Married to Hashimoto’s: A Husband’s Confession – Where I Blew It.

Married to Hashimoto's: A Husband's Confession - Where I Blew It

So often I’ve thought about doing a poll at Hypothyroid Mom, a poll to see how many people with thyroid disease are struggling with issues in their personal relationships.

I haven’t done the poll because…the truth…I fear that the percentage would be even higher than I imagine.

Written by Rock Robbins

I married Stacey in 1989, and 7 years later she got a diagnosis, and I was Married to Hashimoto’s. She didn’t get the light easy breezy, take a pill and call it a day version. She got the misdiagnosed for 2 years, gained 100 pounds, hair failing out, skin bleeding, heart problems, brain toxicity, and we slept in the car outside the Emergency Room night after night for months.

Yeah, we got that version.

Today’s article is sort of my confessional: Where I blew it and what I would do differently if I could go back 20 years.

Seeing as I can’t go back in time, one of the best things I can think to do, moving forward, is to live differently and share my honest story of the lessons I learned so that you can have a shortcut. Not the most flattering portrayal of me, but whatever, if this helps someone get to their health and happiness faster, I’m good with that.

1. Stabilize my family financially

Back 20 years ago, I was not working consistently. I’m not sure why that part of me wasn’t awake in my 20’s like it is for some other guys. Likely, it was that I didn’t have a dad growing up and that my mom took care of everything. Whatever the reason, the result was that it made life more stressful for my capable and healthy wife. I don’t know if your wife or girlfriend is like this, but my Stacey is a rainmaker – super, crazy productive. Back then she was a seriously entrepreneurial, headstrong, ‘make it happen’ force of awesomeness. If a door wasn’t open, she could either get someone to open it for her, or she could force it open. (FYI – that’s not exactly healthy, but that’s a story for another time.) She made it seem so easy when she was feeling healthy and indestructible… so, when I wasn’t pulling my weight financially, she didn’t wait, she just stepped up and made more money happen by overworking. I was in my own world and was okay with the imbalance while she picked up my slack.

Married to Hashimoto's

But the reality is that it was too much for her to work my part and her part financially. If we’re on the teeter-totter of financial responsibility, and I’m not working my side as a young and capable man, that’s a recipe for burnout for her. Which is exactly what happened. When her Hashimoto’s symptoms started kicking in, and she could no longer provide easily, she didn’t just go, ‘Wow, I need some help here Rock, you need to find some work.’ She pushed through those warning symptoms and worked even harder. Unhealthy dynamics on our part, and too much stress, ladies and gentlemen. Just too much stress.

Why do some Hashi women burn the candle at both ends?

Married to Hashimoto's

There are some common issues in Hashi women we’ve seen over the last 20 years. These ladies are uber-productive, caring, and dynamic. They make life happen and are the heart and soul of their families and communities. One of the hard truths is this: A lot of women we’ve talked to with Hashimoto’s have gone through some kind of abuse, neglect or injury in their childhood. So, because of that old baggage, they’ve got their own internal mental circus going on – and one of the main issues they deal with is performing for their worth. That means they’ll bypass their inner signals to ‘stop in the name of health’ and keep going so that she can keep being worthy of love. This is a huge deal for many women.

Other unpleasant side-effects are dealing with issues of trust, self-rejection, fear, perfectionism, control, and guilt that sticks like glue. They’re almost always ‘on’ – taking care of everybody. Sound familiar? And my counterpart to that with Stacey was that I didn’t have to be ‘on’, because she was taking care of it all. Lots of fun for me, not so much fun for her.

Back to the financial thing…

It’s about value. If I value my woman, I’m going to do what I need to do financially so she doesn’t have to overdo it and have that extra burden of stress, which affects her mind and body. We both played our parts, but in owning mine, the first bit of advice to the younger me is to get up and start working it. That will provide the context/stability for the next parts.

2. Stabilize my family emotionally

Married to Hashimoto's

The next bit of advice for my younger self is – be that steady and unflappable presence when life started going nutty. When all the weird symptoms, doctor visits, confusion, hormone changes and frustration were rocking her world, I didn’t need to take it personally and get sensitive about it all. I would be that calm, confident, and protective force in her life. My younger self would have to step up his game and say and do things like…

  • “We’ll work it out together, hon, you don’t have to work it alone.”
  • “Let’s just mark down your symptoms and keep working your health plan.”
  • “I’ll talk to the doctor about why these treatments aren’t working, and we’ll work the next steps.”
  • “Alrighty then, which supplements are you avoiding taking today? Let’s do that now.” (make it fun)
  • “You need to rest, I’ll take care of the …”
  • “Our family doesn’t seem to understand about Hashimoto’s, so I’ll fill them in that it’s a legit health issue – and not that you’re lazy – and that you need more time to heal.”

You get the idea. That kind of consistency when “the fit hits the shan” let’s her know she doesn’t have to be managing everything while she’s dealing with brain fog and a life that’s turning upside down. And that, my friend, helps with the stress because we’re truly being a partner in this, not just along for the ride.

SIDE NOTE #1: For a while, she may still want to jump in anyway, and try to control things that are over on your side. I’ll address that coming up here.

SIDE NOTE #2: This is not permission for you to be criticized by her. Thyroid hormones can make someone be totally out of whack. You can have compassion and not take it personally, but it doesn’t mean that you should be treated like crap either.

3. Focus on our priorities

You know how when life is going well, we have the ‘luxury’ to do other things… we can go to the gym, go kayaking with friends, or go golfing, etc…

But when there’s some big health event, or an emergency, the circle of our big life pulls in and you focus on your core priorities – make sure you and your family are safe, healthy and whole.

I remember trying to take her out when she was the most sick to do the same things we used to, and she couldn’t handle it. The noise of the movies being too overstimulating (anxiety). Having to leave the restaurant as soon as we start eating (stomach issues). Having to cancel plans or leave early (exhaustion).

So, the next thing I would say to young Rock would be, “Rock, you need to prioritize getting Stacey’s health and her treatment plan dialed in. It may not be easy, but if you take care of this now, and invest in her, you’ll get back so much of the fun, healthy, and energetic woman you married. Life may not look exactly the same as before, but it’s worth your focused investment. If you keep putting her health to the side, it will just lead to a lot of years of frustration with one health issue after another, and bouncing from one doctor to another. It’s time to partner with her and take this seriously.”

So, I have the perspective now that the shortest distance to her restored health, is to invest the time now, don’t wait around and just hope it’ll get better by itself.

We are an important part of our wife’s healing.

4. Change our lifestyle

Again, I’m in front of the younger me. “Rock, next up – some things have got to change…

  • First off, you need time for you to recharge and re-center. Make sure you’re eating well, do your exercise early morning, or at night after she’s asleep, or on the weekend. Get enough rest. It’s like those safety drills at the beginning of a flight, make sure you put the oxygen mask on you so that you’ll actually be able to help the important people around you.
  • No more letting ambitious Stacey clog the calendar with one thing right after another – make margins of 2-3 hours between events. Probably no more than 1 or 2 nights out a week until she’s feeling better. If it looks like there’s too much, step in and clear the schedule – even if she protests.

Married to Hashimoto's

  • Make sure she’s doing things that are relaxing, fun, and bring her joy. Painting pottery, watching old movies, watching Food Network – whatever. Make sure she gets out with her friends too for perspective.
  • Take her out to walk around the neighborhood or at the beach and let her talk, talk, talk and talk some more. Gentle exercise helps her body, and the talking relieves the pressure valve on her head where her thoughts are constantly ricocheting around. She’s likely worried a lot about her health and her future and needs some talking it out with you.
  • If there are any contentious relationships that are stressing her out, they have to go (or at least be paused) – even if they’re family! Step in and protect her here. “Sorry, Stacey is resting right now and can’t talk. What do you need?” Then filter the B.S. out of the conversation and share that, or don’t even share that if it’s too much.”The punch line on this, guys, is that you need to take care of you, and you need to help her take care of herself.

5. Call in the troops (family & friends)

I’d tell the younger me to work with Stacey to bring our family and friends into the conversation of what’s going on health-wise. This is one I wish I had done more proactively with my family. They would dig into her for being lazy because they didn’t understand what she was going through. And I’m sad to say I didn’t jump in and help them understand like I could have. Not always an easy task, as so many people believe that Hashimoto’s is as easy as taking a pill, and boom! You’re fixed.

But that’s not always the case.

As a recovering Lone Ranger (where I don’t reach out and try to do everything myself), I’m finally getting how powerful it is to have a network of people who are there for you and your family’s health and wholeness. We both could have used more support that time. So, reach out to your family, your spiritual community, or your network of friends, and bring them into the conversation. There are so many burdens that don’t have to be shouldered alone.

Married to Hashimoto's

6. Get counseling to work on the emotional side

My wife did not start off life as a driven, approval seeking, Type-A personality out of nowhere – she had a family and life history that shaped her into the person she is. And as her partner, I have my complementary issues that fit with her issues – we’re a bit like Yin and Yang – two puzzle pieces that fit together.

My wife was already dealing with Hashimoto’s and addressing her physical issues with food, supplements, sleep, and exercise. That’s just one part of the big picture. It’s also important to address the mental issues that run the show behind the scenes. Stacey’s not just her symptoms. We had to look at – WHY does she push herself so hard? WHY does she push past when her body is telling her she needs a break?

And I had to look at “Why did I let her?”

My wife has been on a journey to work on her whole health – mind, body and spirit. And because life isn’t a one-way street when you’re married, I had to work on mine, too.

Married to Hashimoto's

Wait… what? There’s more? Since my wife and I have been dancing together in life in one certain way for such a long while, when one of the partners changes and learns a new dance of health and wholeness, it affects the old dance we’ve been doing for so long. So, there’s going to be an adjustment time! Woo hoo!! That’s going to mean some stepping on each other’s toes as we learn to be in this new dance. My goal is to be gracious, but I have been known to be a pain the butt in this adjustment process.

So, here’s the deal guys: The truth is that so many of us are really great guys married to really great women. We’re just in unchartered territory with this Hashimoto’s thing. Some of you are already right on task, some of you might be well-intended but asleep at the wheel – like I was, or maybe you’re somewhere in between.

It’s all good and it’s all just a starting point.

The point is that you don’t have to live with 20 years of wishing you had done it differently, you can learn from mistakes like mine and take a better road ahead.

As for Stacey and me, we have a great love and commitment to each other – it helped us get past the crankiness, craziness, and hard times that come in every relationship. The commitment was necessary, because there were times when I wondered if we were going to make it. Looking back, I’m so glad we worked through those hard times, because it paved the way for all the good times.

So, there you go. My 20 year retrospective. I hope that this was a helpful perspective from my past that will help your future – now.

Hang in there.
You’re not alone.

We’re in this together.

Ciao,

Rock

The Guys’ Guide to Hashimoto’sblank

Married to Hashimoto's

(Rock with sons Seth and Caleb, and wife Stacey)

blank About Dana Trentini

Dana Trentini founded Hypothyroid Mom October 2012 in memory of the unborn baby she lost to hypothyroidism. Hypothyroid Mom LLC is for informational purposes only and should not be considered a substitute for consulting your physician regarding medical advice pertaining to your health. To keep the website up and running, Hypothyroid Mom LLC includes sponsored guest posts and affiliate links including the Amazon Services LLC Associates Program and Get Healthy by Healthy Life Enterprises, Inc. These statements have not been evaluated by the Food and Drug Administration.

Comments

  1. I hope that is just a really bad joke. If it’s not – no, you can’t. It’s an autoimmune disease. Try doing a search before asking questions that make you look like a selfish clown.

  2. My name is Ciry, my wife was diagnosed with Hoshimotos a few years ago. We were together for two years, when I started to notice a change in her. She was in nursing school, not acting like herself towards me. It’s almost as if she hated me with the way she treated me without even speaking. I thought it was simply her past abuse and trauma sneaking up on her, her pain and anger being displaced. Yet I never ever gave up on her and us because I was committed in good and bad. Things really spiraled once she graduated. No matter what I did, how romantic and thoughtful, supportive I was, I couldn’t get her completely back. It’s only just recently that I turned to God for help bc I couldn’t grasp what was happening, her behavior. She kept me from her doctors visits bc she didn’t want me to over react and stress his results . And I respected that at times bc I knew how profound my love for her is and how I’d give my life for hers. Biggest mistake ever, it only made it easier for her to detach and leave me 2 weeks prior to Christmas this year. My heart is shattered as it’s been 3 months that we’ve been apart without any communication. 7.5 years lost bc I didn’t have her family’s support and I myself was drowning and don’t have any family. For all you spouses struggling, I plead that you are present for EVERYTHING, seek God in vigorous prayer for you and your loved one. Life is hard, but this disease requires work, love, commitment. Some days will be better than others, but as long as you stay faithful, press on, everything will work itself out because LOVE ALWAYS PRESERVERS!

    I’m still fighting for my wife through prayers, would appreciate yours if it’s not too much to ask. Make sure you’re ALL doing the same for yours.

    You’re ALL in my prayers 🙏🏻❤️

    Ciry

  3. My name is Ciry, my wife was diagnosed with Hoshimotos a few years ago. We were together for two years, when I started to notice a change in her. She was in nursing school, not acting like herself towards me. It’s almost as if she hated me with the way she treated me without even speaking. I thought it was simply her past abuse and trauma sneaking up on her, her pain and anger being displaced. Yet I never ever gave up on her and us because I was committed in good and bad. Things really spiraled once she graduated. No matter what I did, how romantic and thoughtful, supportive I was, I couldn’t get her completely back. It’s only just recently that I turned to God for help bc I couldn’t grasp what was happening, her behavior. She kept me from her doctors visits bc she didn’t want me to over react and stress his results . And I respected that at times bc I knew how profound my love for her is and how I’d give my life for hers. Biggest mistake ever, it only made it easier for her to detach and leave me 2 weeks prior to Christmas this year. My heart is shattered as it’s been 3 months that we’ve been apart without any communication. 7.5 years lost bc I didn’t have her family’s support and I myself was drowning and don’t have any family. For all you spouses struggling, I plead that you are present for EVERYTHING, seek God in vigorous prayer for you and your loved one. Life is hard, but this disease requires work, love, commitment. Some days will be better than others, but as long as you stay faithful, press on, everything will work itself out because LOVE ALWAYS PRESERVERS!

    I’m still fighting for my wife through prayers, would appreciate yours if it’s not too much to ask. Make sure you’re ALL doing the same for yours.

    You’re ALL in my prayers 🙏🏻❤️

    Ciry

  4. My name is Lisa. A few years ago I started putting on weight. I had always been able to maintain my weight as I got older to no higher than 132 and no lower than 126. I had had moments where I was too skinny and moments where I gained too much. But this was different. The weight started Gathering around my middle section. As I was going through menopause, I just assumed it was from this. However my hair started falling out, my mind was so fogged up that I couldn’t grab words that I knew out of the air when I needed them. My memory or short-term memory was non-existent. I had to write myself a note about an upcoming pointment and stick it on my mirror where I brush my teeth so I would remember it. If I got busy doing something I would forget it anyway. I can’t tell you how many finds I’ve paid from missing appointments. When I reached 154 lbs , my hair was falling out and I couldn’t think anymore, my family recommended I get tested for early onset dementia. After a lot of mental test and some blood work it was discovered I had hypothyroidism. I was told once I got on medication it would all clear up. I went on Synthroid and after 6 months another blood work was done. I was told my prescription needed to be increased as it was not helping my thyroid problem. After an increase in my dosage my blood work finally showed it had leveled out. I waited, and waited, and no changes in my body occurred. After reading about Hashimoto’s on the internet, I went back to my doctor and ask him to do another test. After doing the test he told me everything was fine. Here I am, my hair is now so thin it is embarrassing me. I look like I am 8 months pregnant. My skin has gotten so fragile that the least Nick will cause me to bleed. I have ridges on my fingernails that I have been told is due to old age. I am 61. If there is a way to determine for sure one way or the other that I have Hashimoto’s, I would like to know. If I do not have anything further wrong with me, then I need to just hit the gym, buy me some minoxidil and put on a lot of lotion for my thinning skin. I want even go into what my husband thinks or doesn’t think. He never gets sick. Can you help point me in the right direction? By the way, it was very nice to read your post.

    • Have a someone check your thyroid antibody levels. I was responding well, as far as my t3/t4 levels looked on Synthroid but still felt terrible. However, when my antibody levels were checked, even on medication, they were off the charts! I was switched to another medication(Amour). My hair is still falling out, and I am getting bloating again, mood changes, etc, so that tells me my medication needs to be adjusted.

  5. blank Breanna Longtin says

    I am so happy I found this website I could cry. Reading all the posts it’s like “YES! I’m not alone, I’m not crazy and I can fight this!” How refreshing. This shall become my main source of reading material for the next few years. 🙂

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