Undiagnosed symptoms: Hello everybody... - Myalgic Encephalo...

Myalgic Encephalomyelitis Community

2,086 members651 posts

Undiagnosed symptoms

2 Replies

Hello everybody, I'm new to this forum, and I really need help.

I've been sick for one year without a successful diagnosis, my symptoms are: extreme fatigue with brain fog, light sensitivity, weakness in extremities, lately my hands get gripped and my ring finger is twitching all day.

Could somebody help me?, some ideas of what could be affecting me?

Thanks in advance, David.

2 Replies
Iliad profile image
Iliad

Hiya Davjul

Sorry to hear about your illness. This might be a good place to start

nhs.uk/conditions/chronic-f...

Hi Hidden . I did a post recently that might be helpful to you. Lots of things can make people ill like toxins, infections, nutritional deficiencies, poor gut health, diet and lifestyle etc.

The testing system for vitamin b12 has flaws and the guidelines have been changed:

onlinelibrary.wiley.com/doi...

Some of the symptoms of b12 deficiency include, brain fog, fatigue etc. These links should also be useful:

drmyhill.co.uk/wiki/Summary....

drmyhill.co.uk/wiki/Detoxif...

You could also Google Dr Mark Hyman. He used to have chronic fatigue due to mercury poisoning: drhyman.com/blog/2010/05/20...

Heavy metals like mercury and aluminium are in the soil and food chain etc. I just found out I have mercury, aluminium and lead poisoning.

Not what you're looking for?

You may also like...

Covid 19 has it worsen your ME/CFS symptoms?

Good morning all! I was wondering if any of you caught Covid 19 that made their ME symptoms worse....
theia profile image

What was your experience at the doctor on diagnosis?

Hi all, I was diagnosed with CFS in 2015 - and still have it. I remember maintaining at the time of...
Regalbirdy profile image

Who diagnoses ME/CFS?

Hi, I have been researching ME since my GP mentioned that it could be a possible diagnosis about a...
Golfer15 profile image

Advice on pacing

I’m just waiting on formal diagnosis from the ME doctor but had phone call last week from the ME...
Lexilou70 profile image

At my wits end with CFS

I have only had CFS for around 9 months but am already at my wits end. It was bought on by...

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.