What The April Writing Prompts are About & How to Participate
The linkups are a monthly get-together for anyone with a chronic illness, mental disorder, or disability. It’s an opportunity to share, to listen, and to learn from one another through shared writing prompts. I also think it’s a great way to provide insight into life with chronic illness from many different points of view.
All you have to do is write using at least three of the writing prompts listed below, and publish it on your blog, or to a free writing platform like Medium. Then click on the blue ‘Add Link’ button to add your blog post to this page. Voilà, you’re now part of the linkup party!
April Writing Prompts!
We are springing into Spring and Summer around our house. The lilies have popped up and survived the winter storm. I’ve planted basil, cilantro, marigolds in orange and yellow, a red dahlia, two Gerber daisies, one orange, and one in pink. I also have one pick geranium and six tomato plants. Last year we had so many birds dive-bombing the tomatoes we put up shiny green flower spinners this year. They are so fun to watch. Keeps you from getting bored looking in the back of the yard. I planted fewer flowers this year knowing that there’s a chance it would be too much to keep up with during the hot summer days. I’ll write about it in the next paragraph but so glad I planted less because I’ve now scheduled knee replacement surgery for June. Looks like I’ll be having lots of help watering this summer.
I’m enjoying my time before the medical appointments start running back to back. My knee replacement surgery is scheduled for June, it’s been a long time coming. I have yet to start my Plasma Infusion treatments. I’m so frustrated with insurance for taking so long to approve the treatments. I was told last week that insurance turns most around in two days and I’ve been waiting over a week and still no answers. Today they were so busy I couldn’t even get an insurance person in the Infusion office on the phone. I’ve been preparing for my treatments. You spend three to four hours in a lounge chair much like you do while having Chemotherapy but I’ll be having Blood Plasma dripped into the veins. I have a warm blanket, a small travel pillow, downloaded several books to review on the iPad, a new book to start if I need to turn pages, a new mask that has a slot for filters, and of course lots of hand sanitizers. I’ve also bought a new sweater since I think it’s going to be very cold in the room. I had Antibiotic Infusion treatments when I was so sick with Lyme and imagine it will be like that only I had most of my treatments at home. The side effects last three to four days and are all over the place, I have more reading to do on that subject.
I don’t write about my husband very often but he does sustain me, for 20 years now he has sustained me. He never makes me feel pressured or guilty for what I do or don’t accomplish during the day. If I sleep in or need a nap it’s never a problem or the evil eye. We cook together so the burden doesn’t fall all on me and on weekends he usually does all the cooking. He does all his own laundry and has for years, I don’t even remember when that started. One thing that is important to us is to work hard to watch at least one television show together and have time to talk before I go to bed. As I’ve mentioned in several of my Fibromyalgia posts, I go to bed long before he does. It’s my unwind and rest time. I know that whatever comes my way, he’s going to be there, working hard to make everything ok and take the burden off of me.
Are you enjoying the monthly prompt post? Are you learning anything or able to pass anything on to someone who might need the information?