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Q: Has the ALS Association funded any research?
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Research By The ALS Association

One of the main advocacy groups for funding ALS research is the ALS Association. Not only has the association provided funding for research in ALS, but it also has released literature describing the research being conducted in this field.

“Pathways To Hope: The State of Research into Amyotrophic Lateral Sclerosis” is an example of this type of research literature. It is a nineteen- page report released by the ALS Association, describing the research in the treatment of ALS. A free copy of this report can be downloaded at Pathways To Hope.



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ALS Frequently Asked Questions

Has there been a lot of research completed on ALS?

My doctor has prescribed Rilutek. How does this drug function?

Has the ALS Association funded any research?

Can you provide more details about TREAT ALS?

Should I consider participating in ALS Research?

How does Phase III clinical research trials differ from Phase I and Phase II?

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I have been feeling weaknes in my body. Could it be ALS?

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I am scheduled for a CSF analysis. What does this test mean?

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I have heard an Electromyography is important in diagnosing ALS. Can you explain it a little more?

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Is Guamanian ALS only located in Guam?

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What is Amyotrophic Lateral Sclerosis (ALS)?

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I developed muscle weakness and was later diagnosed with ALS. Is it commmon to feel this weak?

What are motor neurons?

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What is the difference between Limb-onset ALS versus Bulbar-onset ALS?

"Spastic bulbar palsy" sounds complicated. What is it exactly?

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I am noticing problems with my speech. Can a speech pathologist help me?

My father who has ALS has stopped eating large meals. What do I do?

I have just been diagnosed with ALS and need to talk to someone. Who do I talk to?

I have heard I will develop problems with breathing. Which type of doctor do I see?

I am a caregiver who needs extra help taking care of my loved one. Should I consider Home Health Care nursing?

What is the purpose of the ALS C.A.R.E. database?



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