8 Reasons For Fatigue Is Your Worst Symptom of My Chronic Illness
When you’re managing none but three chronic conditions, pain is front and center. Every minute of every day. But the worst manifestation for me isn’t a nuisance.
We frequently assume that because I live with multiple chronic conditions — seropositive arthritis rheumatoid, degenerative osteoarthritis, and widespread esophageal fibromyalgia — this pain would be the most powerful symptom of chronic illnesses.
Not necessarily always the situation. Anxiety puts a damper on my own life, to get sure.
Debilitating depression and anxiety also tag along with my physical ailments. But my arch nemesis, both physically and mentally, is fatigue.
All humans go through the feeling of”tired,” but chronic fatigue is a lot more than becoming too little sleep or needing rest at the finish of the day.
Chronic fatigue affects you both physically and emotionally. It doesn’t go away with rest. It’s far more intense than that which I remember out of my healthier (younger) years earlier chronic disease. From the feeling indestructible, staying out all night drinking and dance, afterward moving to work the next day on minimal sleep and also the faint odor of all my toxin was that the evening before on my breath.
Finally, I found events, fun, and work do not always fit. Neither does the practice of chronic disease.
Now I could do next to one day and the following day need to stay during sex with an invisible blanket of fatigue weighing down on me like a lot of bricks. The most ordinary tasks are excruciating and exhausting. I can scarcely handle even showering the next day after an evening outside. I haven’t had a drink in 2 years because it leaves the pain worse.
Fatigue is painful
Sometimes my pain is still manageable, which means it’s there but it’s nothing that I can’t handle — or my medications have kicked in for pain relief. But fatigue is impossible to manage with medication or treatment. I can’t put heat or ice in my own fatigue.
Fatigue is misunderstood
Individuals know”I am in a lot of pain to achieve this” much more easily than”I’m too tired to accomplish this” While I talk about my fatigue being worse than my nervousness, it’s often cut off, while the attention is how much pain I am in. Having people, including caregivers, not believe you when you say fatigue affects your ability to do something just allows you to feel alone, diminished, confused, and lost.
Fatigue makes me flaky
Fatigue annoys others, not simply myself. I am aware I made plans with you two hours before, but sometimes fatigue is sudden and without warning. I despise hearing”Just push it” if my body is fighting itself inside and people are simply judging what they are able to see on the surface. You can’t see my fatigue until I am missing or irritated, back again.
The infection makes self-care difficult
I’m too tired to get ready food — especially breakfast, which makes me even more exhausted. Too tired to bath daily, aside from washing my head, or maintain with a regular beauty routine, that I once did as an esthetician. At least my hair is healthier from being unable to wash it daily. Thank goodness for shampoo.
Looking after your self turns to a full-time job and involves being consistent with rigorous dietary restrictions of sugar, GMOs, and gluten-free (simply because they make you foggier) — also rest, medications, treatments, and physical exercise. Paradoxically, to treat fatigue, I must first create it worse by pushing me to exercise to get my heart rate up, whilst not overdoing it hurting my joints. Really, all I wish to do is eat biscuits.
Fatigue makes me neglectful
Fatigue makes simple things like maintaining laundry or dishes a consistent struggle. I’m balancing my illness, parenting, work, self-care, and also all the housework. That’s overwhelming even without the disease. Fatigue makes me dream about owning a maid or an individual helper.
Fatigue is costly and without a cure
Around I like coffee, it doesn’t touch this fatigue. There isn’t any cure or cure for fatigue. I have spent more money than I want to admit searching for items which work, but I have still come up short — rather tired.
Infection is lonely
When absorbed with fatigue, watching the gorgeous world move by with no feels just like you’re trapped inside your very own invisible prison. Fatigue makes me nervous to meet new folks or have a social living. It forces me to question what I could possibly offer others in a relationship of any kind. Just how can I explain it? I’m scared of forgetting what I had been going to say, or not having the ability to process what somebody else just said, or to be too tired to engage.
The infection makes parenting harder than it currently is
Any parent knows parenting is hard and exhausting. The power of a child and chronic illness don’t match, not really close. Fatigue causes me to feel like a terrible mommy. I fight through the nighttime to even have the energy to read for my 5-year-old son. The guilt is often unbearable, but he loves me and indicates incredible compassion at this young age.
My love for my child moves me only a little faster compared to my standard speed on a number of days. Still, I realize it isn’t about how much that I did this day, but that I put effort into it. I recognize how difficult that is through chronic disease.
I know I am fighting as hard as I could, and it’s really okay if my body needs rest. I have learned to follow its silent cries.