If you’ve followed me for a while, or have read either of my books, you have probably heard me talk about my wife Megan. (You may have even read one of her two previous guest posts for Mind Over Meniere’s.)

She’s been with me throughout my entire journey with Meniere’s disease, helping me through my darkest moments. But today, I’m sitting on the other side of the table, helping to support her through a difficult cancer diagnosis and her own battle with chronic illness.

After much prodding and encouragement, Megan has written another guest post for Mind Over Meniere’s to share some of her struggles as a new mother with chronic illness, as well as some of the lessons she’s learned along the way.

(P.S. if you like her post, let her know in the comments below. We just might be able to get her to come back and write some more!)

Saturday mornings look a lot different than they used to these days.

With my 8-month old son Zack ruling the Schweitzer house, we’ve traded our gym memberships for Gymboree clothes and movie dates for play dates. Today’s goal – make a packing list for our upcoming trip to Sanibel Island, FL next month.

Truth be told, I never used to plan this far ahead for a long weekend. When you have a baby, planning ahead makes everything easier.

But when you are a parent with chronic illness, planning is an absolute must.

As some of you know, I am a recent Breast Cancer Survivor. I was diagnosed at 6 months pregnant, and Zack was only 2 months old when I started chemotherapy.

And now that I am past the hardest parts of my treatment (my last radiation was 3 months ago), I am learning just what it means to live with chronic illness, something my husband Glenn knows all too well.

So as I sit here at the kitchen table, counting out how many onesies I’ll need (and then doubling it, just to be safe) I couldn’t help but wonder – what other habits have helped me as a new mom with chronic illness?

I can come up with a few.

Planning is Everything:

As you undoubtedly know, babies are both predictable and unpredictable. When is he going to need a nap? Or a teether or a diaper change? I don’t know. But I do know it’s as soon as I sit down for dinner.

All joking aside, our diaper bag is always at the ready, and I have found it imperative to bring about 10 things with me wherever I go.

Because of this, I put all of my personal “must-haves” in one convenient pouch that I keep with me always. Glenn calls it a go-bag. At any given moment, I have my medications and supplements (including CBD oil), lotion and anti-bacterial, ID, $20 bill, phone, keys and chap stick. That pretty much covers it.

I feel more secure knowing I don’t have to search every time I go out. I always KNOW that I have my ID, my medicine, and necessary supplies the same way I KNOW I always have a pacifier for Zack.

Lesson Learned: Anyone with chronic illness knows that problems and symptoms can arise at the worst moments. What are the things you can’t live without?

Put your Oxygen Mask on First:

I’ve been flying for as long as I can remember, but it is only this year that this phrase made sense:

“In the event of a loss of cabin pressure, oxygen masks will drop from above your seat. Always secure your mask before assisting others.”

In the days following my chemo treatments, I was unable to care for Zack. But as soon as I felt my strength coming back, usually by day 4 or so, I would try to be Super Mom.

This. Doesn’t. Work.

You cannot care of those around you, especially those that need you most (sick spouses, children) when you do not take care of yourself.

I unrealistically expected myself to magically bounce back after just 3 days and didn’t always give myself permission to “put my mask on” and take a nap or call a sitter.

Lesson Learned: When you are not feeling well, allow yourself to not feel well. If you are like me, and have that voice in your head that says, “You’re fine, you feel well enough, your children need you, society expects this of you, your job needs you”, don’t listen. Kindly tell that voice to take a long walk off a short pier, ask for help, and then go take a nap.

It Takes a (Virtual) Village:

This old adage was especially true for us in a very real sense.

While I was going through treatment, Glenn was still running Mind Over Meniere’s and Rewiring Tinnitus, had a weekly coaching caseload, was taking me to the doctor every other week, and learning to be a new dad every day. We needed a lot of help.

Luckily Glenn’s mom came down to stay with us for every chemo treatment and we had other family and friends that helped out in between.

What I didn’t anticipate was how much help I received from the online community. Reading stories and posts from other young women with cancer, young mothers navigating their unique challenges, and other parents with chronic illness gave me hope and a sense of belonging that nothing else really did.

Being able to share my story and receive love and validation from my peers in return gave me self-worth when mine was waning. Being able to provide support to others gave me purpose when mine was lost.

Getting a like or a comment or a message from someone that REALLY understands was priceless. Especially in my darkest moments.

Lesson Learned: Reaching out for support, guidance, or just to vent to those that really “get it” – even if it’s an online support group – is cathartic in itself. Receiving nods of approval from those that have walked in your shoes is even better. Today, give someone a like or a comment – tell them you have been in that same deep hole – that you understand what they’re going through. It just might change their day, or their life.

(Glenn runs a Facebook Support Group for Meniere’s Sufferers with over 11 thousand members – click here to join!)

Final Thoughts:

This last year has been a challenging one, but it’s in these difficult times that we learn the most. I plan to keep planning, resting and relying on those around me when I need help.

And guess what? As soon as I feel like I have it figured out, Zack is going to start walking…

As Glenn always says – there is so much hope. You are not alone. Never forget that.

  1. Beautiful family. Thank you for sharing your journey through chronic disses. Many blessings to all members of your beautiful family. Do you live in Fort Myers? That is where I live.

  2. Megan, since I learned of Glenn’s and your challenges, I’ve kept your family in my prayers every day. When I see photos of Glenn, Zack, and you, it gladdens my heart! All of you are proof that happy beginnings can occur at any time in our lives, no matter how difficult our past struggles. Thanks to both of you for sharing your personal journeys and giving other people hope.

  3. Hi Megan, I am a mum with Meniere’s disease so I can empathise what it’s like being a parent with a chronic illness. Just wanted to offer support and empathy for your post! The best thing that works for me is staying positive, and reading other people’s positive stories so thanks for your post and Glens too. Mindset plays such a big role! Agree with all the above, and never try to be “super mum” , accept all the help you can and make sure you have guilt free time to yourself, I say guilt free because mums have a tendency to feel guilty about nearly everything! Routine and planning as far as possible essential too! Just wanted to share some positive thoughts. Hope you’re all doing well.

  4. Hi guys, well written Megan. I have Meneries disease. I live in Australia. I was diagnosed 17 years ago and there was not much info on the topic back then. I’ve been symptom free for about 14 years and in Nov 2018 had a major flare up and for past two years have been suffering immensely. Chronic Vertigo, rushing fatigue and debilitating brain fog is my daily. (Which I have written about previously on my blog). A year ago we found a link between My vertigo and a hormone imbalance (I’m very early stages peri-menopause). HRT was used to check if in fact that was the case and I felt great for two weeks whilst taking it, but could not stay on it due to my getting throbbing pain in my leg. To know something worked and no that I cannot take it (and don’t really want to take HRT anyways due to it increased risk of breast cancer, stroke and blood lots) was deflating to say the least. But I soldier on to find new ways to cope on a daily basis. So glad I found your site to inspo. I find the chiropractor and my new naturopath help me too as well as supplements. But on severe debilitating brain fog days I resort to anti-anxiety meds, which I’m hoping to eliminate with ongoing holistic remedies.

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