Tag: dementia

  • Oh Your Just A Glorified Ass Wiper

    I used to be offended when I said I was a health care assistant and people would reply, “oh, so a glorified ass wiper”. I’d struggle to explain to them that it really didn’t matter how much poop I’d see in a day, you forget all about it.

    And what most people don’t understand is, it really IS glorified. It’s the most humbling, tenderhearted experience to be apart of. And call it what you want, but nothing will do it justice.

    Sure, there’s a lot of feces and bed pans, a lot of blood and tubes, a lot of catheters and supps. There’s a lot of hitting and grabbing, punching and yelling. But there is also a lot of love, hugs, dancing and hand holding.

    It’s not all pads, bed baths and poop. It goes a lot deeper than cleaning up after some “senile” Senior.

    What it really is, is breaking the news 15 times in an hour to a devastated wife, that her husband died 30 years ago, each time breaking her heart more and more. Its holding someone’s hand while they scream in pain that they are experiencing mentally, leaving them crippled in bed for days, weeks, months.

    It’s continuously redressing a patient who is confused whether it’s daytime or night time, and maintaining a happy joyful heart as you explain to them that it’s morning time. It’s noticing your patient likes music, but can’t express it- so you sing to them when you get them ready just to see their smile. It’s maintaining a loving heart when you’ve been hitten by your patient because you’ve been trying to clean them, and they’re scared of being hurt.

    It’s wandering around the halls holding your patients hand as they cry out in loneliness and brokenheartedness because their family never comes to visit them, even though their family left 30 minutes prior. It’s remembering their favourite food, snack, drink, it’s knowing their life inside and out and making sure that each person is treated as if they are a person.

    It’s talking about death and helping them prepare, reminiscing on experiences, it’s learning about their life and listening to their sweethearts stories. It’s crying together, laughing together, it’s everything tragic and beautiful at the same time.

    It’s explaining that they might not remember you tomorrow, but assuring them you are coming back to regain your trust and respect every day. It’s working 14 days in a row just to build relationship to make the patients life more comfortable. It’s crying on your drive home because you lost a patient that day. It’s caring about them so much you lay awake at 3am wondering how they’re doing.

    It’s holding back someone’s hair, and scratching their back as they vomit into their bed because their medications make them sick to their stomach.

    It’s reminding them that they are loved, no matter what nasty parts of them you’re experiencing. It’s reminding them that they are heard, valued, noticed and loved regardless of their status, race, origin, or religion.

    There is something so special about being the person that holds someone as they take their last breath. Or knowing that you are possibly the last person they will see before they die. It makes you want to be a better person, it makes you want to give as much of yourself as you can just to make someone’s like a little bit better. Yes, this includes pad changes to prevent skin breakdown, yes, it means giving them a bath as they’ve been covered in their own feces, yes, it means that I will sit for 45 minutes just to help someone drink a small cup of water.

    Yes it means that I will patiently listen to a story from somebody who is incapable of forming sentences. No, I will not strike back when I get called nasty names, or get hit across the arm, or kicked in the leg. I will love this person in a way they can understand, in a way they can feel safe. I will not give up on these people just because their brains are throwing them into defense mode and they are incapable of using words to describe what they need.

    With a happy heart, I will go to great lengths, not because it’s my job, or my title, but because I love my patients as they are my family and want to make a difference in the lives of those I love.

    Being a health care assistant is more work than I ever thought, but I have been immensely blessed with patience and love for the people I am honored to care for. It is pretty damn hard, but worth EVERY single moment.

    THIS is what it looks like to love so deeply every single day.

    Credit https://www.facebook.com/courtneystyba

     

  • Things Need To Change In Uk Care Homes

    I think it’s time to get things changed in care homes to stop abuse and neglect happening to old and vulnerable people who cannot stand up for themselves.

    Care homes need cameras in them ALL OF THEM, to protect residents and staff, they need to be graded as to what level of dementia they can care for.

    Dementia itself needs to be graded so that people are not placed in wrong homes, the staffing levels need to be considerably higher and finally the people working in them need to be vetted more than they are now. Also the owners need to stop making such huge profits because that is all that concerns them .

    So please share to get support I can then go back to the health minister to try to get things changed. Don’t forget you or someone you love might be next

    Credit Ray Ann Lewis

    An investigation by the Daily Mail found four in ten UK care homes had failed inspections in 2017, with residents being forced to live in filthy and squalid conditions, and some locked in bedrooms without any natural light, food was basic with limited nutritional value, paper work was also not accurate.

    Of the 5,300 UK care homes inspected in 2017, 2,314 were dubbed as inadequate or in need of improvement, which is shocking.

    Staffing levels need to increase, better pay, more appreciation, training and shorter working hours would help things.

    Lets stop care home abuse NOW!!!

  • Dementia Should Be Called Failure Of The Brain

    A Neurologist said that dementia / Alzheimer’s should be called “failure of the brain,” because the other names are nebulous and do not show the severity of the disease to most people.

    As the patient’s brain slowly dies, you know they’ve changed physically, and the caregivers are often in shock!! Patients will end up bedridden, unable to move, and unable to eat or drink. But it is the different phases beforehand that are just as painful.

    The day they suddenly forget how to dress themselves, and become confused or combative when you try to fix the shirt, or trousers, they’ve put on backwards. When they repeatedly ask where their life-long mate is while looking straight at her. When they are confused, angry, or frightened, because they are still partially aware of who they were, yet are no longer…

    Most people don’t know what it is to fight or to have a loved one who leads a battle against dementia / Alzheimer’s.

    If you or anyone you know has dementia/ Alzheimer’s please visit https://www.dementiauk.org/ for advice and support.

    Original source unknown

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