What Is The Life Expectancy Of Someone Diagnosed With ALS That Is Described As Being Progressed?
Wed, 14 Oct 2020
Answered on
Wed, 4 Jun 2025
Last reviewed on
Poor outcone in terms of death within months
Detailed Answer:
Hello,
* As per my clinical the Amylotropic Lateral Sclerosis is a Neuromuscular disorder of various types.
* According to the hereditary pattern , it can be familial with multiple family members or sporadic as an isolated occurrence in family
* As per the clinical onset, it can be bulbar or spinal type.
* as per the pathology and physiology aspect, it attacks nerve cells and give rise to progressive muscular weakness.
* In the progressive or aggressive phase, there is rapid deterioration of multiple systems and death occurs within months
* Respiratory failure is usual cause of death in most cases
* There is no cure for the disease till date and she will be having supportive care only to lessen her suffering.
Regards.
Dr Bhagyesh ( MS Consultant Surgeon)
Follow up
Detailed Answer:
Hi
I do understand the agony of pain on side of relatives
* Many bitter facts of medical sciences are very harsh to digest.
* Only exceptions can be from immune response of patient to fight against the deadly outcome, nothing else
Regards
Follow up
Detailed Answer:
Hi
Welcome for follow up.
* The diseases of neurology with rapid onset usually tends to show fast progress and plateau or decline is an unusual miracle of exception when age is elder group
* On the reverse, young patients do show many modalities of hopes via immune response from self as well as external modifying agents.
Regards
Follow up
Detailed Answer:
Hi
* Difficulty in swallowing may be later finding once bulbar muscles are involved, but that does not alter overall disease patho or outcomes to great extent .
Thanks.
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