We posted this poem, “Ode to a Caregiver,” written by the mother of a person receiving home share services, back in March. We are sharing these inspirational words again at the end of our month focusing on posts and resources for caregivers, and we are inviting everyone to join in with us and say: THANK YOU, CAREGIVERS, FOR ALL YOU DO!
Hey everyone, we’re focusing our posts on CAREGIVERS and resources for caregivers this month. We know that one of the challenges faced by many caregivers is…finding sustainable ways to integrate connecting with other caregivers into a busy schedule.
While we’ve posted about the importance of self-care to caregivers, we wanted today’s discussion to be more focused on how connecting with others who have caregiving experience can help fight feelings of isolation and loneliness. With the COVID-19 pandemic changing how we all connect safely with one another, feeling isolated and lonely is more common than in the past. So, since we’ve posted about many ways for caregivers to connect, what’s are we bringing to the table today to try out?
Podcasts! If you haven’t listened to a podcast before, they are like individual radio shows and are usually released in episodes. Podcasts typically target a topic per episode. These podcasts in particular are designed to be relevant to the caregiving experience by those who put them out into the podcast-universe:
- Caregivers Out Loud: A Podcast by Family Caregivers of BC A space to connect, listen and learn with other caregivers.
- The Giving Tree Podcast by Amanda Rocheleau (BSW, MSW, RSW) This podcast is for helping professionals and personal caregivers. … talking openly and honestly about the true hardships of providing care to others while we also talk about sustainable solutions to self-care and personal wellness.
Besides the more obvious benefits of podcasts (running for a set amount of time per episode; covering a breadth of information about a given topic; facilitating discussion with and between people who have relevant experience) they can be a great tool to help caregivers feel that their struggles, challenges, and successes are genuinely seen, acknowledged, and respected. And – we hope! – support caregivers to feel a little less lonely and a little less isolated!
Let us know in the comments if you have a favorite podcast.
Hey everyone, we’re focusing our posts on CAREGIVERS and resources for caregivers this month. We know that one of the challenges faced by many caregivers is…making time and space to take good care of yourself, as a caregiver.
We’ve talked before about the dangers of compassion fatigue, caregiver stress, and burnout , and we posted about the Family Caregivers of BC resources available earlier this week.
It can be hard to know where to start with self-care, so we wanted to highlight the Family Caregivers of BC webinars as one way to start building your toolkit. There’s many webinars to choose from, but why not start with this one? It’s called “Caring for Yourself While Caring for Others” and covers compassion fatigue and how the body and mind deals with chronic stress, as well as what you as a caregiver can do to sustain and nourish yourself.
There’s additional resources available too:
Hey everyone, we’ve been posting a series to celebrate Community Inclusion Month. We have talked about where we’ve been, and about some current issues where we are and how to self-advocate. And so, as we end Community Inclusion Month, we wanted to leave you with some thoughts about where we’re going.
While it’s impossible to know the future, our hope for where we’re going is described best by Cole Blakeway: We are all DIFFERENT, and that’s AWESOME!
Hey everyone, as you know we’ve been posting topics for Community Inclusion month and last week we talked a bit about self advocacy.
A really important part of self advocacy is standing up for your own rights. We have a whole page that talks about rights and responsibilities here, complete with help to understand different kinds of rights, like:
- the Right to Say No
- the Right to Vote
- the Right to Love
- the Right to Have a Job
- the Right to Believe
- the right to be safe — especially, help to Say No To Abuse
Everyone has rights as a person in Canada, and rights as a person in BC. If you have a disability and you are getting supports, you also have rights as a person who uses the services of Community Living BC (CLBC).
With all those different kinds of rights in mind, we thought this would be a good time to remind ourselves about this awesome conversation that helped explore rights and responsibilities:
If you’ve got questions about rights and responsibilities, please let us know or leave us a comment.
Hey everyone, October 24-31 is PRIDE WEEK in Kelowna, and there are a whole bunch of events going on to celebrate 25 Years of Kelowna Pride! You can check it all out here, including the bike derby, trans and non-binary storytelling evening and social, pride festival and pride cabaret.
Hey everyone, we’ve been posting a series as part of Community Inclusion Month. Last week, we talked about where we’ve been in terms of disability rights and inclusion, and the work done by self-advocates who have brought the movement to where we are now. This week, we’re focusing on where we are by exploring some current issues and resources for self-advocacy.
So, what’s self-advocacy?
The BC People First Society (BCPF) talks about self-advocacy being what happens “when we stand up for our needs when they are not being met” and members help each other learn self-advocacy skills. Here is a video of the BCPF Advocacy Committee on Accessibility on YouTube.
Here is an interview from Kelowna Now with Kelowna resident Shelley Decoste that was published on October 7th, to mark Community Inclusion Month. Shelley talks about her experiences and stereotypes about people with diverse abilities.
Here is a news article from CTV News about a young man from Toronto who is part of the Dear Everybody campaign put on each year by a rehabilitation hospital. He (and a team of young people with disabilities) are doing a virtual tour of classrooms and workplaces to talk about ableism.
Here’s how the Dear Everybody website explains it: Ableism is the discrimination towards someone based on their abilities, often favouring those who do not have a disability and seeing less value in those that do. And it needs to stop.
The idea is to get people talking about ableism, in order to end it — and that’s where self-advocates come in! Self-advocates can start great conversations about what’s wrong and how to fix it. You can see the videos made to start the Dear Everybody conversation here.
The Easter Seals website has a great idea on this page that would help start important conversations (like Shelley’s interview and like Dear Everybody). You can invite people you know to watch TED Talks about different disability issues, different people’s perspectives, and different experiences, and the then start a conversation about it, or a video chat, or have a talk on the phone. Or, if you’re interested in exploring another way to safely try out online community, you could post on the video page, a message board, or Facebook page, or post a comment below!
Check out the Easter Seals 10 suggested TED Talks about disability, accessibility, and inclusion to get started (printable list below).
Hey everyone, Plan Institute is offering their Level 1 and Level 2 webinars about the Registered Disability Savings Plan (RDSP) over the next few months.
Check out the info below to see which would be best for you, and click here if you’re interested in signing up!
Hey everyone, CLBC has announced the winners of this year’s Widening Our World (WOW) awards, check it out here!
Hey everyone, we’ve been posting a series as part of Community Inclusion Month. We explored a bit last week about how we can participate in community while we all focus on keeping each other safe and healthy, using tools like technology and online communities.
We also talked about how everyone has a right to be included in their community – and, that this is part of the UN Convention on the Rights of Persons with Disabilities (UNCRPD).
So, why are we talking about it again this week?
We are looking at where we’ve been so that we can see how much progress we’ve made.
Progress on the road to community inclusion — like the UN Convention on the Rights of Persons with Disabilities — can take a long, long, long time. That UN Convention we were talking about? That only happened 15 years ago, in 2006. It’s important to remember what things were like for people with disabilities at the start of the disability rights movement.
If you’re interested in hearing more about what it was like to fight for the rights of people with disabilities, you can check out this video featuring Judith Heumann (a disability rights activist from the US). YouTube is a great resource to find other people with disabilities sharing their stories and experiences.
When we see people and organizations (like CLBC) promoting community inclusion, human rights, and the rights of people with disabilities, we are seeing how far we’ve come thanks to the work of self-advocates all over the world (like Judith) — and we celebrate their achievements as part of Community Inclusion Month!