Tags » Syncope

Blog #1

Hey all! I have decided that the best way to get everybody on the same page (and to take some stress off everyone trying to keep everybody else in the loop) is to just start a blog. 2,032 more words

Cancer

Tree of Hope

Please help me raise funds for Dysautonomia Support Network; an organization near and dear to my heart.

This amazing charitable, non-profit organization helps support patients and increase awareness of an illness of which I suffer. 261 more words

POTS

Dysautonomia & Low FODMAP Electrolyte Drink

Summer is finally here in the UK! It’s quite sad that we get excited when it hits 25°C and everyone floods outside for BBQ’s before it’s jumper weather again! 393 more words

Low FODMAP

Grand Rounds: July 7, 2016

Grand Rounds is back and off to a great start to the new academic year! While we’re sad the class of 2016 has graduated and moved on, we’re excited to welcome the newest members of the DEM family! 227 more words

Conference

Syncope or Seizure?

Studies have now confirmed what some doctors have long suspected — many young people who are given the diagnosis of epilepsy (or seizure disorder) apparently don’t have epilepsy at all. 765 more words

Epilepsy

'FAINT RISK': Canadian Syncope Risk Score

Hot off the press is the Canadian Syncope Risk Score, which takes elements of patient history, ECG/trop and diagnosis to risk stratify patients into their risk of serious adverse events. 31 more words

Literature

Living With Lyme - What Came Next (2)

The Syncope (which I am still calling it Syncope here, because that is what I was told it was), was starting to get worse. I was admittedly in denial about that. 728 more words