Q: How do the different forms of ALS differ?

		Answer(s) to this Question  ( 1 / 1 )
		Distinguishing Between The Different Forms Of ALS There are no ways to tell the difference between sporadic and familial ALS in terms of symptoms. Two patients with either sporadic or familial ALS will both go to their doctor with complaints of weakness and fatigue in a certain area of the body. However, the same cannot be said of Guamanian ALS. There is a noticeable difference in the clinical symptoms of this form of ALS compared to the others. Patients diagnosed with Guamanian ALS will have symptoms of the Parkinson-Dementia Complex with the tremors characteristic of Parkinson's patients, and the memory loss that is commonly seen in Alzheimer's patients. Since the 1960s, the incidence of Guamanian ALS has dropped to worldwide levels.

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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?

Which centers are working on ALS research?

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Are there any upcoming trials to look forward to?

Help me find information on ALS Research?

Which diseases are the differential diagnosis for ALS?

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

I have been referred to a neurologist. What can I expect during this visit?

How important is the neurological exam in diagnosing ALS?

Which laboratory tests are necessary to diagnose ALS?

Will a blood test be taken?

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

Why did the neurologist schedule an MRI for me?

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

I wonder if bone cancer is causing my symptoms?

Are there more than one form of ALS?

Tell me more about Sporadic ALS? How common is it?

What are many chances of getting ALS if my dad or mom had it?

Is Guamanian ALS only located in Guam?

How do the different forms of ALS differ?

Who first made wrote details on ALS?

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Is ALS known as any other names?

What is Amyotrophic Lateral Sclerosis (ALS)?

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What symptoms can I expect during the early stages of this disease?

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

What are motor neurons?

What symptoms can I expect with upper motor neuron involvement?

What symptoms can I expect with lower motor neuron involvement?

Can I expect any other symptoms as I battle ALS?

Which symptoms am I not likely to experience with ALS?

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

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

What can I expect during the end stages of ALS?

Is there a cure for ALS?

Is Rilutek the only medication used in ALS?

Will I benefit from physical therapy as an ALS patient?

Is occupational therapy necessary when diagnosed with ALS?

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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