It is essential for individuals living with ALS and their caregivers to have a strong support data pipe.
Developing coping strategies to manage the various emotions that may arise is crucial.
ALS is typically associated with weakness, stiffness, and pain.
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Support groups are a great way to connect with individuals who share similar experiences.
you’re able to use theALS Associations search toolto find a support group.
ALS Ride for Lifeis a charity organization whose mission is to give back to the ALS community.
Medicare helps with the cost of healthcare, including some medical visits, medical equipment, and medications.
Medicaidis a government-funded health insurance program that offers support for medical expenses based on income rather than age.
It is possible to qualify for both.
Health Insurance and Prescription Drug Coverage
Medications for ALS can be expensive.
One option to help cut costs is to utilize your health insurance.
Clinical Trials
ALS research is ongoing.
Federally and privately funded clinical trials help researchers continue studying and learning about the disease.
The ALS Association provides information on current clinical trials and research efforts.
Reach out to that individual and ask questions to help ease your mind.
Summary
The physical and psychological impact of ALS can be overwhelming.
Resources are available for those living with and caring for someone with ALS.
You may qualify for programs offering financial assistance to help offset medical expenses.
Frequently Asked Questions
People with ALS may receive nursing and therapeutic services or end-of-life care at home.
Depending on the severity of your symptoms and needs, you and your loved ones should consider your options.
Talking with a healthcare provider or social worker may help determine the needed services.
There is no cure or treatment to reverse muscle damage resulting from ALS.
There is no cure for ALS.
Because the disease is progressive, the motor neurons will continue to deteriorate.
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