Experiences with

Chronic fatigue syndrome (CFS)

[i] fatigue syndrome (CFS) is one condition that cannot co-exist with PBC. CFS is always its own diagnosis, meaning it's reached only after all other possible conditions for the fatigue have been explored.

[/u] [i]Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: the biology of a neglected disease[/i] [i]Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a chronic, debilitating disease characterised by a wide range of symptoms that severely impact all aspects of life.

So, have fibromyalgia and now Dr has said I have CFS. Anyone else have experience with CFS with Fibro ? I'm just exhausted with it all Dr said just accept it and get in with my life. Ok thanks ha ha ha ha

Folks just a quickie, does anyone know of hot and cold sweats with fibromyalgia as I am at work now but the pain is bad and I am getting hot and cold sweats

Patients can sometimes be misdiagnosed with other conditions such as stress or anxiety and chronic fatigue syndrome (CFS).

I replied to a comment with this comment, then decided to share it as a post also: As somebody who has been exposed to EBV (mono), I make trying to suppress EBV a leg of my supplement strategy. I need to write up everything I think helps with EBV, but here is a short list: - Lactobacillus

Google CFS - Chronic Fatigue Syndrome. A definite side affect of Elagard! Some of you will be blown away!

I've avoided taking alendronate due to being high risk of stomach and throat cancer. My doctor wants me to try risedronate. Has anyone any experience of taking this?

Hi everyone The question of oe or de is still tbc but id love your thoughts on pgta If we do go straight to DE our Dr in Spain said they don’t pgta test as the donor is younger than me (I’m 45) but the donor age is 35 and below. I won’t get told until day of transfer what their age is. This has left

basic info: 69 yr old female, Parkinson’s diagnosis Jan 2010. The first 7 yrs I lived close to OHSU in Portland OR and received excellent care. Then moved to a remote area 900 miles away with limited choice for PD care. A neurologist here but no movement specialist. The local hospital performs

happy to report that after all the stress & worry over hubby over the last few months re his spinal stenosis, and then all the hassle with the travel insurers last week, we’ve arrived at our gorgeous Singapore hotel en route for Melbourne and he’s doing really well! Well, he was, until he broke

hi, it has been a while since I posted on here, have had ra since I was 34 am now almost 70. I was told by my opthamologist that I had sjorgrens syndrome a number of years ago as I had problems with my eyes. Until recently I thought that condition was just dry eyes, but have recently seen vlogs on YouTube

Good Morning all, Hope you are all well. I am currently experiencing Sjögren symptoms, Dry eyes ,nasal passage , mouth and other areas, outside of eyes skin very dry,cracked and sore. I went to the optician who said my eyes were very dry and advised drops and heat packs, also to go to Dr for diagnosis

Hello everyone, Has anyone found Nifedipine or Minitran patches helpful for Raynaud's? And if you are using these, do you experience really bad side effects? 💚

This past year I have been suffering with an icy cold, sometimes wet feeling, and also burning like frostbite, in my legs and feet, especially the right hand side. It is worse when sitting. I have had a doppler test to check my blood flow is ok, tests for nerve damage, blood tests, and everything comes

I wanted to ask if anyone had to contemplate FET cycle that falls over Christmas? I had failed FET in January it took 12 months to reach this point because I decided to go attend RIF clinic but all the waiting time then treatment to hopefully deal with implant failure has meant my next cycle can start

Part of AI's response to "acetyl-l-leucine anxiety" Elevated lactate levels in the brain can occur with several neurological disorders, including anxiety, major depressive disorder, and Parkinson's disease. High levels of lactate can lower the brain's pH, which can affect neuronal activity and the

I was wondering if others had experienced a slow increase in lymphocyte count in the years following V&O therapy? I’m worried the CLL is slowly relapsing, but my haematologist says I shouldn’t worry and that it may be due to slow recovery of the lymphocytes after treatment. I don’t have any new symptoms

I’ve had CLL for nine years. I was treated (O&V) a couple of years ago, and my numbers are great! Unfortunately, I developed a secondary cancer this past March. I had emergency surgery for a mass removal in my small intestine. I’m wondering if anyone else has Neuroendocrine Tumors (NET)? I’ve been told

Hi all i currently take supplements D3 &k2 ,vitamin C and B12.am considering taking Echinacea for immune system and turkesterone to help beef meback up . I have cll and currently on watch and wait. Any advice greatly appreciated.