We are living in unprecedented times which is making many of us feel quite scared, nervous and anxious about our health as well as that of our families and friends. We wanted to reassure you that Myelopathy.org is run by
THIS SUMMARY IS SUBJECT TO CHANGE AT SHORT NOTICE AS THE GOVERNMENT RELEASES ITS OWN UPDATES – THIS SUMMARY WAS LAST UPDATED MONDAY 23RD MARCH 2020 Dear Friends, These are extraordinary times; coronavirus (COVID-19) represents a nearly unprecedented challenge
Slowly my myelopathy symptoms increased day by day and it quickly came to the point where I developed a new muscular twitch or nagging pain daily. I wasn’t getting much luck with my pain relief and when I had a
The greatest challenge facing those with degenerative cervical myelopathy is understanding and expressing their symptoms and to have a medical practitioner recognize and diagnose the condition early. In my experience neck pain is most often the earliest symptom patients can
Dr Fehlings wins the 2019 Ryman Prize We are very proud to announce that Dr Michael Fehlings, head of the Scientific Advisory board for Myelopathy.org, was this morning awarded the Ryman Prize in recognition of his long career dedicated to
By Max Butler Edited by Ben Davies Delayed diagnosis is a major issue for myelopathy patients (Davies et al, 2018) as delays can be distressing for sufferers, and the condition is likely to worsen without treatment. On top of this,
May 7th was a momentous day for Myleopathy.org, with not one but two landmark events occurring on the same day!
In this blog we cover the financial burden that a chronic condition such as myelopathy can bring. This week we speak to Shirley Widdop, an ex-Nurse that had to give up employment after being diagnosed with Cervical Myelopathy in 2012.
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