ME/CFS
Outcome unclearIll for 14 months
ME/CFS: chronic fatigue, whole body pains, brain fog and weakness, still occasional joint pain
- Condition
- ME/CFS
- At worst
- Not stated
- Ill for
- 14 months
- Last post
- Feb 2025
In their words
- Condition: ME/CFS
I then suddenly developed chronic fatigue, whole body pains, brain fog, weakness and more at the end of 2023
In context ↗ - Began after: a bacterial or tick-borne infection
I do think all ny symptoms were triggered by that original infection in 2020
Summary
Summit 42966 had Lyme disease in 2020; after two initial antibiotics didn't help, a third eventually helped, though some symptoms never fully went away and painful joints came and went. At the end of 2023 they suddenly developed chronic fatigue, whole body pains, brain fog and weakness, which they think the original infection triggered. A repeat Lyme test was negative and by February 2025 they still had occasional joint pain.
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What they tried
Also tried
Their words about each treatment
- antibiotics · Helped
I was then given another antibiotic and eventually I did feel better. But I would every now and then get very painful joints all around my body.
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 |
|---|---|
| end of 2023 | suddenly developed chronic fatigue, whole body pains, brain fog and weaknessI then suddenly developed chronic fatigue, whole body pains, brain fog, weakness and more at the end of 2023In context ↗ |
| February 2025 | still has symptoms and intermittent painful jointsI would every now and then get very painful joints all around my bodyIn context ↗ |
Symptoms mentioned
Their words about their symptoms
- Pain & fibromyalgia
I would every now and then get very painful joints all around my body
In context ↗ - Brain fog
whole body pains, brain fog, weakness and more
In context ↗