
noise dept.

if i look back, i am lost
TVSTRANGERTHINGS
trying on a metaphor
Noah Kahan
Sade Olutola
occasionally subtle

Kiana Khansmith
Aqua Utopiaď˝ćľˇăŽĺşă§č¨ćśăç´Ąă
Mike Driver

d e v o n
KIROKAZE
đŞź
let's talk about Bridgerton tea, my ask is open

pixel skylines
RMH

#extradirty
he wasn't even looking at me and he found me

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@bashful-ash

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Emma Decody in âA Death in the Familyâ
(Ex) boyfriend goals âĽ

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I believe we have a choice in this world about how to tell sad stories. On the one hand, you can sugar-coat it. Nothing is too messed up that canât be fixed with a Peter Gabriel song. I like that version as much as the next girl doesâ itâs just not the truthâŚ
Meet the Red Band Society characters: Kara Souders
This is a bad idea.
You say that about all my ideaâs

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@lovelynataliacipriano @sophie-sage @viennaxconstanzo

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@will-im
Showering While Ill: Beyond Simple Fatigue
Many who experience fatigue as part of a chronic illness or terminal illness, and have dared to express the extent of their fatigue, have been told âEveryone gets tiredâ -the subtext there being âSo stop complaining.â
Everyone does get tired. But the tired a healthy person occasionally experiences -while unpleasant, certainly- is in no way comparable to the fatigue a person with a chronic or terminal illness experiences everyday. It is crushing. And part of the crushing is that you know you will probably always be this fatigued. No amount of sleep or rest will ever dissipate the fatigue -and your illness likely makes even a decent night of sleep elusive. Knowing you will always be crushed by fatigue adds another layer to that fatigue.
To illustrate the point, Iâll take just one of the Activities of Daily Living as an example of how illness can make basic, everyday activities that healthy people can take for granted extremely difficult or impossible: showering.
Catchy and to the point, but the fatigue of chronic and terminal illness goes so much deeper than this implies. Itâs not just the fatigue of the shower itself, itâs all of the things we have to spend our little energy on to make showering possible -if it is possible.
I could range much further than the topic of the difficulties of showering and bathing and hygiene, and describe the many ways illness makes the Activities of Daily Living a monumental struggle of epic proportions, but Iâll stick with it for this list of examples, written in the spirit of the above picture:
*If you donât have to plan for a shower days in advance and recover for days after, you donât understand this fatigue.
*If you donât have to plan your nutrition, hydration, and medication intake Just Right so that they help you and donât impede your shower attempt -if you donât have to think about how nutrition, hydration, and medication affect showering- you donât understand this fatigue.
*If you donât have to have help to shower, you donât understand this fatigue.
*If you donât need assistive devices to shower -if you donât need a shower chair, or to sit or lie on the shower floor, or rails to keep you from slipping, you donât understand this fatigue.
*If you have never been forced to go weeks or months or years without a shower because you needed to preserve that energy just to survive, you donât understand this fatigue.
*If youâve never had to choose between showering and eating for the day, you donât understand this fatigue.
*If youâve never had to keep silent instead of saying âThank you, I love youâ to your spouse for helping you shower because the effort of speech would use the energy you need to shower, you donât understand this fatigue.
*If youâve never had to spend days preparing to shower, then rest all the day of the planned shower, trying to get the energy to shower, and still been unable to shower, you donât understand this fatigue.
*If youâve never had to feel the film and itchy grime of dirt build up on your skin day after day, if youâve never had to let your hair get so oily it could stand on end, if youâve never had to sit or lie in your own filth because of illness, you donât understand this fatigue.
*If youâve never had to cover your feeding tube, or central line, or deaccess that line, or had to forgo showering because the risk of infecting your tube or line was too great to even attempt a shower, you donât understand this fatigue.
*If youâve never passed out or collapsed and hurt yourself in the shower, if you donât have to have someone help you get in and out of the shower and stay with you during because -even seated or supine- you can still pass out and hurt yourself, you donât understand this fatigue.
*If youâve never had to face the reality that you canât both shower and care for your young child in the same day -not just at the same time: itâs a choice between using your energy for the day to shower or to care for your child- you donât understand this fatigue.
*If youâve never had to take an uncomfortably cold shower because just the heat of the water can trigger syncope, you donât understand this fatigue.
*If youâve never been exhausted by a bedside sponge bath, you donât understand this fatigue.
*If youâve never had to wait all day for a CNA to come to your home or room in an assisted living facility to help you shower, only to be too tired to shower by the time the CNA arrived, you donât understand this fatigue.
*If youâve never had to crawl out of the tub or shower and lie on the floor for hours before being able to dry and dress yourself -even with help- you donât understand this fatigue.
Not everyone with a chronic or terminal illness experiences every one of these, but we each experience at least a few, and one is too many.
Those of you who may have experienced some of these due to a temporary illness or injury, please remember what that was like 1) so you can be grateful that you recovered and that this is no longer something you need worry about, and 2) so you will be empathic and compassionate towards those of us for whom these struggles are a daily reality.
Similarly, those of you who have never experienced anything like the above, be grateful for your good fortune, and be empathic and compassionate towards those of us who are not as fortunate.
While writing this list was exhausting, it is far from exhaustive. From your experience as a patient or caregiver/carer, what would you add?