Teresa Pocock’s “Artistic Ability” is featured in The Vancouver Foundation’s annual 2017 magazine, “Gifts of Inclusion”. This is perfect timing as November 1st to 7th is Canadian Down Syndrome Week — a week to celebrate the talents of people with Down syndrome and “See the Ability”. #CDNDownSyndromeWeek.

Read the Vancouver Foundation article by Roberta Staley below…


Artistic 

Ability

Terea Pocock photographed by Zack Embree at the opening of her art show at Gallery Gachet, Vancouver, BC in June 2016

Once forced to live in a senior’s

 care facility, Teresa Pocock has

 created a home, and a body of

 work, in Gastown

By Roberta Staley

VANCOUVER’S GASTOWN NEIGHBOURHOOD, abutting the Downtown Eastside, is known for its red brick 

buildings, cobblestone roadways, graffitied walls, steam

clock, Woodward’s and Dominion buildings, tech cluster

and busy restaurants and pubs. The people who navigate 

its streets are as heterogeneous as their environment:

entrepreneurs, academics, artists and activists, as well as

 those struggling with poverty and addiction.

Seated at a sturdy wooden table in a sleek, minimalist

 Gastown condo is Teresa Pocock. By way of greeting,

 she throws her arms in the air, exclaiming, “I am a self advocate!” 

– a sincere and indisputable declaration. It

 wasn’t an easy journey, but Pocock has learned to express 

herself as an artist and an activist, drawing the attention

 of thousands of people including politicians.

Pocock was inspired to become a working artist 

thanks in large part to a $1,000 Vancouver Foundation 

Downtown Eastside Small Arts Grant in 2016, which 

motivated her to create enough individual works to 

launch a solo show. “It really helped Teresa blossom into 

a professional artist,” says older sister Franke James, with 

whom she lives, along with brother-in-law Bill James, in 

the Gastown home filled with books and art.

Pocock’s inaugural exhibit premiered June 29, 2016 and

 showcased an array of richly illustrated poetry, mounted 

bus-poster size on the walls of Gastown’s Gallery Gachet. 

Opening night doubled as the book launch for Pocock’s

 self-published Pretty Amazing: How I Found Myself in the

 Downtown Eastside, and a selection of the book’s poems and 

illustrations were part of the exhibit. The bold verse, as well as

 

the jewel-coloured art, show an individual who is confident 

about asserting her place in the world, writing in the poem I

 Am Alive: “Redeemed/Okay, I am reborn/In Gastown.”


“Now she can say she’s an artist and a poet,” says Bill.

 “It has given her a huge sense of purpose to her life.”

What makes these accomplishments so significant – 

extraordinary even – is that Pocock has Down syndrome.

As her book title alludes, her life has not followed a simple 

course. In early 2013, Pocock’s elderly father, with whom she

 lived in Toronto, had failing health and was about to move to 

a care home. Several siblings placed Pocock, the youngest of

 seven, in a long-term seniors care facility without their father’s

 approval. Franke and Bill, along with Pocock’s dad, spent 

four days wrangling with government officials, nursing home

 management and even the police to get her out. Pocock 

then went to live permanently with Franke and Bill.

Teresa Pocock is hugged by her sister Franke James; photo by Gerry Kahrmann/PNG for Vancouver Sun and The Province; licensed for use
That wasn’t the end, however. With the help of

 Franke and Bill – who are business partners in the 

communications firm The James Gang, Iconoclasts –

 Pocock made a campaign video for the website change.org

 protesting her confinement and demanding atonement

 while asserting the rights of the disabled. The petition, 

launched on World Down Syndrome Day on March 21, 

2014, called out the Ontario government for supporting 

her placement in an institution that was clearly unsuited to her age – she was then 49 – abilities and temperament. In

 the video, Pocock calls for an apology from the government 

for denying her human rights. “I was crying and scared,”

 Pocock says to the camera. “It’s my right to decide where 

to live … I did not want to be there.” She received 26,000

 online signatures of support.

In November 2016, as a result of public pressure and

 media attention, Ontario Minister of Health and Long-

Term Care Dr. Eric Hoskins wrote a letter of apology to 

Pocock. Franke framed it and hung it in the front hallway.

That wasn’t the only time Pocock has attracted the

 attention of politicians. At the opening of her gallery 

show, a staff member of Vancouver East MP Jenny Kwan

 presented Pocock with a certificate from Kwan, applauding

 her “wonderful drawing, creativity and achievement.” It is

 also framed and hangs in Pocock’s bedroom. Teresa Pocock holding the achievement certificate awarded to her by MP Jenny Kwan

Since the exhibit, Pocock has been drawing nearly

 every day in her artist’s sketchbooks. Her inspiration has 

become Gastown itself, edgy despite its gentrification, noisy

 and raw, a working harbour with cargo ships loading and 

unloading in Burrard Inlet. Pocock draws what is around 

her: the geometric pattern of windows on the Woodward’s

 building; her favourite coffee shop Prado; London Drugs;

 Nesters Market and, most endearing to Pocock, The Flying

 Pig bistro, with its homemade macaroni and cheese, and 

desserts. “I like chocolate cake,” says Pocock, who does 

yoga, plays Scrabble and reads in her spare time.

“Teresa’s art shows what she cares about, what she 

is feeling and thinking and what she’s afraid of and 

excited about,” says Franke. “She shows that she belongs 

in the world.”

Pocock has another project in the works; she is planning

 what Franke describes as “an unconventional, freewheeling 

cookbook” full of her favourite foods. “We thought the 

book could have information about the neighbourhood

 and where Teresa actually gets the food.” As with her 

first publication, it too will be filled with images and

 drawings. “And we’ll go to the Flying Pig,” Pocock adds.

Franke muses on her younger sister’s influence in

 Gastown. “In society, there is a tendency to take people 

who are different and segregate and hide them away. When

 Teresa is out in the world, it brings out good things in

 people. Like at restaurants, they will bend over backwards

 because Teresa is with us. We call it the Teresa Effect.”


To learn more about the Downtown Eastside Small Arts

Grants program visit 

vancouverfoundationsmallarts.ca. You can

 also help support this program with a donation. Call Kristin 

in Donor Services at 604.629.5186 for more information.




CREDITS

“ARTISTIC ABILITY” written by ROBERTA STALEY for the Vancouver Foundation.

Read The Gifts of Inclusion, Vancouver Foundation’s 2017 Annual Magazine. Also available in eReader version. Or download the Adobe Acrobat PDF

PHOTOGRAPHS

Photo by Zack Embree
Photo by Zack Embree

Photo by Gerry Kahrmann for PostMedia (licensed):
Photo by Gerry Kahrmann/PNG

Photos by Franke James:
Teresa reading and enjoying the Vancouver Foundation article October 30 2017. Photos by Franke James Photo of Teresa Pocock by Franke James Photo of Teresa Pocock by Franke James


Help open eyes and hearts to “See the Ability” of those with Down syndrome. Join in raising awareness about the abilities and unique gifts of people with Down syndrome during #CDNDownSyndromeWeek. Spread the word!

Where to buy Teresa Pocock’s book. Pretty Amazing: How I Found Myself in the Downtown Eastside is available on:

Pretty Amazing Cover Kindle

Book Description:
What does Vancouver’s Downtown Eastside look like through the eyes of an artist-an artist who also happens to have Down syndrome? The heart of Pretty Amazing is the unexpected story of Teresa Pocock finding herself as an artist and poet. Previously, Teresa’s artistic expression was discouraged and ridiculed. Her opening poem, I Am Alive, packs added punch when you know that her future was written off a few years ago when she lived in Ontario. Teresa was forced into an Ontario nursing home against her will. The health-care system had wrapped her in-as disability advocate Paul Young aptly describes it -“a cocoon of impossibility.” Against her wishes, Teresa’s liberty and freedom was traded for a single bed in an end-of-life nursing home. It was a violation of her human rights. She did not want to be there. Teresa had things to do, places to go, and people to meet! In the Downtown Eastside of Vancouver, Teresa has found her voice. It is a voice that talks about feeling “butterflies,” but still finds the courage to fly.

Pretty Amazing is available in Paperback or Kindle at Amazon.com and Amazon.ca

About the Artist/Author

Pretty Amazing Cover KindleTeresa Pocock is an artist and poet living in the Downtown Eastside of Vancouver. In 2016, she won a DTES Small Arts Grant from the Vancouver Foundation which enabled her to create her first book, Pretty Amazing: How I found myself in the Downtown Eastside. Teresa exhibited 18 “Pretty Amazing” artworks as 4ft x 5ft posters in her first solo show at Gallery Gachet which launched on June 29, and wrapped up on July 2.

As a self-advocate with Down syndrome, Teresa presented her story, I Love My Human Rights, at the 2016 Canadian Down Syndrome Conference in Montreal. Teresa is a member of the BC Civil Liberties Association, Gallery Gachet, Inclusion BC, Family Support Institute of BC, and the Canadian Down Syndrome Society. She loves chicken pie, word play and spotting the big boats in the Burrard Inlet.

In Canada, buy Teresa’s book at Amazon.ca: Pretty Amazing: How I Found Myself in the Downtown Eastside

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Who is willing to stand up to defend and assert the human rights of the intellectually disabled?

A tragic wrong occurred when Teresa Pocock was forced into an Ontario long-term care home in 2013 against her will. Despite Teresa’s many remarkable achievements since her release, the Ontario government has refused to admit they made a mistake in declaring her “incapable” and forcing her into a long-term care home. The violation of Teresa’s human rights is critically important because there are many, many “Teresas” all across Canada and in the United States. The National Task Force on Living in the Community stated that over 12,000 Canadian citizens (with developmental disabilities) are living in health related institutions such as senior’s facilities, nursing homes, acute care hospitals, long term care facilities and personal care homes, as opposed to ordinary homes in the community.

Thankfully, the British Columbia Civil Liberties Association, (BCCLA) and seven signatories are standing with Teresa.

“We believe and support Ms. Pocock’s statements that she did not want to be put into a nursing home.”

In an open letter sent to the Ontario Minister of Health and Long-term Care, the BCCLA is requesting a formal apology to Teresa from the Honourable Eric Hoskins.

“We are gravely concerned that the government, through its actions, appears to condone the forced placement and mistreatment of developmentally-disabled adults.”

The BCCLA, Canadian Association for Community Living, Inclusion BC, Plan Institute, People First of Canada, Spectrum Society for Community Living, Vickie Cammack, and Al Etmanski have all joined together to send a clear message to the Ontario Government: Teresa Pocock’s forced admission to an Ontario long-term care home violated her human rights.

Please join us in calling for an official apology from the Ontario government by signing Teresa’s Change.org Petition and sharing this letter.

July 12, 2016

The Honourable Eric Hoskins, MPP
Minister of Health and Long-Term Care
Ministry of Health and Long-Term Care
10th Floor, Hepburn Block
80 Grosvenor Street
Toronto, ON M7A 2C4

Dear Minister Hoskins:

Re: Teresa Pocock’s forced admission to an Ontario long-term care home violated her human rights

At age 49, Teresa Pocock was forced against her will into an Ontario Long-term Care Home. The traumatic experience shattered her trust and created psychological distress. These events compelled her to leave her home province of Ontario where she was living at the time. She moved to B.C. where she is flourishing as an emerging artist and is also a BCCLA member.

We believe and support Ms. Pocock’s statements that she did not want to be put into a nursing home.

The BC Civil Liberties Association is concerned that the Ministry has violated Ms. Pocock’s rights, which are protected by the UN Convention on the Rights of Persons with Disabilities, the Charter of Rights and Freedoms, and Ontario law.

We are gravely concerned that the government, through its actions, appears to condone the forced placement and mistreatment of developmentally-disabled adults. We understand that your ministry conducted a 14-month long investigation into Ms. Pocock’s treatment. We understand that, despite uncovering evidence of institutional wrongdoing, the Ministry of Health and Long-Term Care produced a report that concluded that government agencies had done nothing wrong. However, Ministry documents obtained under a Freedom of Information and Protection of Privacy Act (“FOIPPA”) request suggest that the investigation found indications that the law may have been broken in Ms. Pocock’s case, resulting in a violation of her rights.

The information that has been provided to us about Ms. Pocock’s case strongly suggests that Ms. Pocock’s rights under the Convention on the Rights of Persons with Disabilities and the Charter of Rights and Freedoms were violated when she was forced into long-term care against her will.

Ms. Pocock’s right to decide where she lives under Article 19 of the Convention was violated when an Ontario social worker conducted her Capacity Assessment without proper consent and against Ms. Pocock’s written legal directions in her 1995 Power of Attorney. Moreover, the evidence that has been provided to us suggests that the social worker falsely indicated on the consent form that he had reviewed Ms. Pocock’s Power of Attorney when in fact he had not done so.

We are deeply troubled by the findings of the Ministry’s investigation. The documents provided to us through the FOIPPA request that were obtained from your Ministry, in our view, support Ms. Pocock’s assertions that she was wrongly deprived of her liberty.

We urge you to issue a formal apology to Ms. Pocock without further delay.

The following individuals and organizations join the BCCLA in calling on the Ontario Ministry of Health and Long-term Care to uphold the laws of Ontario and Canada to defend Ms. Pocock’s human rights and liberty.

Sincerely,

Josh Paterson
Executive Director of the British Columbia Civil Liberties Association

bcccla_logo

Michael Bach

Vice-President of the Canadian Association for Community Living

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Faith Bodnar
Executive Director of Inclusion BC

Inclusion-Logo_254

Tim Ames
Executive Director of Plan Institute

plan_logo240

Kory Earle
President of People First of Canada

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Ernie Baatz
Executive Director, Spectrum Society for Community Living

spectrun_logo

 

Vickie Cammack

 

Al Etmanski

See the PDF copy of the BCCLA letter to Hon. Eric Hoskins:

“Teresa Pocock’s forced admission to an Ontario long-term care home violated her human rights”

“I Am Alive” is the opening poem from Teresa’s new book, Pretty Amazing. It packs added punch when you know, that just a few years ago, her future was written off. But now Teresa has been “reborn” in Vancouver’s Downtown Eastside. And the unexpected story of how she found her voice — and found herself as an artist and poet — is at the heart Pretty Amazing.

I AM ALIVE

Hello.
Be nice to everyone.
Look, I am alive.
You have to be nice.
I am doing fine.
Thank goodness.
I have to be nice to them.
And to the others.
That’s a brilliant idea!
You’re thinking.
And I’m thinking too.
I think we need to make a list of the things we need.
Right. I’m alive. Nesters. Flying Pig. Prado.
We love it here.
Everybody loves me.
You guys are alright, I know.
You guys, I am born. I am alive.
Redeemed.
Okay, I am reborn.
In Gastown

Teresa_Celebration_2N7A0094lr
Read all about Teresa’s Pretty Amazing book launch which took place at Gallery Gachet on June 29, 2016.

BOOK DESCRIPTION – Pretty Amazing: How I Found Myself in the Downtown Eastside

Pretty Amazing Cover KindleWhat does Vancouver’s Downtown Eastside look like through the eyes of an artist—an artist who also happens to have Down syndrome? Teresa Pocock’s colourful art and poetry let’s us see, hear and feel it from her unique viewpoint.

The heart of Pretty Amazing is the unexpected story of Teresa finding herself as an artist and poet. Previously, Teresa’s artistic expression was discouraged and ridiculed.

Her opening poem, I Am Alive, packs added punch when you know that her future was written off a few years ago when she lived in Ontario. In 2013, Teresa was forced into an Ontario nursing home against her will. The Ontario health-care system had wrapped her in—as disability advocate Paul Young aptly describes it —“a cocoon of impossibility”. Against her wishes, Teresa’s liberty and freedom was traded for a single bed in an end-of-life nursing home. It was a violation of her human rights. She did not want to be there. Teresa had things to do, places to go, and people to meet!

In the Downtown Eastside of  Vancouver, Teresa has found her voice. It is a voice that talks about feeling “butterflies”, but still finds the courage to fly. Teresa has, in her own words, been “reborn in Gastown.”

We’ll have copies of Teresa’s Pretty Amazing book for purchase. (The book will also be available on Amazon, in print and ebook formats.)

Plus… Eighteen 4’ x 5’ original artworks by Teresa will be on display. Admission is free. The artist’s favourite refreshments, cranberry juice and raspberry bars, will be served!

Who made this Pretty Amazing event possible?

Teresa won a DTES Small Arts grant to create the illustrated book. The Vancouver Foundation created the Downtown Eastside Small Arts Grants Program, in partnership with the Carnegie Community Centre, to help DTES artists advance their careers by supporting and showcasing their work.

Vancouver Foundation: Small Arts Grant

Pretty Amazing

Please sign Teresa’s petition at Change.org

Teresa Power Walks: Forced into a Nursing Home at 49. Now She’s Free!

Watch Teresa Pocock ‘power walk’ — and ask yourself how anyone could think she belongs in a nursing home! It is crazy! Who would deny Teresa her freedom?

Unfortunately that’s exactly what happened last November. Teresa who has Down syndrome, was forced against her will into an old-age nursing home, by the CCAC and two of my siblings. Four days later, she was rescued by my 91-year old father who was “adamant” he did not want his daughter living in a nursing home.

But then the nursing home called the police, in a shockingly callous and bizarre effort to force her back.

By signing the petition you can help Teresa get an apology for the harm done to her. Teresa is asking the CCAC to apologize for wrongly taking away her human right to decide where she lives. Teresa is asking the Rekai Centre to apologize for calling the police in a completely unnecessary, intimidating and callous attempt to force her back into their institution.
We need to stand strong to protect the rights of developmentally disabled people so that what Teresa experienced does not happen to anyone else.

Please sign Teresa’s petition, because human rights should never be disabled. Thank you in advance for your support!

Hi I’m Teresa Pocock

Forced into a Nursing Home at age 49.
Now she’s free.

Much better.

Hi I’m Teresa Pocock, I’m 49.

Fighting the system
For human rights.

I’m having fun.

I’m power walking.
I’m power walking.
I’m power walking.

It’s my right.
It’s my right.
It’s my right to decide where I live.

For all the people with disabilities

Please sign my petition at
Please sign my petition at
Change.org
Change.org

Please visit me on the online at
teresapocock.com

Much better.

————
Music Credit: Dan-O at http://danosongs.com/
Song Title: Book of the Monkey

Great story in the Toronto Star by Antonia Zerbisias about Teresa and her adventures “power-walking” toward independent living!

Toronto Star: Teresa Pocock’s passport to a new life with Down syndrome

Teresa’s passport to a new life with Down syndrome

March 29, 2014

Antonia Zerbisias
Posted with permission from Toronto Star

Teresa Pocock is in the dining room, flashing her new Visa card.

She’s proud she can take her brother-in-law, Bill James, out for coffee and doughnuts after they power-walk through their Bedford Park neighbourhood.

On the other side of the table, her older sister, Franke James, props up her iPad, which is playing a video of Teresa applying for that card at the bank.

Asked to share her PIN, Teresa is shocked: “It’s personal. I’m not supposed to tell.”

At 49, Teresa is finally handling money. For the first time ever, she knows the price of orange juice. She can distinguish between bills and coins.

“She just never had any training,” Franke explains, adding that Teresa has, despite attending many day programs, been “cocooned” all her life.

Now that she’s living with Franke and Bill, Teresa has been getting lessons on independent living. Not that she will ever be on her own. She was born with Down syndrome and, despite her boast that she “can walk faster than a speeding bullet,” she faces mobility as well as other challenges.

But not nearly as many challenges as Teresa and Franke’s four other older siblings — all but one have asked not to be named in this story — believed she had when their elderly father Joseph could no longer care for her in the condo they shared. Teresa had lived with him since her mother died in 1999.

That’s why, on Nov. 27, and against her father’s wishes, those siblings had Teresa admitted to Toronto’s Rekai Centre, a long-term care facility filled mostly by people much older and less able than she is.

Franke and Bill believe Teresa was made out to be less capable than she is now proving to be. They charge that Teresa’s siblings worked to get her on a “crisis list” that would move her into “a nursing home.”

They claim the Community Care Access Centre (CCAC), which deemed her eligible for long-term care, “ignored” its own positive observations about Teresa’s behaviour. They say the system that moved her into the Rekai Centre so quickly was “manipulated” to manufacture a crisis that didn’t exist.

“The fact is, Teresa’s human rights were taken away,” insists Bill. “We want to share her story because we want people to know the truth about how the system works.”

Bill and Franke, both writers and artists who work at home, are angry — angry at the social service agencies that assessed Teresa as showing signs of dementia, angry that she was placed in “a nursing home,” angry at Teresa’s family.

Now they want apologies on Teresa’s behalf — and last week they got one. Toronto Central CCAC CEO Stacey Daub posted one on a petition Teresa and Franke put online.

“My siblings were desperate, but they didn’t have to be because we had offered to take care of Teresa for the rest of her life,” says Franke, producing a stack of emails between her and the rest of the family.

“If you had asked me a year ago to take her, I would have said, ‘No, let’s look at other options,’” she continues. “But once I got the sense that they were serious about putting Teresa in a nursing home, we stepped in.”

In January, Franke took Teresa’s case to the provincial Select Committee on Developmental Services, where she testified that the consent and capacity laws are “easily abused” and that “disabled and disadvantaged people are getting hurt.” She has even filed a complaint with the Human Rights Tribunal.

None of this is a knock on Teresa’s other siblings, who have doted on her all her life, taking her to their cottages, making sure she makes it to medical appointments, having her over for meals and holidays. In fact, every year, her two dozen nieces and nephews make a “Christmas calendar” for her, marking off the days they will each take her to a movie, or shopping, a hockey game or on some other outing.

But now the anger and resentment — on both sides — are palpable.

A misunderstanding? Miscommunication? “Manipulation?”

Depends on whom you talk to.

Three of Teresa’s siblings would communicate solely by email. Only her sister Joanne Mills spoke on the record with the Star. She maintains that the Rekai Centre was just a temporary stop for Teresa, until a suitable group home could be found.

“The real story here is that there should be more group homes,” she insists in a brief interview, adding that the family acted out of concern both for Teresa and their father. “Because no family member stepped forward to say that they would take her — we truly did not know that (Franke) and her husband would take Teresa — and no group homes were available, there was nowhere else for Teresa to go.”

It’s an all-too-common situation when parents of adult children with Down syndrome grow too old, or too ill, to care for them, despite government supports, community programs and social services. That’s because people with Down syndrome are living longer — so much longer that even their siblings are themselves ailing or otherwise unable to take them in.

“We have an aging population of Down syndrome clients,” notes Julia Oosterman, director of Communications and Stakeholder Relations at Toronto CCAC. “Appropriate housing — supported living, group homes etc. — is an area that we need to plan for as our population ages. Long-term care, while it may be the only available option, may not be suitable, and the health-care sector needs to consider how we plan for this.”

For her part, Mary Hoare, chief executive officer of the Rekai Centres, writes in an email: “It may not be ideal, but the top priority is always to ensure that, if someone is in urgent need and we have the space and capability to take them in, we will do so, and they will be safe and well cared for.”

But Bill and Franke say there was no urgency for Teresa.

“We offered four times to take Teresa, but the CCAC was never informed,” Franke said.

According to Dr. Terri Hewitt, vice president of community programs and adult services at Surrey Place Centre, the need for group homes is urgent. She counts 215 adults in Toronto on the waiting list. Of those, 102 are “ready” for placement now, while 59 are considered urgent and high-priority.

“If you’re in long-term care because you don’t have somewhere to live, then you become high priority,” Hewitt explains, avoiding the specifics of Teresa’s case. “If you’ve been transferred temporarily to long-term care placement to keep you safe, you would be escalated on our priority list. We would be actively looking for something. The more high priority you are, the more you are identified when vacancies come up.”

Hewitt can’t provide figures for how many adults with Down syndrome end up, at least temporarily, in nursing homes — but many do. Some for good.

“Even the most caring of families can have differences of opinion on how to proceed,” she admits. “It’s a difficult road to follow and preparation is the best thing that you can do.”

This particular story has a happy ending.

Unaware of the storm around her, Teresa is thriving in her airy new home. Since Dec. 1, when her father, Bill and Franke removed her from the Rekai Centre, she has been learning photography. She loves to play Scrabble. She cooks and she’s been hitting the road.

A new capacity assessment in January found Teresa to be “capable” enough for things like granting Franke and Bill her power of attorney for personal care. In February, she accompanied them to Washington, D.C., and all this month, she’s been on the West Coast, where she met David Suzuki.

“We’re really enjoying her,” says Franke. “It’s been an eye-opener.”

And for Teresa, it’s a wide new world.


Toronto Star

Reprinted from Toronto Star, in the “com.smg.cq.components.page.SectionImpl@1b838653” section.

[iCopyright]2014 Torstar Syndication Services. All rights reserved. Licensed by Mrs Franke James on March 29, 2014. You may obtain additional permissions to reuse this article at the following iCopyright license record: http://license.icopyright.net/3.7212-51078. Torstar Syndication Services and Toronto Star logos are trademarks of Torstar Syndication Services. The iCopyright logo is a registered trademark of iCopyright, Inc.

See the Toronto Star: Teresa’s passport to a new life with Down syndrome