33 episodios

Neuromyelitis Optica Spectrum Disorder (NMOSD) and Myelin Oligodendrocyte Glycoprotein antibody disease (MOGAD) are neurological autoimmune diseases that cause blindness and paralysis. While NMOSD and MOGAD are rare diseases, autoimmune diseases are common, and so is finding scientific and medical jargon tricky to understand. In this podcast, The Sumaira Foundation works to simplify the science associated with NMOSD, MOGAD, and related neuro-immune disorders, bringing together patients and experts.

Demystifying NMO & MOG The Sumaira Foundation

    • Salud y forma física

Neuromyelitis Optica Spectrum Disorder (NMOSD) and Myelin Oligodendrocyte Glycoprotein antibody disease (MOGAD) are neurological autoimmune diseases that cause blindness and paralysis. While NMOSD and MOGAD are rare diseases, autoimmune diseases are common, and so is finding scientific and medical jargon tricky to understand. In this podcast, The Sumaira Foundation works to simplify the science associated with NMOSD, MOGAD, and related neuro-immune disorders, bringing together patients and experts.

    Episode #33 | From Patient to Practitioner w/ Roselyne

    Episode #33 | From Patient to Practitioner w/ Roselyne

    This week's episode offers a compelling narrative for both patients and clinicians as we delve into Roselyne's extraordinary journey. Diagnosed with Neuromyelitis Optica (NMO) as a young adult, she would later decide to pursue a career as a physician.
    Throughout her journey, Roselyne grappled with the psychological impact of straddling the roles of both clinician and patient, navigating feelings of guilt and obligation along the way.
    Roselyne emphasizes the importance of patient-provider communication and empathy in healthcare. She highlights the need for clinicians to convey diagnoses in a clear and compassionate manner, drawing from her own experiences of receiving life-altering news with nonchalance.
    Tune in as Roselyne shares her hard-won wisdom on navigating the complex intersection of healthcare and chronic illness.

    ABOUT US:
    The Demystifying NMO and MOG podcast is a Sumaira Foundation (TSF) project and
    was made possible with the generous support of Genentech.

    SOCIAL & WEBSITE:
    Roselyne
    Instagram - https://www.instagram.com/roselyne_trains
    Demystifying NMO podcast
    Instagram - https://www.instagram.com/demystifying_nmomog
    Twitter - https://twitter.com/DemystifyingNMO
    The Sumaira Foundation
    Website - https://www.sumairafoundation.org
    Facebook - https://www.facebook.com/TheSumairaFoundation

    TIMESTAMPS/TOPICS:
    00:01:00 Roselyne
    00:01:28 The Path to Being a Physician
    00:04:29 Educating Others
    00:06:14 Guilt and Obligation
    00:10:03 Self-care in a Demanding Profession
    00:14:48 Managing a Career with NMO
    00:17:23 Improving Clinician - Patient Relationships
    00:25:33 Learning to Accept Illness

    SUPPORT THE PODCAST
    Donate to Illuminate
    https://www.sumairafoundation.org/advocacy/donate/

    CREDITS:
    Producer & Host - Brian Dawson
    Music - Denys Kyshchuk from Pixabay

    • 29 min
    Episode #32 | Beyond Words: The Silent Support of Animal Companions

    Episode #32 | Beyond Words: The Silent Support of Animal Companions

    In this emotional episode, we delve into the profound relationship between pets and mental health.
    Starting with the TSF AMbassador for New Mexico, Marie Abrego talks about the recent loss of her dachshund Bambi while traveling to raise awareness about NMO.
    Then, we are joined by TSF Ambassador for Illinois, AnneMarie Nawrocki, a licensed social worker and TSFs ambassador for Illinois; they explore the multifaceted benefits of pet ownership for individuals with disabilities and chronic illnesses. From reducing stress and providing emotional support to promoting opportunities to enhance physical health and promoting social connection, pets play a crucial role in improving overall well-being. The discussion also touches on coping with the loss of a beloved pet, highlighting the unique grieving process and the importance of support from friends and family. Through personal anecdotes and expert insights, this episode celebrates the transformative power of the human-animal bond in navigating life's challenges.

    ABOUT US:
    The Demystifying NMO and MOG podcast is a Sumaira Foundation (TSF) project and
    was made possible with the generous support of Genentech.

    SOCIAL & WEBSITE:
    Marie Abrego
    Website - t.ly/ndARI
    Twitter - https://twitter.com/nmo_marie
    AnneMarie Nawrocki
    Website - t.ly/RN2TD
    LinkedIn - www.linkedin.com/in/annemarie-nawrocki-5426b7120/
    Demystifying NMO podcast
    Instagram - https://www.instagram.com/demystifying_nmomog
    Twitter - https://twitter.com/DemystifyingNMO
    The Sumaira Foundation
    Website - https://www.sumairafoundation.org
    Facebook - https://www.facebook.com/TheSumairaFoundation

    TIMESTAMP:
    00:01:03 Marie Abrego
    00:04:06 Marie & Bambi
    00:20:42 AnneMarie Nawrocki
    00:23:37 Pets & Wellbeing
    00:27:13 Physical benefits
    00:35:57 Loss of a Pet
    00:39:29 Coping with the Inevitable
    00:42:03 Supporting a Grieving Pet Owner

    SUPPORT THE PODCAST:
    Donate to Illuminate
    https://www.sumairafoundation.org/advocacy/donate/

    CREDITS:
    Producer & Host - Brian Dawson
    Music - Denys Kyshchuk from Pixabay

    • 47 min
    Episode #31 | EUPATI Education in Action: Leda's Path to Patient Advocacy

    Episode #31 | EUPATI Education in Action: Leda's Path to Patient Advocacy

    Episode #31 | EUPATI Education in Action: Leda's Path to Patient Advocacy
    In this episode, we delve into the world of patient advocacy with Leda Bresnov. Leda shares her transformative journey following her NMO diagnosis and the pivotal role patient advocacy and education played in reshaping her life. From her initial involvement as the Denmark Ambassador with the Sumaira Foundation to her experiences in EUPATI’s Patient Academy, Leda's dedication to raising awareness and empowering fellow patients is making a significant impact in healthcare. Join us as Leda offers her insights into the power of patient involvement in healthcare decision-making, highlighting the importance of education and advocacy in shaping the future of healthcare.

    ABOUT US:
    The Demystifying NMO and MOG podcast is a Sumaira Foundation (TSF) project and
    was made possible with the generous support of Genentech.

    SOCIAL & WEBSITE:
    Leda Bresnov
    Website - https://www.sumairafoundation.org/ledas-nmo-story-i-want-to-live-while-i-live/
    Instagram - https://www.instagram.com/bresnov/
    Twitter -https://twitter.com/Bresnov

    Demystifying NMO podcast
    Instagram - https://www.instagram.com/demystifying_nmomog
    Twitter - https://twitter.com/DemystifyingNMO

    The Sumaira Foundation
    Website - https://www.sumairafoundation.org
    Facebook - https://www.facebook.com/TheSumairaFoundation

    TIMESTAMPS/TOPICS:
    00:01:14 Leda Bresnov
    00:04:36 EUPATI Patient Expert Training Programme
    00:07:21 Patient Expert Training Programme
    00:11:02 Patient Input and Drug Development
    00:23:39 Self-Advocacy & Involvement in Healthcare Decision-Making

    LINKS:
    EUPATI - https://eupati.eu/
    European NMOSD Toolkit - https://www.nmosd-in-focus.com/-/media/Themes/Horizon/nmosd-in-focus-com/nmosd-in-focus-com/Documents/European-NMOSD-Patient-Toolkit.pdf

    SUPPORT the Podcast
    Donate to Illuminate
    https://www.sumairafoundation.org/advocacy/donate/

    CREDITS:
    Producer & Host - Brian Dawson
    Music - Denys Kyshchuk from Pixabay

    • 39 min
    Episode #30 | Navigating NMO in Challenging Circumstances: Global Inequities in Care

    Episode #30 | Navigating NMO in Challenging Circumstances: Global Inequities in Care

    In recent years, we have seen healthcare systems collapse under the strain of natural disasters and armed conflict and hundreds of millions of people being forcibly displaced. So, how do we meet the healthcare needs of people in humanitarian disasters, let alone those living through these nightmares with a rare disease such as NMO?
    To talk about the unique challenges of diagnosing and treating rare conditions like NMO in these low-resource settings, we are joined by Dr. Farrah Mateen.
    She highlights common barriers such as lack of disease awareness, limited diagnostic testing availability, and restricted treatment access. Dr. Mateen also proposes concrete goals to better support patients facing the most challenging circumstances.

    ABOUT US:
    The Demystifying NMO and MOG podcast is a Sumaira Foundation (TSF) project and
    was made possible with the generous support of Genentech.

    SOCIAL & WEBSITE:
    Farrah Mateen, MD, PhD
    Website - https://doctors.massgeneralbrigham.org/provider/Farrah+J+Mateen/255866
    Global Neurology Research Group - www.massgeneral.org/neurology/research/global-neurology-research-group
    Twitter - https://twitter.com/FarrahMateen

    The Sumaira Foundation
    Website - www.sumairafoundation.org
    Facebook - www.facebook.com/TheSumairaFoundation

    LINKS:
    Mateen FJ. Neurological disorders in complex humanitarian emergencies and natural disasters. Ann Neurol. 2010 Sep;68(3):282-94. doi: 10.1002/ana.22135. PMID: 20818788.
    Mateen FJ. Neurocritical care in developing countries. Neurocrit Care. 2011 Dec;15(3):593-8. doi: 10.1007/s12028-011-9623-7. PMID: 21863357.
    Mateen FJ, Hanafi I, Birbeck GL, Saadi A, Schmutzhard E, Wilmshurst JM, Silsbee H, Jones LK Jr; AAN Quality Committee. Neurologic Care of Forcibly Displaced Persons: Emerging Issues in Neurology. Neurology. 2023 May 16;100(20):962-969. doi: 10.1212/WNL.0000000000206857. Epub 2023 Mar 1. PMID: 36859408; PMCID: PMC10186241.
    Mateen FJ. Rectifying global inequities in neuromyelitis optica diagnosis and treatment. Mult Scler. 2023 Jul;29(8):932-935. doi: 10.1177/13524585231179108. Epub 2023 Jun 10. PMID: 37300419.

    SUPPORT the Podcast
    Donate to Illuminate
    https://www.sumairafoundation.org/advocacy/donate/

    CREDITS:
    Producer & Host - Brian Dawson
    Music - Denys Kyshchuk from Pixabay

    • 54 min
    Episode #29 | Caregivers: Nobody Fights Alone

    Episode #29 | Caregivers: Nobody Fights Alone

    We kick off Season 4 of the Demystifying NMO & MOG Podcast with a very special guest, Candice Galvan.
    Candice became an Ambassador for The Sumaira Foundation after her daughter was diagnosed with NMO. She joins us today to talk about her path to becoming an advocate and how she is helping care for others through her work as program manager for TSF’s Human Collective Project.
    ABOUT US:
    The Demystifying NMO and MOG podcast is a Sumaira Foundation (TSF) project and
    was made possible with the generous support of Genentech.
    SOCIAL & WEBSITE:
    Candice’s Story
    https://www.sumairafoundation.org/bellas-nmo-story-in-this-family-we-fight-together/
    Demystifying NMO podcast
    Instagram - https://www.instagram.com/demystifying_nmomog
    Twitter - https://twitter.com/DemystifyingNMO
    The Sumaira Foundation
    Website - https://www.sumairafoundation.org
    Facebook - https://www.facebook.com/TheSumairaFoundation

    TIMESTAMPS/TOPICS:
    00:01:34 Candice's Story
    00:11:28 Becoming an Advocate
    00:14:42 Explaining NMO to a 9-year-old
    00:17:57 Medical Marijuana
    00:22:10 TSF's Human Collective Project

    LINKS:
    Human Collective Project (HCP) Support Group Meetings
    https://www.sumairafoundation.org/community/human-collective-project-2/

    SUPPORT the Podcast
    Donate to Illuminate
    https://www.sumairafoundation.org/advocacy/donate/

    CREDITS:
    Producer & Host - Brian Dawson
    Music - Denys Kyshchuk from Pixabay

    • 38 min
    Episode 28 | Financial Assistance For NMO & Critical Insurance Updates w/ the Pan Foundation

    Episode 28 | Financial Assistance For NMO & Critical Insurance Updates w/ the Pan Foundation

    As we wrap up Season Three of the podcast, we are speaking with Amy Niles of the PAN Foundation. Amy is the Chief Advocacy and Engagement Officer, where she dedicates her time to building relationships, public policy, and advocacy initiatives. She joins us to discuss how PAN helps people manage the financial burden of chronic illnesses. Amy also explains important updates to Medicare and some new insurance practices that can be harmful to patients with life-threatening, chronic, and rare diseases.
    ABOUT US:
    The Demystifying NMO and MOG podcast is a Sumaira Foundation project and
    was made possible with the generous support of Genentech.
    SOCIAL & WEBSITE:
    Amy Niles & The PAN Foundation
    Website - https://www.panfoundation.org
    Facebook - https://www.facebook.com/PANFoundation
    Instagram - https://www.instagram.com/pan.foundation
    Twitter - https://twitter.com/pan_foundation
    Connect With Us
    Website - https://www.sumairafoundation.org
    Facebook - https://www.facebook.com/TheSumairaFoundation
    Instagram - https://www.instagram.com/demystifying_nmomog
    Twitter - https://twitter.com/DemystifyingNMO

    TIMESTAMPS
    00:02:02 Amy Niles & The Pan Foundation
    00:04:16 A Day in the Life
    00:05:54 Serving the NMO Comunity
    00:06:29 Eligibility Criteria
    00:09:03 The Application Process
    00:11:30 The Fund Finder
    00:14:58 Medicare Updates
    00:20:37 Copay Accumulators
    00:24:49 Alternative Funding Programs
    00:30:54 Do You Have a Copay Accumaltor?
    00:32:32 Legislation to Protect Patients & What You Can Do

    LINKS:
    Fund Finder - https://www.panfoundation.org/find-disease-fund
    Find help with FundFinder - https://www.panfoundation.org/fundfinder
    Neuromyelitis Optica Spectrum Disorder - PAN Foundation - https://www.panfoundation.org/disease-funds/neuromyelitis-optica-spectrum-disorder
    Everything you need to know about Medicare reforms - PAN Foundation - https://www.panfoundation.org/everything-you-need-to-know-about-medicare-reforms
    Ask your elected officials to support The HELP Copays Act and ban copay accumulator programs - https://www.panfoundation.org/end-copay-accumulators

    CREDITS:
    Producer & Host - Brian Dawson
    Guest Photo - The PAN Foundation
    Music - Denys Kyshchuk from Pixabay

    • 38 min

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