『Navigating Disability with Me』のカバーアート

Navigating Disability with Me

Navigating Disability with Me

著者: Meghan & Pam
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A conversational podcast that empowers Canadians with disabilities (and those supporting them) by cutting through the complexity of the system. Featuring authentic lived experiences and insights, it brings together essential resources and real voices to guide, inform, and inspire2025
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  • Being an Advocate Part II: Conflict and Self Care
    2026/05/21
    A continuation of episode 15's discussion of being an advocate, covering topics around conflict and self care. Sound quality on Meghan's mic is poor - it's been fixed as much as possible. Apologies! Guest: Linsey, a healthcare worker who has also been a health care advocate for a family member. Feedback: navigatingdisabilitywithme@gmail.com Links: Dr. Kristen Neff: https://self-compassion.org/BCalm: https://bcalm.ca/Family Caregivers of BC - including virtual and support line, art therapy, elder care, workers etc etc: https://www.familycaregiversbc.ca/family-caregiver-support-groups Tips When is it appropriate to push back? This is not about being difficult, this is about protecting the alignment between the patient/client and the care team.Facilitate communication - whether that's a language barrier or a communication difficulty - to be clear about patient/client's values, and help with alignment.Always keep patient/client's values centered!Take time to process new information before pushing back.How do you escalate concerns without alienating the team? This is loaded wording as it's the team's job to look after you. Always remain polite but other than that it is not the patient's family/friends' jobs to tip toe around the care team. The care team should be trying to understand YOU.An example that we're seeing in hospitals in Vancouver is how care teams are shifting to recognize and support indigenous patients with indigenous care teams as part of cultural safety.Most hospitals have spiritual practitioners, language interpreters etc. to facilitate religious or language needs.Share your/your loved one's story with the care team to flesh out who they are and what your concerns are. Stories are powerful! But remember that the care team's time is limited.Share the "why" of your questions to explain where you're coming from.How do you advocate when you feel intimidated by the medical system? Who are the people in the system you could go to? Social worker, nurse, case worker, GP. Start with whoever knows the patient/client the best.For clarity: around minute 22 Linsey refers to "Cerner". That is a type of electronic charting used in the Vancouver region. The electronic chart may not contain everything that was in the patient/client's old paper chart.Stories can reveal important medical details. Advocate for yourself by reading through your own lab results/imaging interpretations. Things do get missed!How can patients with cognitive or communication impairments still have their voice centered? There are many technological advancements but something as simple as writing down a basic alphabet chart (in any language) helps a lot. Patient can point out letters, or to "Yes" and "No".Occupational Therapy and Speech and Language Pathologists can help with technologies or strategies. iPad interpreters are in hospitals now, with well over 100 languages available.How should families handle situations where the patient's wishes conflict with what the team recommends? There's usually time given after plans are discussed, for everyone to process and ask questions. Ethics teams exist for when the care team's recommendations conflict with the patient/advocates wishes (if they can't come to a resolution together), but they are a last resort (before the courts). Care teams will try to resolve conflict without turning to boards/courts.Get your wishes down on paper (a representation agreement etc.) to help navigate conflict (but also make sure you discuss your wishes with your family/friends/advocate).How do you balance being a supportive advocate versus taking over? Center the patient/client! Advocacy can slip into control, due to fear. Watch yourself, as the advocate. "Am I amplifying my grandma's voice or am I replacing it with my fears?"Hospitals are becoming more respectful of language and cultural needs. Just ask about what you want to do, you will likely be welcomed to do any practice etc.Any financial barriers? Just ask the social worker! They'll have access to all sorts of resources and programs.Public Guardians are in use if a patient/client has no family or friends to act as advocate. This is largely for financial matters. They usually leave medical decisions to the care team.What was hardest about being the family instead of the professional? Linsey's response was masking her own fear, making decisions quickly, dealing with so many family members, wondering if she was doing the right thing according to her family member's wishes.Build your own resilience with rest/sleep, eating well, seeing friends, doing something else etc.What signs of burnout should families watch for? Emotional: irritability, short tempered, numb, teariness. Physical: exhaustion, headaches, getting colds etc. Relational: shortness with family/loved ones, withdrawing. Pay attention to if a good friend points out issues with how you're behaving.Look into Dr Kristen Neff's (University of Texas at Austin) work on self compassion. Treat yourself ...
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    49 分
  • Episode 15: Advocating for Family (with guest Linsey)
    2026/04/13

    Summary: A rambling conversation with Linsey about the challenges, both emotional and systemic, of being an advocate for a loved one who becomes ill or disabled.

    Guest: Linsey, a healthcare worker who has also been a health care advocate for a family member.

    Feedback: navigatingdisabilitywithme@gmail.com

    Notes:

    1. How do many families feel when facing being an advocate? Family members want to provide love and safety so they may feel anxious and vulnerable, or feel out of control. They're being asked to make important decisions for a loved one when they are in shock themselves.
    2. Write things down - team meetings, updates from staff etc.
    3. Take time to process new information but also don't hesitate to ask questions.
    4. Most hospitals/organizations will ask you to appoint one person as the advocate/decision maker.
    5. How do you think one should go about selecting an advocate? What values should they have and what discussions should you have with them ahead of time? Is a medical professional necessarily the person to choose?
    6. If you can select an advocate ahead of time make sure they share your values. Are they strong under pressure? Do they have good communication skills? Are they able to ask questions and stand up for you? Medical knowledge is a plus but not a necessity. Ask yourself how does this person emotionally regulate? Can they stay grounded when stressed?
    7. Advance directives/living wills can be temporarily overridden or delayed by grieving families. Which is why you need a grounded advocate with good communication skills to look out for your wishes.
    8. Talk to your family/advocate about your values and wishes!
    9. As a health care worker, what do you wish families understood about our health care system?The system is stretched and it's imperfect. Both money and practitioners are stretched thin.
    10. Gaps are not intentional - whether it's in care or communication. Practitioners are doing the best they can.
    11. Families often have to ask the same question more than once due to the fragmented system. Try to not get frustrated!
    12. It's not fair but families and clients have to be patient and polite. Remember that staff often feel like their hands are tied in being more effective due to workload.
    13. As a granddaughter, what surprised you about how the system actually feels?
    14. Waiting for things feels like it takes forever. The impact of emotion is so much bigger when it's your family member. There's a struggle with what the outcome will be. It's hard to let go of staying at her bedside overnight when you know all the steps that must be taken for high quality of care, to trust that they'll all be done.
    15. What did you think you knew professionally that turned out to be incomplete when it was your own family?
    16. You understand the process but it's exhausting to live through the emotional impact. Big time decision fatigue. Gave new understanding of why family/advocates need time to make decisions. Surprised by how much support other family members would need. The stamina needed was significant. The experience built empathy for patients and families.
    17. The importance of trauma informed care became obvious. Frankly all people/professions could benefit from trauma informed care training
    18. What are common mistakes families make when advocating?
    19. It's the care team's job to lead and react, not the family's job to be "easy". But don't wait too long to speak up with questions and concerns! Always be polite and non-aggressive. The team knows that the aggression/yelling etc. is from a place of fear and loss of control, however, it makes a tense situation worse.
    20. Any aggression is flagged and all team members are made aware, so don't get yourself flagged this way.
    21. Look out for yourself through all this: sleep, food, sunshine etc. Talk to someone about what you're going through.
    22. Look to the social worker for help on emotional but also practical issues.
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    35 分
  • Episode 14 - Canada Disability Benefits, Credits and Rebates
    2026/03/29

    Summary: A review of some of the remaining federal programs for disabled people: the Canada Disability Benefit and the Canada Caregiver Tax Credit, as well as the GST/HST rebate. Actual topic starts at 10:06 post all sorts of chat on various topics.

    Feedback: navigatingdisabilitywithme@gmail.com

    Links:

    1. Tody app: https://apps.apple.com/ca/app/tody/id595339588
    2. Canada Disability Benefit
      1. Apply online: https://www.canada.ca/en/services/benefits/disability/canada-disability-benefit/apply.html#h2.2
      2. Calculator: https://www.canada.ca/en/services/benefits/disability/canada-disability-benefit/amount.html#h2.5
    3. Canada Caregiver Tax Credit:
      https://www.canada.ca/en/revenue-agency/services/tax/individuals/topics/about-your-tax-return/tax-return/completing-a-tax-return/deductions-credits-expenses/canada-caregiver-amount.html
    4. GST/HST tax refund:
      https://www.canada.ca/en/revenue-agency/services/child-family-benefits/goods-services-tax-harmonized-sales-tax-gst-hst-credit.html
    5. North Shore Disability Resource Centre resource guide for a good list of all federal benefit/tax programs: https://nsdrc.org/resource-guide/

    Tips:

    1. Canada Disability Benefit: In Canada, over 1.5 million people with disabilities lived below the poverty line in 2022, representing 1 in 6 people with disabilities. This benefit is supposed to help lift disabled people out of poverty.
    2. The official poverty line is a set of 66 different thresholds based on the Market Basket Measure which determines the cost of a basic modest standard of living. Calculated to be approximately $2000-$4300/month, depending on where you live in Canada.
    3. These "poverty lines" are often not very realistic as compared to actual cost of living.
    4. Maximum income to get full benefit of $200/month is $23000 for a single person and $32500 for a couple.
    5. If you're working they give an exemption for the first $10000 for a single or $14000 for a couple of income.
    6. For 2025-2026 if you make more than this you won't qualify for the CDB:
      • Single Individual:
        • $35,000 or more (if you have no working income).
        • $45,000 or more (if you have at least $10,000 in working income, utilizing the maximum exemption).
      • Couple (Only one person eligible for CDB):
        • $44,500 or more (if no working income).
        • $58,500 or more (if you have at least $14,000 in combined working income).
      • Couple (Both eligible for CDB):
        • $56,500 or more (if no working income).
        • $70,500 or more (if you have at least $14,000 in combined working income).
    7. Qualifying: must have the DTC, have filed tax returns and have Canadian residency.
    8. There can be back payments of up to 24 months
    9. Wouldn't it be nice if the federal government just had one central application for all disability benefits???
    10. Canada Caregiver Tax Credit is a non-refundable tax credit.
    11. Who qualifies: Caregivers supporting a spouse, child, grandchild, parent, grandparent, sibling, aunt, uncle, niece, or nephew with an impairment.
    12. Amount varies based on who you're supporting and how old they are. For 2025, you can claim anywhere from $2687 plus an additional $8601 depending on household circumstances. Varies if the dependant is a child vs and adult dependent vs a spouse. (Actual dollar amounts cut from episode as it was too confusing).
    13. The CRA may require a signed statement from a medical professional confirming the impairment.
    14. GST/HST refund - not disability specific but low income. A federal tax-free quarterly payment that helps individuals and families with low or modest incomes offset some of the GST or HST they pay. Eligibility is determined automatically each year when you file your tax return.
    15. North Shore Disability Resource Centre has a good resource guide of all federal benefit/tax programs. Look for similar in your city.
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    36 分
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