Thank You, COVID, I’m Back!

It is no secret I have fought hard not to let PCOS define me. It is no secret I suffered a SCAD heart attack while thin, causing me to be sent home during a said heart attack because “I didn’t look like someone having a heart attack.”

Fast forward to today. I get the gift of COVID while attending an outdoor music festival. This festival celebrated that I survived 17 units of college while working and being a mom to two kids, well, three by the end of the semester. I attended the festival to start my week off before summer school, and then a facial would end my week. No, instead, I’m writing this post and changing things.

I have done pretty well with my friend COVID. I have not had a fever since Friday am, and other than being tired, I was good. I received the call yesterday that my doctors want me on a prescription called Paxlovid. They said I am considered high risk. I have Fibromuscular Dysplasia and have a dissection in my neck right now. I figure, though, they assume I’m an untreated diabetic because I take metformin and Victoza. So this little visit from COVID now woke my body dysmorphia.

I wish I had the calm in me like those who accept their bodies for how they are. It would be awesome to feel good about my body like Lizzo. I am not anywhere near feeling good about my body. The previous judgment for either being thin or obese has shown me the judgment one can receive based on their body size or physicians not reading an individual’s medical history.

I write this because I don’t want to go to a dark place. I write this because I know I am not the only one who has felt judged by the medical field. I write this because I do not like my body today. I write this because these feelings are not facts. I will keep writing on my journey: the good and the bad. My hope is one day, I can be happy in my skin and not worry about judgment. It looks like it took a COVID medication to get me writing. So be it.

IBS C/D OH MY!

Something I’ve kept to me because, let me be honest, admitting that you have IBS isn’t the kind of thing that people just discuss.

I have grown accustom to planning my medications based on what I am doing that day.

For instance, today, I knew I would be out with my daughter and my mother. I skipped my Linzess. I wanted to be sure that I did not get an upset stomach when I was out because it is never fun to be sick when you are out. Especially if you are unsure that there is a restroom available and one that is private.

Like a gift that keeps on giving, my IBS D decided to visit anyhow. I hate that I need to rush to a restroom, and I’m embarrassed when I leave the bathroom because I’m sure that they know I’ve just been sick.

I realized today how debilitating IBS can be. I don’t take the Linzess, and IBS C happens, and with the Linzess, my body goes to the opposite, and IBS D becomes a problem.

Things I’ve avoided the past couple of years due to this gift that keeps on giving:

  • Hikes through the Hollywood Hills
  • The beach for day trips
  • Long car rides through the desert or up the coast
  • Dance classes

I felt it was time to share this. The point of my blog is to show others they aren’t alone with conditions that they may feel uncomfortable with. I hope that sharing this helps others to know they’re not alone. I do hope that over time these issues will not stop me from living the life I want to live.

It has to get easier

Twenty-Nine days in, and I am still stuck in body dysmorphia. Why can’t it just be easier to lose weight? I get it, I have PCOS (Polycystic Ovarian Syndrome), FMD (Fibromuscular Dysplasia), and I am not twenty anymore. I understand it is harder for me than others to lose weight, but it does not make me feel any better about the situation. It is a hard day today, and here are some of the roadblocks I have found that I do in which the journey is even harder:

  • I feel punished. I cannot eat like other people because I am supposed to eat gluten and dairy-free. With PCOS, it is suggested not to eat a “poor man’s diet,” and although I find that term off-putting, the way it was described to me was not to eat white bread (high carbs), potatoes (starches), and high sugar fruit and snacks. I feel like I will never be able to eat these things, and then I do. It is not that I eat a ton, but even a little for me is too much. I have to remember I am not being punished for having PCOS and other medical conditions. There are people allergic to nuts and other foods, and they are not being punished either. I need to remember my body is just different.
  • I am too concerned with the scale. I weigh myself daily, which can impact my mood. I try not to but then, even when I am doing the right things, but the scale is not showing the results, it can make me feel even worse about myself. I realize I give this object too much power.
  • I have a drawer filled with the clothes I wore before my health issues began in 2016. I am not that same person from five years ago.

I am learning to be in acceptance which I see as an ongoing journey. I am making progress, not perfection, with the way my body is today. I have a partner who accepts me for me, and he loves my body no matter what, and he tells me that I need to see my body is perfect as it is. He means well, but this journey for me has been a long and hard one.

A new step I have taken to being kinder to me is I have just started the podcast “Body Image with Bri,” which I hope will help me be in more acceptance within my body no matter what I weigh or what size I wear.

Growth can be hard but without it you remain stuck and I want to grow. We only have this one life to enjoy.

Until next time….