The Importance of Movement

It’s fall, which means colder weather makes it difficult to get moving to either exercise outside or make it to the gym. Perhaps because of the season, it is more important than ever to keep moving. As we head into winter, chances of weight gain increase along with seasonal mood changes that might be mitigated with some form of exercise.

Yesterday, researchers released a study regarding the importance of exercise and health. It’s something I’ve known a long time from health class and personal experience: exercising makes me feel better. If I sit still long enough (even in the span of a few hours), I start feeling bad.

That was the point of this study: the longer we sit during the day, the more danger we put on our health in the long-term. Sitting for vast spans of time and maintaining a sedentary lifestyle is worse than smoking. This study wasn’t providing new information, this article from 2014 discusses how dangerous sitting for hours on end is for our bodies. But this study was another confirmation of what researchers were saying: movement is important for maintaining a healthy lifestyle.

While the studies weren’t talking about the emotional impact of a sedentary lifestyle, more of the long-term impact, aerobic exercise is a form of anti-depressant for those suffering from major depression. A person should never quit their drug-regimen in favor of running without consulting their healthcare professionals first, but adding running or some other high-aerobic workout to the routine might increase the anti-depressant impact for mental health management.

This information is great to have to make informed decisions without an autoimmune disease that impacts fatigue levels, but living with MS, getting out of bed can be a hardship some mornings.

What to do when your body works against you?

I count myself lucky with my MS: my disease is rather benign and easy to manage compared to someone with PPMS, SPMS, or even some versions of RRMS. But it can cause my mood to swing, my depression to kick into high gear, and send my fatigue into overdrive for no reason other than “just because.”

Getting out of bed to go for a run some mornings is particularly rough when my body just does not want to move. Additionally, I’ve suffered from being overweight and depressed, so I understand how each individual factor can impact personal motivation and ability.

So what can you do?

  1. Speak with a trusted healthcare professional about what you can do to increase movement in relation to your particular health concerns or limitations. You want to find an expert who will be sensitive to your situation to provide positive encouragement, but also one who will point you in an appropriate direction for the types of exercises needed to get you started.
  2. Even if your doctor is providing you with generic information, use that information as a starting point with your own research.* Find simple exercises you can do from bed or the couch while watching television. From there, you can build up your type of exercise and the amount of time spent.
  3. Drink water. Water helps energize muscles to help prevent fatigue, protect joints and the nervous system (a huge plus for MS), and decrease MS symptoms.
  4. Keep your goals reachable and manageable. If you know that getting out of bed will be difficult most mornings, see about adding a different type of exercise that can be done from bed until you have a good day.
  5. If you have to miss a day or forget, just plan to restart tomorrow. Don’t look at a day off as a failure, but just something that happens. Try to maintain an attitude of moving forward rather than dwelling on forgetfulness. Don’t overdo it if you do miss a day – with MS that can set you back from exercising tomorrow.

*Note: your own research must be done with extreme caution and consideration to your ability levels. Do not put yourself at risk.  Read my disclaimer about health advice here.

Lack of Motivation

I find that the lack of motivation is my biggest obstacle to exercising. I wish I could write, “do this and you’ll always be motivated!” but the truth of the motivation obstacle is this: it varies from person-to-person and moment-to-moment. What keeps me motivated may not apply to another person and what keeps them motivated would never work for me.

When dealing with a chronic illness, motivation can run thin, sometimes without being the individual’s fault, but because of the way the illness impacts brain function. Having physical impairments stacked against you can be depressing on its own.

So how to combat this?

It’s never going to be a “snap your fingers and get over it” solution. That is not possible and won’t work. Rather, figure out what is important to you at the moment. Is it disease management? Depression management? Having more energy day-to-day? Wanting to see the numbers go down on the scale? Figuring out that primary starting place may be enough to get the ball rolling and sometimes that’s all it takes.

Having reports released about the importance of exercise are validating for me on my health journey because it shows that I am on the right path, especially on days when my energy and motivation are at its lowest. I just have to move forward and try not to be discouraged by a bad day or my MS.

What prevents you from exercising? What keeps you motivated to exercise? Relate your stories below in the comments section.


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Featured photo credit: Michelle Melton


Good for the Nerves: Fall & MS

MS is a disease that’s affected by the weather, particularly extreme temperature variables. Summer and wintertime can be particularly rough because of the temperature swings on either end of the thermometer. The temperate or more moderate weather of the spring and fall can offer some relief for those who need it.

I know that for myself when it’s a consistent mid-70’s with low humidity, I am at my most comfortable. I find that I have more energy, able to sleep better at night and find the need for a midday nap to be lower. I still need naps because I have an energetic toddler, but I can skip the nap with minimal impact on my evening energy levels.

I know that my MS situation is different from others, so what is comfortable for me to function may be uncomfortable for others. That’s the unfortunate truth about MS – while fall is the ideal season for me to be my best, it can make others miserable. If fall isn’t your season, that’s okay because there’s bound to be another season that works best with your illness.

Fall Weather & MS (in the South)

All of this is to say that the fall weather makes me happier. I feel like we get more temperate days in the fall than we do in the spring, though if I looked at the temperature statistics I am probably wrong.

In the South, fall means that while we may still get 90-degree days, it feels like the day’s heat dissipates faster in the evenings and takes longer to be oppressive in the mornings. It also brings more rain during the hurricane season, which is less helpful because of the humidity, but ideal in keeping temperatures lower.

More Activities to Keep Moving & Healthy

As discussed on Tuesday, fall festivals are a great way to get out and enjoy the outside with family and friends. Going on hikes, particularly in the South, are more pleasant because the leaves haven’t dropped just yet, so there’s enough shade from the sun in the forest.

Walks are more pleasant to take in the evening, more importantly, less of a mental hassle when you don’t have to consider bringing a bunch of cooling supplies to keep from overheating (for me: ventilated shoes, water, and a hat).

As a runner, I find that some of my best personal records happen between the months of October and April because of the milder weather. I also don’t run into the issues of dehydration headaches after a race that I get in the hotter month. I get these headaches no matter how much I hydrate before, during, or after the race.

If physically able, yardwork is less oppressive as well. Raking leaves is a great cardio activity to get moving, as is trimming bushes.

While hydrating is still extremely important for those of us with MS, I find that it’s not as imperative as it is in the hotter weather. I also find my means of hydrating open up: I am a huge tea drinker and love drinking herbal tea in the fall. While drinking straight water is always recommended, drinking herbal tea is easier to swallow than straight, boring water.

Relaxing Atmosphere: Less Stress, Less Flare-Ups

Scientifically speaking, fall is a more relaxing time of year: we’ve been conditioned to enjoy it at least in the United States. Fall elicits cozy feelings, warmth, and togetherness ahead of the holiday season. The idea of sitting by a fire pit with a cup of mulled cider, a blanket, and good company is extremely relaxing.

My happy place is Pumpkin Spice Lattes which are a huge indicator of fall. That first sip of the year always relaxes me in the  “ah, fall is finally here” sort of way.

Stress is a huge factor for flare-ups, at least for myself, so having relaxing evenings helps minimize my stress. Any stress that comes during the fall is usually the kind I enjoy, i.e. planning gatherings, parties, events, and outings.

While my first flare-up happened at the beginning of December nearly six years ago, most of my flare-ups happen in the winter and summer months. I think because I have worked hard to make fall a relaxing time of the year for myself.

If you have MS or a chronic illness that is affected by the weather, what do you do to help manage it during your favorite seasons? What is your favorite season and why? Leave a comment with your thoughts below.


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Featured photo credit: Michelle Melton


Talking to others about MS

There comes a time to reveal a difficult diagnosis to those outside the immediate family.

This can be a stressful or liberating experience. Friends may have suspected all along or been completely surprised by the information shared with them.

Revealing your diagnosis is an intimate act because you are sharing something personal with a friend in the hopes they will be supportive.

Because we cannot control others’ reactions after such a revelation, waiting until you are ready to talk is extremely important for your emotional health.

When to Say Something

First of all: you do not owe an explanation for your health. If you choose to divulge your diagnosis, that is a decision only you can make. Do not let anyone else force the matter from you.

If someone is visibly unwell and been so for a while, it may be harder to keep diagnostic information from others, particularly if treatment starts. It may be a relief in telling others because there is finally some information to share, but don’t be surprised if holding onto that information a little longer is more important.

While there might be a temptation to tell people immediately after the diagnosis, waiting until the information is processed is best. It allows for better preparation both with reactions and questions. Knowing which friends can handle the information with care and sensitivity helps in deciding who gets what information first.

But there may be some friends, despite waiting until you are ready, that may scale back the friendship because they don’t know how to handle your diagnosis. This hurts, but being ready for it will help mitigate the pain versus being blindsided. I made this mistake a few times and each time I wish I had waited to reveal my diagnosis or not bothered at all.

Only you will know the right time to divulge information, there isn’t a magic number or “best by” date to tell others.

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Advocating for Your Health


I am not a medical professional and the information provided in this post is intended for your general knowledge only and is not a substitute for professional medical advice or treatment for specific medical conditions. You should not use this information to diagnose or treat a health problem or disease without consulting with a qualified healthcare provider. Please consult your healthcare provider with any questions or concerns you may have regarding your condition.


Something is wrong.

You don’t know what it is, but something isn’t right with your body. You may not have gotten an MS diagnosis yet, but you might suspect that it’s MS or something similar.

Going to WebMD tells you one thing, but you know that self-diagnosing is not the final stopping point. You call your General Practitioner and set up an appointment to begin the investigation process.

You’ve made it this far, but what is the next step to make sure you get some answers?

Healthcare Failings

Unfortunately, simply going to the doctor isn’t going to get you an immediate answer or an answer at all. This shouldn’t discourage you from going: in fact, it should encourage you to go even more and advocate for yourself.

But it is important to go into the process prepared.

Not everyone will have a smooth experience when talking to the doctor about health issues. If you are a woman, you are more likely to be dismissed for pain complaints. MS can cause pain, as can a number of other autoimmune diseases, so walking into the office may feel like preparing for battle: will my health care professional take my complaints seriously?

The answer depends. They will hopefully jump at the chance to figure out what is going on, but some may surprise you and be resistant to exploring your situation.

This post isn’t meant to disparage the medical system, but to shed light on the possibility that you may need to engage in personal advocacy. Being an advocate is important regardless, but having tools and a contingency plan will streamline and hopefully speed up the process of getting answers and treatment.

It is important to remember this: going in with a calm attitude and willingness to listen will help disarm any potentially defensive healthcare professional, but make sure to come in with questions and ready to assert yourself for answers if necessary.

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