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Giving Girls A Voice To Change The World

When I spoke with Angela Patton a few months ago, I was struck by how direct and open she was. We discussed the CAMP DIVA program she founded in Richmond, Virginia in 2004, its merger with non-profit Girls for a Change and her current role as CEO of that organization. Her passion for her work was clear, from her constant reference to program participants as “my girls” to the story she told of networking and making contacts while on a family vacation because you have leap at the opportunities that present themselves.

Not only has Patton leapt at the opportunities that have come her way, but she has tried to facilitate opportunities for her girls to advance themselves, improve their communities and feel empowered to make their voices heard.

The article that I wrote about Patton, CAMP DIVA and Girls for a Change appeared in the May 2017 issue of The Advocate, the newsletter for Virginia Union University’s Center for the Study of the Urban Child. You can read it here.

Angela Patton
Girls for a Change CEO and CAMP DIVA founder Angela Patton

 

 

#WeNeedDiverseBooks

Last week I spoke with mother and son authors Betty K. Bynum and Joshua B. Drummond about their recently released title, I’m a Brilliant Little Black Boy! Bynum is also the author of two titles for girls, I’m a Pretty Little Black Girl! and I’m a Lovely Little Latina! 

The story that I wrote appears in the latest issue of the Urban Views Weekly. (more…)

Chaeli Mycroft: Hope in Motion

Michaela (Chaeli) Mycroft became the first female quadriplegic to summit Mount Kilimanjaro in September. But this is only one of many interesting facts I learned when I met the 21-year-old South African and her mother Zelda on campus recently.

Chaeli and Zelda were at Quinnipiac University at the invitation of David T. Ives, executive director of the Albert Schweitzer Institute, to speak about Chaeli’s experiences with cerebral palsy and her work as an ability activist.

Chaeli gave her presentation three times before the day was over, the second time without the aid of her slideshow. At the end of each talk, students were given time to meet Chaeli, who is a student herself at the University of Cape Town. These informal interactions were among her favorite parts of the day.

Chaeli spoke about her own desire for mobility and independence as a youngster. Wheelchairs were expensive and fundraising for a motorized wheelchair would wind up being the start of The Chaeli Campaign, a non-profit organization she co-founded as a 10-year-old, along with her older sister Erin and their three best friends, Tarryn, Justine and Chelsea Terry.

In 2004, the five girls came up with an idea to raise money. They would sell cards featuring Erin and Chaeli’s artwork and Sunshine Pots, miniature pot plant kits that included seed and soil. Chaeli got permission from her school to take orders from students and their families, and the girls began to sell. Within seven weeks, the girls had the money for Chaeli’s wheelchair, but orders were still coming in.

Zelda suggested the two families could start a non-profit organization to help other children with disabilities, if the girls wanted to keep being involved. The organization, proud to have been founded by kids, is now in its eleventh year.

The Chaeli Campaign helps about 3,000 South African children a year to receive assistive devices and therapies. It also operates a number of programs designed to create inclusive environments for children with disabilities. A basic tenet of the organization is this:

Physical/intellectual impairment is self-evident and can be dealt with. Disability is created by the way in which society responds to the impairment.

Often, Chaeli said, people with disabilities are seen as a burden within their community, taking up time, energy and space.

“Disability is inconvenient for them to deal with,” Chaeli acknowledged. But it’s important to remember that it is an inconvenience for the disabled person as well.

“Disabled people are still people who have the same needs and the same rights as everyone else,” Chaeli pointed out. “You can’t just give people a wheelchair and think, ‘Cool, my job is done,’”

This is why inclusive environments are so important. They reinforce the message that being different is okay and help to change people’s perceptions about disability and what ability means.

As Chaeli talks about her life, she uses humor to engage her audience. It makes her incredibly relatable, even as she challenges what people might believe are the limitations of a disabled person. Take for example her story about sandboarding.

When she went, no one was sure what would be the best way for Chaeli to ride down the sandy hill. The first option had Chaeli sitting at the front of the board with her ride partner behind.

“It was a bad plan,” Chaeli laughed. “Don’t put a disabled person with balance issues on the front of a sandboard.”

Chaeli had a great time and is thankful to her parents for the bravery they showed in letting her do it, despite the possibility she might get hurt. Like many things in her life, it was tough sometimes, but it helped that her parents always focused on the positives, which fostered her can-do attitude. It’s like Zelda said to me later:

You can’t learn inclusion, you have to live it.

Living a life of inclusion has led Chaeli to many interesting adventures. She gave a few examples, like wheelchair dancing. Chaeli started at the age of 11 and competes with current partner, Damian Michaels.

Or cycling. Her friend, Grant Kruger, introduced her to the idea and she joked about her initial response. “My legs don’t even move; you’re ridiculous,” Chaeli says she told him. “Eventually I was convinced by his face. It was nice.” The pair competed in the Cape Argus Pick n Pay Cycle Tour.

Building on these experiences led to the the idea for something grander in scale, or as Chaeli put it, “a little more epic” – climbing Mount Kilimanjaro.

The climb was four years in the planning, and Chaeli needed a custom built wheelchair, and an incredible team to make it happen.

Chaeli celebrated her birthday on day two of the climb. “They made me a cake on a mountain,” she said. “It was phenomenal.”

But on day three she realized what she’d really gotten into. There were many challenges, not least of which was the cold. By day five, she was starting to get frostbite in her feet.

“It’s not like I need my feet, but I like having them,” she laughed.

The group learned many lessons about planning, being creative in the face of problems, bravery and admitting weaknesses. In short, it was an amazing experience.

The whirlwind schedule Chaeli and Zelda have planned for the next couple weeks sounds like it will be pretty amazing as well. They arrived in the U.S. the day before the talks at Quinnipiac, and they were flying out the next day to visit Earth University in Costa Rica.  After that, they are scheduled to take part in workshops at the International Children’s Peace Prize ceremonies in the Netherlands before heading to the 15th World Summit of Nobel Peace Laureates in Barcelona.

Chaeli herself won the 2011 International Children’s Peace Prize, and she was also awarded the first ever Peace Summit Medal for Social Activism at the 2012 World Summit of Nobel Peace Laureates. She has met famous people from Archbishop Emeritus Desmond Tutu to Bill Clinton to Malala Yousafzai, who won the International Children’s Peace Prize in 2013.

But these are not what she is most proud of achieving.

“It’s more the small things,” Chaeli said. She recalls a young boy in a South African township whose bedridden parents had not left their home for seven years. The Chaeli Campaign was able to get wheelchairs for them.

To be able to give something that is a pretty small thing in the big picture … for them it was everything.

The Chaeli Campaign is about changing lives by focusing on mobilizing the minds and bodies of children with disabilities. It is also about hope. Following Chaeli’s lecture, Zelda spoke about some of the programs of The Chaeli Campaign that focus directly on nurturing hope and opportunity.

One is the Pay-It-Forward Ambassadors Program. The program was started in 2009 in order to ensure that The Chaeli Campaign, which was started by kids to address the needs of kids, would be able to maintain the voice of youth leaders as its original founders continued to age.

Children aged between 9 and 14 are invited to invest a year of their time to promote The Chaeli Campaign while learning about social entrepreneurship and how to run their own projects – including fundraising and awareness campaigns within their own communities.

Another program is the Bhabhisana Baby Project. This newly launched independent project is operating under the umbrella of The Chaeli Campaign’s therapies programs.

Their mission is assess babies (0-2 years) who are at risk of developmental delay and disabilities. Where a need is identified, the project aims to provide multi-disciplinary therapy for the child and support and empowerment to family members and carers, so that every baby may reach their individual potential. The Bhabhisana Baby Project saw its first baby on September 29.

Zelda also spoke about The Chaeli Campaign’s Vocation and Rehabilitation Program. Disability is particularly difficult for older children and young adults, she said. Once a disabled person turns 18, they can find themselves in a vacuum where programs that can help with socialization and skill development are absent.

The Chaeli Campaign holds weekly workshops targeted at intellectually and physically disabled young adults to provide them with an opportunity to learn skills and practice them in a work situation.

Sometimes, Zelda said, it can be difficult to raise funds for these ongoing therapeutic programs, but each one is an important piece in helping to change the lives of people living with disabilities and their families.

After listening to Chaeli’s presentation and spending some time speaking to her afterward, Quinnipiac occupational therapy graduate student Samantha Wondsel summed it up nicely.

“[The Chaeli Campaign] takes a holistic approach – bringing in family, leisure, sports and education,” Wondsel said. “It’s really about putting the person first rather than the disability.”

Chaeli Mycroft, her mom Zelda, and David T. Ives, the executive director of the Albert Schweitzer Institute. Photo Credit: Nicki Dakis-Gallagher

Chaeli and Zelda along with David T. Ives on Quinnipiac’s campus. Photo: Nicki Dakis-Gallagher

Caring Leadership Teaches Reverence For Life

Quinnipiac University students in QU 301 sat wherever they could find an empty seat on the first day of fall classes. The room at the back of the Albert Schweitzer Institute is not exactly a classroom, but it is where “Combating the Causes of Poverty” will be meeting for the semester. Professor David T. Ives teaches the class. His long white hair is receding at the front and caught in the back in a loose ponytail. Tall and broad with a warm, easy manner he resembles a big teddy bear.

Ives goes through the roll and promises to work on remembering names before asking everyone to introduce themselves and share why they are taking his class.

“It’s okay to say because it’s a requirement,” he adds with a chuckle. “I know that’s why some of you are here.”

As the students take turns speaking some admit to it, although they all say the class sounded interesting as well. But many of them say they signed up for this class because of Ives. Different versions of ‘someone I know had you for a class and said you were great’ tell the story of why maybe a dozen of the nearly 30 students in the class are there.

Ives is okay with that. He knows the goal of the institute is to promote the values of Albert Schweitzer on a worldwide basis with an emphasis on peace, humanitarian values and health. He also knows that to do that, he needs students in the classroom. If they were all there for heartfelt reasons that would be ideal, but required service learning and classes may mean getting to reach students who otherwise wouldn’t be there at all.

If Ives could have his way then young people would spend a gap year living in poorer countries. He knows that getting them outside of their own experiences and into the world can be life-changing, not just because about 91 percent of the students that go on a Quinnipiac service trip abroad come back feeling the experience has changed them. No, Ives knows from his own life how experiences can change us.


Changes, even difficult ones, sometimes result in benefits unimagined. Albert Schweitzer once said that each person can do a little to help end misery for others. A physician and humanitarian, Schweitzer believed passionately that by practicing reverence for life we would help others, but we would also help ourselves to become good, deep and alive.

The institute named after him was founded in 1984 and became affiliated with Quinnipiac University in 2001. Ives was brought on as executive director in January 2002. Since then he has sought to cultivate a desire to help those in need in the hearts of Quinnipiac’s student body in a number of ways including arranging and leading service trips to developing countries. It was on one of those trips that Ives found a way to benefit others from a difficult personal experience.

In January 2012, Ives was traveling with a small group of occupational and physical therapy students in Guatemala. They set up a small clinic in a classroom of the local school in the village of Joya de las Flores. Two people came to the clinic that day. One of them was 14-year-old Pablo Enrique.

(You can click here to watch the documentary “Esperanza Lograble (Hope Within Reach): Uniting a Community Through Occupational Therapy.” It records the earlier experiences of a group from the Albert Schweitzer Institute and the Occupational Therapy Department at Quinnipiac University who traveled to San Lucas Toliman, Guatemala in July 2009.)

Pablo suffered from a physical disability and initially the Quinnipiac group believed it was to do with a fall he had three years earlier. The family had sought treatment for him then, but quickly exhausted their meager finances. It had now been many months since Pablo had seen a doctor. As they learned more of Pablo’s history; however, something started to click with Ives. When the family said that doctors years ago had mentioned Pablo might have Guillian-Barré syndrome, Ives became very emotional.

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Pablo and his father. Photo courtesy David Ives.

Guillian-Barré is rare. In fact, only about 1 person in 100,000 is afflicted with it. Amazingly, it was a disease Ives had personal experience with. At 41, Ives had been diagnosed with Guillian-Barré syndrome and rushed to the hospital for treatment. He spent the next several months in hospital. “One night,” Ives recounts, “I almost did die.”

Because of this, Ives knew what Pablo needed to do. He was able to send a walker, crutches and canes when the group returned to the United States. He also sent exercise manuals so that local staff could assist Pablo with his therapy.

Just two years later, the same group was overjoyed to witness Pablo walk out to greet them completely under his own power.

“We gave him the gift of walking again and for me, it doesn’t get any better than that in terms of what I do.”

Ives shares personal experiences like this very openly. It is something about him that creates a lasting impression. A former student, political science major Danielle Tomlinson, 20, recalls first listening to Ives speak. “He had a wealth of life experiences,” she said. “He had seen much more than any normal person had seen.”

How much more becomes apparent the more Ives opens up. Although his life begins in the usual way, his telling is certainly unique. “I was born rather young,” Ives begins. “I was in the same room as my mother at the time.”

The room was a hospital room in Lake Placid, New York. The year was 1951. The first two babies born at the brand new hospital received welcome gifts. Ives was born third. Within a few years his father Leland, a landscape designer, decided to become a minister. He moved his family and enrolled in the Gordon Divinity School, a few hours north of Boston.

“That’s probably where one of the more seminal incidents happened, although I didn’t realize how seminal it would be,” Ives recalls about being diagnosed with polio. He was 4 years old at the time and the doctors said he would never walk again. His mother, Dorothy, did not accept that.

“It took about nine months from the time I collapsed in front of the toilet and was diagnosed with polio until I took my first step unaided.” Not surprisingly, Ives said, “That was a big day in our household.”

When Leland Ives got a pastorate, the family packed up and moved to Pierpont, Ohio. “It was a growing metropolis of about 250 people and about 3,000 cows,” Ives explains, only half in jest. “It was kind of a Norman Rockwell existence.”

Surviving polio didn’t afford him any special treatment at home, at least not from his mother. Ives was given typical chores including mowing and cleaning. “My mother,” Ives explains laughing, “was also an initial feminist. When I told her I didn’t want to clean the bathroom because that was ‘women’s work,’ guess what I did for the next six months? I still hated doing it, but I wasn’t dumb enough to say it again!”

Growing up in a small town taught Ives a lot about community and helping others. He remembers how every farmer in town chipped in some of their own store to replace the hay of one farmer that was destroyed by a fire. And he credits seeing the gratitude of families receiving a Thanksgiving turkey through his father’s pastoral work as cementing the idea that he wanted to grow up and help people like that.

Another thing that made a real impression on a 10-year-old Ives was John F. Kennedy.

“I admired him as a young person. He seemed so full of life, of vim and vigor,” Ives said. “I knew I wanted to join the Peace Corps since I was about 10-years-old when John F. Kennedy recommended it, started it in 1961, I think it was.”

When Ives was 16, his mother was instrumental in arranging a family trip to South America. It was there that Ives saw real abject poverty. He remembers a family home they went to that contained a single soggy mattress shared by everyone, the walls made out of laboriously unrolled tin cans.

“Seeing that really changed my life,” Ives shared. “But it didn’t do it right away.”

He enrolled at Ohio State University after high school, but Ives says he really settled on a degree in social work because he didn’t need to take a language. During his freshman year, tragedy struck. Dorothy Ives was killed by a drunk driver and Ives admits his 19-year-old self did not handle her death well. He drank too much and his grades suffered, but he did find a path he enjoyed, planning programs and doing counseling as a resident assistant. When he was accepted into a master’s program, Ives finally began to deal with his anger.

“The master’s program had a counseling aspect to it and part of the deal was that you had to get therapy yourself,” Ives said. “So that’s when I talked about my mother for the first time in-depth.”

Once he had his master’s, Ives worked for five years before finally realizing his dream of joining the Peace Corps at 29. He was assigned to Costa Rica and taught agriculture to the locals, helping them to plant gardens and improve their health through better nutrition. As he worked in the different communities Ives began to realize he wanted to look at issues on a more macro level. It is good to work on the micro level of the Peace Corps, building a pond or planting a garden. When a child eats the produce from the garden then yes, Ives said, their health is helped. But what, he began to wonder, about the tens of thousands of children under the age of 5 who die every day?

This thinking was influenced by another seminal moment in Ives’ life. In a remote area accessible only by boat, a young girl was having trouble breathing. She was severely malnourished and it was clear she desperately needed medical attention. Ives went ahead to hold the boat as the family made their way more slowly behind. The captain did not want to wait and Ives had to resort to threatening to throw the man overboard to get him to hold the boat, but finally they were all on board. Ives held the little girl during the ride, but sadly she did not survive the trip. Her death has stayed with him and often motivates his efforts to help.


Ives met many people through the Peace Corps. One of them was his future wife Barbara, who also served as a volunteer in Costa Rica. When her service period ended, Ives arranged to leave his posting about a month early so that he could go home and chase her. He confesses it took him a little while to catch her though.

“When we were in the Peace Corps,” Ives reveals, “she had a boyfriend. She was the only one in the whole Peace Corps that did not know I was interested in her. To everybody else it was pretty obvious.”

The two were married on May 7, 1983. Within a few years they expanded their family when they adopted their son, Taylor, from the Philippines in 1986. Two years later they adopted daughter Kelsey from the Philippines as well.

In 1989, Ives took a job as executive director of The Louis August Jonas Foundation and settled his family in Rhinebeck, New York, not far from where he ran Camp Rising Sun, a national leadership and training program focused on bringing together young people from countries that have a history of conflict and try to show them how to relate to each other as individuals without violence.

Despite his experience traveling the world and dealing with people of many ethnic and cultural backgrounds, Ives still worried about being culturally sensitive to his children. At 4, son Taylor asked a question about the difference between their skin colors.

“He asked me, ‘When I grow up, will I be white too?’”

Unsure how to answer, Ives said he rambled on for at least 10 minutes discussing heritage and the varying shades of skin color. He spoke about diversity and even mentioned that white people often tan to try and darken their skin to look like Taylor’s.

“Can you believe I used the word diversity to a 4-year-old?” Ives asks, shaking his head at the memory. Taylor went off to play but returned a little later with a question that made it clear the nuanced cultural conversation had gone over the boy’s head.

“This time he asked me, ‘Dad, did you leave me out in the sun too long?’” Ives laughs delightedly at one of his favorite personal stories.

He also shares some of the more deep and meaningful exchanges he had with his own father, albeit when he was much older. During his time in the Peace Corps, Ives began to question some of the political ideals he had shared with his father. Ideals he had even once held sacrosanct. His growing disillusionment with the role of the United States in Latin America was sometimes a bone of contention in correspondence with his father at the time.

Ives felt that not every American working in Costa Rica was there for altruistic motives. Many made no attempt to understand the root causes of why people viewed communism as a good alternative. He saw companies “raping the land” and insecticides leaching into the groundwater. He saw workers in the fields, once including Barbara, being sprayed with DDT. And America held itself forward as “a beacon on the hill” even while some of their covert actions were “a moral abomination.”

Returning to the United States, Ives found it disturbing that many Americans were ignorant about what was happening outside of their own country. He wanted to work at the macro level, but discovered he needed to start at the micro level because of people’s limited knowledge of the wider world.

“I found when I would talk about my experience in Costa Rica, the first thing I had to do usually, if they were really interested, is explain where it was and why I went there.”

Typically Ives’ students have to learn some world geography early in the semester. He believes they need to be able to find a place on the globe and have some basic knowledge of a country in order to understand the problems it faces.

“I could shoot the person that took geography out of the high school curriculum,” Ives states. But once students begin to gain that basic understanding, he feels they become capable of profound thinking on the world’s problems. He works in the classroom to challenge students thinking. He wants to hear their opinions and gives each person his attention to ensure they get the most from the experience. Ives also makes a point of hearing from everyone, every class. He genuinely believes they all have something unique to offer. It’s a big part of why students love his classes.

Elaine Martinez, 20, is a health science studies major and former student of Ives.

“In class he is very intuitive. He’s very open to a lot of different opinions,” she said. “Instead of shutting your ideas down like some professors do, he builds on them.”

Tomlinson agrees. “He sincerely cares about each and every person, each and every student, regardless of their situation, or their attitude, or their views. He truly wants to inspire students and give them the best opportunity possible to achieve the things they want to in their lives.”

His colleagues recognize these same attributes in Ives. Professor Renée Tursi is an associate professor of English. She met Ives shortly after she started at Quinnipiac in 2004. She found him to be very warm and open-hearted, admiring his sense of a personal mission in the world.

“David is one of the people at Quinnipiac who has, single-handedly, changed more students’ lives than anyone else. Faculty, we all love to think that students are never the same after taking one of our courses. But David connects with these students.”

Tursi has traveled to Nicaragua with Ives for several service trips. The trips, she says, are so moving that had she gone on such a trip as a young student, “I might have chosen a different path.”

For Crystal Brian, professor of theater at Quinnipiac since 2001, the impact of Ives was twofold.

“I met him early on and it made a big difference to why I wanted to keep working here,” Brian said. “When he started talking about what he’s done throughout his life to try and take care of people it was so interesting to me.”

Their conversations were one of the motivators for Brian to change her whole idea about the theater program and led to the development of a changed B.A. at Quinnipiac – Theater and Community; something she believes no other college or university in the country has.

But Ives’ impact in Brian’s life goes beyond the professional. In 2013, she suffered a stroke and was in the hospital for more than a year. Ives came to see her on numerous occasions, talking to her when she couldn’t even hear him and sharing his experiences with rehabilitation.

This caring beyond the classroom and the workplace was repeated by Tomlinson. When she was sick last year, Ives went out of his way to make sure she had access to the medical care that she needed, which helped her to stay in school. He also went a step further, taking the time to reassure her parents in Kingston, Jamaica, that she was getting taken care of and contacting Tomlinson and her family over the summer to be sure that everything was going well.

Ives definitely understands what it takes to overcome health issues. Besides his bout with polio as a boy and Guillian-Barré in his forties, Ives, now in his sixties, has been diagnosed with Parkinson’s disease. It affects his speech at times and he has some tremors as well.

“I can cover up my disability for most people and that’s sometimes why I tell jokes to kind of distract from that,” Ives confesses. “But my hand still shakes a bit and we can’t tell if that’s from the polio, post-polio syndrome, Guillian-Barré syndrome which turned me into a quadriplegic for a time, or like right now with my Parkinson’s.”

And when he is working with people of different cultures, humor serves another purpose for Ives. “I break down barriers with that,” he adds. “It makes me more human.”

It may be a device at times, but Brian gives another reason for the jokes.

“He’s very funny.”

It seems to be an assessment everyone agrees with. “He has the most amazing sense of humor and buries us in puns,” Tursi notes. “He just must stay up late thinking these things up.”

But it is his genuine sincerity that makes the biggest impression.

“He doesn’t have a mean bone in his body, and he doesn’t lie,” Tursi reflected. “He never falters from his sense of purpose. He’s just completely committed and he wants to make the world a better place. It sounds trite, but it’s never come in a more sincere package.”

This warmth and genuine ease may best be reflected in a story from another student, Andrew Chestney, 19, who has traveled with Ives to Guatemala twice. When asked to share something that he felt summed up Ives as a person, Chestney related how during last year’s trip to work on a school for the disabled in the country, Ives and the students visited the homes of some of the students with disabilities in order to meet the people they had been working to try and help.

At one home, a young disabled girl was very excited by their visit. The girl’s family has recently had another child who was still a newborn. Chestney shared the image of Ives, sitting in this humble home, holding the infant in his arms while its sister was standing beside him, hanging off every word. Ives spoke jokingly with the family trying in jest to convince them to name their new child David.

“That,” Chestney said, “is David. He cares about everyone and he doesn’t treat them different. He’s not making them feel like he’s sorry for them, he’s just doing what he can to help.”

The need to help others is the most important thing to Ives. “I would hope that you would do things for altruistic reasons,” he explains. “But if not, do it because helping others is good for you personally and also for your own country.”

As for Ives, he takes his motivation from the small successes and believes they outnumber the frustrations of his job.

“I haven’t been able to bring peace to the world yet, but I’ve got little pockets of positive energy that we helped place around the world,” he said. “I’m probably going to have to be satisfied with that.”