Magic Valley Adults in Motion Society

Magic Valley Adults in Motion Society This is a support resource for adults with disabilities and their caregivers to promote life skills, social interaction, and community involvement.

The month of April is Autism Awareness Month, and April 2nd is World Autism Awareness Day. In honor of this month we are...
04/02/2026

The month of April is Autism Awareness Month, and April 2nd is World Autism Awareness Day. In honor of this month we are gong to “light it up blue” and ask all of our friends to do the same. Please help bring awareness and acceptance to children and families with loved ones on the spectrum. We need and appreciate our support!

03/29/2026

In 1915, a princess was born with Down syndrome into one of Europe’s most powerful families.

The expected response was immediate and brutal: hide her. Institutionalize her. Erase her from photographs, from history, from memory.

Instead, her family made a different choice.

A choice that would one day save her life.

On April 7, 1915, Princess Alexandrine Irene of Prussia entered the world. Her grandfather was Kaiser Wilhelm II, ruler of the German Empire. Her father was Crown Prince Wilhelm, next in line to the throne. Within weeks, her parents realized their newborn daughter had Down syndrome.

In that era, the script for aristocratic families was clear. Eugenics was rising. Disabled children were labeled “unfit,” “burdens,” “defective.” Many royal and noble families quietly removed such children from public view, sending them to institutions where they were often forgotten. Society whispered that their very existence brought shame.

Alexandrine’s family refused to follow the script.

They called her “Adini.” They kept her at home. They included her in official family portraits that were distributed across Germany — a princess with Down syndrome standing visibly beside her brothers. Her mother wrote that Alexandrine was “the sunshine of our house.” In an age of shame and silence, this simple act of visibility was revolutionary.

Then the world collapsed around them.

In 1918, the German Empire fell. The throne vanished. The family lost their status, their wealth, their future. But they never lost their devotion to Alexandrine. From ages 17 to 19, she attended Europe’s first school for children with disabilities, the Trüpersche Sonderschule in Jena — a place where she could learn and grow.

But 1939 brought darkness unlike anything the world had seen.

The N**i regime launched Aktion T4 — a systematic program to murder disabled Germans. Doctors identified victims. Buses arrived at institutions. Gas chambers disguised as showers killed them efficiently, quietly. Between 1940 and 1945, over 200,000 disabled people were murdered.

Most victims came from institutions.

Alexandrine wasn’t in an institution. She lived privately with her family in Bavaria, protected by the love that had surrounded her since birth and, ironically, by the very visibility that had been so radical in 1915. While genocide consumed disabled people across Germany, she survived.

Her brother Wilhelm died fighting in France in 1940. The empire her grandfather built crumbled into fascism, then rubble. But Alexandrine endured, year after year.

For decades after the war, her brother Louis Ferdinand — head of a family without a throne — made the journey to visit his sister near Lake Starnberg. He came faithfully, year after year, until he was the only sibling left.

On October 2, 1980, Princess Alexandrine Irene died peacefully in Bavaria at age 65.

Pause and consider what that means.

In 1915, life expectancy for someone with Down syndrome was less than 10 years. Today it’s around 60. Born into a world that wasn’t ready for her, living through two world wars and a genocide targeting people exactly like her, Alexandrine outlived nearly every medical prediction of her time.

She was buried at Hohenzollern Castle beside her parents. The photographs still exist — a baby in christening clothes, a child among her brothers, a young woman in her confirmation dress. In every image, she is there. Present. Visible. Unmistakably part of the family.

Her family wasn’t perfect. Her father initially supported Hi**er before turning against him. They once ruled an empire built on conquest. But they made a choice that transcended their flaws and their era. When the world said hide her, they showed her. When society said she had no value, they said she was their sunshine.

Alexandrine didn’t change laws or lead movements. She lived quietly, loved deeply, visited faithfully. Her life wasn’t a grand political statement. It was something more powerful: proof that acceptance, offered without apology or condition, can sustain a person through 65 years in a world not built for her.

She was born a princess of an empire. She died something far more precious: a person with Down syndrome who lived her entire life visible, valued, and loved.

That choice her family made in 1915 — to simply love her openly — didn’t just define her life. It saved it.

03/14/2026

📅 Save the Date!

Join us April 18th for the 2nd Annual Walk-A-Thon supporting the Twin Falls Special Olympics Teams!

Bring your family and friends for a fun community walk while supporting our athletes and their fundraising campaign. Enjoy a hot dog and great company while helping make a difference.

Every step you take helps empower local athletes and supports the mission of Special Olympics Idaho—creating opportunities for individuals with intellectual disabilities through sports, inclusion, and community programs.

We hope to see you there!

03/13/2026
03/10/2026

As we move closer to World Down Syndrome Day on 21 March, we want to share why the way we describe Down syndrome is so important for building an inclusive world.

Down syndrome is a genetic condition that happens by chance at the moment of creation. It is not a disease or an illness. When we use medicalized language like "suffering from" or "afflicted by," we unintentionally suggest that the person is unwell or in a state of constant struggle.

The Facts:
💛A Genetic Reality: People with Down syndrome simply have an extra copy of the 21st chromosome—giving them 47 instead of 46. 🧬
💛 A Part of Identity: Having Down syndrome is just one part of who a person is.
💛 Empowering Language: By saying someone "has" Down syndrome, we acknowledge their genetic makeup without defining their entire life by a medical label.

Using accurate language helps dismantle the stigma that leads to loneliness and exclusion. When we stop seeing Down syndrome as a "disease" to be cured and start seeing it as a "condition" to be supported, we open the door to true belonging.

Let's stand by speaking with clarity and respect.

02/22/2026
02/21/2026

We are starting something new...Quarterly IEP 101 sessions—live on Zoom!

📅 Perfect for parents who are new to IEPs, need a refresher, or want to better understand their child’s supports.

💡 Learn how the IEP process works and get practical tips for collaborating effectively with your school team.

🗓️ Upcoming sessions:

November 13, 2025
January 8, 2026
April 9, 2026
August 13, 2026

⏰ 6:30–7:30 PM MT (5:30-6:30 PM PT)
🔗 Register here: https://www.tfaforms.com/5198846

(Flyer reads:

Quarterly IEP 101
2025 - 2026
Sessions Live on Zoom!

NOV 13 - IEP 101
6:30 PM – 7:30 PM MT
JAN 8 - IEP 101
6:30 PM – 7:30 PM MT
APR 9 - IEP 101
6:30 PM – 7:30 PM MT
AUG 13 - IEP 101
6:30 PM – 7:30 PM MT

Sessions are perfect for parents new to IEPs or those needing a refresher.
Learn how the IEP process works, understand your child’s supports, and get tips for effective collaboration with the school team.
Open to all parents and families of students with IEPs.
IDAHO PARENTS UNLIMITED INC.
Engage + Educate + Bridge + Lead
Register here:
https://www.tfaforms.com/5198846

02/17/2026

Talking about loneliness can be really hard, but we don't have to do it alone. On World Down Syndrome Day, we use the campaign to help us speak up! We wear our brightest, boldest, or even mismatched socks to say, "Listen up, the Down syndrome community has something to say!".
The Lots Of Socks campaign works best when everyone takes part. You can help us be heard and bring people together by:
💛Holding a 'Lots Of Socks' day: Ask your school or workplace to wear bold socks and make a donation.
💛 Starting a competition: Give a prize for the best socks or have a contest to design your own using our template.
💛 Getting creative: Color in sock sheets or turn your designs into sock bunting to decorate your space.
💛 Sharing a 'Lots Of Socks' selfie: Post a photo of your socks on social media with the hashtag to join the global conversation.
Every pair of socks helps us share our messages and build a world where we are .
Learn more about Lots Of Socks: https://www.worlddownsyndromeday.org/lots-of-socks-campaign

02/10/2026

A Single Global Voice
On World Down Syndrome Day, our community speaks up together. We create a single global voice to tell the world about our rights, our inclusion, and our well-being. It is a day to make sure the voices of people with Down syndrome are finally heard. This is important because many of us still feel left out and lonely. We want to change that. Will you join us?
Find out how you can get involved: https://www.worlddownsyndromeday.org/

10/16/2025

Parenting kids with disabilities is particularly overwhelming right now - let my book Overwhelmed & Grateful- help get you through: https://amzn.to/45fhRLp

🎃👻 The wait is over—tickets are on sale now for Building Hope with A Haunt! 👻🎃Join People for Pets MVHS, Inc. for a spoo...
10/05/2025

🎃👻 The wait is over—tickets are on sale now for Building Hope with A Haunt! 👻🎃

Join People for Pets MVHS, Inc. for a spooky-good night you won’t forget. Come dressed in your best costume and enjoy an evening of delicious finger foods, music from the incredible DJ V3ROS, fun prizes, and a lively costume contest!

This event kicks off our Capital Campaign to expand the Twin Falls Animal Shelter—because every pet deserves a safe, loving space. All proceeds go directly toward the expansion, helping us meet the growing needs of our community one wag and one purr at a time. 🐾

Bring your friends, bring your best costume, and most importantly, bring your love for animals. Together, let’s make this a night of haunting fun and hopeful beginnings! ✨

📌 Event Details
📅 Date: Saturday, October 25
🕕 Time: 6–10 PM
📍 Location: 360 Main Event Center
🎟️ Tickets: $25 in advance | $30 at the door (each includes a drink coupon)
🎶 Entertainment: DJ V3ROS, finger foods, prizes & costume contest

Address

Twin Falls, ID
83301

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Community Connection

As many young adults with disabilities age out of the public school system, they find their world to be smaller and more limited. Many of the adults, parents/guardians, caregivers, or other support sources find it difficult to make connections in the community to resources, activities, peers, and other important information. As one of those parents, I am creating this page so we will all have a location to share ideas, resources, up-coming events, and overall to build a supportive network as our adults with so many abilities move into this next chapter of their lives.