ME/CFS
No benefit
ME/CFS getting worse over a very hard year; CBT gave no benefit
- Condition
- ME/CFS
- At worst
- Not stated
- Ill for
- a few years
- Last post
- Jan 2017
In their words
- Condition: ME/CFS
I was diagnosed a few years ago with cfs/me
In context ↗ - Now: No benefit
This year has been so hard on me and it seems to only be getting worse.
In context ↗
Read from 1 of their posts and comments; links to the one this page draws on
Summary
Stone 83885 was diagnosed with CFS/ME a few years before 2017, while still under 18, and was referred to a child psychologist for CBT, which they said never helped. After turning 18 they were dropped from paediatric care to a GP they described as uncaring, who told them to go to the gym, leaving them without CBT or regular professional support. At the time of writing they said the past year had been very hard and their illness seemed to be getting worse.
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What they tried
Also tried
Their words about each treatment
- CBT · No change
they refered me to a child psychologist for CBT and it never helped me
In context ↗
Their path
They say too little about how ill they were at each step to draw it on the severity scale, so the steps are listed as they describe them. Dates are when they posted.
| When | What happened |
|---|---|
| a few years before 2017 | diagnosed with CFS/ME while under 18I was diagnosed a few years ago with cfs/meIn context ↗ |
| 2017-01-16 | discharged from paediatric care to an unsupportive GP, still worseningThis year has been so hard on me and it seems to only be getting worse.In context ↗ |