Welcome to 2017 friends!
I hope your holidays were filled with lots of family and love. I had a wonderful break spending time with those who matter most.
Anyways, if I had to guess based on the title of this post, you are probably are expecting this post to be all about losing weight or having a positive body image of yourself. I’ll go ahead and stop you there. Although I could probably write a post about that, one of the reasons that I started this blog was to not only share projects that Matt and I have done around our first home, but it was also started to raise awareness for those suffering with Crohn’s Disease. To learn more about my diagnosis, you can click on the tab labeled Living with Crohn’s Disease at the top of the page.
March of this year will mark the 5th Anniversary of my diagnosis. Has it gotten easier, you ask? Yes. No. There’s really not a way for me to easily answer that question. Every 15 days I have to inject myself with a Humira shot. Although, I’m really not in pain any more, it doesn’t mean that the inflammation and pain will never come back. Right now, it’s a managing game. I will say, this last year was probably the most “normal” that I’ve felt since being diagnosed almost five years ago.
Although, I’ve felt “normal” doesn’t mean my body isn’t fighting against me. It seems the only thing my body like to do is fight against me. It’s probably the most frustrating thing and really not a thing that I share because people around me can listen, but really have no idea what the frustration is really like.
Fall/Winter time is when most of my yearly doctor appointments roll around. This year those appointments have turned into return visits. You see, in November I had my 6 month visit at my gastroenterology clinic. Prior to that I had to have blood drawn. Of course, my luck, some of that blood work came back abnormal, which led to more blood work and the scheduling of my annual colonoscopy/endoscopy. Now I’ll be going back in for another visit towards the end of the month.
During this time, I’ve also had some other health concerns that I had to bring up at my annual gynecologic appointment. Of course, this led to more blood work and an ultrasound. Two visits later and I am now being treated for Polycystic Ovarian Syndrome (PCOS.) Does it hurt? No, really it’s just messed with hormones and other womanly functions. More than anything it’s just annoying. Is it related to my Crohn’s? No, I really don’t think so. But now not only do I have to take medicine to manage the Crohn’s, but now have to add another regimen of medicine for the PCOS. Seriously…
I look normal on the outside, but inside my body gets to just decide to work against me. Like it would be great if it would ask permission before making that decision..ha! Now this post isn’t about wanting pity, I simply began this blog as a way to reach out to others struggling with Crohn’s and for the last year I haven’t had anything to really write about because I’ve felt fine. There haven’t been any ER visits, hospital stays, etc. It’s honestly just something that has been on my mind. I feel fine. I’m not in pain right now, and I am able to do anything that any other person is able to do.
Although, my body seems to want to work against me and hate me, I’m choosing to love it. You can say we have a love/hate relationship. Is that a thing? Can I seriously have a love/hate relationship with my body? Yes. I am choosing to have that relationship because although I have plans for my life, in the end my body gets to choose whether some of those plans are possible. So for now, I’ll love it. I will go to the gym, drink more water, take my medicine and vitamins, etc. I will lean on my faith and trust that by loving my body all things will work out how and when they are meant to.
Thanks for reading! Matt and I do have a few projects in the work so check back soon.
Ashley