At Can Do MS, we know that the power of knowledge can transform lives and expand beliefs about what is possible.
These articles are written by our nationwide team of program consultants - renowned healthcare professionals dedicated to educating people living with MS and their support partners. You will find valuable information and approaches covering our Six Dimensions of Wellness- Emotional Well-Being, Cognitive Well-Being; Home & Work; Diet, Exercise & Healthy Behaviors; Relationships; and Spirituality.
These articles are provided as general educational resources and should not be interpreted as diagnoses, prognoses, or treatment suggestions. Information and perspectives represent the views of the individual author(s); Can Do Multiple Sclerosis is not responsible for the accuracy or currency of the responses. Readers should consult with their healthcare team.
By: Abbey Hughes, PhD and Stephanie Singleton, OTR/L
Over a few short weeks, the coronavirus (COVID-19) pandemic has become a constant presence in our lives. We have experienced rapid shifts in our daily activities, including how we work, socialize, exercise, eat, pray, receive medical care, and care for others. Fatigue and sleep disturbance are common in MS and can worsen during periods of stress.Continue Reading
By: Juliann Hanson-Zlatev, OTR and Patty Bobryk, MHS, PT, MSCS, ATP
Many people find fatigue to be one of the most complex and challenging of the symptoms they face with MS. It is often called an “invisible” symptom since it cannot be seen on its own. To make matters worse, friends, family, and associates may not understand the severity of MS fatigue and expect you to simply “push through it.”Continue Reading
By: Allison Shadday, LCSW, Can Do MS Programs Consultant
How do you cope with something that you can’t see? For many of us, dealing with the invisible symptoms of MS can be extremely challenging. Issues with fatigue, depression, cognition, intimacy and self-esteem often go undiagnosed, under treated and misunderstood.Continue Reading
By: Beth Bullard, OTR, Can Do MS Programs Consultant
Around 60-80% of individuals living with M.S. experience heat intolerance, particularly during the warmer summer months. Simply explained, when the body’s temperature elevates nerve conduction is slowed or blocked causing a temporary worsening of symptoms. The effects are as unique as we are with each individual having their own threshold and response to heat and humidity. It is important to note, heat does not cause an exacerbation of the disease process. The effects are temporary with symptoms returning to their normal level as the body cools.Continue Reading
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