Greetings Membas!
This post is informational and it is about fatigue.
I have been reading quite a few posts about fatigue and how it is/might be different for stroke survivors. I may have missed the help that is available to stroke survivors, but in my mind, the impression I get is that this something that (all) stroke survivors experience and there is not much that can be done about it.
If the last part of the previous sentence is true i.e. “**there is not much that can be done about it **” this could be my misunderstanding or it may be the view/experience of stroke survivors.
Assuming it is true, I find this unacceptable and would challenge this belief. I am of the opinion, there are always things that can be done, just that we may not always know it when we need it.
I am a carer for my Mum who is severely impacted both physically and mentally by the damage the stroke did, but in caring for her we treat her as a “normal” (non-stroke affected) person. We don’t think she is a stroke survivor and so this can be done or can’t be done. We try to understand what is bothering her, what she needs help with and try to give it.
The idea behind this is to be non-discriminatory. She has already been discriminated against on various levels by the healthcare professionals and they continue to discriminate, but we do not. We do the best we can sometimes with some token help, but more often than not, by ourselves.
This works for us and it works for Mum. Any guests, visitors are encouraged to do the same i.e. not treat Mum as a stroke survivor, which sometimes they (guests) find difficult, but nevertheless that is what we encourage.
Following on from the above and having seen a few posts on stroke fatigue, I did some research and found some articles on the internut and I have selected a few that I believe might be from reliable sources. These are for information and they may also help those who are plagued with fatigue.
I would also recommend having a blood test done to see if there might be some deficiency that is causing or contributing to the fatigue.
In addition, I would not want to worry about the term “stroke fatigue” - I have seen several posts that say “my GP does not recognise Stroke fatigue or does not accept stroke fatigue exists”.
OK, so it doesn’t exist by the name “stroke fatigue”, but fatigue does exist and no doctor however ignorant they might be will try to deny that. So when you see a GP and he/she says Doctor: “There is no such thing as stroke fatigue, or words to that effect”,
your response "Fine, treat the normal fatigue that I am experiencing - you call it what you like. I am experiencing fatigue and I would like you to treat it.
Don’t get hung up on terminology - discuss aliment and symptoms and get the help you need instead of being fobbed off.
Articles to read for professional help.
UK NHS
fatigue-after-stroke_nov23.pdf
Fatigue management – Bradford Teaching Hospitals NHS Foundation Trust
OTHER ORGANISATIONS
Fighting Through Fatigue | American Stroke Association
Why am I so tired after my stroke? - PMC
Namaste|
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