A thread on what people with ME/CFS need in the way of service

[Trish]

Some of us don't live anywhere near a major university research hospital where research and leading clinics are likely to be centred. I fear we will be left out of any specialist doctor led care services which are being rightly described as needed. The difficulty with travel becomes magnified when the nearest such centre might be 100 km away. We therefore need a whole medical specialism to take on ME/CFS as part of their responsiblity in every area of the country, and to have specialist nurses able to travel a wide area to visit patients, and consultant willing and able to do home visits too.

Basic need:

Consulatant diagnosis and annual checkup if wanted accessible for all severity levels.

Specialist nurses working with the consultant

• acting as as contact point for patients available by phone and email and able to do home visits
• to advise on activity management,
• liaise with schools and employers,
• write reports or see that the consultant does them for benefit claims,
• assist with getting home carers
• and OT assessment for equipment,
• and ensure timely referrals to counsellors and dieticians well before the need for either of these becomes critical.

Well informed hospitals with priority for single rooms for very severe cases who need to be in hospital, 'hospital at home' where possible.
Maybe arrangement with hospices for some very severe cases who need nursing care.

NO BACME clinics.

No separation in services for mild/moderate and for severe/very severe. Especially important for continuity of care as any individual is likely to cross over between severity levels over their lifetime.

 

[OrganicChilli]

Can we get dental home visits? What about preventive checks like cancer screenings?

 

[alex3619]

Well here it is folks. Get posting.

I think they need to be referable to a clinic with a physician in a standard medical speciality (not rehab) for an assessment of their problems with a waiting time of around 2-3 weeks on average.

I am facing this kind of thing in about three and a half hours for Australia's MyAgedCare support, but with a public servant who will run me through a very long interview process designed mostly for just older people, not people with complex disability. Setting up specialized assessment services have been needed for a long time. However it will take a lot of analysis, consultation and ongoing dialogue to get the services that we really need on an individual basis. Probably a few field trials and published papers as well.

 

[Utsikt]

Can we get dental home visits? What about preventive checks like cancer screenings?

Eye exams as well. Anything that can be done at home for the severe.

 

[Eleanor]

I wonder if it would be interesting to find examples of briefs for NHS services for other long-term disabling conditions, maybe to borrow ideas but also when it comes to presenting some kind of wish list to decision makers - to be able to say "look, this is the provision that people with other conditions can expect, and people with ME/CFS deserve an equal level of care".

 

[Eleanor]

For example, here are parts of what NHSInform says about motor neurone disease (I have a friend who has just been diagnosed with it, so I was looking at this recently). https://www.nhsinform.scot/illnesse...ves-and-spinal-cord/motor-neurone-disease-mnd

After you’re diagnosed you should be provided with contact details of an MND care specialist. These are healthcare professionals with specialist experience caring for people with MND. They’ll be able to give you (and your family) extra support after the diagnosis and during your time with the illness.

Although there’s no cure for MND, there are treatments available to help relieve the symptoms.

A team of healthcare professionals will work together to help care for you. This multidisciplinary team typically includes:

• a neurologist and an MND care specialist
• a specialist in breathing (respiratory specialist)
• physiotherapists to advise on mobility aids
• occupational therapists to assess the need for adaptations to living environments
• speech and language therapist to provide help with communication and swallowing
• dieticians to support nutrition

As the conditions advances, you might also need palliative care.

Research and drug trials​

You might be given the opportunity to take part in research, including drug trials. Your MND care specialist and neurology consultant can provide further information on this.

Advice for carers​

Caring for someone with MND can be both physically and emotionally demanding. It’s likely you’ll need a wide range of support.

 

[Felis Catus]

Can we get dental home visits? What about preventive checks like cancer screenings?

I can only speak for the UK. Depending on where you live, there might be private mobile dentists and some private dental practices might offer home visits. I saw in a Facebook group people mentioning NHS dental visits but I've never seen an NHS dentist, so it didn't even cross my mind to check. You might need a referral for it.

My GP surgery told me they were going to start offering at home smear tests this year.

Eye exams as well. Anything that can be done at home for the severe.

UK - yes, Specsavers for free for those who are housebound. They didn't ask me for any documents to confirm that but maybe it depends on whom you speak to.


I just thought I'd share this in case it helps someone. The goal would be to have those options everywhere.

 

[Kitty]

I think for newly ill people, a diagnostic service led by a physician who:

• has the training to exclude alternative diagnoses;
  
  
• explains that some people recover, but others don't;
  
  
• tells them they can sometimes help with specific symptoms, but there is no treatment yet for the underlying disease;
  
  
• refers them to good quality sources of advice;
  
  
• signposts patient advocacy and support platforms;
  
  
• makes notes detailed enough to contribute medical evidence if the person has to go through ill-health retirement or claim benefits;
  
  
• sees them maybe once a month for the first six months, then again for a full review after a year;
  
  
• ideally, is interested enough in ME/CFS to want to contribute to a better understanding of the natural history.

Also, I wonder if a peer advice project would be useful, where people who've been ill quite a long time could contribute paragraphs about the journey they went on. For instance:

• clinging to the belief there must be something that helps, followed by trying anything and everything to no avail;
  
  
• suspecting they may have made their illness worse by trying too hard to keep up their lives;
  
  
• discovering there are patients who've been harmed by inappropriate advice, which was given to them by reputable healthcare institutions and medical professionals;
  
  
• learning that most ME/CFS research ranges from useless to fraud-adjacent, and it doesn't take long to get the hang of how to spot it;
  
  
• realising people who claim to be experts usually aren't – real experts admit they know almost nothing;
  
  
• grasping the sheer scale of crappy alternative medicine that is thrust in our faces at every turn, most of which is useless and some of which is risky;
  
  
• the whole internet thing – misinformation from other patients, private doctors offering expensive and unproven treatments, the mushrooming of so-called syndromes.

Charity websites sometimes have pages like this, but they tend to be pretty anodyne and are rarely detailed enough to be satisfying. People who've recently become ill often feel a drive to do something, and this kind of peer learning is useful. If it's done well it can be more convincing than doctors; patients sometimes feel their GPs are overly conservative or suspect they don't want to offer some treatments because they're very expensive.