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UK: DIY dentistry and 'no teeth left to chew with' as people go almost a decade without check-up. (news.sky.com)
submitted 8 months ago by to c/worldnews@lemmygrad.ml
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"The crisis in NHS dentistry is so bad that a charity set up to run clinics in poorer countries is now spending more time working in the UK."

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[–] [S] 7 points 8 months ago (7 children)

It was a side effect of my cancer treatment. And what really pisses me off is that I wasn't warned about any of the side effects. I had two options for treatment, radioactive iodine, which they admitted had side effects, or "over treatment" with thyroxine, which means taking a higher than necessary dose of thyroxine for life, to supress any remaining cancer cells and stop it from spreading again. They said this option didn't have any side effects, so i chose that. Well it turns out it does have many side effects including strokes, heart problems, development of food intolerances, temperature regulation issues, skin problems, mental health issues, exhaustion and brain fog and many other things, all of which I have developed. It can also apparently cause other cancers, that's the only side effect I haven't had yet. And of course with all the health problems it's caused it has also condemned me to a life of poverty and loneliness as I can no longer work or have a social life.

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  • [–] 5 points 8 months ago (6 children)

    😳 It's extremely frustrating that therapies, treatments, medications can have five pages of fine-print side effects, and doctors seldom seem aware of, let alone consider, when treating patients or getting consent (informed consent seems so passé), or contraindications, with or without other medications someone may be taking. Thank you for abiding my nosiness, I know people who are high risk for stroke, with poorly managed risks, usually because of costs. Cancer is also prevalent in my area, presumably because of a lack of waste, chemical, and industrial regulation; one of them is really struggling with treatment side effects, which does include taking a daily medication. I will be inquiring about the name of that in short order.

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  • [–] [S] 5 points 8 months ago (5 children)

    It's infuriating that I've ended up on so many meds I can hardly manage them, and it's all because of side effects. The cancer meds caused me to have a stroke so now I am prescribed two stroke meds. It also caused food intolerances so i can eat very few foods without getting sick, so I've developed deficiencies and been prescribed vitamin injections and pills. One of these vitamins (folic acid) gives me terrible UTIs so I need antibiotics and bladder meds. These also have side effects. These issues have wrecked my skin so now I have eczema (so bad I've been hospitalised multiple times when it gets terribly infected), dermatitis and infected foot ulcers. It's caused chronic migraines so now I take migraine meds which have side effects, and many others.

    And with the folic acid, it took seeing multiple doctors before they accepted that the folic acid was causing my UTIs. A simple google search would have shown them that folic acid is known to cause UTIs and other bladder issues but most doctors are too arrogant to even check something they haven't heard before and just dismissed me. And the latest bladder med they prescribed, in the side effects it lists UTIs, bleeding in urine and bladder pain as side effects! I've been begging to see a urologist for ages but they just keep fobbing me off with pills.

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  • [–] 3 points 8 months ago (4 children)

    I understand! I'm getting frustrated, following your nightmare journey. And yes, doctors are extremely arrogant. Add that on top of whatever constraints imposed on them (time management, restricted formulary from which prescription is permitted, etc) by the system, and I can imagine wanting to throttle someone!

    But you said something that made me wonder... Often FNPs or even LPNs are more knowledgeable than MDs, and I wonder if for primary care management, that's a workable possibility for you? I'm sorry if it's another useless idea, I am unfamiliar with your healthcare system, other than what I've read online.

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  • [–] [S] 3 points 8 months ago (3 children)

    A lot of the time, if I actually manage to get an appointment, it's not even with a GP but a nurse, or now they even have paramedics and other similar people doing appointments at the surgery. These have been even worse than the GP. The nurses always say they don't understand blood test results and have to ask a GP and get back to me, and usually no-one gets back to me and I have to chase them up. When my folate deficiency symptoms started and we had no idea what was causing it, I was first given an appointment with a nurse who said she would ask the GP what to do and get back to me. She never did. Months passed as I waited, always expecting a call and my symptoms got much worse, in the end I kept trying to get an appointment with a GP and eventually got one and they said "Oh it looks like the nurse just forgot to follow it up."

    One time I went with a UTI and was given an appointment with a paramedic. He was extremely unprofessional, made inappropriate sexual remarks, didn't know which part of the body was affected by a UTI and refused to give me antibiotics so my situation deteriorated. I actually ended up making a complaint about him but nothing came of it.

    It's just utterly impossible to get any adequate treatment at all.

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  • [–] 4 points 8 months ago (2 children)

    😲

    I have a hypothesis, but without a detailed whistleblower report, it's just a hypothesis.

    I'm sorry you're going through this. What a wicked system.

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