I undertook a self selecting survey about NHS care for children and young people with ME and received 151 responses. I am particularly interested in this at this time due to the Parliament debate on ME this January (2019)
Steve Brine, Health Commissioner dismissed the ideas that : 1. People with ME are dismissed by their doctors 2. People with ME are coerced to do Graded Exercise Therapy
My last article Policy funnels families into unwarranted child abuse shows how refusal to force a child to undertake Graded Exercise or failure of the child to *improve* whilst doing this dangerous and debunked therapy, leads directly to child protection and false allegations of fabricated and induced illness. Clearly, young people with ME are coerced into doing Graded Exercise Therapy, regardless of the wording of the NICE guidelines. Steve Brine quoted these guidelines and the fact that they clearly say that a patient can refuse
treatment and that this refusal will not affect their ongoing care, to dismiss this very real problem of abuse of people with ME. However, we can see that unwarranted and false child abuse investigations are used in order to coerce GET engagement.
GET is the idea that increasing exercise by 10% every other week can cure you of ME/CFS, a condition that is characterised by Post Exertional Fatigue, that is, any exercise causes a massive increase in fatigue and other symptoms and/or an exacerbation or "crash". Despite the study behind GET being debunked, it remains in the NICE guidelines and the vast majority of those surveys had been prescribed GET. The NICE guidelines are now under review, however NICE have refused to remove GET from their recommendations in the mean time, stating that patients have the right to refuse.
Pie chart "Have they/you been prescribed Graded Exercise Therapy?" 149 responses 38.3% No 61.7% Yes
Just a reminder that this is a therapy that is debunked and has shown in further studies by the ME Association to actually harm people with ME.
Many felt that their refusal to do GET and CBT affected their care, despite it being stipulated in the NICE guidelines that this should not happen
Pie chart "If GET and/or CBT was refused, do you feel this refusal affected your care?" 89 responses 47.2% NO 52.8% YES
Pie chart "If you/they were prescribed Graded Exercise Therapy, was it prescribed after 21st June 2018?" 115 respondents No 77.4% Yes 22.6%
Pie chart "Have you ever been told by an NHS medical professionals that they "Don't believe in ME"? 150 responses 58% No 42% Yes
Another common phrase heard in ME circles is "Everyone gets tired", I don't know of a single phrase that is so hurtful and dismissive when uttered to a child struggling with a condition that has been shown to have a worse quality of life than those with cancer.
“ME/CFS is as disabling and has a greater impact on functional status and well-being than other chronic diseases such as cancer. The emotional burden of ME/CFS is felt by lay carers as well as by people with ME/CFS.” Nacul et al (2011a) The scary thing is that many NHS professionals seem to think that this is a phrase which it is totally reasonable to say to a child with ME
Pie chart "Have you every been told by a NHS professional that "Everyone gets tired"? 150 respondents 63.3% Yes 36.6% No
Pie chart "Have you been referred to children's services ?" 147 responses 75.5% No, 13.6% Yes for school attendance, 4.1% yes to the disability service, 4.1% yes for fii, 2.7% yes for abuse/neglect related to having ME
Bar chart "Have you/they been offered medication for symptoms?" 50 responses 45.3% Melatonin for sleep, 31.3% pain relief, 20.7% anti sickness 30.7% other medication, 27.3% No medication offered
The NICE guidelines specify that ME/CFS diagnosis should be made only when after other possible diagnoses have been excluded and symptoms have persisted for more than 3 months (4 months in adults). The vast majority, 92% had blood tests before being diagnosed, but only 24% had ct head and 5% had sleep clinic. Of the respondents, 63% were diagnosed after blood tests only.
Once a diagnosis of ME is made, despite the professional attitudes that they either "don't believe" in ME or seem to think its *just* feeling a bit tired, many young people find other symptoms and conditions are dismissed as relating to ME. Indeed a low but significant percentage reported injuries being dismissed as ME/CFS. Bar Chart "Have any other illness/injury and or symptom that isn't ME been dismissed as related to ME?" 146 responses 26.7% Yes another illness, 20.5% Yes other symptom from something else, 3.4% Yes from injury, 57.5% No
In fact, securing any medical care for any condition when you have a diagnosis of ME/CFS becomes increasingly difficult, with young people with ME/CFS reporting they are refused referrals for other conditions.
Bar chart " Gave you been refused referral for other health needs due to it being dismissed as ME?" 142 respondents 2.8% yes refused mental health referral, 15.5% yes refused referral to specialist for something else, 66.2% No, 21.1% Yes refused referral for POTS, 8.5% yes refused referral for EDS
I will be sending this information to Steve Brine and my local MP and can only hope that they don't dismiss the plight of people with ME.
Update: Steven Brine has quit due to other matters, but I'm still hopeful that we will receive a response from his replacement when they are appointed
originally published 30 March 2019