A few weeks ago, a friend asked if I was finished with this blog. He wondered if he should delete the icon from his desktop. For some time, I did feel like Not Going Gently was done. I felt I had nothing left to say. But lately, I've had some swirling thoughts asking to be written. So, Big John, if I'm still up there, don't delete just yet please.
One of the things rattling around in my brain is my health journey these last few months. I had the delightful opportunity to lunch with a dear friend recently, and she asked me about it. Really asked me, wanting details and dates. And I could not remember clearly. I'm pretty sure I gave her inaccurate information, so here for the record is the timeline:
September 6 -- Tightness and pain starting in left shoulder and spreading through chest and back; shortness of breath; went to see doctor; diagnosis of pleurisy. Home with steroids.
September 11 -- Symptoms return, more extreme; doctor sends to emergency clinic; diagnosis of pleural effusion. Home with antibiotics.
September 18 -- Symptoms return, not as severe; doctor prescribes more antibiotics, sets up appt. with pulmonologist.
September 24 -- Pulmonologist says please come see me any time something is wrong with your lungs. (This is not that time.)
October 2 -- Still fatigued; further bloodwork with doctor which reveals nothing except low Vitamin D levels.
October 25 -- Appointment with functional medicine doctor. She recommends low dose of thyroid, gluten-free diet, treatment for yeast overgrowth, megadose daily of Vitamin D. Sends me home with test kit for hormones/adrenals.
Within days of starting thyroid medication, I felt SO MUCH BETTER. Unbelievably better. Like magic.
So much better that Dave and I were able to go on a getaway to Montana that we had planned months before, but were beginning to wonder if I could make it. We had a delightful time together with friends who moved to MT, rested a lot, remembered that we liked each other, and made it through a travel adventure to get home the day before Thanksgiving. We spent Thanksgiving at home instead of with extended family because Nate came down with the flu the day before we returned.
And then the following Monday, I returned to work with my students at Brighter Vistas. Three weeks later was finals at school (which we fondly refer to as "Hell Week") and then, wham, it was Christmas. Somewhere between Thanksgiving and Christmas, I received word from the functional medicine doctor that I did indeed need adrenal support, so I added DHEA to my daily cocktail of supplements. I have continued to feel really really good. (With the exception of yesterday afternoon and today--holiday exhaustion? virus? allergies? Who knows.) I even wake up thinking purposefully and positively about my day, instead of trying to imagine just dragging myself out.
My takeaway from this whole health experience? I wish I had known. I wish I had gone to see Dr. Caldwell at the beginning of full-time caregiving just as a preventative measure. I wish I had not waited until I had inexplicable health issues that stopped me in my tracks and robbed me of six weeks. Caregiving, loss, and grief are hard, hard work. They drain our emotions, our souls, AND our bodies. We can only soldier on for so long without support.
So here's my Public Service Announcement: Get thee to a functional medicine doctor. Have your levels tested, see where you need to get support, and make changes. Taking care of yourself is not optional; it's a necessity. Really.
Postscript:
What is functional medicine?
How can I find a functional medicine doctor?
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