FUMS: Giving Multiple Sclerosis The Finger

FUMS 038 – MS Stories From Around the World #3: Katrine Bonde (Denmark)


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This episode is the third installment of our international series where Kathy talks to MS’ers from around the world, to see how their diagnosis and treatment experiences differ from our own.

Today's guest is Katrine Bonde, a university student from Aarhus in Denmark. Denmark has one of the highest rates of Multiple Sclerosis in the world (only San Marino and Canada have a higher prevalence).

Now aged 24, Katrine was diagnosed with MS in June 2014.

 

Topics covered include:

  • Katrine's diagnosis and initial symptoms
  • Availability and cost of care and treatment in Denmark, including DMTs and ancillary treatments
  • Workers' rights, protection and sick-pay in Denmark
  • Danish protocol for MS relapses
  • Availability of medical marijuana in Denmark
  • How to say FUMS in Danish!

 

Resources mentioned in this episode (clickable links):

  • Parts  one and  two of the international podcast series
  • The Visit Aarhus website
  • The Danish Multiple Sclerosis Center website
  • If, like Katrine, you would like to link up with other MSers, Shift.MS is an international social network for people with Multiple Sclerosis. Their MS forum has thousands of members worldwide and it's free to join.
  • Temperature conversion! 
    • To change Fahrenheit to Celsius, deduct 32, then multiply by 5, then divide by 9
    • To change Celsius to Fahrenheit, multiply by 9, then divide by 5, then add 32

 

** Sign up for the FUMS Friday Night 6 Pack at FUMSnow.com. And for more information about Patients Getting Paid, get on the email list at  FUMSnow.com/PatientsGettingPaid.

**If you get value from the FUMSnow Podcast Show, please consider leaving a rating or review wherever you get your podcasts. Reviews are really important and help to spread the word about what we do. It’s quick and easy to do and we have some instructions here. Thanks for your time and support!

**Don’t forget to join us on the FUMS Facebook Page and on Twitter at FUMS. Have an idea for a topic or someone to interview? Perhaps YOU?? Send me an email at [email protected].

And remember to speak to this stupid disease as it deserves: tell it FUMS every day!!

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FUMS: Giving Multiple Sclerosis The FingerBy Kathy Reagan Young

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