Civic Duty

For the month of November, I am taking each day to highlight some element in my life that I want to express my gratitude about. This could be something deeply personal or just a passing appreciation for something more superficial. 


Today, in the United States, is the mid-term elections. So I wanted to express how grateful I am to have the opportunity to vote.

I remember learning about voting through elementary school and about the suffrage movement at the beginning of the twentieth century. I grew up knowing that being able to vote was a right, but as a woman less than one hundred years away from the Nineteenth Amendment, it was also a privilege of sorts. My great-grandmothers would have gone part of their lives unable to vote whereas I knew that once I turned eighteen I could register.

As soon as I was able to, I registered to vote. Every time I moved I switched my registration. If I knew I wouldn’t make it to the polls for a particular election, I filed for an absentee ballot or moved heaven and earth to make it home. I can confidently say that I have not missed a single November or Primary election. I even try to go to the smaller ones for the local elections.

If I ever missed an opportunity to vote, I can count them on one hand.

Voting is extremely important to me. I recognize the sacrifice that the women underwent so many years ago to make sure I had that right to vote that I don’t want to ever waste that opportunity. I feel that I am able to honor these women by standing in line and waiting my turn to cast a ballot. By going to my polling station it’s an act of gratitude for all of those who went before me to make it possible.

I also recognize that my ability to vote and the fact that my vote counts, is a privilege. Not everyone has free and fair elections even in my own country. While there is a lot of vitriol out in the US political climate right now, our elections are still relatively free. Racially, I am part of two groups of people who have historically been disenfranchised, so each time I walk up to get my card I am nervous that I might run into some conflict with a poll worker.

My state is currently under national scrutiny for the disenfranchisement of some voters over the course the current mid-term elections, so getting out to vote was extremely important to Ash and me.

So important that with the exception of the 2016 elections (Jai was only one month old at the time), I make a point to bring Jai with me to vote. I want him to see that this is his right and if he wants to help bring about change, he needs to see how that happens. Right now he’s enjoying the sticker at the end, but when he gets older I want him to enjoy watching Mommy or Daddy pressing buttons on the screen and watching the card spit out after the vote is cast.

I will start explaining what each election is about, who is running in it, what they are running for, and explain why I am voting the way I am. I hope he’ll ask me plenty of questions along the way and more importantly, I hope it gets him excited to go out and vote as soon as he can at eighteen.

So while it may be a minor thing to be grateful for, I truly am glad that I have the opportunity to play such a small role in how my country is run. Sometimes it feels as though my voice isn’t heard or ignored, but I know that I did what I could regardless.

Do you enjoy voting? What’s your favorite part of the process? Share your thoughts and any fun stories in the comments below.


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Featured photo credit: Photo by Element5 Digital on Unsplash


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


black cat cuddling baby

Breastfeeding Struggles

For today’s post, I featured a photo I took when Jai was 3 months and my favorite cat used Jai as a bed. This doesn’t make for an easy nursing session and while it’s fun to show off silly pictures of cats making nursing difficult, struggling with breastfeeding is no laughing matter.

I struggled at first and then it got better. And then I struggled again and that got better.

This was my personal experience, so what worked for Jai and myself may not work for everyone, nor will you have to deal with the same issues I did. Please take what is contained in this post as suggestions/anecdotal evidence and not as universal fact. Please speak with a professional if you have any major concerns regarding breastfeeding.

Something to Remember

Prior to giving birth, I attended a breastfeeding class, took a bunch of notes because it is hard to shut the academic off most of the time, and requested a lactation consultant (LC) once I was in the recovery room. One thing that was never mentioned in the class or in the hospital, and this may be a failing on my birthing hospital’s part, was that there are two people in the process of breastfeeding.

It was only Jai and me.

I had the intellectual or logical knowledge of what to do and he had the instinctual knowledge. Unfortunately, I brushed aside instinct in favor of logic so I asserted what I thought was best on Jai. This is to say that when the LC came into the room, she shoved my breast into Jai’s mouth and snipped at me to listen for a swallow while holding his head to the breast. I tried to copy her aggressive manner of shoving the nipple into Jai’s mouth and keeping his head close so he wouldn’t move and prayed I would hear that swallow to indicate a latch.

Needless to say,  this manner of feeding was ineffective and did not work.

Both he and I got frustrated. I was frustrated because I wasn’t feeding my child and he was frustrated because he was hungry. I began to stress about my milk not coming in, that he’d be underweight and they wouldn’t release us from the hospital, the nurses were already getting judgemental over each box of newborn formula they brought in, and my hormones were working in overdrive.

I don’t remember crying, but I do remember feeling like a failure as a mother.

But the moment I shut out the intellectual learning and trusted my son to know what to do, he latched and within days my milk eventually came in strong. We were on our way to breastfeeding.

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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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The First Couple Days…Weeks…Months…


This is a conversation I wish someone gave me when I first received my diagnosis. While it is tailored specifically to MS, I hope some of the thoughts are universal enough for any difficult medical diagnosis.

CW: Discussion of suicide, self-harm, and depression within this post. If you or someone you know is feeling suicidal, please contact Lifeline at 1-800-273-8255. If you are in crisis, text CrisisTextLine to connect with a crisis counselor. You are not alone.


After I got my MS diagnosis I went through a period of shock and relief. I was shocked that it was MS but relieved to finally have an answer. Ultimately, the shock overpowered the feelings of relief and I found that my emotions spiraled out of control.

I don’t remember the first couple days, I think I was numb from trying to process the information: it was like finding out a loved one had died. Every couple of minutes I’d get distracted enough to forget, but as soon as I turned my mind to it, my heart sank and it felt devastatingly fresh again.

The numbness I felt was me unable and unwilling to process the news. 

I was aware of MS since High School because my art teacher had it. I remember my mom telling me about MS, explaining why my teacher may seem fatigued or snappy towards the end of an afternoon class. I also remember sitting in the art room, watching my teacher gush about Cezanne and thinking two things to myself: one, “Oh god, I hope I never get MS;” and two, “it would be the end of my life if I ever got it.”

I was wrong on both thoughts. I may have MS, but my life isn’t over.

So You Have MS

Welcome to Club MS where no one wants membership. 

Right now you’re searching online for meaning and information. There is a lot of information out there and I understand that this post is going to add to the noise. I wrote a simplified post about MS, but I recommend checking out the NMSS for thorough information on the disease if you want specific medical details about MS.

I am not going to offer advice on how to cope with the news of the diagnosis, but provide insight into what I went through to normalize your experience to a certain extent. While working through a diagnosis is unique to each individual, there are certain aspects to the process that is universal. You are not alone in this journey.

There’s a good chance you will go through a range of emotions like I did. Hopefully, relief will be one of them because there is a sense of calm with finally having an answer to what is going on with your body. It makes what is intangible – tangible. What was presumed to be just in your head is now externally acknowledged by a medical professional.

These feelings of relief probably won’t comfort you past the first 48 hours or so. But it is something to keep in the back of your mind for later as you move through your coping process.

The next set of emotions may be frustration and betrayal.

I was frustrated that my body was attacking itself but equally betrayed by it. Here I was, at the end of my 20’s looking at a lifetime of disease; where Ash would have to take care of me if I progressed past a certain point; and I would be a physical, mental, and emotional drain to all of my loved ones.

As a younger person, the idea of having a disease or getting sick was something that happened to other people. I took what was presumed perfect health for granted. I remember thinking to myself: I lived my life relatively well, I was a good person, I did what I was supposed to, why is my body punishing me? What wrongs was I atoning for? This does not happen to good people.

I sank into a deep depression. I was completely lost about what I was facing, how I would face it, and how I would get through it. I felt completely selfish because I could only think about myself. I couldn’t and didn’t want to think about anyone else.

I went to a very dark place and stayed there for several months. There were moments where I was suicidal over the whole situation. If I killed myself, I would regain control of an out-of-control situation. More importantly, I would be able to remove myself from Ash’s life and no longer be a burden to him. The sooner I did it, the sooner he could move on and find a healthier partner.

I never acted on it, never made any serious plans. Instead, I pushed it down the road: if I start to be a burden for my loved ones – then I would do something about it.

I am not saying, nor am I recommending entertaining these thoughts, but by pushing the desire back it helped give me the clarity to healthfully resolve my thoughts on the matter and get to a point where suicide was no longer a viable option at any point in time.

It was around this point that I realized I was going through a form of grieving after getting the diagnosis. Grieving a medical diagnosis for yourself is, in fact, normal. It helped contextualize what I felt in the months after my diagnosis. It also helped me move through the stages more effectively because I now knew what I was experiencing was normal.

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