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Symptoms: Slurred Speech (Dysarthria)

Can ME/CFS cause slurred speech? This is something that I occasionally have to cope with – especially when I am very feeling very tired and/or haven’t slept well and am not able to concentrate properly. Should I see my doctor about it?

Symptoms: Slurred Speech (Dysarthria) Read More »

Can ME/CFS cause slurred speech? This is something that I occasionally have to cope with – especially when I am very feeling very tired and/or haven’t slept well and am not able to concentrate properly. Should I see my doctor about it?

Symptoms: Cognitive Dysfunction

I know that cognitive dysfunction/’brain fog’ is one of the key symptoms of ME/CFS and that it can vary in severity – just like most other ME/CFS symptoms. But I’m concerned about what seems to be a slow and progressive worsening in the problems I have with memory, concentration, mixing up words and the ability to process information. I’ve also noticed that my memory for events in the past is now being affected. Otherwise, most of my other ME/CFS symptoms are fairly stable. But the frustration with not being able to properly function mentally is starting to make me feel depressed.

I went to see my GP a few months ago, and he felt that my cognitive problems were probably ‘just another part of having ME/CFS’. So is this sort of progressive decline in mental functioning something that other people with ME/CFS report and just have to live with?

Symptoms: Cognitive Dysfunction Read More »

I know that cognitive dysfunction/’brain fog’ is one of the key symptoms of ME/CFS and that it can vary in severity – just like most other ME/CFS symptoms. But I’m concerned about what seems to be a slow and progressive worsening in the problems I have with memory, concentration, mixing up words and the ability to process information. I’ve also noticed that my memory for events in the past is now being affected. Otherwise, most of my other ME/CFS symptoms are fairly stable. But the frustration with not being able to properly function mentally is starting to make me feel depressed.

I went to see my GP a few months ago, and he felt that my cognitive problems were probably ‘just another part of having ME/CFS’. So is this sort of progressive decline in mental functioning something that other people with ME/CFS report and just have to live with?

Treatment: Apheresis

Are you aware of a new treatment called apheresis that is being given to people with Long Covid? It is supposed to remove small blood clots that are involved in causing Long Covid. Some of the overseas clinics that are treating people with Long Covid are also offering apheresis to people with ME/CFS and I know of several people who have travelled abroad to have apheresis – with mixed results. So why isn’t apheresis also being made available to people with ME/CFS here in the UK?

Treatment: Apheresis Read More »

Are you aware of a new treatment called apheresis that is being given to people with Long Covid? It is supposed to remove small blood clots that are involved in causing Long Covid. Some of the overseas clinics that are treating people with Long Covid are also offering apheresis to people with ME/CFS and I know of several people who have travelled abroad to have apheresis – with mixed results. So why isn’t apheresis also being made available to people with ME/CFS here in the UK?

Vaccine Damage Payment Scheme

There was an interesting item on the BBC news ( https://www.bbc.co.uk/news/health-61898694 ) about the first payment being made under something called the vaccine damage payments scheme (VDPS) to the relative of someone who had suffered a fatal adverse reaction to the Oxford Astra Zenca COVID-19 vaccine.

The BBC article also referred to a lady who “…..was unable to work for a year after developing VITT (vaccine-induced immune thrombotic thrombocytopenia) and struggles with chronic fatigue, migraines and brain fog and fears her job could be at risk – but believes she will not be considered 60% disabled”.

As someone who has had a significant and prolonged (now over a year) relapse of ME following this vaccine do you think it is worth making a claim? And does this scheme also cover people who have developed ME after other types of vaccination?

Vaccine Damage Payment Scheme Read More »

There was an interesting item on the BBC news ( https://www.bbc.co.uk/news/health-61898694 ) about the first payment being made under something called the vaccine damage payments scheme (VDPS) to the relative of someone who had suffered a fatal adverse reaction to the Oxford Astra Zenca COVID-19 vaccine.

The BBC article also referred to a lady who “…..was unable to work for a year after developing VITT (vaccine-induced immune thrombotic thrombocytopenia) and struggles with chronic fatigue, migraines and brain fog and fears her job could be at risk – but believes she will not be considered 60% disabled”.

As someone who has had a significant and prolonged (now over a year) relapse of ME following this vaccine do you think it is worth making a claim? And does this scheme also cover people who have developed ME after other types of vaccination?

Treatment: Vitamin D & Safety

Following on from the question in the Summer issue of ME Essential about the risk of developing osteoporosis in ME and the use of vitamin D supplements, I was concerned to see a newspaper report about someone who had been recommended to take a vitamin D supplement by a nutritionist which had caused serious side-effects and resulted in hospital admission.

So should people with ME/CFS be taking vitamin D supplements? Or any vitamin supplement? And is it safe to do so?

Treatment: Vitamin D & Safety Read More »

Following on from the question in the Summer issue of ME Essential about the risk of developing osteoporosis in ME and the use of vitamin D supplements, I was concerned to see a newspaper report about someone who had been recommended to take a vitamin D supplement by a nutritionist which had caused serious side-effects and resulted in hospital admission.

So should people with ME/CFS be taking vitamin D supplements? Or any vitamin supplement? And is it safe to do so?

Symptoms: Overactive Bladder (OAB)

I’m female, in my early forties, and have had moderate ME/CFS for about five years. More recently, I’ve been having a number of bladder symptoms – in particular a frequent and sudden urge to pass what are only quite small amounts of urine. I am also having to go to the bathroom on several occasions during the night.

My doctor thought I might have cystitis – even though I don’t have any pain. However, there were no signs of infection on repeated urine tests. My GP now says that I probably have an “overactive bladder”, and that while there are drugs that can definitely help to calm down an irritable bladder they can cause side-effects, including drowsiness.

Is having an overactive bladder more common in ME/CFS? And is there any other form of treatment – as this is causing me a lot of distress and restricting what I’m able to do outside the house.

Symptoms: Overactive Bladder (OAB) Read More »

I’m female, in my early forties, and have had moderate ME/CFS for about five years. More recently, I’ve been having a number of bladder symptoms – in particular a frequent and sudden urge to pass what are only quite small amounts of urine. I am also having to go to the bathroom on several occasions during the night.

My doctor thought I might have cystitis – even though I don’t have any pain. However, there were no signs of infection on repeated urine tests. My GP now says that I probably have an “overactive bladder”, and that while there are drugs that can definitely help to calm down an irritable bladder they can cause side-effects, including drowsiness.

Is having an overactive bladder more common in ME/CFS? And is there any other form of treatment – as this is causing me a lot of distress and restricting what I’m able to do outside the house.

Non-Alcholic Fatty Liver Disease (NAFLD)

I’ve recently been feeling more fatigued than usual. I’ve also lost a bit of weight and had some tummy pains – which are higher up than the sort of spasmodic pain I sometimes get with my irritable bowel.

My GP did some blood tests – all of which were OK apart from some minor abnormalities in my liver function tests. To cut a long story short I then had a visit to hospital and an ultrasound scan of my liver. It turns out that I have what the hospital doctor calls a fatty liver. He says it’s a fairly common condition – especially if you have diabetes, high blood pressure or are overweight and possibly ME/CFS. Could this be connected to having ME/CFS as well? As I’ve only put on weight since developing the condition.

Non-Alcholic Fatty Liver Disease (NAFLD) Read More »

I’ve recently been feeling more fatigued than usual. I’ve also lost a bit of weight and had some tummy pains – which are higher up than the sort of spasmodic pain I sometimes get with my irritable bowel.

My GP did some blood tests – all of which were OK apart from some minor abnormalities in my liver function tests. To cut a long story short I then had a visit to hospital and an ultrasound scan of my liver. It turns out that I have what the hospital doctor calls a fatty liver. He says it’s a fairly common condition – especially if you have diabetes, high blood pressure or are overweight and possibly ME/CFS. Could this be connected to having ME/CFS as well? As I’ve only put on weight since developing the condition.

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