This post was recently shared on MyID’s T1D blog, but it is important to me to make sure it has a home on my blog as well. This is my journey…
Everyone has moments in life that rock them to the core, ones that change their thinking or put them on a whole new path. For some, those moments are joyous things like marriage or the birth of a child. For others, those moments might be shrouded in challenge like the loss of something or someone important. I think those challenging moments are essential to living because you never know what you are capable of without them. Like many people, I have had numerous positive and challenging moments that have stopped me in my tracks, but my daughters Type 1 Diabete diagnosis brought me to my knees.
I have been actively managing my own T1D since my diagnosis over 26 years ago. The management of my T1D has just been a daily thing to do like getting dressed or making my bed. I didn’t go out of my way to share the literal ups and downs of living with T1D. My mentality was “it just is what it is” but I also thought the act of sharing would result in people sympathizing or pitying me for something that was my reality. I didn’t want people to feel bad for me, I wanted them to see past my T1D and see me. Of course, if someone asked me about giving myself an insulin shot or taking my blood sugar levels, I would talk with them about what I was doing and why but for the most part I keep my invisible disease invisible.
This all changed when my daughter was diagnosed with T1D in December of 2018 at the age of 18 months. Suddenly, I realized that I couldn’t continue to be quiet about life with T1D. I realized that sharing is a critical part of the journey with this autoimmune disease – the more I share, the more people know, and the more they know, the more they understand what’s its like to live with T1D. Without this basic understanding, there is nothing – no support, no love, no fight for a cure.
When I tell people about Nora’s diagnosis, generally the first response is “she’s so lucky to have you”. I give a smile and a nod but think to myself “I’m lucky to have her”. Her moment has changed me – the way I think about this disease, the way I interact with it, the way I talk about it. Now, I’m shouting from the rooftops that we have T1D and that we will continue to rise up and do our part to educate and fight for a cure.
I am so excited!! My journey with T1D was recently featured on MyID’s T1D blog. Go check it out at https://shop.getmyid.com/blogs/myid-diabetes-community/how-seeing-my-daughter-get-diagnosed-changed-my-view-on-diabetes
While you’re there, check out MyID’s medical ID products. They have been a part of my sharing journey and I couldn’t be happier!
I might be in the minority when I say that I am sad Spring Break is over. We didn’t do anything extraordinary or travel someplace exciting, but each day of break the girls and I something fun. We tried a new restaurant with friends on Monday, visited the Crayola Experience on Tuesday, played at the mall playplace on Wednesday, played at the park on Thursday, and the girls went to the zoo with my parents on Friday. I would even go so far as to say that most of those things are pretty everyday for us, depending on the week. So why am I sad that break is over?
Honestly, I miss Kaelyn. She went back to Kindergarten today and is hopefully having all the fun telling her friends about her spring break adventures. I hope as she is swapping stories with her friends, her eyes twinkle and her face lights up the same way it did when we visited the Crayola Experience for the first time, or when I surprised the girls with lunch at Chick-fil-a. I hope as she is playing on the playground during school today, she is remembering how much fun she and another friend had swinging on the tire swing at the park last week. I hope the joy she experienced during her ordinary adventures is displayed loud and proud.
As a parent, it’s hard to not always have the opportunity to do the super fun things. Finances, time, and to do lists are very real roadblocks. Is there a part of me that wishes we could have traveled to a new place? Sure, but I also think it’s healthy for a child to be bored or to participate in normal day to day activities like running errands or meal planning. It teaches them the use their imagination, to be an active participant in their life, and to find the extraordinary in the ordinary. Am I disappointed in our spring break adventures- absolutely not! It was ah-mazing to not have to wake anyone up to do multiple school drop offs and pickups or to not have to remind my girls again and again to get ready for school and sometimes in a loud voice.
So today, while I am going through my ordinary day, I will miss the simplicity and joy of spring break. I will however, relish in the opportunity to find the extraordinary in the ordinary.
I’m sitting here waiting for my oil change to be done and thinking about how much life has evolved for me over the last few months. Last year, my days were filled with diapers, snacks, errands, and all the adulting. Now they are filled with all of that plus carb counting, needles, and more technology than I ever expected. Nora’s T1D diagnosis last December lit a fire in my belly – a fire I needed more than ever. Now don’t get me wrong, I would LOVE for her to lead a life without T1D. I would love to lead a life without T1D too! It’s not something either of us had a say in, but we move forward and make the most of our circumstances while trying to have a little fun along the way.
I think this is why I have become more active on social media and sharing our T1D stories. I am having fun educating and helping people understand the literal ups and downs with this chronic disease. I’ve been following others on their journey and I can totally relate to the stories they share. I hope that the stories I post are ones others can relate to or can learn from, but for me sharing our story on social media helps keep me accountable.
If you are a parent you understand that you need to fill your cup before giving to others. I STRUGGLE with this on the daily! Not just with self-care, but, before Nora’s diagnosis, the daily management of my T1D. I would eat when I could, forget to take my lunch time bolus, or just generally be lazy with the day to day management of my T1D. But then Nora was diagnosed and she forced me to be better…be better for her management AND mine. I need to ensure I am taking the best care of myself so that I can continue to help her through her T1D journey.
So thank you social media for helping to keep me accountable and for bringing us a little closer to those who have similar experiences.
For those readers that are new to Type 1 Diabetes, it is a disease where the body attacks itself and can no longer make its own insulin. Insulin is a necessary hormone whose main job is to convert food into usable energy. People with T1D rely on getting this hormone in their body from an outside source through an injection or shot. It’s a fascinating (and sometimes frustrating) disease that requires the daily micro-management of food, exercise, and insulin. Even more fascinating is that there is a blood test that screens for T1D. This test looks at a persons blood for the autoantibodies that are associated with T1D. Positive results for these autoantibodies indicate that said person is at a high risk for developing T1D.
I first learned about this screening when Nora was diagnosed last month. Before then, I had no idea it existed. While in the hospital, her endocrinologist and diabetes educator asked me if we would like to have our other two daughters tested. “Thank you, but no thank you” was my immediate response.
Later that night when Nora had finally fallen asleep, I put more thought into why I said no and more importantly why I said it so quickly. I mean, our family tree is scattered with T1D. Besides myself, and now Nora, I have a cousin and an uncle who both have T1D. How is it that the youngest person in our respective core families came to be persons with T1D? Well, the exact cause of T1D is unknown and generally thought to be brought on by a combination of factors including environment and genetics. So if the cause of T1D is multifaceted, what is there to gain by knowing if my big girls have these autoantibodies? First and foremost – research towards the goal of finding a cure. But for us, with Nora’s diagnosis still being so very raw, there would be a lot of unnecessary worrying and second guessing of everything.
Would you want to know if you kiddo was at high risk of developing a disease knowing there was nothing you could do to stop it? Or would you rather soak in the moments of blissful ignorance? There’s no right or wrong answer, but for my family – we choose blissful ignorance…for now.
A couple of people have reached out and asked me why I’ve decided to reboot my blog for a third time 😳. “Third times a charm”, I say with a big smile hiding the fact that I really didn’t know the answer to that question. But that’s the beauty of following your heart – sometimes it takes a while for your head to catch up.
Driving home from this mornings preschool drop off, I had been talking with one of my best girls about building my social media presence and she told me to tell my story the rest will fall into place. My story, huh? What is my story? I thought about this question during my entire short (and cold!) run. As I was cooling off, my head finally caught up to my heart.
When Nora was diagnosed with Type 1 Diabetes on December 17th, 2018 I sat in the hospital room that first night unable to sleep. My head was spinning, my heart was grieving. At 3:00 am, I finally gave up on sleep. I texted a couple of my best friends to let them know about Nora’s diagnosis which ended up being a big step of acceptance for me. After that, I googled everything I could related to young children with Type 1 Diabetes. I was looking for someone, anyone, who could share in my current situation and in their own words tell me that everything is going to be ok. Much to my dismay, all I found was clinical and factual information related to kids and Type 1 Diabetes. I know these types of websites are exceptionally helpful for families who haven’t had any experience with Type 1 Diabetes, but I’m different – I’ve been managing my own Type 1 Diabetes for over 25 years. But even with this significant experience, I was still looking for a connection to someone who might have had the same feelings I was while sitting in a dark and lonely hospital room, someone who might have some tips or tricks in managing this disease in a person as young as Nora. I hope that I can be the person I was looking for, and never found, when I was most vulnerable.
Type 1 Diabetes is not a death sentence – I’m living proof of this, but it is still a difficult and overwhelming disease to manage no matter if you’re 36 or under 2. Here’s to building a community, sharing in experiences diabetes related or not, and finding the extraordinary in the ordinary.