ME/CFS
Moderate → no benefit
Worsening exhaustion with ME/CFS and less energy, no improvement
- Condition
- ME/CFS
- At worst
- Moderate (mostly housebound)
- Ill for
- Not stated
- Last post
- Apr 2024
In their words
- At worst: Moderate
at least I still have a window of time during the day that I can get out and do something ... am not completely bed bound
In context ↗ - Now: No benefit
Since getting back I’ve watched my exhaustion get worse and worse.
In context ↗
Summary
In April 2024 they said they had been depressed about their health and that their exhaustion had worsened steadily since moving back to the United States, a move that was hard on them physically and mentally. They were not completely bed bound and still had a window during the day to leave the house for appointments, but had noticeably less energy than when they lived overseas.
Ask Miruvor AI
What they tried
Also tried
Their words about each treatment
- Botox · Helped a lot
It would literally freeze my facial muscles but it worked for nearly three months at a time. It was AMAZING. I wasn’t able to get it for a few years and when I started again, they had changed the type of Botox they used. Unfortunately it didn’t really help much.
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 | Where they were |
|---|---|---|
| — | ill while living overseas, with noticeably more energy than laterWhen we were overseas I had so much more energy than I do now.In context ↗ | Not stated |
| 2024 | moved back to the United States; exhaustion steadily worsenedThe move back to the states was really hard on me, both physically and mentally. Since getting back I’ve watched my exhaustion get worse and worse.In context ↗ | Moderate |
Symptoms mentioned
Their words about their symptoms
- Anxiety & low mood
I’ve been really depressed about my health lately.
In context ↗