Be Prepared. Where is Your Stash?
Most of us have them and some of us even forget where they are due to the lovely fog that comes with Fibromyalgia and other conditions! I currently have five different locations that I stash emergency Spoonie supplies.
1. My nightstand is the primary place where I keep all of my medicines. I normally keep a weeks’ worth made up in my pill organizer, which gives me enough time to go to the pharmacy for refills. I have two drawers filled with medicines, vitamins, supplements and braces. It’s sad, really, but a reality for so many of us.
2. I use three different purses or shoulder bags depending on the day and my pain threshold. Each of these has a small container of my pain medicine for breakthrough pain. Pain can unexpectedly come on, and it’s not a good idea to be stuck somewhere without being able to take necessary medicine. I also have an extra day worth of medicine, in case I forget to take it with me, or in case of emergency.
3. I use forearm crutches for stability, but right now I’ve been fortunate to use only one, more like a cane function. Where is my other crutch? In my husband’s truck of course!
4. The kitchen. I live in a Loft, with the master bedroom being upstairs. Once I’m either up or downstairs, that’s where I stay for the majority of the time since stairs can be incredibly difficult for me. Thus, I have extra medicine downstairs in the kitchen so I don’t have to hike upstairs to my nightstand next to the bed.
5. My desk at work. I’m currently on short-term disability (with an unknown return to work date), but on my first day at my desk I brought an extra two sets of daily medicine, in case I forgot to take my daily pill container with me, as well as pain medicine, ace bandages, pain patches, Tylenol, band aids and other general first aid supplies. There is also makeup to cover up any Lupus rashes because I break out with them randomly!
I’ve had acquaintances ask me if this is really necessary, because to some it may seem extreme. Unfortunately, this is the reality for most of us. Whenever I go out of town, I don’t want to take all of my pill bottles, so I normally take what I need PLUS an extra few days.
Article written by staff writer, Ashley Morgan
Ashley has been diagnosed with Fibromyalgia since 2005 after spending five years undiagnosed and many misdiagnoses. Other secondary diagnoses include: Lupus, Hyper-mobility Syndrome, and Sjögren’s Syndrome. Originally from Glendale, California, she now calls San Antonio, Texas home. In her spare time she enjoys volunteering with youth at her Church and spending time with her husband and step-sons. She can be found on Twitter at @Ashiemorgan
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