your child is newly diagnosed, navigating ongoing symptoms, or you’re simply looking for a better understanding of pediatric neuroimmune diseases, this webinar is designed with families in mind.
Monday, September 21 | 5:00 PM PT / 8:00 PM ET
https://us02web.zoom.us/webinar/register/WN_ICZaFGZ2TB2koEcKAkfaww
Live Q&A: Those who attend live will have the opportunity to ask Dr. Fisher their questions directly.
Made possible with support from Amgen.

Miami Patient Day for Rare Neuroimmune & Related Disorders
2026-09-26 10:00 - 17:00 (America/New_York) | 16701 Collins Avenue, Sunny Isles Beach, Florida 33160, 16701 Collins Avenue, Sunny Isles Beach, FL, 33160, United States
We’re coming to Miami!
Are you or your loved one impacted by: CIDP*, MG*, MOGAD*, or NMOSD*? You’re invited to our event on Saturday, September 26th.
Join us for a day of education, community and fun to:

Meet local patients, partners, care-partners and clinicians
Ask experts questions in real time about symptom management, treatments and therapies, comorbidities and more
Learn about updates on the latest research and findings from local key opinion leaders

This event is being organized in collaboration with The University of Miami and in partnership with MG Holistic Society.
Registration is free and lunch will be served.
https://www.eventbrite.com/e/miami-patient-day-for-rare-neuroinflammatory-related-disorders-tickets-1994071513576?aff=oddtdtcreator
We can’t wait to see you in Miami!
The Sumaira Foundation team
—
CIDP stands for chronic inflammatory demyelinating polyneuropathy
MG stands for myasthenia gravis
MOGAD stands for myelin oligodendrocyte glycoprotein antibody-associated disorder
NMOSD stands for neuromyelitis optica spectrum disorder

Día del Paciente sobre Trastornos Neuroinmunes y Relacionados Raros
2026-09-26 10:00 - 17:00 (America/New_York) | 16701 Collins Avenue, Sunny Isles Beach, Florida 33160, 16701 Collins Avenue, Sunny Isles Beach, FL, 33160, United States
¡Nos vemos en Miami!
¿Usted o un ser querido vive con CIDP*, MG*, MOGAD* o NMOSD*? Lo invitamos a acompañarnos en nuestro evento el sábado 26 de septiembre.
Acompáñenos a disfrutar de un día de educación, comunidad y convivencia para:
• Conocer a pacientes, aliados, cuidadores y profesionales de la salud de su comunidad.
• Hacer preguntas en tiempo real a expertos sobre el manejo de los síntomas, tratamientos, terapias, comorbilidades y mucho más.
• Conocer las últimas investigaciones y los hallazgos más recientes presentados por líderes de opinión de la región.
Este evento se organiza en colaboración con el University of Miami y en alianza con MG Holistic Society.
La inscripción es gratuita y se ofrecerá almuerzo.
https://www.eventbrite.com/e/dia-del-paciente-de-miami-sobre-trastornos-neuroinflamatorios-raros-tickets-1994072435333?aff=oddtdtcreator&keep_tld=true
¡Estamos deseando verlo en Miami!
El equipo de The Sumaira Foundation
—
CIDP significa polineuropatía desmielinizante inflamatoria crónica
MG significa miastenia gravis
MOGAD significa enfermedad asociada a anticuerpos contra la glicoproteína de oligodendrocitos de la mielina
NMOSD significa trastorno del espectro de la neuromielitis óptica

Financial Health Workshop Series - How to Set Goals, Build a Budget & Save
2026-09-28 18:00 - 19:00 (America/New_York)
Managing your finances can feel overwhelming, especially when living with the added costs and uncertainty that can come with a rare disease. In this first session of our three-part Financial Health series, Angelica Civilus, Vice President, Community Manager with Chase Bank, will share practical money skills to help you feel more confident about your financial goals.
Together, we’ll explore how to set realistic financial goals, create a budget that works for your life, and find ways to build savings—even when your resources may feel limited. Whether you’re just getting started or looking for ways to strengthen your current financial plan, this session will offer approachable tools you can put into practice right away.
Join us Monday, September 28th at 3pm PT / 6pm ET and take the first step toward feeling more confident about your financial future.
Register HERE.

Juniors in Neuroimmunology: Meet the Expert – II Edition
2026-10-01 - 2026-10-03 | Complesso di Sant’Andrea delle Dame – Aula Affreschi, Italy
Juniors in Neuroimmunology: Meet the Expert – 2nd Edition
Il corso, dedicato a giovani neurologi e assistenti in formazione, si propone di fornire una formazione aggiornata sulla diagnosi e sul trattamento delle principali patologie autoimmuni a carico del Sistema Nervoso Centrale e Periferico (incluse NMOSD/MOGAD, encefaliti autoimmuni, miastenia gravis, neuropatie autoimmuni, miositi, sindromi paraneoplastiche e neurotossicità associate agli inibitori dei checkpoint immunitari).
Il programma prevede lezioni tenute da esperti nazionali e internazionali ed una seconda parte, invece, caratterizzata da sessioni pratiche altamente interattive focalizzate su neuroimaging, diagnostica di laboratorio, neurofisiologia e discussione di casi clinici.
La partecipazione è riservata a medici italiani under 40, specialisti o assistenti in formazione in Neurologia o Immunologia Clinica.
Iscrizione e opportunità di supporto
La quota di iscrizione ordinaria è fissata in € 300,00 + IVA. È prevista la possibilità di richiedere l’iscrizione a titolo gratuito, subordinata alla valutazione del curriculum vitae da parte della segreteria scientifica. Il numero massimo di partecipanti ammessi è pari a 30.
Inoltre, per i partecipanti provenienti da regioni italiane diverse dalla Campania, sarà disponibile un rimborso per viaggio e alloggio fino a €300. Il supporto economico è limitato e sarà concesso ai partecipanti selezionati in base al Curriculum Vitae ad i 15 richiedenti con migliore/più attinente CV.
Il numero massimo di partecipanti ammessi è pari a 30.
Come candidarsi
Le candidature dovranno essere inviate entro il 10 giugno 2026 tramite il modulo di registrazione disponibile sul sito dell’organizzatore:
eventi8adv.it – Juniors in Neuroimmunology Meet the Expert II Edizione
I candidati selezionati saranno informati indicativamente a partire da circa 10 giorni dopo la scadenza delle candidature.

Financial Health Workshop Series - Improving Credit and Managing Debt
2026-10-05 18:00 - 19:00 (America/New_York)
Credit and debt can sometimes feel complicated, confusing, or even stressful—but understanding your options can be an important step toward greater financial confidence.
In the second session of our three-part Financial Health series, Angelica Civilus, Vice President, Community Manager with Chase Bank, will break down the basics of credit and share practical strategies for managing debt. We’ll talk about what can impact your credit, ways to work toward improving it, and helpful approaches to managing debt without feeling overwhelmed.
Whether you’re building credit for the first time, working to improve your credit, or simply want to better understand your financial options, this session is designed to meet you where you are.
Join us Monday, October 5th at 3pm PT / 6pm ET for an approachable conversation about building stronger financial habits and taking steps toward your goals.
Register HERE.

TSF HCP Caregivers - Family Caregivers
2026-10-11 12:00 - 13:00 (America/New_York) | Virtual: Global
