That's fantastic @josepdelafuente very best of luck with it :)
oh dear, thats a bit cringeworthy 'magnificent significance'.
So sorry to hear of your ordeal Sally i cant offer any advice really as i've been as ill as you are now for upwards of a decade, but it wasnt...
So what time of day is it saying is best to get vaccinated? i cant pick out the key point through all that information
oh... very good!:rofl:
exactly... If i, while having a broken leg (for example), went to the doctors in huge distress reporting i was hearing voices telling me to kill...
yes! thank you
The other thing about having help is that if you do it all on your own they may use that against you - they may make the argument that if you can...
I had lumbar puncture originally during investigations - 20 odd yrs ago, & the CSF pressure was very high they said - the dr doing it even cried...
I'd missed that detail in your original post Joseph. And while it is certainly still possible for them to mess with your UC if your PIP doesnt go...
:rofl: perfect
My advice would be to join (subscribe) to the website www.benefitsandwork.co.uk It costs £20 a yr but is worth 10 times that in my experience....
thats impressive @IanMcPhee :) your Dad would be proud of such a scientific appraoch :heart: edited to tag
yes i can relate to that, like everything within you is telling you SUFFERING, like the signals are generalised rather than specific like pain...
Eh? what things? is my concentration impaired that i can answer but can i concentrate on certain things... which things? reading? watching tv? an...
yes i know, i agree, my point was that you need to be careful when you call it 'aversion'. Thats not an optimal term because it is oft used by...
THIS.
My experience chimes with @Trish I think we need to be careful about calling it aversion, because the BPs theory is all about us feeling avoidant...
precisely indeed. This is one of the issues, because its human nature for people to think that whichever 'version' of, or whichever...
Yes one of the things i find most frustrating is because so many researchers (even outside the BPS crowd) dont seem to understand what ME/CFS even...
Separate names with a comma.