Miruvor
Sign up
ME/CFS Somewhat better

ME/CFS, somewhat better with methylphenidate and heart-rate pacing

Condition
ME/CFS
At worst
Not stated
Ill before improving or writing
Not stated
Last post
Oct 2018
In their words
  • Condition: ME/CFSThat started me on another path that led me to a CFS/ADD(I) diagnosis. In context ↗
  • Now: Somewhat betterit helps me get by In context ↗
  • Began after: stress or burnoutit may have even been the catalyst for CFS In context ↗
Read from 4 of their posts and comments; links to the 4 this page draws on

Request to remove this story

Summary

Acorn 49006 described having CFS. Antidepressants made them worse; one with norepinephrine reuptake inhibition fixed nothing but made things different and led to a CFS/ADD(I) diagnosis. A B12 injection from their CFS specialist brought no change. Methylphenidate helped them get by, though with tolerance issues, and they paced using a Fitbit heart rate monitor within a conservative estimate, which they found positive.

Ask Miruvor AI

Asking aboutAcorn 49006’s story

What they tried

Their words about each treatment
  • antidepressants · WorseI've found antidepressants make it worse. I lucked onto one with norepinephrine reuptake inhibition, which didn't fix anything, but made things different. In context ↗
  • B12 · No changeB12 was the first intervention my cfs specialist prescribed. ... No change in me, but I would still recommend giving it a go. In context ↗
  • coffee · HelpedIt didn't work, but helped, before I was better medicated. Would have between 10 and 15 a day, now 1 to 3. In context ↗
  • methylphenidate hydrochloride (Ritalin) · HelpedI'm on methylphenidate hydrochloride (Ritalin) and it absolutely helps. ... it helps me get by. In context ↗
  • Fitbit heart rate monitor · HelpedI've been using a Fitbit heart rate monitor for the last 6 months. My resting HR is 63 bpm, when upright I range from 72 - 86, and when active, up to 115. In context ↗
  • working within a conservative heart rate estimate · HelpedMy practice has been to, as you suggested, work within my conservative estimate; this has been a positive methods in my experience. In context ↗

Approaches: Pacing · Stimulants

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.

WhenWhat happenedAfter
—CFS, possibly after ADHD burnoutit may have even been the catalyst for CFS In context ↗
2018Ritalin helps them get byI'm on methylphenidate hydrochloride (Ritalin) and it absolutely helps. In context ↗Methylphenidate (Ritalin, Concerta)
2018-10-25pacing with a Fitbit heart rate monitorthis has been a positive methods in my experience In context ↗Pacing and the energy envelope

Adverse events

Symptoms mentioned

Their words about their symptoms
  • Post-exertional malaiseit triggers post-exertional malaise and activates my sympathetic nervous system response In context ↗

Ask Miruvor AI

Asking aboutAcorn 49006’s story

Similar stories

  • Bedbound with ME/CFS after COVID, some improvement with low-dose naltrexone and ivabradine

    Somewhat better Crocus 16327 ME/CFS Severe at worstIll 15 years before improving or writing reddit.com Oct 2026

    She had 15 years of gradual ME/CFS symptoms with teenage EBV and crashes during her PhD, then became bedbound after COVID in early 2024. Diagnosed with ME/CFS, POTS, MCAS and hEDS in 2025, she credits low-dose naltrexone, ivabradine, H1/H2 antihistamines and…

  • Bedbound with ME/CFS after a two-day CPET, much better with MCAS treatment and pacing

    Much better Tide 69091 ME/CFS Very severe at worstIll 3.5 years before improving or writing reddit.com Oct 2026

    A woman in the Netherlands with ME/CFS became bedbound after a two-day CPET in November 2022. LDN, Mestinon and amitriptyline made her worse and she stopped them. Later MCAS treatment (quercetin, cromolyn, antihistamines), escitalopram and pacing helped; by…

  • Bedbound over a year with ME/CFS, much better and moderate after gabapentin and kratom

    Much better Summit 17500 ME/CFS Very severe at worstIll 4 years before improving or writing reddit.com Oct 2026

    They traced their ME/CFS to 2018, when abuse, antipsychotics and a cold left them mildly ill; COVID in 2021 made them severe overnight and they spent over a year bedbound, barely able to lift an arm. Gabapentin and later kratom, plus their unsupportive…

  • Unable to work much for 10 months with ME/CFS, somewhat better with vitamin C and Cortef

    Somewhat better Crocus 36923 ME/CFS Severe at worstIll 7 years before improving or writing reddit.com Oct 2026

    A US patient on the ME/CFS spectrum tipped into CFS after travel vaccinations and a later flu shot around 2019, and was able to return to work after a first bad vaccine reaction before a second reaction left them unable to work much for about 10 months.…

A little hope, every Sunday

New recovery stories and data-driven research on ME/CFS and long COVID. Ideas worth considering, and the evidence behind them.

Free · Unsubscribe anytime