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Message: <blockquote data-quote="Rabdos" data-source="post: 2542453" data-attributes="member: 402888">HelloAfter COVID, it's been now more than 6 months that dyspnea, fatigue etc are still present with no improvement.I was hoping that dyspnea could exclude ME/CFS but I read that 50% of ME/CFS have severe dyspnea with other concurrent symptoms that I have too.So, I think I will need to get diagnosed with ME/CFS as soon as possible.Do you know what is the process? I do not think my GP even know what that is, he never mentioned it and from other discussions he probably doesn't know it.How can I get diagnosis?What help is available?Will it even improve or go away?It really looks like a life sentence of almost constant unbearable pain and fatigue. If this will be the case from now on, it will be a huge disability that puts in risk all life aspects, work, family, health, etc.Thanks!</blockquote>

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