Lea Menninger – That’s how she rolls

Which day or moment in your life do you particularly like to remember? And why?

Lea Menninger: I especially treasure the days when I could simply feel “normal.” I have always been supported, and everything was done to make little Lelly happy – thank you for that! It’s extremely important to me to try things out: ice skating, roller skating, skateboarding, climbing. That’s how I find out whether something works for me – or not.

What has been the biggest challenge in your life so far and how did you overcome it?

Lea Menninger: 

• Not slipping into depression
• The key questions I kept asking myself: Why? How? For what reason?
• Staying optimistic and not letting myself be dragged down
• The "battle with my family"

Which assistive devices are essential in your everyday life, and why?

Lea Menninger: In my daily life, I use crutches (GANYMED®), functional electrical stimulation (FES), and my car. For new or longer routes, my wheelchair is also essential – especially when I don’t know what to expect.

What do you wish for from society and those around you in how they interact with people with disabilities?

Lea Menninger: More education and genuine inclusion instead of pitying stares. I wish people wouldn’t look away or ignore us, but rather understand the value of genuine consideration. Instead of staring at their smartphones, sometimes all it takes is an open, attentive look.

It’s especially frustrating when non-disabled people misuse accessible parking spaces or toilets – and then argue about it. These facilities aren’t a convenience, they’re a necessity. Many forget how costly participation in everyday life can be for people with disabilities. We put in a lot of effort to be part of it.

Lately, I’m often asked what people should actually call us. The term "disability" apparently sounds negative. What does the community think?

Are there any particular issues relating to people with disabilities that are especially close to your heart?

Lea Menninger: It’s important to me that rare or unclear diagnoses receive more attention: instead of leaving people in uncertainty, we need more education, clear explanations, and genuine support. Chronic pain and the often underestimated dependency on pain medication should also be taken more seriously – I’ve experienced it myself.

Greater support for people with disabilities is urgently needed: we all have potential – in everyday life, in sports, and in our professions.

And please: leave accessible parking spaces, toilets, and changing rooms for the people who truly depend on them. Every step is a gift – don’t forget that.

Tell us something about yourself that might surprise us.

Lea Menninger: I had my pain point tattooed so that therapists immediately know where to start. And yes, I’m a bit of an organisation freak. With my condition, I learned early on how much planning everyday life requires.

Many of the pieces of furniture in my home I’ve restored myself. It may take me twice as long, but I value each one all the more.

In 2024, I earned my swimming badge and, in February 2025, joined para swimming. Since then, it’s become my little addiction: discipline, ambition, energy, and calm.

What does REHACARE mean to you?

Lea Menninger: REHACARE brings together people with and without disabilities. It’s a place to discover new things, exchange ideas – and sometimes simply laugh or cry together.

Is there anything else you’d like to share?

Lea Menninger: Be proud of everything you have, and of everything you can do and achieve! Enjoy every single day.