Homecare Beds, Surfaces, Lift Systems, Medical Supplies- We have it all!
RAMS provides high-quality and customizable solutions for mobility needs. We carry adjustable beds, full-motion homecare beds, bariatric beds, as well as advanced wound-therapy and micro-climate managing systems.
& Sleep Surfaces
& Home Supplies
Power Wheelchairs, Manual Wheelchairs and Mobility Scooters
We provide a wide variety of configurations suited to individual needs. Smarter drive controls, better seating systems that can memorize the way you want to sit, and Bluetooth integration for compatible devices are our capabilities and expertise. Our experts and technicians will evaluate your medical needs and custom configuration so you can get back out there.
Beds & Sleep Surfaces
Beds and Sleep surfaces that provide multiple positioning and transfer configurations.
There are many choices in bed types, each with their own benefits, and we work with our customers to find what works best. We provide adjustable beds, full-motion homecare beds, bariatric beds, as well as advanced wound-therapy and micro-climate managing systems from trusted brands like Span-America, Burke Bariatric, Accora, and Carilex.
A ceiling lift serves the same purpose as a roll-around patient lift, however, ceiling lifts use ceiling-mounted track which makes transfers easier in confined spaces and anywhere else a roll-around hoist may not work.
Ceiling lifts make transfers easier in confined spaces and anywhere else a roll-around hoist may not work. Hoist lifts can be cumbersome and labor-intensive that cause fatigue for both patient and caregiver. The power traverse systems use motorized wheels to move the patient along the track, and are controlled via attendant remote. Many feature a "return to charger" function which sends the lift motor back to its charging base at the push of a button.
Seating & Positioning
Alternating Pressure Cushions, Air Cushions, Gel Cushions, Back Supports and much more!
Seating and Positioning is very important for individuals limited in mobility in order to maintain postural support, balance and prevent and treat potential pressure sores. From alternating pressure cushions, air cushions, gel cushions and custom support, we provide trusted brands as well as services through our expert to make sure that your medical needs meet comfort and quality of sitting.
Medical & Home Supplies
Forget about driving to a medical supply store or pharmacy. We understand that it is inconvenient to those facing mobility challenges.
We stock a complete line of name-brand care products that you trust for sanitation, wound care, incontinence, hygiene, monitoring, and more! We offer free delivery both by our own delivery staff, or by postage where necessary
If you don't see what you're looking for on this page, please submit a request below or call our helpful supply representatives at 800-655-4920 to see if we have your product in stock.
Connect to our experts or submit a reorder so our team can get back to you within 24 hours!
Under Michigan’s new auto insurance law, everyone loses, except big auto insurance companies.
Rehab and Mobility Systems supports the action against the new auto insurance law. Our products and services have benefitted thousands of customers and significantly improved their lives. We continue to enable mobility services to many more in need. Unfortunately, this might not be possible under the new Michigan law.
The Coalition for Protecting No-Fault Auto provides deeper insights into the law and it's effect on:
Drivers who purchase policies with PIP caps who sustain catastrophic injuries will spend their benefits within a few weeks, if not sooner. Yet many of those drivers will require care for the rest of their lives. Meanwhile, any dollars saved through reduced PIP premiums will likely be offset by increases in liability premiums required under the new law.
Seniors on Medicare who opt out of injury protections will lose access to long-term care, residential treatment programs, case management services, vehicle modifications, and more.
PEDESTRIANS AND CYCLISTS
The new law caps at $250,000 the amount of care you will receive if you’re a pedestrian, cyclist, senior who no longer drives, children riding in uninsured vehicles, or anyone involved in a car accident who doesn’t have auto insurance.
The post-acute care industry, which provides rehabilitation services to victims after they leave the hospital, will be destroyed by the arbitrary fee schedule imposed by this law. It will force many care providers to close their doors and layoff thousands of employees, hurting Michigan’s economy.
The reduction in PIP premiums is based on the statewide average. So, if you live in an area with historically high rates like Detroit, the reduction you’ll see will be significantly less than residents in other areas.
The new law eliminates guaranteed lifetime coverage for motorcyclists involved in car crashes—instead, if they are in an accident, their level of care will depend on the level of coverage carried by the car driver who caused the accident – regardless of the level of PIP coverage they purchased under their own auto policy.
Michigan businesses renewing their fleet insurance are already experiencing significant increases in their premiums due to the legal exposure the PIP choice options create. In addition, healthcare insurance will likely increase as health insurers will need to shoulder the costs of auto accident injuries.
With fewer benefits available, more accident victims will be forced into medical bankruptcy and onto Medicaid, which is paid for by Michigan taxpayers.
The new law will limit reimbursements for family members who care for accident victims to 56 hours per week. Many of these victims require around-the-clock care, and family members often have to quit their jobs to care for them. Now they will be forced to hire outside agencies to care for their loved ones and allow strangers in their homes.
The night of my injury is a night I will not forget, and neither will my family or friends who experienced it with me. On August 31, 1984, I had a motorcycle accident that left me laying in an apple orchard with a broken back and a collapsed lung for 14 hours through the night, surviving a thunderstorm that brought hail and high winds. Amazingly, I was found by a friend in his helicopter the next morning. Later at the hospital, I learned I was paralyzed. The doctor explained that paralysis meant that I would never walk again, and that having sex and children were impossible. The doctor told us that because I wouldn't be able to take care of myself, my parents should be looking for a nursing home for me, that my life expectancy would be 45. I looked at my mom and dad and told them to bring my gun. Life as I knew it was over. I was 19.
But, my parents didn't accept that future for me. They had me air-lifted to the University of Michigan Hospital where I had back stabilization surgery and three and a half months of rehabilitation. And, I was assured that what was said to me before was not true. Still, at 19 I was holding on to what I had already heard: my life was over.
Being a paraplegic at 19 also meant that I had to learn quickly about my new life in a wheelchair in addition to the life as a young adult. Day-to-day routines were suddenly harder than I had imagined. I had to learn about a daily bowel program and had to re-learn basic hygiene routines that would keep me healthy long-term. Some of the typical things that able-bodied youth are challenged by, like dating and sex, were even more stressful for me, and a romantic life seemed out of reach.
I'm blessed that my family and friends were there, pulling me through that mindset. In addition to treating me like the person I always had been, they helped me to remain active in the things I had loved before, like snowmobiling, 4-wheeling, hunting, and canoeing. But no matter how hard they tried, I was still feeling alone in the wheelchair. I felt that as able-bodied people, they couldn't possibly understand what life was for me now.
Those first few years were difficult for sure. But then I met Lee, who I now see as my first mentor. Though Lee's situation is different than mine, he was the first person I met in a wheelchair, who could understand more of what I was going through. He introduced me to wheelchair sports like basketball and tennis. I met a host of individuals in wheelchairs, both athletes and non- athletes. He introduced me to peer mentoring by taking me with him while he volunteered at the local rehab hospital. He instilled in me the importance of giving back by mentoring and sharing my story and experiences with others. Through my interactions with others in wheelchairs, I finally felt understood. This gave me the much-needed confidence I didn't have when I was first injured.
However, the road was not always so smooth. I found myself masking my pain and insecurities with alcohol. I used it to gain the courage needed to meet people and try new things, to accept myself for who I am in a world that would never accept me in my wheelchair - or so I thought at the time. In 2010, I was introduced to a new group of peers: those who dealt with addiction. Through their stories and their commitment to sobriety, I was able to get sober. This process helped me to see more deeply how people can have many different kinds of problems, and again that I was not alone, and that my wheelchair did not define me. I learned the power in listening, and being open to sharing our own stories in the process of healing.
Over time, and with the help of my mentors, my my friends, and my family, it seemed as though the limits I had invented in my mind had melted away.
Now, I lead a healthy, active, and independent life. I travel across the country to compete in handcycle racing. I ski in the mountains in Colorado and I water ski. I captain my boat all over Lake Michigan. I drive four-wheelers. I hunt deer. I am a happy, healthy 55-year old, outliving the doctor's prediction by 10 years. I have a 20-year old son, and a happy love life. In short, I have proven that first doctor wrong, and I can do whatever I set my mind to.
But most importantly, I have been blessed to be a mentor by sharing my experiences - both failures and success - as a lifelong athlete and outdoors enthusiast. For over 30 years, I have been involved in various programs to help others learn to be physically active and involved in sports such as the Junior Wheelchair sports camps, and the Mary Free Bed Company handcycling team. I have helped the others learn to ski and try many other sports for the first time, or to re-learn a sport played before their injury. I also advocate for the larger community by serving on various boards of of organizations for people with disabilities.
Through the Perspectives program, I see great potential we have as a collective of people with similar challenges, but who also have stories of empowerment and hope. My goal is to bring groups of people together to share these stories, to learn from each other about how to adjust to even the simplest of things, to find solutions to things we first see as complicated, and to develop self-confidence and strength, as I was taught from my earliest mentors. - Steve Chapman
On June 16th, 2003, my life was instantly changed forever. I was involved in a motorcycle accident that left me paralyzed from the chest down when a vehicle pulled in front of me less than a mile from my home and I was thrown through the car's windshield at 55mph. Suddenly the things I took for granted instantly became crystal clear. The value I placed on my surroundings, my priorities, the quality of relationships, what kind of person I was. If this was to be my end, what image and memory was I leaving behind for people to remember me by?
What was previously familiar and safe seemingly overnight turned into dark unfamiliar spaces. Friends, family, even the place I called home all looked different and inaccessible. Simple things like pouring a glass of water or walking down to get the mail, taking out the trash suddenly were TASKS. Things like balance, security, coordination, going to the bathroom - all once second nature - had to be relearned or were completely lost altogether. Instead of the normal college curriculum I was used to, foreign terms like catheters, bowel program, autonomic dysreflexia, were now taught in classroom-like settings, but in hospitals.
After a catastrophic event there is no folder or resource guide handed out to provide patients with perfect referrals, good reputable companies, or groundbreaking new advancements with medical procedures. Suddenly, things like selecting wheelchair seating, transfer techniques, and even things like re-learning how to get yourself dressed became critical. For many of us, we learn from making our own mistakes, through trial and tribulation.
In the years following my accident, I learned the importance of involving myself in my own plan of care. I learned the importance of being my own advocate and learning from my mistakes... and there were a lot of them. I've learned how to take seemingly impossible tasks and create shortcuts to make them not only possible but manageable. How to live more "capable" than I ever thought possible.
I've been lucky enough to experience things I never would have had the opportunity to experience before my accident. From being the 30th person in the world to undergo an experimental olfactory nerve cell transplant in Portugal, to sharing my story in front of hundreds of medical professionals and sitting bedside in hospitals talking with patients and their families, offering resources and answers to possible questions.
To me, being a peer mentor is simply listening and sharing my story. We all have different stories, different struggles, and different walks of life. Sharing our stories empowers us all and brings us closer together, and realizing that, as different as we all may be, we are now on a similar projected journey. I was told I was a peer mentor before I even realized it, just by sharing my story, talking to other newly injured people, discussing and overcoming hardships we encountered. Exchanging rehab advice, workout techniques, motivating others and being motivated by others alike. The journeys and struggles were fought and overcome together. I now engage in things like public speaking and giving seminars to hospital staff, physical therapy students, nurse case managers-even neurosurgeons-on real life events seen through the eyes of a spinal cord injury patient. Explaining things that were not, and can not, be taught in books or classrooms. Things like finding alternative doctors and treatments, or driving a lifted truck instead of a minivan, because why not? I've tried things like skydiving, rock climbing, scuba diving, self defense classes, hunting, or fishing - all great alternatives to lying in bed, dwelling in self pity. I am always looking for hobbies that excite me, and more importantly, dating, relationships, and convincing patients and their families that life isn't over.
Questions everyone has after an accident or catastrophic event are usually related to the most basic human functions, anything from bowel and bladder function to, of course, sex. The small things we take for granted become the most important and life controlling aspects of our new life. One thing I've learned; newly injured people are simply scared and need answers to the many questions about what comes next.
This is how the Perspectives program came to fruition. Too many people don't see the light, don't understand options available to them, don't look at the the possibilities in front of them, and instead focus on the loss and the darkness, because that is all they are reminded of on a daily basis. This program is based on and thrives off of client empowerment and interaction through directly involving the client and their family with their own plan of care. Giving them hope for the future instead of focusing diagnoses and labels. Giving them hope for the future instead of focusing on the glaring hardship. Moving forward we cannot change the past or what may have happened, we can only choose to overcome and keep perspective on our outlook on what lies ahead. Maybe start to focus on the things that we probably once took for granted. Rehab and Mobility Systems and the Perspectives program want you to know YOU ARE NOT ALONE ON THIS JOURNEY. - Billy Vickers