The disappearance of ME/CFS

In Canada I was diagnosed with 'post-viral fatigue syndrome' in 1992. The billing code in my province was changed to ME/CFS in 2010 and also includes FM in the mix. I wonder if doctors are even aware of it because I just go for my yearly physicals and don't mention ME at all for the last 25 years.
 
Mij said:
My new GP wanted me to come in to assess my walking. I've had ME/CFS for 34 years, and she's not going to collect any data by watching me walk down the hallway. sheesh.
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I observe a critical state in many systems needing radical reform yesterday. Some breakthroughs broke through ugh trugh some programmed rearguard actions, so maybe your new GP is conducive, but:

Is it necessary to have a walking assessment?

If not, then is there any problem if one says: no thankyou?

Or if one asks: why?

If one is not in danger of falling. If one did not report stumbling legs, or shaky vision. If one is already assessed and diagnosed with a condition limiting mobility.

If not suspected of geriatric or other incompetence, and not currently asking for a mobility aid, domestic or nursing help, an income top-up, or a medical exemption.

And If no authority, professional or relative wants what re-assessed.

And there is nothing you don't know about on offer

Frankly, is this a mobility assessment to review the diagnosis, maybe suspected of being out-dated? Super-superseded? With precedence?

If so a review is not necessary, because the symptoms remain, and remain consistent with the current diagnostic criteria, too.
 
@bicentennial

I wrote about the issue I have with my new GP in more detail on another thread. She is very young, early 30s, she replaced my GP of over 35 years. She has only met me three times, the last time was 2yrs ago so she doesn't know much about me. I have a CFS diagnosis, I saw it on the computer screen but I'm not sure she's aware of that or even knows much about it. I never discussed it much with my retired GP, only when she asked how my 'fatigue' was doing. She understood that I was disabled though.

To make a long story short, I need to get my disability tax credit renewed every 4yrs, and when I spoke to the receptionist to get the process started, she went to inform the doctor. The doctor asked if I had "mental health issues". I explained to the receptionist, no, that's not my problem and that I have a physical and cognitive energy deficit- a recognized chronic illness since 1992. My GP still wanted me to come in to assess my walking.

I decided to upload information about ME/CFS to their secure portal to provide more info, so my GP agreed to a phone appointment. I hope she reads what I sent in, otherwise she won't understand the nature of my disability.
 
Mij said:
@bicentennial

I wrote about the issue I have with my new GP in more detail on another thread. She is very young, early 30s, she replaced my GP of over 35 years. She has only met me three times, the last time was 2yrs ago so she doesn't know much about me. I have a CFS diagnosis, I saw it on the computer screen but I'm not sure she's aware of that or even knows much about it. I never discussed it much with my retired GP, only when she asked how my 'fatigue' was doing. She understood that I was disabled though.

To make a long story short, I need to get my disability tax credit renewed every 4yrs, and when I spoke to the receptionist to get the process started, she went to inform the doctor. The doctor asked if I had "mental health issues". I explained to the receptionist, no, that's not my problem and that I have a physical and cognitive energy deficit- a recognized chronic illness since 1992. My GP still wanted me to come in to assess my walking.

I decided to upload information about ME/CFS to their secure portal to provide more info, so my GP agreed to a phone appointment. I hope she reads what I sent in, otherwise she won't understand the nature of my disability.
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It sounds like she thinks disability means 'can't walk good'.
 
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