Chronic Illness Life is a Lonely Life

I was told about the symptoms of myasthenia gravis (MG). I was even told you about the possible side effects of the treatments I was put on (like prednisone and weight gain). But no one told me that I’d get a dose of chronic illness loneliness.

If you have a chronic illness, the fact that it can lead to loneliness shouldn’t be surprising. We’ve all had to leave a party early, bail on dinner last minute, or skip a girls night out because a flare up was on the horizon.

Us spoonies know that with diagnosis comes a deep sense of isolation feels. Our lives take a major detour. It’s like entering the twilight zone. You can see your old life happening around you but it’s like you’re on your own little island.

There’s a wall up or something. You feel detached from the life you used to live, from your old self and your old friends and family. It’s as if you’ve entered a different realm, a strange, uncharted land that sets us apart.  Yes chronic illness loneliness is real.

Chronically Ill and Lonely AF

Ill People Want to Be Left Alone

Let’s be clear that there is a difference between being alone and being lonely. I grew up as an only child so I am no stranger to being alone. I love my own company. Some, like my mom, may argue a bit too much.

I never really felt alone or lonely, until I was diagnosed with MG. It was a natural reaction for me to retreat inward to cope with everything that was going on. But this time I truly felt alone because I didn’t know who I was anyone. I was spending time with a stranger basically. And truth be told chronic illness lonely is a different type of lonely.

You may say well that’s your choice for isolating yourself. Yes and no. Let me explain. A chronic illness diagnosis is a very confusing and stressful time. Everyone responds to it a little differently.

You may not understand what exactly is going on with your body and what it really means for the rest of your life. Some people get angry or go numb. Some rely heavily on their friends and families for support and some withdraw even if there are people present to support them.

It’s a toss up. I clearly was the latter. 

How I Became Chronic Illness Lonely

It wasn’t a conscious decision to add chronic illness loneliness to my life. From the moment of my diagnosis, I harbored resentment toward my body for not cooperating with the life I wanted to live.

I wanted to still be out living my best life. Not in the my den, struggling to make it to my bed. I wanted to take trips to all the places I haven’t been, not trips to the various ERs in my areas and being admitted for long stays.  

In all honestly, I was ashamed of my illness and was hiding from the world. On the rare occasions that I did go out, it wasn’t an enjoyable experience. “What’s the point?” was pretty much my thought.

I could stay home and be labeled as a flaky friend or force myself to go out and suffer the consequences of being too active instead of resting. I was embarrassed by the physical side effects of my illness (prednisone weight gain and acne).

The anxiety of not knowing when a symptom would flare was also enough to keep me inside. Didn’t want to have to explain to people why my eye is dropping or why my speech is slurred.

So I decided it would be best to stay home. I built a comfort bubble of isolation. My safe place. Where the only person subjected to my illness was me.

Being Friends with “Normies”

I have a few friends who will check in on me from time to time. I had friends who would constantly invite me out places to have some fun.

One I’m no longer really friends with. She didn’t understand my new reality. She wanted pre-MG Morg.

The one who was always down for impulsive trips to the beach or unlimited mimosa brunches followed by day party turn up. She consistently made me feel bad when I said I didn’t feel up to it. I was “lame” to her.

I had one friend always invite me places but made sure to do health checks and remind me to not overdo it. She still does it to this very day. 

Feeling Disconnected

I can’t lie and say I didn’t have major moments of FOMO while scrolling social media and seeing everyone do amazing things. The greatest accomplishment of my day would be making it to my bedroom. At the time I feel like I made the best choice for myself and that’s all I could really do.

However, I can say I wish my friends and family made more of an effort to be present, to check in on me, just come over and watch TV in silence. Laughter is good for the soul and I NEEDED positive vibes and good times. Not alone time to sit and dwell on everything that’s happening. 

Now that I’m “doing the work” as Iyanla would say, I’m pulling myself out of the hole. I realize that life went on without me and I don’t feel connected to my friends anymore.

Scheduling time to get together seems to be more difficult than a Rubik’s cube.  We live completely different lives now. And while I can empathize with the perils of motherhood and they can ask me questions about my illness, it’s not evenly yolked.

Some things can’t really be adequately expressed. Spoonie life is something you don’t understand unless you’re the spoon. 

I don’t think my friends mean to separate themselves from me. I honestly believe this is uncharted territory. Most of the time, people don’t know what to say when someone is facing a hardship.

They probably want to support and aren’t sure how. I feel as though I put forth effort into maintaining my relationships but it’s difficult waters to navigate. Maybe too much time passed when I was in my hole.

No New Friends

I’ve tried to open up about these feelings to my friends and family over the years about how I miss them and I feel disconnected. Not in a whiny way, just in a hey I miss you/us way. Not much has changed though.

Yes they will tell me I’m being a bit irrational and may make a short lived effort to be more inclusive. Relief was short-lived. Each missed outing, each milestone birthday or celebration, every new medication or a trip to the ER just widens the gap between the old me and the new me and subsequently my friends/family and me. 

When I felt myself being detached from my old loves ones I looked for new communities to join. So I went on a search for support groups in my area of those with the same illness as me.

While they offered some relief because hey they were ill too, the age gap too wide. They could relate to being ill but they couldn’t relate to lifestyle struggles of being young-ish and ill. So it didn’t do much in terms of filling that social interaction void from my friends but being around others with the same illness helped me feel a little less alone.

My search then turned electronic. I went to the internet searching for blogs, IG pages, FB groups, anything that could foster that sense of belonging, acceptance and community that I was craving. I joined and followed as many as I could but I haven’t found many blogs for myasthenia gravis (which is part of the reason I started this one. 

Coping with Chronic Illness Loneliness

Interestingly enough, my chronic illness journey has catapulted my holistic wellness journey. I don’t remember the exact day I made the mindset shift but I can say that it was possibly the best part of being diagnosed.

I’ve spoken in depth about mediation and gratitude. When I get frustrated or things are just going haywire I’m able to recenter myself from going down the pit of despair by taking a few deep breaths and thinking of all the things I have to be grateful for. Sometimes it’s as simple as “I woke up today”. 

By choosing gratitude, I’m accepting what is, releasing what was and embracing what will be. I have faith that even though things aren’t picture perfect, everything works together for a purpose greater than my understanding. 

You can’t change your illness (Trust me, I’ve tried) or how people treat you. You can change your mindset. As always perspective is key.

So while I have no cure for chronic illness loneliness just like I don’t have a cure for my chronic illness I can say that it does get better with time, honest and communication. You’ve got to be honest with yourself and take some responsibly if you isolated yourself from people.

I definitely suggest letting your friends know that you are in need a little TLC. Then allow the situations to play out as it’s supposed to. Release expectations that people ow you anything, including their time & support. Accept the reality and navigate your relationships to the best of your ability.

Y’all know I keep it a bean on YT. Check it out.

Morgan Greene is a Maryland chronic illness and holistic wellness lifestyle blogger. After years of struggling with her autoimmune disease diagnosis, Myasthenia Gravis, she decided to combine two of her favorite things…writing and informing others was created to have unfiltered discussions about having a chronic illness. It has since become a place to inspire and create a sense of community among women with autoimmune diseases. Morgan loves trying new things and sharing with other spoonies how to live an ill life on their terms.

When she’s not blogging she is probably reading a book, drinking a Coke Slurpee or listening to music.

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