A Look Back at the First Quest Product Guide of 2026
By MDA Staff | Wednesday, May 27, 2026
The MDA Quest Media Product Guide is designed to help you find the products you need to live a more independent, stylish, fun, and all-around great life. All the products you see here were chosen by MDA Ambassadors, who shared exactly how each product helps them in their daily lives. Find something for yourself, or for someone else in your life who you want to get a thoughtful gift for.
With new guides uploaded throughout the year, we’ve created a space for you to be able to access past lists of our thoughtfully curated products and timeless recommendations, because we LOVE you and because we LOVE things that make your life just a little easier.
These items are recommended by MDA Ambassadors, but MDA does not receive any portion of the proceeds.
Meet our Ambassadors and their favorite products
MDA Ambassador Andy A.
Andy enjoys playing video games and writing in his free time. As a child, he attended MDA Summer Camp where he was able to connect with other kids living with a neuromuscular disease. He is passionate about sharing the positive impact MDA has on those living with a diagnosis and how funding research helps the neuromuscular disease community find new cures and treatments.
It gives me more independence to call people, set the perfect temperature, and control the lights in the house. Every day I’m finding more uses for it.
I have limited dexterity and regular utensils are difficult to use. Plastic utensils with long handles weigh less and have more reach.
I am unable to lift cups; extra-long straws are essential so that I can drink independently.
These shoes are easily adjustable, comfortable, and don’t squeeze my feet.
This sheet has slippery material on one side and bedsheet material on the other. It makes it easier for my parents or caregiver to reposition me in bed.
MDA Ambassador Rebecca G.
For Rebecca, being diagnosed with LGMD clarified years of uncertainty and fueled her passion for patient advocacy. She joined the Board of Directors for the LGMD Awareness Foundation in 2021. Rebecca is also a contributing writer and volunteer for other neuromuscular disease focused non-profits, including MDA. Inspired by her husband and two daughters she models resilience and persistence, ensuring that challenging times do not define her journey.
Dr. Scholl’s® Soothe & Revive Foot Mask
These single use, warming booties soothe muscle tension with essential oils and Epsom salt. It’s like getting a pedicure without having to leave your house.
These are the cutest option for compression socks! And they are so super soft and comfortable that I forget I’m wearing them.
Bracelet making has become my go-to hobby. It keeps my hands active, especially with the small beads, and I feel like my dexterity has improved because of it.
Need a pick-me-up? This beautifully scented body powder is perfect after physical therapy or just a long day. The cocoa butter in it makes your skin soft, too.
Med Massager Foot Massager Plus
This massager helps activate and enhance blood flow. As a wheelchair user, I’ve found this medical-grade massager vital for helping with my foot atrophy.
Hairbrush & Straightener Combo
This two-in-one product is a game-changer. It’s lightweight and combines both tasks, making hair styling much easier without having to hold multiple devices.
An adjustable wheelchair leg strap is a vital accessory for dignity and comfort. The Velcro strap keeps my legs together while providing stable, secure support.
For people with limited dexterity, magnetic clasps are an accessible alternative that make it easier to put on and take off jewelry independently.
MDA Ambassador Mike H.
Mike has many hobbies, including reading, watching movies and documentaries, music, astronomy, and collecting vintage skateboards. He is also a lifelong LA Dodgers fan. Mike volunteers with several organizations within the disability community, including MDA. He shares that it is truly rewarding to be able to give back and hopefully serve as an example of “the possible” to others within our community.
This is a small, collapsible male urinal that can be used for travel or on the go and is easily hidden in a personal bag.
These come in a variety of sizes and colors with stainless steel or lighter-weight plastic options. They open and close easily and have a built-in straw.
ROHO Inflatable Wheelchair Cushion
These provide better pressure relief and comfort than standard cushions. With a variety of sizes, consult with your wheelchair provider for appropriate size.
Adjustable Wrist & Ankle Weights
These are great if you can exercise with light weights. They weigh one pound each but can be adjusted all the way down to 1/4 of a pound.
To maintain flexibility or increase range of motion with low impact, these exercise balls come in a variety of sizes and both peanut and round shape.
This device helps increase range of motion and has a variety of supports to keep hands and arms in place. These are expensive but may be covered by insurance.
I like these because they provide a lot of flexibility, a good grip, and keep my hands warm. I use them for driving with my hand controls in the cold.
UA ColdGear Fitted Crew Shirts
These provide warmth without excessive bulk. They can be layered or worn alone. I order a size up for layering and easier dressing and undressing.
Telescopic Extendable Back Scratchers
For those with limited reach, these allow you to reach parts of your extremities and body. And the claw shape makes it useful to pull things toward me.
MDA Ambassador Elizabeth M.
Elizabeth loves hanging out with friends, going on family trips, and just being herself. She enjoys attending MDA Summer Camp; it is one of her favorite weeks of the year. She has learned how to adjust and make life accommodate her instead of the other way around. She found her voice and started speaking not just for herself, but also by talking to medical students and doctors about what it is like to live with a rare disease and how much they can learn from their patients. Someday, she wants to be a neuromuscular doctor so kids like her can get the right answers sooner.
Audiobooks (Audible/Libby/Kindle)
Audiobooks allow me to keep learning and enjoying books when I develop double vision and eye fatigue or muscle weakness. I never have to stop reading!
This flexible phone mount clamps to almost anything. I can use my phone hands-free when my arms are weak. I use it for homework, research, and to watch movies.
Suction Phone Grip / Case Mount
The suction grip lets me stick my phone to my laptop or mirror. It makes Zoom calls, school, and watching tutorials easier when my hands or arms are weak.
MDA Ambassador Jeff T.
Jeff T. lives with Oculopharyngeal muscular dystrophy (OPMD), a rare, adult-onset neuromuscular disease. He enjoyed spending much of his life active and outdoors, with a fondness for competitive mountain biking, before beginning to experience progressive muscle weakness. While OPMD is progressive, Jeff is comitted to adapting, advocating, and moving forward with resilience. Throughout his journey he has been empowered by the unwavering love and support of his wife, his family and friends, and the life they continue to cherish together.
Walgreens Flex & Go Folding Cane
These are lightweight, have great shock absorption, a large supportive base, and fold easily. They fit in a plane’s overhead bin or below the seat for travel.
Lightweight and comfortable with large and small pockets to hold daily essentials, including my iPad. Great for travel and the design accommodates my pacemaker.
This sleek, insulated vest has spacious pockets, is easily packable, and fits comfortably over a sweatshirt or jacket for extra warmth and storage on the go.
Tough, stretchy, and non-metallic, this easily adjustable belt with a contoured buckle is ideal for everyday use and travel.
MDA Ambassador Skye A.
Skye is passionate about raising awareness and advocating for accessibility. She loves cheering on the Carolina Hurricanes, creating art, partaking in new experiences, and spending time with her friends and family. Through sharing her experiences living with facioscapulohumeral muscular dystrophy (FSHD), she aims to empower others living with a neuromuscular disease and drive positive change in society.
This is one thing I use to help manage my body pain. The heat and vibrations work together to relieve tension, making me feel more comfortable.
This electric razor with multiple attachment options makes shaving easier and safer. The ergonomic handle provides control. It can be used on wet or dry skin.
This helps me reach high items, pick things up from the ground and low shelves, and pull objects closer to me. It’s a tool that has made daily tasks easier.
Smart Plugs and Smart Lightbulbs
Paired with Alexa, smart plugs and lightbulbs let me control lights and devices hands-free. They make daily tasks easier, safer, and more accessible at home.
Hanging my clothes up and getting them down in the closet has become a struggle, but this pole has made the task easier and less stressful.
I keep this at an accessible height and I don’t need to bend or balance like at a traditional oven. It makes meal preparation safer, easier, and more efficient.
This battery-operated mirror is portable and provides helpful lighting, making makeup application and general hygiene easier and more accessible.
This bra provides support and I don’t have to twist or reach behind to clasp. It makes getting dressed simpler, more comfortable, and more manageable.
Satin pajamas reduce friction, making it easier to move while in bed. I can reposition with less effort while still feeling comfortable and feminine.
MDA Ambassador Sara Z.
Sara is a wife and mother living with Charcot-Marie-Tooth (CMT) disease. Although having a disability presents its challenges, it didn’t stop her from going to college, having a successful career in social services, and raising her family. When she’s not advocating or spreading positivity, she enjoys cooking, gardening and adaptive yoga. As an MDA Ambassador, she hopes to bring awareness to the programs and services that MDA provides to the neuromuscular disease community.
This is my favorite possession. Large buttons make it easy to turn on/off and adjust settings. It’s soft and cozy, and the warmth soothes my muscles.
I love to cook and this peeler makes food prep so easy. The soft rubber handle makes it easy to hold, and I can use it without straining my hands.
My hands have trouble with switches; this is a great alternative to a standard lamp. This model also has an AC adapter outlet and phone charging outlets.
This Wi-Fi thermostat is a game changer. I can control my heat and AC settings on my phone from anywhere, whether I’m lying in bed or out of the house.
I use this kettle for tea every day. It’s lightweight, boils water quickly, and has a great handle for pouring.
This is a great solution if you are unsteady in the shower. With this belt, I stay safe and secure on my shower bench and don’t have to worry about falling.
MDA Ambassador Jessery P.
Jessery is a strong advocate for accessibility, pushing for more research and sharing her story so others feel seen and supported. She graduated with a degree in psychology and is working towards her master’s in elementary education. Teaching and advocating for students has become a big part of who she is. Jessery recently became a parent for the first time. She hopes to share her experience so that more people understand what pregnancy with a neuromuscular disease can look like.
UnbuckleMe Car Seat Buckle Release
This tool reduces the nine-pound force required for buckles, allowing me to unbuckle my baby independently and confidently without my hands hurting afterward.
It’s hard for me to sit on the floor next to the bath. This stand brings the tub to waist height, making baby bath time painless and possible to do alone.
I can easily grip the wider base of this bottle with my whole hand, which helps me feel more secure and confident when feeding my infant.
This car seat swivels 360 degrees. It eliminates the need to reach/twist, allowing parents with limited mobility to load and unload their children more easily.
Standard clippers require high precision and fine motor control. This electric file is easy to grip and safely trims tiny nails through vibration.
This ergonomic seat puts the baby’s weight on your hips, allowing you to support your child with much less arm and hand strength.
MDA Ambassador Micah T.
Micah is a bright, spirited 5-year-old who lives with LAMA2 muscular dystrophy. From the moment he wakes up in the morning, his curiosity and cheerful spirit light up every room. His heart is full of bravery, joy, and an unshakable love for life. Micah and his family believe in making the most of every day. With a gentle smile and a determined soul, he shows others that life with a neuromuscular disease is not defined by limitations, but by the love, hope, and resilience you carry in your heart. Through his journey with MDA, Micah wants to be a voice for kids who face similar challenges. He hopes his story can offer courage to other families – a reminder that even when the road is tough, you are never alone.
Height Adjustable Overbed Table
We use this table for daily activities, coloring and drawing, eating, and more. It can be used sitting or standing and is easy to maneuver.
Sit to Stand with Self Propulsion
Micah sits in this daily and stands in this daily and uses the controls independently. The self-propulsion system allows him to safely move around the house.
These shoes look good and are easy to put on and take off, especially with AFO and SMO type braces. We have multiple pairs!
This cooling, memory foam pillow is soft and great for sleeping and support/positioning on the couch. It increases comfort and prevents muscle tightness.
This positioning device is used daily when sitting. It provides postural support, conforms to individual posture, and alleviates pressure.
Next Steps and Useful Resources
- Browse the current Product Guide here!
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Disclaimer: No content on this site should ever be used as a substitute for direct medical advice from your doctor or other qualified clinician.
