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ME/CFS Moderate → no benefit

ME/CFS and POTS, wheelchair help; physiotherapy resistance exercise gave no improvement

Condition
ME/CFS
At worst
Moderate (mostly housebound)
Ill for
Not stated
Last post
Dec 2025
In their words
  • At worst: ModerateI’m moderate to severe so it’s not too bad but it’s not invisible. In context ↗
  • Now: No benefitrecently that hasn’t been going well and I keep overdoing it(things that definitely wouldn’t overdo it before) In context ↗
Read from 8 of their posts and comments; links to the 6 this page draws on

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Summary

An under-18 with ME/CFS and POTS who uses a rollator, manual and power chair and got their first wheelchair at 14. Physiotherapy that pushed resistance exercise left them in crying pain every night, and they have been overdoing it recently. In late December they went to the ER, which was not very helpful, and were admitted. They can travel only with wheelchair help and long sleep-ins.

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What they tried

Their words about each treatment
  • mobility aids / conserving energy · Helpedtaking a power chair walk outside makes me feel the best. In context ↗
  • physical therapy: resistance bicycle and leg pushes · WorseAt my pt she mad me do bicycle with resistance for 6 mins and push 75 with my feet and more. I have been in crying pain every night since. In context ↗
  • migraine cocktail · Not saidI really only got a migraine cocktail and then admitted which I thought was bc they were going to do testing 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 wereAfter
age 14already ill enough to need a wheelchair for a family weddingI first started using a wheelchair when I was 14 and we were invited to a wedding. In context ↗Moderate
2025-11-03physiotherapy pushing resistance exercise, flare where they could not walkI have been in crying pain every night since. In context ↗SeverePhysical therapy / physiotherapy
2025-12-02travels only with wheelchair and long sleep-insI’m moderate to severe so it’s not too bad but it’s not invisible. In context ↗Moderate

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseI keep overdoing it(things that definitely wouldn’t overdo it before) In context ↗
  • POTS & dysautonomiaMy pots hates it In context ↗
  • Pain & fibromyalgiaI have been in crying pain every night since. In context ↗
  • Headaches & migraineI really only got a migraine cocktail In context ↗

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