Fern Cohen is a freelancer who makes multiple efforts to help others facing debilitating symptoms, such as the ones she faces with ALS (amyotrophic lateral sclerosis). She is also working on writing a book and she does this, not letting her ALS, or Lou Gehrig's disease, diagnosis interfere.
"Up to age 12, I lived with my family in a NYC housing project in Brooklyn. Then, my parents followed the 'American Dream,' bought a home, and moved us out to Long Beach, Long Island," she said. She went on to earn her bachelor's degree in both French and Spanish and became certified to teach both. Fulfilling the job of a teacher would come later. First, she would pursue a life-long dream to be a "woman of the world." "I wanted to travel, and I had heard that if you worked for an airline, you could get free or discount travel," Fern said. In 1977, she began what would become an 11-year career in the airline industry. Fern enjoyed the many positions of this career, which took her all over the world. Eventually, she would end up earning a master's in travel and tourism. "In 1997, I decided to return to my roots and give back to society," she said. This is when she made use of her teaching degree, teaching at a public high school in East Harlem, N.Y. She taught French as well as Spanish here, until 2004, when she left fully tenured. During this same time, she also studied collage and mixed media art in NYC. She was thoroughly enjoying managing and living her life. At the beginning of 2003, she felt the first symptoms. Experiencing extreme fatigue after normal activities, like bicycle riding and exercising, came first. Next came a loss of balance, causing her to trip and fall regularly. As a foreign language teacher, the symptom of slurred speech was one of the hardest. Then came the breathing difficulties, which were shrugged off as a symptom of her asthma and allergies. It was January of 2004, after going through numerous doctors and a long period of tests, that Fern got the devastating diagnosis of ALS. The symptoms she had been living with finally had a name. Cohen continued to teach for the remainder of the school year. However, when she put in a request to teach at a school without steps, due to the fact that steps were nearly impossible for her to endure, the request was not fulfilled. She was told by the Department of Education that her needs could not be accommodated. It was then that she was forced to resign and collect disability. Not being used to staying at home, Fern had a hard time managing this new life. ALS did not change who she was on the inside. She still had the intellect that would have allowed her to continue teaching. However, it wasn't seen that way by others. In Fern's words, "I find that they see the wheelchair and don't see that there is a person sitting there." For Fern, isolation is the most devastating of ALS symptoms. Many of her friends have disappeared since her diagnosis with ALS and she says that even family members can be uncomfortable in her presence. However, the friendships she lacks in that area are greatly outnumbered by the ones she has acquired through the Internet. Most of the positive impact she has had on others has come from her outreach efforts in meeting people on social sites for those with disabilities, as well as through her blog. While having ALS has forced Fern to use a communication device for speaking and to make use of aides for various tasks, it has not stopped her from looking at positive aspects of life. On this she said, "ALS has forced me to slow down, mentally and physically and see things I never stopped to look at before... Always fiercely self-sufficient and independent, I have had to learn to ask for and accept help. And with all the medications I take, there is no room for carelessness. If I could communicate with every ALS patient, I would say: Don't wait to die; live in a way that allows you to realize a dream. And don't dwell on what you can't do, but rather make the best of what you can still do." She definitely lives up to that statement every second of every day. *I originally published this on the former Disaboom via the former Yahoo Contributor Network.
by Lyn Lomasi, Write W.A.V.E. Media Staff
More and more companies are noticing the need for accessible and universal design in a wide variety of products and projects. Consumers can now find options for accessible homes and even accessible tree houses. One organization making a difference in the arena of universal living is the Center for Inclusive Design and Environmental Access (IDeA). Located in Buffalo, New York, this company is involved in some innovative ideas and projects.
What is IDeA? IDeA is an organization dedicated to design improvements on products and environments. The goal with these ideas is to create a universal design that is accessible to everyone, including those with disabilities. What is the Purpose of IDeA? IDeA strives to create new and innovative ideas on accessible design through universal accessibility options. These ideas can be implemented in accessible products and structural designs for the home, as well as the entire living environment and even entire cities. IDeA also seeks to inform as many individuals as possible about these ideas in the hopes of creating a more accessible environment for all. How Does IDeA Help People With Disabilities? The goals and solutions developed by IDEA can help those with disabilities by promoting designs that are accessible to everyone. Universal accessibility is very important to those with certain disabilities. A universal design in a structure or project creates an accessible design for those who have limited access to similar products and structures, making these projects easier to use for those with disabilities. What are Some of the Projects and Products IDeA is Involved in? Home Modification is one program IDeA has developed. In this program, consultation services are offered to families, social service agencies and other nonprofit organizations. Through the Home Modification program, there is an extensive amount of information available on accessible solutions through universal design. Universal Design Education Online is a Web site available to teachers and students interested in learning more about accessible living through universal design. The Web site can be found at udeducation.org. Another program developed by IDeA is called Universal Design Identity Project. Through this program, IDeA seeks to learn more about the general public's perception of accessible and universal design. Universal Cities is a program that makes resources easily accessible to builders, public officials, the general public and designers. This is done in an effort to eventually design entire cities around universal design. IDeA has developed plans to make New York City a universally accessible city. The Passport Kitchen Cabinet Line, made by KraftMaid, is an example of an accessible kitchen product with a universal design. This line features a raised dishwasher for extra toe or wheel space underneath, lower cabinets , lowered upper cabinets and much more. The universal design is easy to access from a wheelchair. The Soft Bathtub is an accessible bathtub with a universal design that is comfortable for anyone to use. Its soft covering helps provide fall protection, and the non-slip design helps prevent slipping. The Soft Bathtub has even been featured on ABC's Extreme Makeover Home Edition. These are just some of the many projects, products and programs associated with IDeA and its dedication to accessibility through universal design. *I originally published this via Yahoo Contributor Network by Lyn Lomasi, Write W.A.V.E. Media Staff ![]() Circuit training is becoming increasingly popular among people of all walks of life. It is known for its quick results as well as versatility in adaptation to many exercise forms. Circuit training is an exercise method that can be adapted to fit most forms of exercise and can even be used for those with a disability. In fact, circuit training is being used in most popular gyms and exercise programs. Circuit training is simply a set of exercises performed quickly in small increments, generally timed and categorized. Because the exercises used can be adapted to any exercise program, circuit training can be a good fit for someone with a disability. This method of exercise can be used for injury rehabilitation, weight loss, boosting energy levels, to adapt to disability and life tasks, for strength endurance, routine fitness maintenance and most any other exercise form. One of the main reasons circuit training is so useful is that it causes the body to adapt to different movements and positions than normal. It can exercise areas that may not be used otherwise. Further benefit, of course, lies in the ability to adapt the method to anyone's specific needs and to any form of exercise. From beginner to expert, most anyone can use circuit training in combination with various exercises at their appropriate level. Those with disabilities will appreciate the flexibility of this customizable way to adapt to life tasks. A very important aspect of circuit training in relation to disabilities is that it can actually help some people adapt to their specific disability. The Miami Project to Cure Paralysis at the Miller School of Medicine, University of Miami is using Circuit Resistance Training (CRT) to help patients with spinal cord injuries. So far, the documented research shows promising results, with those who used the CRT reporting that certain life tasks become easier to perform after using the CRT. Reported benefits include increased fitness, as well as strength in muscles that are not paralyzed, showing that patients were able to better adapt to their disability. Currently, the research on this is a continuing effort. Circuit training has been used in many different fitness activities for those with disabilities. In addition to CRT, water fitness is used to help someone with a disability adapt. Water fitness is relevant to those with disabilities, as some conditions (such as paralysis) may require an exercise that needs very little weight bearing down on the person. When in the water you can feel weightless, which makes it much easier for those with certain disabilities to adapt to the exercise. In turn, the exercise provides benefits that also help a person with a disability adapt to their disability as well as certain life tasks. There are many different ways to incorporate circuit training into an exercise program for those needing to adapt to a disability. Anyone considering this should first consult with a medical professional, as every form of exercise is not for everyone. However, due to the flexibility, it is possible that circuit training could be the answer for many needing to adapt to a disability. *I originally published this via Yahoo Contributor Network by Lyn Lomasi, Staff Writer ![]() To help along a grassroots cause, fundraising is generally required. In the case of persons with disabilities, this is no different. In some cases, this fundraising source will come in the form of a grant. In order to get any grants, a proposal will need to be written. When grant-writing in the form of a proposal, it is very important to know your cause, have a general plan that you can refer to, as well as know the expected outcome of the community project at hand. It is also important to have an idea of what the final costs of your cause for persons with disabilities will be. Some community development projects can change course midway, but be sure to at least have an outline of the possible outcome available as reference. This way, the proposal for any needed grants will be easier to write with accuracy. What is Your Cause? A potential grassroots fundraising source will need to understand what exactly your cause is, such as which group of people with disabilities you wish to help and how, and why their available grants could help. Be sure to make it known in detail in the fundraising proposal, but with simplicity, so that it is not difficult to tell what your organization's specific needs are. For example, if you simply state that you want to help people with disabilities, this gives the fundraising source very little information. If you state that you want to provide a group home to foster children who are in wheelchairs, this is much more specific. Of course, you would also include in your proposal how you plan on doing this, as well as estimated costs. Laying Out the Proposal The Foundation Center notes that a grant proposal needs to be laid out specifically under the directions that the funding source provides. Under an example that the foundation provides, the first part of the fundraising proposal could be an umbrella statement and summary, one page long. The second part could explain the reason why the community development project must be carried out. Two pages is the recommended length for this section. Next, you could discuss how the project will be carried out and monitored. Three pages should cover this well. Financial Plan and Conclusion The budget is the next discussion item mentioned. Laying out the financial plan (including grants, other fundraising, and available funds) with any necessary notes on one page could follow. Next may be the history of your organization (or it's governing organization). Include the purpose of the community development organization, as well as who it serves and how, such as "service dogs aid those in wheelchairs." This may take up one page. The final component of the grant proposal could be a conclusion that sums up all the key factors. This could be two paragraphs. Finalizing the Proposal Once your grant proposal is written, be sure to get a few opinions from colleagues and friends. At times, someone else can notice an error or a missed point that otherwise may have gone unnoticed. Having several sources for this will ensure that the proposal is well-written and representative of your specific community project. *I originally published this via Yahoo Contributor Network by Lyn Lomasi, Staff Writer ![]() When learning they will be attending a camp, some children will be ecstatic, while others may be much less enthusiastic. In either situation, it is a good idea to emotionally and physically prepare your child for camp. Kids with disabilities, as well as parents preparing them, may sometimes face even greater challenges in this area than others. Dealing With Emotions Some children may not be very excited to attend camp. They may be concerned about being away from the parents or friends for a long period of time. They may also be concerned about spending so much time with strangers. To ease a child's concerns and fears, discuss the positives of the camp, such as any fun activities your child might enjoy doing. If it is a camp for kids with disabilities or special needs similar to those of your child, let your child know he or she will get to meet children with similar needs as their own. Another thing to remember is that kids can be cruel to each other. There may be some teasing involved. With disabilities involved, it may compound that issue. Do some research and be sure your child is prepared to possibly deal with this. Even children who are overly excited will still need to be prepared for attending a camp. It is a big adjustment to be away from family and home life. Focus on the positive aspects of the camp to emotionally prepare your child for this rewarding experience. What To Tell the Camp The camp will need to know a variety of things about your child. As the parent, it is your job to be sure you inform the camp of any special needs or accommodations your child might have. One of the most important necessities a child attending camp will need to have is an emergency contact list. For kids with disabilities, this list may be even more important. Ideally, an emergency contact list should include how to the mother and father of the child, backup emergency contacts in case the parents are not available, as well as phone numbers for doctors, caregivers, and any other pertinent contacts. Kids with disabilities may have extra contacts on this list, such as caregivers and specialists. The camp should be alerted of all allergies, medical conditions, disabilities, special needs accommodations, or other pertinent information pertaining to the child's safety and well-being. Transportation Arrangements Some camps provide transportation. However, not all of them do. Even if the camp you have chosen provides transportation, it may not always be accommodating for kids with disabilities. Check with the camp your child is attending to see if they provide transportation and if so, what the mode of transportation will be. Ask questions about the accommodations and do not be afraid to be specific. If the camp does not provide the type of transportation your child will need, look into alternative modes of transportation. If you cannot bring the child to the camp yourself, see if a family member, friend, or relative is willing and has the appropriate accommodations to do so. Be sure that whichever mode of transportation is selected is available for the return trip as well. *I originally published this via Yahoo Contributor Network ![]() by Lyn Lomasi, Staff Writer Wheelchair sports are growing more and more popular as those with disabilities realize that they can do anything anyone else can. Sometimes it may require creative thinking and some adaptive technology, but it's definitely possible. Adaptive sports can be found all over the United States. One only has to look. Accessible bowling is one of the adaptive sports that has grown in popularity and may continue. There are accessible bowling alleys and even leagues especially for those with a disability. Some could feel more comfortable in a league that specializes in wheelchair and adaptive sports. Although a good number of traditional bowling alleys do have accessible lanes. Either way, this is an adaptive sport that can be easily enjoyed by people with disabilities. Bowling is naturally a very accessible sport. However, some people with disabilities who require the use of a wheelchair may still enjoy an even more authentic way to enjoy adaptive sports. That's when they can use adaptive technology, such as the IKAN Bowler. The IKAN Bowler actually allows the bowler to release the bowling ball much in the same way as a person who stands to bowl, rather than one who is seated in a wheelchair. There are many other types of equipment and accessories that are approved for, and can be used to, make bowling even more of an adaptive sport. Some of those include special ball ramps that attach to a wheelchair or walker, as well as the front of the bowling lane. There are also special ball pushers for getting the bowling ball to roll down the lane while seated in a wheelchair. Accessible bowling exists both for adults and kids. It even exists in the Special Olympics International, or SOI. SOI allows people with varied disabilities to participate in a variety of adaptive sports. Bowling is actually an official activity of not only the SOI, but also the United States Deaf Sports Federation (USADSF), the National Disability Sports Alliance (NDSA), and the American Wheelchair Bowling Association (AWBA). Getting involved in accessible bowling sports is as simple as finding a bowling alley or league that you want to participate in, which is not very hard at all, considering how accessible bowling truly is. Many bowling alleys are accessible, even if they do not advertise themselves that way. In addition to bowling, there are many other accessible and adaptive sports available to those with disabilities. *I originally published this via Yahoo Contributor Network |
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