Ella

“For me, when I was diagnosed with type 1 diabetes (t1d) I flipped the switch immediately. I went back to life right away – surprising many people by doing so. But I had no choice! There were so many exciting events and milestones happening – the last thing I wanted was for this new illness to prevent me from doing anything.

And it didn’t! I accomplished many goals and dreams of mine in that short period of time. But, reflecting now, I wish I gave myself more time to process this new lifestyle. I’ve had many scary medical events after my diagnosis, each of them having a specific place in my mind and won’t go away.

It’s extremely hard to call a body home that once protected you and now turned on you – forcing you to adapt and do everything you can to make it through each day gracefully. Which – is really hard!! It’s really really hard when people don’t understand what you’re going through. When people don’t understand the fight and the battles you’ve gone through to be standing here today. It’s hard having discrimination and judgement over a part of you that isn’t going anywhere. It’s hard accepting a ‘new you’ – and I wish I took time to reflect and acknowledge my feelings so it wouldn’t be as hard as it is now.

Making physical health a priority is a big switch to make, and with that mental health should also be prioritized. It’s okay to feel your emotions, it’s okay to grieve a life you once had and has now changed forever, it’s okay to be mad at the universe for giving you this illness, it’s okay to be mad when people are not willing to understand/relate/empathize towards your experiences, it’s okay to feel it out. Healing takes time, everyone has their own pace.”

Ella
United States

Similar Posts

  • JenVon

    “Living with Epilepsy for the past 36 years hasn’t been easy. The hardest part of my journey has been accepting and living my truth. As a child living in Washington D.C. I was attending school and one day a classmate stabbed me in the eye with a pencil. The pencil lead was lodged in my…

  • Matthew

    “I was diagnosed with Multiple Sclerosis (MS) in March of 2020, after about 9 months of searching for answers to everything I had been experiencing. Several trips to my doctor, completed blood tests, various types of scans, and visits to the ER kept leading to no answer, until I was in the right place at the…

  • Lucy

    “I first began experiencing symptoms of endometriosis when my periods started, around 12 years ago. I would always have painful periods and heavy bleeding and occasionally had to miss school. I just thought that this was normal, and everyone’s period was like mine. When I was growing up, I had a lot of male friends,…

  • Katie

    “I have the urge to share my journey with as many people as possible. To raise awareness, to educate, and to help others so they don’t ever feel alone like I did in the beginning of my journey. My story has been long, like many others, but it’s also full of hope and gratitude. My husband and…

  • Shelley

    “My story with chronic illness began in early October of 2003. Earlier in the year I had gotten an infection. I really thought nothing of it. I took an antibiotic to get rid of the infection and then that October I got a cough. Again, I thought nothing of it because I had never been…

  • Mason

    “When I was 11 years old, a psychiatrist asked me if I blamed myself for having a disease. I am pretty sure I had a bit of side-eye at that question, but then looked her in the eyes and responded, ‘Not at all. I don’t wonder why this happened to me or blame anyone, of…