I thank all who continue to read my ramblings every week and I apologize for the delays. Saturday blog days turn into late blog nights, but eventually, I get them done and posted. I lollygag and I lose my train of thought. I like to just go with whatever is in my head, remembering things here... Continue Reading →
Remicade Infusion Day #4
After Saturday's post, Another MRI for Mary, my weekend went as per usual, filled with marinating on the couch, finishing homework, filling my pill case, and, writing for my blogs - yes, plural. I can't believe it. It is still quite nice to know that I am out there sharing on multiple outlets and bringing... Continue Reading →
Another Week with My Crohn’s Disease
Saturday blog days. This is still so new and odd to me. I find myself stressing for Fridays, still, and I worry about scheduling appointments or making plans. I keep having to remind myself that I have another whole day and that I can take my time on Saturday to write, have coffee, and, enjoy... Continue Reading →
MRIs and Valentine’s
Hello to all, I hope you had a great week. I know this post comes late, but since my IBD News Today column goes live on Fridays, I will be posting on Saturdays from here on out. After last Friday's blog posts went live, both Early Signs and Symptoms of My Crohn's Disease and Eggshell... Continue Reading →
Eggshell Days
Friday night after my last blog post, It Could Be Worse, Philip and I went out to dinner for 'date night' at a restaurant nearby. The restaurant itself was nice, but I was slightly let down because the food was highly overrated. While they boasted their fried chicken, they had overcooked ours, and it came... Continue Reading →
It Could Be Worse
For this week, it is all about 'it could be worse'. This is my message. My motto. My catchword. We began the weekend with some insomnia Friday night, and we began Saturday with our new weekly movie date. Philip and I went to see La La Land, a completely spectacular movie. If you haven't, I... Continue Reading →

