I have lacked the energy (and emotional stability) to post much the past few days (sorry for missing Music Monday) but I wanted to give a quick update on my current medical journey. Continue reading
Yes, yes, and yes. AMEN!
Have you recently been tired? Have you recently been endo-tired? If yes, you’re very likely to know the difference. Explaining how you feel to the rest of the world is a different matter altogether.
“It can’t be endometriosis that’s making you feel so tired. Are you sure you don’t have cancer or something?”
“I’m too busy to ‘rest’ like you do.”
“I admit you’re not well, but stop ‘revelling’ in it.”
Renunciation and attack are common reactions. Onlookers simply refuse to believe that a person can be so excessively tired because of endometriosis, so they come up with alternative explanations: You’re lazy. You’re feigning it. You’re exaggerating it. You’re just feeling sorry for yourself. You don’t want to face up to your life. There must be something else wrong with you.
My experience has been that most people, including me, the sufferer, are, initially at any rate, unaware of this…
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Well, I said I would follow-up on the last leg of my medical journey, which I started explaining in a prior post titled Doctor Appointment #Infinity.
I must admit that I was wrong about my doctor. At this moment, my faith in him has been restored. My husband was also right when he said that God works in mysterious ways and there may have been a reason that I needed to have the abdominal CT scan, which I believed would be a waste of time and money.
The CT scan revealed a variety of issues, none of which were a stomach ulcer. It appears that some of the symptoms I have been blaming on Endometriosis, may be related to an entirely different problem.
My abdominal CT scan came back abnormal with punctuate calcifications in my spleen, extrahepatic biliary (up to 8 mm) and pancreatic duct dilation, enhancing gallbladder walls, hypodensity of the left hepatic liver lobe, thickening of the ascending colon, probable scattered leiomyomata within the uterus, and a left adnexa cyst. The report mentioned several possible causes such as gall stones, colitis, chronic cholecystitis, a genetic disease (for the spleen calcifications), as well as some even more scary possibilities that I’m trying not to think too much about just yet.
I (ironically) didn’t feel well enough to attend our wellness meeting at work today, but a caring co-worker told me about this video that they watched during it. I really needed to watch something like this today.
In light of some worrisome news that I received this week (I’ll elaborate on that more when I’ve had time to digest it), I really needed to see something positive. This video inspired me and I hope it inspires you.
❤ Wishing you all a low pain level day ❤
I have felt it on the horizon for days now and, without invitation, it’s here. The excruciating Endometriosis flare-up that is becoming more and more frequent and is the one thing that I can count on to stop me in my tracks and bring my life to a stand-still for a 3 to 5 day stretch every 4 to 6 weeks.
Don’t get me wrong, the Endo monster is very much present on a daily basis, in one way or another. However, flare-ups like this are a very different level of agony.
I am celebrating a small victory in the timing of this one, because it just so happened to start yesterday, which was Friday, at about 3:00 pm so it didn’t cause me to miss any work (yet).
At this point, I have made it 5 consecutive weeks without calling in sick. That may not seem like much to a normal, healthy person but to those who work each day with severe chronic pain, debilitating fatigue, and a plethora of other unpleasant symptoms, making it through 5 weeks of work actually IS an accomplishment.