@liamsLCjourney@DrRebeccaRyan Thank you - very helpful to know. A lot of people ask and it’s been difficult not having even observational data vs case based reports. Informing people about the risk when searching for benicial treatments is so important.
Hello all, I am working on a project about #ME and looking for physicians who have ME that would be willing to be interviewed about having ME.
Comment, reply, send a message, forward, etc
Dr Lana Dyment, BSc MD CCFP FCFP
BC-CLMF
@surf4children@Sabrina_Poirier Yes, I have just begun seeing children with ME and related central sensitivity conditions. It is heartbreaking that even if they do get a diagnosis they don’t get treatment. Definitely pushed me forward to do more. We can do better.
@NgocThach74 Not Celine in the wheelchair - but it is a woman who suffers from similar illness and has less money to fight the disease - both are rich in love from their families. I wish them both love.
@drkeithsiau Yup, air way such as bronchus with something like heterobilharzia. My rescued dog had it from swimming in the mountain waters of South Georgia. Larva enter via the skin and take a ride back to the lungs via the venous return. If not treated fast and hard the outcome is poor.
@Rainmaker1973 Better than three words… three letters that equal three words: PEM
Post exertional malaise is the hallmark symptom of myalgic encephalomyelitis, also known as Chronic Fatigue syndrome, which is another nightmare.
@ThrillaRilla369 All the time when I had my own panels of patients in family practice, did obstetrics and OR assists. Doctors get a lot of bashing but we try hard to meet the needs of our community in good faith.