Local disability activists lead Abilities Expo’s community outreach efforts through ambassador program
Abilities Expo has appointed Ambassadors—members of the local community of people with disabilities and their families—to spearhead community outreach initiatives. These individuals will meet face-to-face with rehab institutions, independent living centers, local manufacturers, service providers and local associations to generate excitement and increase attendance at each event.
Meet the impressive individuals who have chosen to represent Abilities Expo to the Community:
It was at the University of Houston-Downtown that Ana Calvo became the president of the student organization for people with disabilities and, through this role, that she discovered her love for advocating for the rights of others with disabilities.
Ana received her Bachelors in Arts of Social Science with concentrations in Psychology and Sociology and a Minor in Political Science in 2002. She went on to get her Masters in Social Work from the University of Houston College Of Social Work in 2007.
Over the last decade, she has been the subject of much media attention. When she received her undergraduate degree, Ana was featured in the Texas Magazine for her accomplishments. In addition, she appeared in the Houston Chronicle in 2002, has done numerous television appearances locally—including the Patricia Gras PBS show and Telemundo with Marcelo Marini—and was recently featured in HTexas Magazine.
Ana currently works at the Houston Community College Vocational Advancement and Social Skill Training (V.A.S.T.) Department as director of transition services where she prepares young adults with cognitive and physical disabilities to lead a healthy, productive and independent life. She is very active in the community and also serves as Chair for the City of Houston’s Commission for People with Disabilities.
In May 2008, Ana was awarded the Dorothy Caram Commitment to Leadership Award from the United Way Foundation. At the Ms. Wheelchair America pageant in August, she received the Nicki Ard Award for her advocacy accomplishments. Recently, Ana was also recognized as one of the 100 Houston Latinas Women in Leadership.
As Ms. Wheelchair Texas 2009, Ana promoted her platform of helping the youth to embrace their disabilities and achieve their dreams through education, employment and community involvement and will continue to be an advocate for people with disabilities.
A native Houstonian, this former Ms. Wheelchair America (2009) and Ms. Wheelchair Texas (2008), graduated Summa cum Laude from the University of Houston and earned her Master's degree in Health Promotion from the University of Texas School of Public Health. Born with spina bifida, Michelle has used a wheelchair since the 6th grade, but those who know her don't think of her as "disabled."
With her background in health research, Michelle emphasizes the importance for everyone to make their own health a priority. She reminds us that those of us who have physical limitations can still be healthy and active. She herself stays active with daily exercise at her gym, and through recreational activities such as snow skiing, wheelchair sports, kayaking and Taekwondo.
Through her volunteer work, Michelle is an active advocate for all people who have disabilities, not just those who use wheelchairs like herself. From 2003 through 2007, Michelle served as a commissioner on the Houston Commission on Disabilities before being appointed that committee’s chair. She also served on two other city commissions and coordinated efforts to better serve Houstonians with disabilities. Michelle is also the winner of the prestigious Jefferson's Award in recognition of her volunteer service which includes her involvement in Playgrounds Without Limits, Houston's first inclusive playground for all children.
In addition, Michelle previously served as Executive Director of the Houston's Mayor's Office for People with Disabilities and, in that capacity, led a number of successful disability initiatives. Thanks in part to her efforts, Houston was honored by the National Organization on Disability as the recipient of the 2007 Accessible America Award. Michelle currently works at a major cancer center and continues to volunteer as a disability advocate on collaborative initiatives. She also recently joined the Colours Wheelchairs team, a manufacturer of innovative and stylish wheelchairs.
Michelle’s philosophy is to never refuse a true adventure. In her spare time, she races her MINI Cooper in autocross competitions, and has even taken first place in her class and "Driver of the Year."
Olga L. Guerra
My name is Olga L. Guerra and I am a parent of an 11-year-old child who has cerebral palsy. I am a very involved parent and have been advocating for Araceli since she was diagnosed at the age of six months.
Araceli was born “normal,” but as she grew she was not meeting developmental milestones. Her pediatrician suggested we see a neurologist, so we did. Dr. Bohan diagnosed Araceli with microcephaly, but he explained that he was going to label her with CP so she could access more resources. This was Greek to me but I agreed. Little did I know that having the CP label was a good thing. As she grew, she was also diagnosed with mental retardation, speech impairment, an orthopedic impairment and a physical impairment.
As a first-time mom, it was very difficult for me to be told that the child I thought I was going to have, I was no longer going to have. I felt all the emotions that we all go through when there is a great sense of loss. But, I had to pick up the pieces and move forward because my daughter needed her mommy and, gosh darn it, she was going to have her mommy!
Thus my quest began to ensure that she would receive any and all services she needed to be successful. This also meant making sure she had devices and equipment that would assist her in being the best that she can be.
I did not think Araceli would ever walk but she had other ideas. A few years ago, she just got up and walked from one room to another. This, of course, comes because of therapy, a gait trainer, leg braces and endless doctor appointments. Araceli is non-verbal, but she does have lots of communication so I was able to get her a DynaVax MightyMo through the Specialized Telecommunications Assistance Program (STAP) in Texas. This is an augmentative communication device which allows Araceli to convey her desires. For example, when Araceli wants French fries, she can press the corresponding picture and it says, “French fries.”
She has a Tandem trike from Freedom Concepts thanks to The Heart of Variety organization. She has gone to Disney World courtesy of Make a Wish. I could go on and on but, bottom line, there are many resources, services and equipment that will help our children with challenges get that much closer to being “normal.” I tell parents all the time that all they have to do is ask. The worst thing that could happen is that the answer will be “no” and you are no worse off than when you started. What if the answer is “yes?”
I believe in allowing all children with disabilities to be the decision makers as to what they can or can‘t do. Granted, Araceli may not become a rocket scientist, but who I am I to put any limitations on her abilities?
Part of my job as her mother is to ensure that ALL doors will always be open for her. Araceli will be the only one who will decide if she can or can’t do anything.
Karen Kain—a parent of a medically fragile, vaccine-injured child named Lorrin for fifteen years—teaches parents how to enjoy their children no matter their abilities. She shares how she bridged the gap from special needs to mainstream experiences in all arenas of life: best friends, slumber parties, concerts, camping, beauty pageants, Girl Scouts, school dances, musicals and endless travels.
Karen is committed to helping children who are living a unique life experience by supporting their parents. In 1994, Lorrin was severely vaccine injured and at that time Karen’s world fell apart. Life as she knew it was put “on hold” as she tried everything that she could to “heal” Lorrin and give her the best life possible.
Karen was forced to overcome massive rejection and isolation as she hurdled obstacles and adapted her life to find success as a parent of a unique child. What Karen did not expect on this journey was that she herself would learn, grow and even heal from her experiences. It turned out that Lorrin was always the teacher. She taught Karen that life is full of magic, how to love herself, not to pass judgment, to be present in the moment whether it be at the hospital or Disneyland, beauty comes from within, and that we are all one and each soul is important no matter their ability. Lorrin was totally comfortable with who she was, even though she was cortically blind, nonverbal and a quadriplegic who lived with uncontrolled seizures for her entire life.
When Lorrin was 3, Karen made a pivotal choice to embrace Lorrin’s uniqueness and enjoy all areas of life, living without rules and boundaries. Karen overcame life’s massive roadblocks as she raised Lorrin. Together they held their heads high as they paved the way to giving all parents permission to explore and enjoy life. Karen found that the solution to winning in this life of parenting a unique child started with being committed to having a great attitude and perspective regardless of their situation.
Through her keynotes sessions and workshops, Karen shares the principals that made her parenting experience a success. Her message is simple:
“It is my mission to share our life story in hopes it will support other children and their families who are living a unique life experience. It is my goal to raise awareness of the power and importance of all unique souls. I believe that Lorrin was here to pave the way to a grander attitude of love and acceptance for all. It is my honor as her parent to help spread her life’s message of love and forgiveness.”
Learn more about Karen at www.lorrinsworld.com.