Severe fatigue and brain fog destroying my life!
I know that this is a Pernicious Anaemia group, so I'm sure people are going to say YES!...
Chronic fatigue trial results 'not robust', new study says
Just seen this article on the BBC News site - I imagine there will be similar on other sites. [ b]Chronic fatigue trial results ' not robu...
•Feel like I move extremely slow now both mentally and physically •Dizziness upon standing often •Extremities/body parts feel so utterly exha...
Crippling fatigue and brain fog ruining my life
Male, 23, 5’10, 165 lbs, White Hello, My health has felt like it’s been in the crapper for way too long. When I was 12-13 I was diagnosed wit...
Severe fatigue and brain fog destroying my life
Hello friends, I have been dealing with these same issues for far too long! Little long, but here goes: Starting when I was 16, I woke up one...
I have just been diagnosed with Chronic Fatigue Syndrome and I just want some advice from the community. I have painful headaches every day a...
Exercise therapy in Warwick, UK
If so I would like to let you know about the therapy programmes and classes specifically for people with PD coming soon. I am an OT with many...
Graded Exercise Therapy (GET) is declared ineffective and potentially harmful for ME CFS patients
Wow! As a physio I never understood why the fatally flawed PACE trials and others were not judged harshly by Cochrane and other safeguards of...
Hi, I have normal T4 and TSH but a benign part cystic / part solid nodule and symptoms of hypothyroidism....
Faith to be healed and made whole
I always have considered life a journey. We have met up with anxiety, depression, post traumatic stress disorders and other disorders on our ...
Chronic fatigue and brain fog ruining my life!
I would say my anxiety levels are about a normal human amount, at least not enough to perpetually feel like this •Never have had issues with ...
Just need some hope
Hey all, It's been 8 months since my last afib attack. Well, it's the last that I know of....
Life is a living hell from worsening chronic fatigue and brain fog
Have ME/CFS? Write to your local MP about current NICE Guidelines for ME
For those who have already signed ME Association’s petition, there is something else you can do – write to your MP. ' NICE guidelines are bad...
Thyroid crew: Thank you for your support.
Despite being hypothyroid and on Levothyroxine for over 15 years, I've learned more about the condition since I joined this website than I ha...
Bring me to life without chronic fatigue syndrome
Hello everyone, I'm new here. My name is Jane and I had an ordinary life: a good job, a loving family, finally I paid the mortgage....
Support DR Myhill eat al re ME PACE Please read
You do NOT have to have been diagnosed or have fallen ill with CFS/ME after PACE was published [ March 2011 ] to support this complaint....
EULAR Guidelines for Fibromyalgia July 2016
so quickly Hope you are all as well as you can be as we all live with this illness Fibro and it's various symptoms plus associated ailments?...
The first step out the door is always the hardest!!!
This morning a battle took place in my house, a battle so epic that Morgan Freeman should have done the commentary... ( of course I am joking...
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