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ME/CFS Severe → no benefit

ME/CFS and lymphoma chemo left constant fatigue and brain fog, now unable to work or study

Condition
ME/CFS
At worst
Severe (mostly bedbound)
Ill for
Not stated
Last post
Jun 2026
In their words
  • Condition: ME/CFSMy doctor settled on CFS when I was a teen In context ↗
  • At worst: SevereI need to sit or lay down all the time to recover from exhaustion after relatively little exertion. In context ↗
  • Now: No benefitIt’s just getting worse with time. In context ↗
  • Began after: nothing they could nameAll of this was going on for years before I was diagnosed with cancer at 22.
  • Says they never had: Pain & fibromyalgiaI experience no physical pain from it
Read from 1 of their posts and comments; links to the one this page draws on

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Summary

Diagnosed with CFS as a teenager, Bramble 86582 worked full-time factory shifts in their early twenties despite daily exhaustion, long sleep and muscle weakness. Stage 2 Hodgkin's lymphoma at 22 and twelve ABVD chemo infusions left them much worse, with brain fog, memory loss and constant fatigue, now unable to work or study. In remission at 23 they were applying for disability and described near-daily suicidal thoughts.

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What they tried

Their words about each treatment
  • antidepressants · No changewe’d tried multiple antidepressants and I remained fatigued regardless of how much sleep I got or how much my mental state might’ve improved In context ↗
  • Adderall · HelpedIt helps with the fatigue. Without it I’m in bed all day. With it, some days, I can get out of bed. In context ↗
  • estrogen HRT · WorseI was very, very sleepy and depressed when I was taking it, more than usual, for the few months I was able to be on it. In context ↗
  • ABVD chemo · Much worseThe cancer definitely didn’t help the fatigue but the chemo has made it so, so much worse. In context ↗
  • pacing · Not saidI have to really pace myself with minor physical activity (even bending over) or I will get smacked with symptoms either immediately or soon after. In context ↗

Their path

Very severeSevereModerateMildNear normalRecovered

How ill they were on the ME/CFS severity scale, estimated from what they describe at each point, in the order they describe; they don’t give enough times to place each step. Hover or tap a point. Dates are when they posted. What the levels mean.

Show as a table
WhenWhat happenedWhere they were
as a teenagerdiagnosed with CFS as a teenager after antidepressants did not help the fatigueI was diagnosed with it as a teenager many years ago, I’m 23 now In context ↗Mild
age 22stage 2 Hodgkin's lymphoma and 12 ABVD chemo infusions worsened the fatiguethe chemo has made it so, so much worse In context ↗Moderate
June 2026, age 23in cancer remission but nonfunctional, unable to work or study, applying for disabilitynow I’m more nonfunctional than I’ve ever been, even at the height of cancer and chemo In context ↗Severe

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseI have to really pace myself with minor physical activity (even bending over) or I will get smacked with symptoms either immediately or soon after In context ↗
  • Brain fogThe brain fog, memory loss, muscle weakness, and exhaustion from chemo In context ↗
  • Sleep problemsthe amount I slept (12-15 hours on good days, all day on bad days) In context ↗
  • Muscle weaknessthe symptoms of daily muscle weakness (I even feel it in my bones, they feel weak like jelly) In context ↗
  • Anxiety & low moodAll of this combined has left me extremely depressed and thinking about suicide In context ↗
  • Hair lossdepression, from hair loss, scars In context ↗

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