American and Canadian Health Care

November 6, 2009

This is a special guest blog post by our Executive Director, Alanna Hendren, on health care in Canada and the United States, and how it relates to people with developmental disabilities.

health symbolThe Health Care debate in the U.S. is providing some great opportunities for positive changes in federal and state legislation regarding people with disabilities.    The current bill proposed by the Senate Finance Committee, called “America’s Healthy Future Act” is a mix of individual responsibility, government subsidies and the creation of a health-exchange.  Insurance reforms such as eliminating pre-existing conditions clauses are also included.

It is difficult for us Canadians to imagine a system where people do not have universal access to healthcare services, particularly for people with developmental disabilities.  In the U.S., Medicaid is the only program where non-senior citizens can get payments for their health care needs, but in order to qualify the proposed legislation would standardize eligibility for Medicaid for all parents, children, pregnant women and adults at or below 133% of the Federal Poverty Level, or $30,000 for a family  of four – $14,400 for an individual.  Prescription drug benefits would also be extended to all Medicaid beneficiaries under the proposed plan.

Recognizing that qualified health care providers are in low supply in the U.S., the Senate bill also includes provisions for two demonstration grant programs that benefit the work force.  One program provides financial and supportive assistance to eligible low-income people who are receiving education for health care jobs, including direct-care and community support positions.  The second program will develop a set of core training competencies and certification programs for personal and home-care aides throughout the country.

The Federal Office of Disability Employment Programs has also provided major funding for the Campaign for Disability Employment, which aims to encourage employers and others to “recognize the value and talent that people with disability bring to the workplace.”  The Campaign is the result of lobbying by the American Association of People with Disabilities, Special Olympics, the National Business and Disability Council and the U.S. Business Leadership Network.  The website for the Campaign is at http://www.whatcanyoudocampaign.org.

The U.S. Department of Education has also received $11.37 billion for elementary and secondary education, Individuals with Disabilities Education, and Vocational Rehabilitation.  Of the $11.37 billion in funding, $6.1 billion has been released for Individuals with Disabilities Education and will provide states, school districts and early intervention service providers with additional funding to improve outcomes for infants, toddlers, children and youth with disabilities and will also stimulate the economy.  $270 million in Vocational Rehabilitation funding will improve employment outcomes for people with disabilities.

In Canada, the federal government has virtually no involvement in services or supports for people with developmental disabilities and in British Columbia, we have seen the direct-care and community workforce decrease substantially in favor of “home-care” or other models that do not require pay much over minimum wage.  Funding for special education and early intervention continue to be insufficient to meet the needs of children who are on waitlists or receiving diluted services.  Although Community Living BC (CLBC) is stressing ‘jobs first’, there has been nothing more than token funding invested to make jobs a sustainable reality for adults.  Vocational rehabilitation used to be an area where the federal government played a fundamental role, but now these supports have been passed on to the provinces to provide, with predictable results.  Affordable housing is another area where families, self-advocates and service providers continue to face major obstacles in both the U.S. and Canada.

The economy is certainly no worse in Canada than it is in the U.S., so it is particularly disturbing that we have seen cuts during good times and now we will see more cuts during bad times.  The great blessing is that we all have healthcare, so families can at least have the security of knowing that treatments for physical disorders are fully funded.  What families also need, however, is to know that their loved one is maximizing their full developmental potential and is supported to live a safe life in the community – two areas where we are falling behind our neighbors to the south, east and many places around the world.


Just Singin’ Round

November 4, 2009

Last night, I attended the monthly Just Singin’ Round (JSR) event hosted by the Synergy Foundation. I was joined by Raul and Grace and my friend Jenn at this event. As usual, it was a fantastic showcase of musical talent, good food, and excellent company. For a minimum $25 donation admission fee, it’s definitely worth the food, fun, and hours of entertainment. Additionally, the $25 along with any raffle tickets sold at the event, go directly towards funding a different charity every month. This month’s featured charity was the Vancouver Adaptive Snow Sports.

JSR Performers

JSR Performers
Raul and Grace
I finally remembered to bring my camera to JSR again after going for the past many months. For more information on JSR, you can view the JSR website, read up on JSR at Raul’s post on his blog, or view my previous entry on JSR.


National Down Syndrome Awareness Week

November 2, 2009

The week of November 1 – 7 is National Down Syndrome Awareness Week – a week where inclusion is celebrated and people with Down syndrome can be recognized.

Recently, I came across an article on from ABC News on parenting and Down Syndrome. The article opens with a powerful introduction:

After prenatal testing, Boston filmmaker Melanie McLaughlin faced the likelihood that her 12-week-old fetus had Down syndrome, or a heart defect.

She prayed for the heart defect.

Who would think that a heart defect would be comparable to Down syndrome? Melanie McLaughlin, later fell in love with her daughter after learning more about Down syndrome. Down syndrome, the most common genetic condition in the United States and one of the most common conditions in Canada, is often feared, but feared out of lack of education.

cover5For parents who may have a child with Down syndrome or are curious about what Down syndrome means; local celebrity, Tamara Taggart articulates her journey, challenges, and happiness, with her son Becket, who was born with Down syndrome in an article posted on her CTV blog. For more information, you can read the full article on the Urban Baby & Toddler website.

I’ve had the pleasure of meeting Tamara on a couple of occasions and I can attest to her congeniality and her dedication and devotion to her family and children. The above articles definitely helps demystify the issues regarding raising a child with Down syndrome.


United Way Campaign 2009

October 30, 2009

We’ve kicked off our 2009 United Way Campaign today at our Halloween potluck. Not only did we get to snack on delicious homemade “Hallowe’en” food, but we also got to hear a meaningful message.

United Way Loaned representative, Emma

Emma, a United Way loaned representative came and talked to us about the importance of programs funded by United Way and also showed us an inspiring movie clip.

We’re holding a raffle this year for our United Way Campaign. Prizes include $50 to Cincin Ristorante + Bar, CTV prize pack, $150 Photobooks and much more! This year, we’re trying to beat the amount we’ve raised last year for United Way with this raffle. It means a lot to us at DDA to raise money for the United Way as our programs are partially funded by United Way!

We will continue to show our support, and hope that you will also support United Way of the Lower Mainland and its causes.


Playhouse Halloween Party 2009

October 28, 2009

This morning, I had the pleasure of attending Playhouse’s Halloween Party. Playhouse is one of the Developmental Disabilities Association’s Child Development Centre’s nestled in the quiet neighborhood on Brant and East 27th.

This was my first Halloween party of the year, and my first time attending Playhouse, so I brought along my camera to take some pictures of the Halloween party. Kim Looi, the Manager at Playhouse, did a fantastic job organizing the party with her staff. The entire Child Development Centre was decorated with pumpkins, smiling faced paper ghosts, fake cobwebs and other Halloween themed decorations. Most of the children were also dressed in Halloween outfits.




The party started off with some excellent guitar music and singing with all the kids clapping and singing along. After the music came pumpkin pancakes and cantaloupe for the children.


Once the children were done their snacks, they headed off trick-or-treating at the different rooms at Playhouse. They’d knock on the door, yell “trick-or-treat”, and someone would open the door and give the kids healthy Halloween snacks.

The Halloween party was plenty of food, fun, and songs, with plenty of smiles on the faces of all the children. For more photos of Playhouse’s Halloween Party, view the Developmental Disabilities Association’s flickr site.

Playhouse (East Vancouver) – Children 6 months – 3 years old
4107 Brant Street, Vancouver 604-873-6448
Hours of Operation: 7:45am – 5:30pm
playhouse@develop.bc.ca


Disability Services Awareness Day Recap

October 26, 2009

Over this past weekend, Joyce and I managed a booth at the Disability Services Awareness Day event held by SUCCESS and the Richmond Centre for Disability. Also attending and speaking at the event were a variety of other service providers in the Lower Mainland, along with MP Alice Wong, MLA Rob Howard and Mayor Malcolm Brodie. This was a great opportunity for us to meet some new people and educate them about our services. People were impressed by the variety of workshops offered by the DDA (like the RDSP and workshop on sexuality we hosted recently), in addition to our programs, such as our Family Support program. Most importantly, people were impressed that all our workshops and our Family Support program, were all free.

Disability Services Awareness Day

Disability Services Awareness Day

Joyce and I @ Disability Services Awareness Day

Both Joyce and I enjoyed the Disability Services Awareness Day and look forward to attending next years. See you all again then!


How it feels to have H1N1

October 22, 2009

This is a special guest blog post by our Executive Director, Alanna Hendren. Unfortunately, she has H1N1 and has only been able to work from home. We wrote about H1N1 recently to in another blog post – stay healthy everyone, and we hope you get better soon, Alanna!

vaac3If anyone has looked for me around the office lately, you’ll have noted my absence (I’m sure its been quieter).  I have H1N1 and if I can use the experience for any positive good at all I hope to encourage as many of you to get vaccinated as possible.  H1N1 sucks.  This is the worst flu I’ve ever had and I can now understand how feared such epidemics must have been in earlier centuries.

The symptoms vary between people, but mine started with an extreme fever, chills, sweats, vomitting, an unbelievably severe headache and muscles that were so sore I could not figure out what was happening to me.  I didn’t have much of a cough or sore throat, so I thought it was something else, but I was still taking antibiotics for another infection, so that may have been why.  My fever was so high I was in a semi-hallucinatory state so I easily collapsed into a heap of denial.  But as this went on, I realized my immune system was not going to shrug this off easily.  I was also tormented with the notion that if I went to the doctor, I could easily infect others.  Besides, I was too sick and too cold to leave the house.

When you have this thing, there is nothing you can do but stay away from your loved ones or else you’ll pass it on and they could potentially die.  My kids are in the age group that is getting most severely impacted – college aged.  Clayton, has extraordinary good  health and luck as a rule so he’s still fairly oblivious to the whole thing.

Each hour drags by, fever rages. Dreams take on bizarre qualities and day turns into night without much difference.  TV is a constant recap of balloon boy and I can’t tell if that’s a product of my fever or American TV journalism is really that bad.

Finally, I phoned my doctor and he confirmed my suspicions and basically said there’s nothing that could be done and my body would just have to fight it off on its own.  Had it been caught within 48 hours, Tamiflu could have been prescribed, but there are mixed reviews on its effectiveness.  People vary widely in their reaction to this thing so its hard to predict what will help.

So here I sit – I must be feeling a lot better because I can actually type but I am still so sick.  For the last few days I haven’t been able to read or even watch TV.  My eyeballs were so hot it was hard to open my eyes.  I’m constantly nauseated and queasy.  My face is still grey and my tongue is all spotted and blotchy.  If that image alone isn’t enough to make you want to get a double dose of vaccine then you too may be doomed to suffer the curse of the swine.  Take care!

[On a side note, Donna Cain, our Assistant Director of Operations, will be setting up a time for free vaccinations for all DDA employees in the coming weeks.]


Better Business Bureau Torch Award Gala

October 21, 2009

Last week, Joyce and I, along with some of our Board Members and some of the Developmental Disabilities Association’s Senior Management Team attended the Better Business Burea’s Torch Award Gala. The DDA was nominated in the Green Award Category along with 7 other socially responsible and environmentally responsible organizations. Although we unfortunately did not win the award, we were privileged to be one of the finalists. Congratulations to spud! for winning the award.

Congratulations to all the winners and finalists, and we look forward to next year!


Bridge to a Cool Planet

October 19, 2009

This coming Saturday, in addition to participating at the Disability Services Awareness Day, the Developmental Disabilities Association will also be in attendance at Bridge to a Cool Planet. We’ll be there to promote our recycling and sustainability initiatives that effectively help prevent climate change. Everything starts at 1pm. For more information visit the Bridge to a Cool Planet website.

You can also follow Bridge to a Cool Planet on Twitter @B2CP.


MAPCL Art Show

October 16, 2009

Last night, I attended the Mainstream Association for Proactive Living (MAPCL)’s 5th Annual Art Show for BC Artists with Developmental Disabilities. This event was a fantastic showcase of talented BC artists and their amazing work. Works included Watercolours, acrylic, tile mosaics, textile art, glass, pottery, photography and more. I was amazed by the caliber of work at this event, and the number of people who attended it. Undoubtedly, the art presented at the art show exemplifies the genius, talents, gifts and abilities that each artist has.



The event was definitely a success, with catered food, wine and beverages, as well as a raffle and silent auction. All the best to the artists, and I look forward to attending next year’s art show! To see more photos of the artwork at the show, visit the Developmental Disabilities Association’s flickr page.