3 Reasons Why You’re Not Getting Better From M.E/CFS - Comment Recover Below For The Free Training.

[@carolineroberts9743]

So true! A holistic approach is key.

[@CFSHealth]

100%

[@Milliemollym]

Crappy Doctor....that made me laugh....the first doctor told my mum that 'She' was a hypochondriac when I first got ill in the 70s.... Didn't even bother to ask me how I felt...Poor mum tried but there was no info out there back then....it's taken until the advent of the internet before anything remotely useful came to the fore... Needless to say I only visit the doctor as a last resort for the easy stuff they can prescribe for.. Now I am 60 I am finding people who have only become ill recently with Post Viral Fatigue after Covid, are telling me not to bother trying to get well.... they've no idea what it's like to have this your whole life... God bless the lady who joined you in her mid 80s s and is now well...that's the example I am determined to follow

[@sushilaananda3365]

Or, as is the case with my doctor, there is absolutely no interest in either discussing ME/CFS or even attempting to mitigate symptoms.

[@Milliemollym]

I had a doctor like that....he wouldn't even let me have a £10 blood test.....so I asked him ..I said "I'm curious , are doctors now a first point of call to be referred onto consultants and the like...or do they still try to make people well?" He amazed by saying he liked to try to help people get well... He did at least read the book I gave him on Adrenal Fatigue but said it wasn't the science he had learnt....no discussion re how I felt or was I feeling better... nothing.. Id had ME almost 40 years at this point and only ever asked for a blood test to check my iron...I was a pretty low cost patient. At least he never gave me any hassle and retired soon after

[@NamirasAcolyte]

My brother in christ, i can't afford decent food, i can barely get around. Im american, i dont have universal healthcare, im living off canned food and buscuits. This condition is complex, simply saying "change how you eat, get your energy and sleep right" isnt enough. This condition is far more complex than just fixing your sleep and food. Its a bonecrushing fatigue that never goes away. Some are so sick they need feedin tubes. This isnt some sunshiney walk in the park condition that can be fixed with some lifestyle modifications and positive thinking

[@janetholmes]

There is hope. I'm remembering the heartbreak of the man at the pool of Bathesda in John 5 and the faithfulness of Jesus to find him where all else had failed him. We have eternal hope in the Lord. While no one has got us into the pool yet, Jesus is for us and with us. He is well able to heal and there's many beautiful testimonies of Him setting others free from ME/CFS. This isn't incurable, and we know the Healer. One day we will be healed. I don't say any of that to negate any of the pain, isolation and abandonment you've endured. Some lifestyle adjustments can help a bit, but I think the root of this condition is prolonged trauma and heartbreak, which really only God can heal. Thank goodness He is with us. 💖We're in this together! Keep up the good fight :)

[@katharinedavis4947]

Recover. . I've been getting worse and worse, and I no longer push and crash. I can't push any longer . I used to in order to have any quality of life. I'm 79 , I don't expect to be like 30 again, but even like 70 would be great . K

[@CFSHealth]

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[@Earthenergy100]

I'm feeling good for like a week I even forget I have it then I crash with flu like symptoms then I get better again and would say the rash can be every 3 weeks around can anyone relate

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[@CFSHealth]

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[@HBIC-te7me]

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