Pay it Forward For ME

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Here’s my letter from my awesome doctor (Dr.Levine) to my college for my accommodations. 
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Here’s my letter from my awesome doctor (Dr.Levine) to my college for my accommodations. 

    • #cfs
    • #chronic fatigue syndrome
    • #myalgic encephalomyelitis
    • #m.e
    • #chronic illness
    • #invisible illness
    • #spoonie
    • #dysautonomia
    • #Postural Orthostatic Tachycardia Syndrome
    • #pots
  • 8 months ago
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My updated video about all of my illnesses! Please watch even if you can’t contribute. I worked hard on this and hopefully my personality came through! (: 

    • #Postural Orthostatic Tachycardia Syndrome
    • #cfids
    • #cfs
    • #chronic fatigue syndrome
    • #chronic illness
    • #dysautonomia
    • #ehlers danlos syndrome
    • #invisible illness
    • #pots
    • #eds
  • 9 months ago
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May 12th is International NeuroImmune Invisible Disease Awareness Day!

May 12th dot org want you to email them your story, photographs, poems, art, video’s to be put up on the May12thDotOrg YouTube channel 

Contribute your story now to may12globalaction@gmail.com 

We want to be swamped with stories!

Pay It Forward For ME !

    • #May 12
    • #CFS
    • #ME
    • #myalgic encephalomyelitis
    • #chronic fatigue syndrome
    • #Chronic Immune Dysfunction syndrome
    • #POTS
    • #Postural Orthostatic Tachycardia Syndrome
    • #Epstein Barr Virus
    • #Epstein Barr Virus
    • #EDS
    • #eh
    • #Ehlers Danlos syndrome
    • #dysautonomia
    • #lizzie fall
    • #sarah whitestone
  • 1 year ago
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Hey! We need everyone to start Paying It Forward For ME. We can make change happen! Please call you Senator’s or Congressman’s office today. It only take a few minutes. Tell them your story. Ask the politician what they are doing for specifically To make more treatments available and more funding for research for a CURE! http://payitforwardforme.tumblr.com/makeadifference
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Hey! We need everyone to start Paying It Forward For ME. We can make change happen! Please call you Senator’s or Congressman’s office today. It only take a few minutes. Tell them your story. Ask the politician what they are doing for specifically To make more treatments available and more funding for research for a CURE! http://payitforwardforme.tumblr.com/makeadifference

    • #CFS
    • #ME
    • #chronic fatigue syndrome
    • #Chronic Immune Dysfunction syndrome
    • #myalgic encephalomyelitis
    • #Epstein Barr Virus
    • #epstein barr
    • #POTS
    • #Postural Orthostatic Tachycardia Syndrome
    • #EDS
    • #dysautonomia
    • #Lizzie Fall
    • #sarah whitestone
  • 1 year ago
  • 11
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Photo credit to Getty Images.
I have POTS as well as ME/CFS. There was a story in ABC News. What do you think?
Do you feel they got the story right? 
http://abcnews.go.com/blogs/health/2012/02/29/what-astronauts-have-taught-doctors-about-fainting/
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Photo credit to Getty Images.

I have POTS as well as ME/CFS. There was a story in ABC News. What do you think?

Do you feel they got the story right? 

http://abcnews.go.com/blogs/health/2012/02/29/what-astronauts-have-taught-doctors-about-fainting/

    • #pots
    • #postural orthostatic tachycardia syndrome
    • #dysautonomia
  • 1 year ago
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I’m having a bad day!

    • #CFS
    • #cfids
    • #dysautonomia
    • #pots
    • #chronic fatigue syndrome
    • #m.e
    • #myalgic encephalomyelitis
  • 1 year ago
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Pay it Forward For ME

About

Who's your ME/CFS doctor?

We created this blog in order to help spread awareness of the debilitating illness Myalgic Encephalomyelitis -Chronic Fatigue Syndrome.

Pages

  • About Lizzie
  • You Tube Videos
  • Tell The Media To Do A Story
  • Make A Difference
  • Contact Senate Decision Makers
  • Contact House Decision Makers
  • CFSAC Testimony 11/11
  • Chronic Fatigue Syndrome Advisory Committee
  • CFSAC Committee Recommendations
  • Resources

Me, Elsewhere

  • @payit4ward4ME on Twitter
  • myinvisibleillness on Youtube

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