Lena Armstrong-Strober is the founder and creator of The Down Syndrome Office and Resource Center (DSORC) and a longtime advocate committed to creating more inclusive, informed, and connected communities for individuals with Down syndrome and their families throughout New Mexico.
Lena’s advocacy is deeply rooted in both her personal and professional life. She is the proud mother of two daughters, Aleeya and Zoelle. Aleeya, who has Down syndrome, serves as a New Mexico Ambassador for the National Down Syndrome Society (NDSS). Together, Lena and Aleeya have used their voices to advocate for greater inclusion, access, opportunity, and
representation for people with Down syndrome.
Lena previously served on the Board of Directors for the Rio Grande Down Syndrome Network (RGDSN), where she created and chaired the organization’s Advocacy Committee. Through this work, she helped strengthen relationships with policymakers, community leaders,
families, and disability organizations while creating opportunities for individuals and families to become more engaged in advocacy.
Her commitment to disability advocacy extends across New Mexico. Lena serves on the board of New Mexico Allies for Advocacy and works for The Arc of New Mexico as Outreach Coordinator for the Gonzales Trust Fund, connecting individuals with Down syndrome, families, and organizations with resources and opportunities available through the fund.
A graduate of Partners in Policymaking, Lena continued her leadership development through the Leadership Education in Neurodevelopmental and Other Related Disabilities (LEND) program, graduating in May 2026. She now continues her work as a LEND Fellow. She has also completed specialized training in inclusive practices through Illume Learning,
strengthening her ability to advocate for environments where people of all abilities are welcomed, valued, and given meaningful opportunities to participate.
Lena is also a public speaker who brings together the perspectives of a mother, advocate, community leader, and lifelong performer. A member of SAG-AFTRA and Actors’ Equity Association, her background in performance has helped shape her approach to public speaking, storytelling, and advocacy—using authentic stories and lived experience to inspire others to find their voices and take action.
Outside of her disability advocacy work, Lena is deeply involved in New Mexico’s festival and event community. She is the co-producer of the Southwest Chocolate & Coffee Festival and has served as Box Office Manager for wine and lavender festivals, bringing extensive experience in community engagement, event production, outreach, and relationship building.
At the heart of Lena’s work is a belief that meaningful change happens when families, self-advocates, organizations, professionals, and communities work together. She created DSORC to help build those connections and to ensure that individuals with Down syndrome and
their families have greater access to information, resources, advocacy, leadership opportunities, and community.
For Lena, advocacy is more than speaking up—it is about creating spaces where people belong, developing new leaders, opening doors, and building communities in which individuals with Down syndrome are recognized for their abilities, their voices, and their right to live full and meaningful lives.
Hollye has been an occupational therapist for over 25 years.
She loves working with individuals faced with challenges and supporting
their growth and development. She is passionate about equity and opportunity
for all people, focusing on inclusion in schools and community settings.
Hollye has built and run her own therapy clinic, as well as a variety of programs for
community agencies. She hosted the Education Rx Podcast for 3 years.
Hollye has sat on the board of directors for Rio Grande Down Syndrome Network and
participated in the planning and execution of large-scale events to support members and the
community. Hollye holds a master’s degree in Instructional Design and Technology, focusing on how individuals learn and retain knowledge, as well as technology that supports access to all.
Board Member
Jack Fanburg is a writer, producer, filmmaker, and community advocate who brings a diverse background in youth development, creative project management, communications, and relationship-building to the Down Syndrome Office and Resource Center (DSORC).
Jack’s experience includes working as a Behavioral Interventionist in a kindergarten classroom, where he supported children with a range of behavioral, social, and educational needs. He has also worked with the Boys & Girls Club, helping young people build confidence, develop independence, and thrive in supportive environments. These experiences strengthened his commitment to inclusion, individualized support, and ensuring every child has the opportunity to succeed.
As a writer, producer, and filmmaker, Jack understands the power of storytelling to raise awareness, inspire action, and bring communities together. He brings valuable skills in communication, collaboration, and project development, along with a strong professional network that can help DSORC expand its outreach, partnerships, and fundraising efforts.
Jack is passionate about creating a more inclusive society where individuals with Down syndrome have access to the resources, opportunities, and respect they deserve. As a DSORC Board member, he is committed to listening, learning, and using his creativity, experience, and connections to help advance the organization’s mission and make a meaningful difference in the lives of individuals and families.
I am a senior undergraduate at UNM with a double major in Speech and Hearing Sciences and Psychology. I work in a research lab that specializes in working with patients on stroke Aphasia recovery, and I also work as an assistant teacher for a children’s choir AGC. I have previously worked for a crisis line and have over 44hrs of crisis intervention training.
My future goal is to work with individuals who have neurological disorders in terms of treatment and recovery but also help advocate for these individuals to receive the same amount of support and access others receive as well.
Jessica McArthur is a dedicated disability advocate whose work has been shaped by personal experience, community leadership, and, most profoundly, her sister, Cari, who has Down syndrome. Inspired by Cari and their family’s journey, Jessica advocates for the rights and inclusion of people with Down syndrome and other intellectual and developmental disabilities. Her experiences have also shaped her understanding of the importance of inclusion, accessible services, strong communities, and responsive public policy.
Jessica serves as an Ambassador for the National Down Syndrome Society, and is a member of Down Syndrome International, National Down Syndrome Congress and the Global Down Syndrome Foundation. She is also an advocate for the Auburn University BraveHeart Center for Place and Purpose. Jessica participates annually in World Down Syndrome Day at the United Nations NYC, hosted by Down Syndrome International, joining advocates from around the world in advancing the rights, inclusion, and visibility of people with Down syndrome.
Jessica is the founder of Project Cari, an emerging initiative inspired by and named for her sister. Through creative projects, partnerships, and collaborative efforts, Project Cari will raise awareness, foster purpose, and give back to individuals and organizations within the disability community.
As a LEND Fellow at the University of New Mexico, Jessica continues to strengthen her leadership and deepen her understanding of interdisciplinary approaches that improve outcomes for individuals with developmental disabilities and their families.
As a board member of the Down Syndrome Office and Resource Center (DSORC), Jessica is committed to helping build a resource that empowers individuals with Down syndrome and their families through its mission .
Jessica brings empathy, persistence, and a collaborative spirit to everything she does. At the heart of her work is the belief that every individual deserves to be valued, supported, and given the opportunity to thrive.
Rachelle Renteria was born in New Mexico. She holds a Masters in Special Education from the
University of New Mexico, and a Bachelor’s in Social Work from New Mexico Highlands
University. In her twenty five years as a New Mexican educator, Rachelle Renteria has been
privileged to work with students, their parents and teachers and administrators in a variety of
Special Education Pre-K/K classrooms as a level 3 licensed teacher. She has worked as an
educational assistant, classroom teacher, and a district itinerant special education preschool
teacher. Rachelle completed her UNM LEND (Leadership in Education in Neurodevelopment
and Related Disabilities) certification in May 2026.
Currently, Rachelle volunteers with the New Mexico Make-A-Wish Organization Rachelle is
willing to collaborate, and communicate with fellow stakeholders to maintain the vision and
integrity of New Mexico’s First Down Syndrome Resource Center.
Rachelle’s work is rooted in one of her favorite quotes, “Be the Change You Wish To See In the
World.”
Born and raised in Las Cruces, New Mexico, Michelle Roybal is the proud owner of
Magnets-n-More by Michelle, where she creates fun and inspiring magnets, pins,
stickers, and more using her graphic design skills.
Michelle has always loved being creative and active. She began Kindermusik at age
2, danced with Verdi Academy of Dance from ages 10 to 21, and performed in ballet,
modern dance, and musical theater. Her passion for singing and dancing continues
today.
After graduating high school in 2018, Michelle helped inspire the creation of the
Career and Life Skills Academy at Doña Ana Community College, providing
educational and career opportunities for people with different abilities. She is also a
certified Improvaneer graduate, teaching personal expression through improv.
Today, Michelle stays active in her community. She volunteers with the Community
Foundation of Southern New Mexico, serves as the Event Planning Officer for Best
Buddies NMSU, and participates in Special Olympics New Mexico, where she
enjoys golf, cornhole, and bocce ball. She is also involved with the RGDSN of New
Mexico and continues singing and dancing with a private instructor.
Michelle is creative, determined, talented, and passionate. Through Magnets-n-More
and her daily life, she loves meeting new people, making friends, spreading
awareness, and most importantly, celebrating people of all abilities!
I am a proud native New Mexican, born and raised in Albuquerque. Throughout my life, I have called Santa Fe, Pecos, Hobbs, and Las Cruces home, giving me the opportunity to experience the many unique communities and lifestyles that make New Mexico special.
I am a retired middle school educator and coach with 27 years of experience. Although I retired from the classroom, teaching never really ended. Today, my most rewarding and gratifying teaching role continues through my daughter. She has learned multiple technology skills and, although she is very articulate, she is also fairly fluent in sign language.
Together, my daughter and I helped inspire the creation of the Career and Life Skills Academy at Doña Ana Community College, which provides educational and career opportunities for people with different abilities.
We continue to give back to our community by volunteering with the Community Foundation of Southern New Mexico and participating in Best Buddies and Special Olympics New Mexico, where I serve as a Unified Partner. We are also involved with the Rio Grande Down Syndrome Network (RGDSN) and participate in activities whenever possible.
Through education, advocacy, volunteering, and our everyday lives, my daughter and I are passionate about creating opportunities, building inclusion, and celebrating the abilities of every individual.
Co-Founder & Board Member
Dean Strober brings more than 30 years of experience in business management, nonprofit leadership, community engagement, marketing, and large-scale event production to the Down Syndrome Office and Resource Center (DSORC).
As the founder of Blue River Productions, Dean has created and produced some of New Mexico’s largest community events, including the Southwest Chocolate & Coffee Fest. His professional background also includes Broadway theater management and serving as Director of Events for the New Mexico Wine Association. Throughout his career, he has focused on building partnerships, supporting small businesses, and bringing people and communities together.
Dean’s commitment to disability advocacy is deeply personal. As the father of Aleeya, his daughter with Down syndrome, he has experienced firsthand both the joys and challenges of navigating education, healthcare, and community resources. Together with his wife, Lena Armstrong-Strober, he helped establish DSORC to make information, support, and opportunities more accessible to individuals with Down syndrome and their families.
Dean brings his experience in organizational development, communications, fundraising, and community outreach to DSORC, helping build a sustainable organization dedicated to empowering families, advancing inclusion, and creating meaningful opportunities for individuals with Down syndrome.
Lena Armstrong-Strober is the founder and creator of The Down Syndrome Office and Resource Center (DSORC) and a longtime advocate committed to creating more inclusive, informed, and connected communities for individuals with Down syndrome and their families throughout New Mexico.
Lena’s advocacy is deeply rooted in both her personal and professional life. She is the proud mother of two daughters, Aleeya and Zoelle. Aleeya, who has Down syndrome, serves as a New Mexico Ambassador for the National Down Syndrome Society (NDSS). Together, Lena and Aleeya have used their voices to advocate for greater inclusion, access, opportunity, and
representation for people with Down syndrome.
Lena previously served on the Board of Directors for the Rio Grande Down Syndrome Network (RGDSN), where she created and chaired the organization’s Advocacy Committee. Through this work, she helped strengthen relationships with policymakers, community leaders,
families, and disability organizations while creating opportunities for individuals and families to become more engaged in advocacy.
Her commitment to disability advocacy extends across New Mexico. Lena serves on the board of New Mexico Allies for Advocacy and works for The Arc of New Mexico as Outreach Coordinator for the Gonzales Trust Fund, connecting individuals with Down syndrome, families, and organizations with resources and opportunities available through the fund.
A graduate of Partners in Policymaking, Lena continued her leadership development through the Leadership Education in Neurodevelopmental and Other Related Disabilities (LEND) program, graduating in May 2026. She now continues her work as a LEND Fellow. She has also completed specialized training in inclusive practices through Illume Learning,
strengthening her ability to advocate for environments where people of all abilities are welcomed, valued, and given meaningful opportunities to participate.
Lena is also a public speaker who brings together the perspectives of a mother, advocate, community leader, and lifelong performer. A member of SAG-AFTRA and Actors’ Equity Association, her background in performance has helped shape her approach to public speaking, storytelling, and advocacy—using authentic stories and lived experience to inspire others to find their voices and take action.
Outside of her disability advocacy work, Lena is deeply involved in New Mexico’s festival and event community. She is the co-producer of the Southwest Chocolate & Coffee Festival and has served as Box Office Manager for wine and lavender festivals, bringing extensive experience in community engagement, event production, outreach, and relationship building.
At the heart of Lena’s work is a belief that meaningful change happens when families, self-advocates, organizations, professionals, and communities work together. She created DSORC to help build those connections and to ensure that individuals with Down syndrome and
their families have greater access to information, resources, advocacy, leadership opportunities, and community.
For Lena, advocacy is more than speaking up—it is about creating spaces where people belong, developing new leaders, opening doors, and building communities in which individuals with Down syndrome are recognized for their abilities, their voices, and their right to live full and meaningful lives.
Hollye has been an occupational therapist for over 25 years.
She loves working with individuals faced with challenges and supporting
their growth and development. She is passionate about equity and opportunity
for all people, focusing on inclusion in schools and community settings.
Hollye has built and run her own therapy clinic, as well as a variety of programs for
community agencies. She hosted the Education Rx Podcast for 3 years.
Hollye has sat on the board of directors for Rio Grande Down Syndrome Network and
participated in the planning and execution of large-scale events to support members and the
community. Hollye holds a master’s degree in Instructional Design and Technology, focusing on how individuals learn and retain knowledge, as well as technology that supports access to all.
Jack Fanburg is a writer, producer, filmmaker, and community-minded professional with experience working with children, supporting youth development, managing creative projects, and building relationships across a diverse professional network. He brings a combination of direct experience with young people, strong communication and organizational skills, and a genuine commitment to creating inclusive opportunities for individuals and families.
Jack’s experience as a Behavioral Interventionist in a kindergarten classroom gave him firsthand experience supporting young children with different behavioral, social, and educational needs. Working directly with students taught him the importance of patience, individualized support, positive reinforcement, and creating an environment where every child feels valued and capable of succeeding. It also gave him a deeper understanding of how early support and strong relationships can influence a child’s development.
Jack has also worked with the Boys & Girls Club, where he supported young people in a community-based setting. This experience reinforced his belief in the importance of mentorship, positive role models, safe environments, and providing children with opportunities to develop confidence and independence.
Professionally, Jack has built a career as a writer, producer and filmmaker, developing projects from initial concepts through production and completion. While his creative background is not the sole reason he would be an effective board member, it provides several skills that could directly benefit DSORC. His experience communicating ideas, managing complex projects, collaborating with diverse teams, and developing stories for audiences could help the organization strengthen its public outreach and communicate its mission in compelling and accessible ways.
Jack also understands the power of storytelling in building awareness and inspiring people to become involved in a cause. He could help DSORC develop compelling narratives around the experiences, achievements, and contributions of individuals with Down syndrome while ensuring those stories are presented with dignity and authenticity. These communication skills could be particularly valuable as DSORC continues building programs, expanding its resources, and reaching individuals with Down syndrome, families, educators, employers, healthcare providers, and the broader community.
Another significant asset Jack would bring to the Board is his strong network of potential donors and community supporters. Through his professional and personal relationships, he has connections with individuals who may have an interest in supporting DSORC’s mission. Jack would be eager to leverage those relationships responsibly by introducing potential supporters to the organization, helping cultivate donor relationships, and identifying opportunities to expand DSORC’s fundraising capacity.
Jack is interested in serving on the Board because he believes strongly in creating communities where individuals with Down syndrome have the resources, support, opportunities, and respect necessary to live fulfilling lives. DSORC’s commitment to equitable access to education, healthcare, housing, meaningful employment, and other resources strongly aligns with his belief that every individual deserves the opportunity to reach their full potential.
As a Board member, Jack would bring direct experience working with children, an understanding of behavioral and developmental support, strong communication and relationship-building skills, creative problem-solving abilities and access to a network of potential donors. He would also bring the perspective of someone who understands how to turn an idea into an organized, public-facing initiative and how to communicate its value to different audiences.
Most importantly, Jack would approach board service with a willingness to listen and learn from individuals with Down syndrome, their families, educators, advocates, and other members of the community. He sees the opportunity to serve on the Board not simply as a professional opportunity, but as a chance to contribute his skills, relationships, and experience toward building a stronger organization and expanding opportunities for the people DSORC serves.
I am a senior undergraduate at UNM with a double major in Speech and Hearing Sciences and Psychology. I work in a research lab that specializes in working with patients on stroke Aphasia recovery, and I also work as an assistant teacher for a children’s choir AGC. I have previously worked for a crisis line and have over 44hrs of crisis intervention training.
My future goal is to work with individuals who have neurological disorders in terms of treatment and recovery but also help advocate for these individuals to receive the same amount of support and access others receive as well.
Jessica McArthur is a dedicated disability advocate whose work has been shaped by personal experience, community leadership, and, most profoundly, her sister, Cari, who has Down syndrome. Inspired by Cari and their family’s journey, Jessica advocates for the rights and inclusion of people with Down syndrome and other intellectual and developmental disabilities. Her experiences have also shaped her understanding of the importance of inclusion, accessible services, strong communities, and responsive public policy.
Jessica serves as an Ambassador for the National Down Syndrome Society, and is a member of Down Syndrome International, National Down Syndrome Congress and the Global Down Syndrome Foundation. She is also an advocate for the Auburn University BraveHeart Center for Place and Purpose. Jessica participates annually in World Down Syndrome Day at the United Nations NYC, hosted by Down Syndrome International, joining advocates from around the world in advancing the rights, inclusion, and visibility of people with Down syndrome.
Jessica is the founder of Project Cari, an emerging initiative inspired by and named for her sister. Through creative projects, partnerships, and collaborative efforts, Project Cari will raise awareness, foster purpose, and give back to individuals and organizations within the disability community.
As a LEND Fellow at the University of New Mexico, Jessica continues to strengthen her leadership and deepen her understanding of interdisciplinary approaches that improve outcomes for individuals with developmental disabilities and their families.
As a board member of the Down Syndrome Office and Resource Center (DSORC), Jessica is committed to helping build a resource that empowers individuals with Down syndrome and their families through its mission .
Jessica brings empathy, persistence, and a collaborative spirit to everything she does. At the heart of her work is the belief that every individual deserves to be valued, supported, and given the opportunity to thrive.
Rachelle Renteria was born in New Mexico. She holds a Masters in Special Education from the
University of New Mexico, and a Bachelor’s in Social Work from New Mexico Highlands
University. In her twenty five years as a New Mexican educator, Rachelle Renteria has been
privileged to work with students, their parents and teachers and administrators in a variety of
Special Education Pre-K/K classrooms as a level 3 licensed teacher. She has worked as an
educational assistant, classroom teacher, and a district itinerant special education preschool
teacher. Rachelle completed her UNM LEND (Leadership in Education in Neurodevelopment
and Related Disabilities) certification in May 2026.
Currently, Rachelle volunteers with the New Mexico Make-A-Wish Organization Rachelle is
willing to collaborate, and communicate with fellow stakeholders to maintain the vision and
integrity of New Mexico’s First Down Syndrome Resource Center.
Rachelle’s work is rooted in one of her favorite quotes, “Be the Change You Wish To See In the
World.”
Down Syndrome Office & Resource Center
Resources, support, and advocacy for individuals with Down syndrome and their families.