When you or a loved one is facing an amyotrophic lateral sclerosis (ALS) diagnosis, a good first step is to arm yourself with information. From understanding the importance of early treatment to separating fact from fiction, the articles below will help you to understand ALS and assist you in making informed choices about managing the disease and maintaining quality of life for as long as possible.
The best way to manage amyotrophic lateral sclerosis (ALS) is through a multidisciplinary care plan tailored to a person’s specific medical needs. This includes ALS medications, supportive therapies, and symptom management.
Whether you have been diagnosed with ALS or are a caregiver, it’s important to know the facts. Here are some common myths about the disease and the truth about each claim.Â
A multifaceted care and treatment approach started as soon as possible after an ALS diagnosis can help maintain independence for longer and improve quality of life for both those with ALS and their caregivers.
Understanding how your ALS treatment plan evolves over time with the progression of the disease will enable you and your caregivers to make informed decisions about your care.
Financial planning can help with managing expenses related to living with ALS, so you can focus on your health and well-being. Working with a financial adviser or navigator can help you find health insurance, along with financial assistance programs.
After an ALS diagnosis, some useful next steps include educating yourself, putting together your care and support team, weighing your financial options, and looking at the variety of resources available to you.
There can be a lot of variation in the order in which ALS symptoms appear and how quickly the disease progresses. However, as ALS advances, patients go through several stages of progression.
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