My name is Pam, and next week will mark the 1 year mark for my official diagnosis of being gluten free. It was a long journey for me, I was living in Africa and got really sick one weekend. For about a year and a half I was sporadically ill. Seeing as I was living in a 3rd world country we assumed I had some sort of parasite, amoeba, or strange illness and treated myself for all of them, with no luck. After a year and a half I found myself in a doctors office in the states and was introduced to Celiac's Disease. And life changed forever.
It's been a year since I officially ate gluten free full time. I was one of those who in the process of trying to figure out what was wrong with me cut out wheat for a time, which I know is exactly what the Doctors tell you not to do, but I didn't know at the time. It has been an eventful year, but I can say, 100% worth it to have a diagnosis and treatment plan. It is a wonderful thing to feel healthy, to have energy, to not be in a mental fog and to not have eczema patches on my skin. Yes, it is frustrating to have to be so careful about what I eat, but the outcomes are so worth it.
This post is supposed to be an introduction of myself. And one thing that I have fought this year, is the idea that my diagnosis does not define who I am. In the first year of diagnosis changing this mental perspective is difficult because it seems like everything revolves around the "g word" and so it is so easy to let it define you. Yes, it places boundaries on my life, BUT, I am so much more than a person living without gluten.
I am Pam, I live in Cary, I love hiking, kayaking and anything that gets me outdoors, I serve on staff as a missions Pastor at a local church, I relieve stress through creativity in my kitchen, have a deep love for the continent of Africa, and yes, I live gluten free. I look forward to getting to know you better, and letting you into my crazy world of living Gluten free in Cary, and wherever life takes me.