Progressive: A poll asking do you get... - Ramsays Disease

Ramsays Disease

568 members470 posts

Progressive

Effort profile image
7 Replies

A poll asking do you get progressively worse ?

cortjohnson.org/forums/thre...

Written by
Effort profile image
Effort
To view profiles and participate in discussions please or .
7 Replies
Dunnlyn profile image
Dunnlyn

Mixed feelings ticking boxes then so many experiences are the same not so isolated in a new world adjusted and adjust again without realising.

ringading profile image
ringading

Without treating a cause deterioration seems almost inevitable and all the more surprising any recovery can be found.

Ian123 profile image
Ian123

Progressive or relapsing remitting will be of more interest for researchers I think as coping with each day is easier with the belief tomorrow is a better day.

Moonlightshadows profile image
Moonlightshadows

Whatever the truth of recovery and progression my own preference is knowing the facts I found the disbelief from test results prolonged acceptance of health issues.

Seascape profile image
Seascape

Progressive but feel more up and down than the poll suggests.

budgiefriend profile image
budgiefriend

I agree with #Moonlightshadows . Without tests, we are left to wonder what is going on. I try to take some tests myself and write down the results. But I have difficulty interpreting them or fitting them together to make a picture.

I am not trained in any kind of science. I am trained in Fine Arts. Really out of my depth with all this.

I know what constitutes good research, I can get the gist of any article or research paper, but I will forget details and struggle with any complex or multi-stage line of thought.

My cognitive dysfunction is worsening in this regard. I can't do math problems beyond basic arithmetic in my head. When I am in pain, I can't even do that.

I do appreciate that we have scientists in the ME and Fibromyalgia communities who write blogs and report on the latest science. That interpretation of these studies and news helps so much. But even their blog articles are often too complicated to be of much use to me.

When will doctors be taught about these illnesses? When will they be required to do proper investigation online if there are areas they know nothing about and they need to know how to diagnose or refer or treat a patient?

I do not understand this at all. Is there anything we can do to make this possible?

Mistymooring profile image
Mistymooring in reply tobudgiefriend

Predicted three separate groups of equal size (approximately) polling results ask researchers use science updating knowledge.

Not what you're looking for?

You may also like...

Progressive brain changes

A long term study of white matter changes...
Ian123 profile image

Please ask your MP to attend the APPG on ME Wed May 11th

If you have not already done so please ask your local MP to attend the All-Party Parliamentary...
ukmsmi4 profile image

Support Dr Sarah Myhill

We want people who have been harmed by PACE to write in support of this complaint. You are free to...
Effort profile image

Request to sign a petition to the government for funding for ME research

This is on behalf of a fellow ME sufferer on the fibromyalgia HU forum, but as an ME and...
ukmsmi4 profile image

New to this !

Hi all I am awaiting diagnosis for this my dr has referred me to someone but i was having a...
cowre profile image

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.