What is Post Exertion Malaise in ME/CFS

We’re a clinic focused on making invisible illnesses visible - join us on this journey!

We help people overcome complex health conditions including:
🔹 Fatigue Syndromes such as ME/CFS
🔹 Dysautonomia such as OI & POTS
🔹 Pain Sensitisation such as Fibromyalgia & Chronic Widespread Pain
🔹 EDS & HSD Syndromes
🔹 MCAS
🔹 Sleep Disorders
🔹 Related anxiety & depression.

Use the hashtag #ahcmillions to help us on our way to impacting one million lives by 2022.

[kwillo]

That was lovely! Thank you! Congratz on recovering! I just found out CFS exists after 5 years of struggle and calling it a burn-out. Hearing from others really feels helpful, KEEP GOING

[dfisher]

I think i have this, bout two years now, been to hundreds of appts they cant find anything wrong with me but days i feel like im dying after just writing on paper or standing up

[bluewolf]

I'm literally crying right now, because I've been fighting for years for doctors actually listen to me and stop saying that it's all in my head... Time is passing by and I keep getting worse! I'm reaching a point where I don't know what to do anymore. I need help.

[DanaRToliver]

are there any doctors out there willing to make the connection between mycotoxicosis (systemic fungal infection / mold illness) & ME/CFS, MCAS, MCS, POTS along Vaccine Injury? Why won't the medical community ever look at vaccine injury & fungal infections / mycotoxic exposure as a cause of these illnesses?

[Kattykat]

Where do you go to get diagnosed for cfs. I'm a single 60 yr old women who has had this all my life. I dont have the money or time to miss work with a ton of doctor visits only to be told that they dont know what to do other than workout and eat healthier. Seclusion is the only comfort i have.

[joannedevine]

Why is my PEM worse second day out from activity?

[hillsofwi]

Any thoughts at all on expanding the energy allotment? I've tried everything I can imagine without success. And the price paid for each experiment is usually extreme.

[anvime]

To which kind of doctor do you recommend me to go to get a possible diagnosis of CFS and to get advice about pacing or supplements? My GP and psychiatrist know nothing about chronic fatigue and want me to do more exercise (which I know it’s bad) and failed to tell me to which kind of doctor I need to go. Neurologist?

[allaboutstress]

What s the bio chemical cause pem? Knowing that means I can do something about it. Thank you