Search 5,000,000+ questions and answers.

Frequently Asked Questions

Is There Hope For People With ALS/MND?

Frequently Asked Questions
ALS/MND wreaks a devastating effect on patients as well as their families. As they struggle to cope with the prospect of advancing disability and death, it consumes their emotional and financial reserves. It is a costly disease in its later stages, demanding both extensive nursing care and expensive equipment. But there is always hope. Recent medical discoveries have led to new drugs which seem to slow the progression of the disease.
Related Questions

Is there hope for people with ALS?

What is ALS - ALS Description
curren; back to top ¤At the moment, there is a drug trial being conducted that may prolong life minimally. Research is looking to find not only the cause of the disease so that a cure can be developed but also other medications or treatments that can help until a cure is found. With improved knowledge about ALS, healthcare providers and families can help people living with ALS live life more fully.
Related Questions

Can creatine help people with ALS and what are the potential side effects?

Patient Services Frequently Asked Questions - The ALS Associ...
with any medication or dietary supplement, it is important to check with the physician managing your ALS care to discuss the pros and cons of adding any new drug or supplement. Creatine is a dietary supplement and is sold in most health food stores. A variety of companies produce creatine. Because it is not a drug, creatine does not fall under the control of the FDA for product claims or manufacturing purity.
Related Questions

How many people have ALS?

FRONTLINE: so much so fast: what's als? | PBS
It is estimated that 30,000 people in the U.S. have ALS at any given time, with approximately 5,600 new cases diagnosed annually. More than 5,000 people die from the disease each year.
Related Questions

What Is ALS?

Patient Services Frequently Asked Questions - The ALS Associ...
Amyotrophic Lateral Sclerosis (ALS) is a motor neuron disease, first identified in 1869 by the noted French neurologist Jean-Martin Charcot. Although the cause of ALS is not completely understood, the 1990's have brought a wealth of new scientific understanding about the physiology of this disease.
Related Questions

How can I find a doctor knowledgeable and experienced in taking care of people with ALS?

Patient Services Frequently Asked Questions - The ALS Associ...
Selecting a physician to manage your ALS care will often be influenced by what is covered by your health insurance plan. If necessary, contact your insurance company to request approval to receive care at an ALS specialty clinic or center. Finding a doctor who is a "match" for you and your family is important. Individual styles and approaches to care will vary - despite equal medical skill and competence.
Related Questions

How can people get more information about ALS and The ALS Association?

Media Frequently Asked Questions - The ALS Association
The ALS Association has a toll-free information and referral service available to patients, caregivers and family members, staffed by The ALS Association Patient Service Coordinators. The ALS Association Information and Referral number is 1-800-782-4747. To reach The ALS Association's Patient Services department by e-mail, contact alsinfo@alsa-national.org.
Related Questions

What Is ALS/MND?

Frequently Asked Questions
Amyotrophic Lateral Sclerosis, a.k.a Motor Neuron Disease-is a rapidly progressive, fatal neuromuscular disease. It attacks motor neurons in the spinal cord and lower brain which transmit signals from the brain to the voluntary muscles throughout the body. When motor neurons die as a result of ALS, the ability of the brain to control muscle movement is lost. When muscles fail to receive messages, they weaken, atrophy, and die. There is no known cure.
Related Questions

How Is ALS Diagnosed?

Frequently Asked Questions
present there is no definitive means of diagnosis of ALS/MND. Most diagnoses are made by eliminating all other possibilities--ailments whose symptoms resemble those of ALS/MND. Neurologists use a number of clinical tests to establish a profile, including blood testing, EMG, MRI, etc;
Related Questions

Is ALS painful?

Frequently Asked Questions
Some of the pain ALS may cause are pressure sores, muscle aches or cramps, swelling feet, and muscle contractions.
Related Questions

How long do people with ALS live?

Amyotrophic Lateral Sclerosis ALS: rockin for a cure
Persons with ALS who go on a ventilator may live for many years, but once on a ventilator, 24-hour care MUST maintained by qualified nursing care.
Related Questions

Is creatine beneficial for people with ALS (Lou Gehrig's disease)?

Creatine FAQ
Studies have shown that creatine may be beneficial for ALS. Studies have shown that creatine can cause an increase in strength in people with such disorders. Researcher M. Flint Beat of Cornell University Medical Center published work on the issue in March of the 1999 for the issue of Nature Neuroscience.
Related Questions

Where can people buy HOPE BOOKLETS?

World Trade Hope
We appreciate and applaud organizations like the Red Cross who strive to meet the most immediate physical and emotional needs of people. The issue is not to help in a better way; rather, we are helping in a different way. Jesus is in the business of healing hurting people. He will meet people where they are. Christ brings the most important kind of healing, spiritual healing, to those who call out to Him in faith.
Related Questions

What is ALS - ALS Description
curren; back to top ¤ALS stands for Amyotrophic Lateral Sclerosis, sometimes called Lou Gehrig's disease. It is a rapidly progressive and fatal neuromuscular disease that is characterized by degeneration of a select group of nerve cells and pathways (motor neurons) in the brain and spinal cord. This loss of motor neurons leads to progressive paralysis of the voluntary muscles. The heart is not a voluntary muscle, and therefore, remains unaffected by the disease.
Related Questions

Is there hope for people with BPD? Can they recover?

BPD Central - borderline personality disorders - frequently ...
Yes. The Stone New York State Psychiatric Institute did an outcome study of 206 BPD clients admitted between 1963 and 1976 who spent three months or more in inpatient unit. Follow-up study showed: Two-thirds of sample patients now in their 30s and 40s were rated as "good" or "recovered" on the Global Assessment Scale, a tool used by clinicians.
Related Questions

What is Project Hope?

Team Discovery TSC FAQ - dslreports.com
bull;Project Hope status: Twenty Six blades are currently crunching under five hosts and plans are continually in the works for expansion. Please follow developments in the Team Discovery forum and the Project Hope forum. bull;Project Hope is a Team Discovery project pioneered by slava ryklin to create a farm of TSC and UD crunchers that will be hosted at various locations. bull;Project Hope is run by the members of Team Discovery and without donations, the project will fall apart.
Related Questions

What is hope?

alt.support.cancer FAQ - Miscellaneous
quot;I used to get hung up on statistics and numbers, but not anymore. Have lots of hope. .... Do you know what hope is ? ... It's magic and it's free... It's not in a prescription ... It's not in an IV ... ... It punctuates out laughter ... It sparkles in our tears ..... It simmers under sorrow ... And dissipates our fears ... ... Do you know what hope is ? ... It's reaching past today ... It's dreaming of tomorrow ... ... It's trying a new way ....... It's pushing past impossible ..
Related Questions

D6 What technology is available for people with ALS/stroke?

ATA-Family Place in CyberSpace-FAQ Disability
Many technology options are available for people with ALS or stroke. These include infrared controls, switches Home | About | ATA Community | Join the ATA | Donate to ATA | Initiatives | News | FAQ | ATA Resources | Related Resources | Member Area
Related Questions

What devices and technologies are available to help people with ALS?

FRONTLINE: so much so fast: what's als? | PBS
In the beginning stages of ALS, patients may use walkers or canes before progressing to a wheelchair. There are power wheelchairs available that can be controlled by the head or chin or by a "sip-and-puff" mouth device. Transfer boards and patient lifts are also available to help maneuver the patient's body. And there are a multitude of devices -- from elastic shoelaces to silverware aids -- available to help with daily tasks.
Related Questions

Amyotrophic Lateral Sclerosis ALS: rockin for a cure
Amyotrophic Lateral Sclerosis (ALS) is a fatal neuromuscular condition characterized by progressive muscle weakness, muscle wasting, fasciculations and increased reflexes, resulting in total paralysis of all voluntary muscles. ALS is a rapidly progressive, fatal neuromuscular disease that attacks motor neurons in the spinal cord and lower brain, which transmit signals from the brain to the voluntary muscles throughout the body.
Related Questions

Patient Services What Is ALS?

Patient Services Frequently Asked Questions - The ALS Associ...
Amyotrophic Lateral Sclerosis (ALS) is a motor neuron disease, first identified in 1869 by the noted French neurologist Jean-Martin Charcot. Although the cause of ALS is not completely understood, the 1990's have brought a wealth of new scientific understanding about the physiology of this disease.
Related Questions

Got A Question? Ask Our Community!


More Questions >>

© Copyright 2007-2008 QueryCAT
About • Webmasters • Contact