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Helpful Advice from Homewatch CareGivers

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord.

ALS will cause changes in a person’s ability to eat, communicate, and exercise. Care for someone living with ALS can require a great deal of patience and understanding.

ALS & Communication

ALS (Lou Gehrig’s disease) does not affect the senses (sight, smell, taste, hearing, and touch). Caregivers for someone living with this disease will need to be patient when waiting for a reply to a question or other interaction and not assume that the person did not see or hear something.

Speech is affected by Amyotrophic lateral sclerosis (ALS) at some point during this progressive neuromuscular disease. More commonly called Lou Gehrig’s disease after the famous baseball player who was diagnosed with it in 1939, ALS affects the muscles used for movement, speech, breathing, and eating.

A family caregiver or professional caregiver can help with communication with doctors and others, and there are many communication devices to choose from when it becomes too difficult to talk.

If you or someone you love is seeking home care services, call (888) 404-5191 or complete our online form.

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Our In-Home Caregivers Can Make Eating Easier

Because of changes in the ability to swallow, a caregiver to someone living with ALS will need to assist with pureeing or modifying foods. In addition, the person with the disease should be sitting upright during mealtimes. Amyotrophic lateral sclerosis (ALS), often called Lou Gehrig’s disease, causes muscle weakness and affects an individual’s physical function. This includes the ability to swallow and this difficulty can, in turn, lead to malnutrition and dehydration. People living with ALS need to choose foods that are not only nutritionally appropriate but also have the appropriate textures.

Our In-Home Care Experts Recommend to Keep Moving

As muscle movement deteriorates progressively with ALS, our in-home caregivers can assist with mobility and transferring the person living with the disease from a sitting or lying down position to standing or getting in and out of a wheelchair.

“Part of maximizing your function and comfort lies in preventing or minimizing joint discomfort and addressing any painful areas quickly,” state the authors of the ALS Association manual, “Living with ALS: Functioning When Your Mobility is Affected.”

The Muscular Dystrophy Association (MDA) explains that exercise in the earlier stages of ALS can provide “physiological and psychological boosts.” Note that people diagnosed with ALS should consult with their healthcare provider to discuss what type of exercise is best and safe. For some people living with ALS, a daily walk may be all that is possible and advisable and other might prefer water-based activities in a supervised pool for cardiovascular activity.

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<p>Because of changes in the ability to swallow, a caregiver to someone living with ALS will need to assist with pureeing or modifying foods. In addition, the person with the disease should be sitting upright during mealtimes.&nbsp;Amyotrophic lateral sclerosis (ALS), often called Lou Gehrig&rsquo;s disease, causes muscle weakness and affects an individual&rsquo;s physical function. This includes the ability to swallow and this difficulty can, in turn, lead to malnutrition and dehydration.&nbsp;People living with ALS need to choose foods that are not only nutritionally appropriate but also have the appropriate textures.</p>

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ALS Caregiver Tips

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<p>If you or someone you love is seeking home care services, call&nbsp;<a target="_blank" class="c-link" data-stringify-link="tel:8884045191" data-sk="tooltip_parent" href="tel:8884045191" rel="noopener noreferrer">(888) 404-5191</a> or complete our online form.</p>

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<h2>Our In-Home Care Experts Recommend to Keep Moving</h2> <p>As muscle movement deteriorates progressively with ALS, our in-home caregivers can assist with mobility and transferring the person living with the disease from a sitting or lying down position to standing or getting in and out of a wheelchair.</p> <p>&ldquo;Part of maximizing your function and comfort lies in preventing or minimizing joint discomfort and addressing any painful areas quickly,&rdquo; state the authors of the ALS Association manual, &ldquo;Living with ALS: Functioning When Your Mobility is Affected.&rdquo;</p> <p>The Muscular Dystrophy Association (MDA) explains that exercise in the earlier stages of ALS can provide &ldquo;physiological and psychological boosts.&rdquo; Note that people diagnosed with ALS should consult with their healthcare provider to discuss what type of exercise is best and safe. For some people living with ALS, a daily walk may be all that is possible and advisable and other might prefer water-based activities in a supervised pool for cardiovascular activity.</p>

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<h2>Helpful Advice from Homewatch CareGivers</h2> <p><em>Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord.</em></p> <p>ALS will cause changes in a person&rsquo;s ability to eat, communicate, and exercise. Care for someone living with ALS can require a great deal of patience and understanding.</p> <h2 data-item="i" data-key="242">ALS &amp; Communication</h2> <p>ALS (Lou Gehrig&rsquo;s disease) does not affect the senses (sight, smell, taste, hearing, and touch). Caregivers for someone living with this disease will need to be patient when waiting for a reply to a question or other interaction and not assume that the person did not see or hear something.</p> <p>Speech is affected by Amyotrophic lateral sclerosis (ALS) at some point during this progressive neuromuscular disease. More commonly called Lou Gehrig&rsquo;s disease after the famous baseball player who was diagnosed with it in 1939, ALS affects the muscles used for movement, speech, breathing, and eating.</p> <p>A family caregiver or professional caregiver can help with communication with doctors and others, and there are many communication devices to choose from when it becomes too difficult to talk.</p>

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Our In-Home Caregivers Can Make Eating Easier