I’m having a bad day!
Just to let you all know, my mom helps out with the blog posts on here. (: So, yeah! it may not be me all of the time on here, but don’t hesitate to message me on my personal tumblr which I’m pretty sure most of you know… shhhhh. So yeah!
Young People Have The Power to Make Change →
All you have to do is believe and get to work!
For the chronically ill, details are all. To cope with chronic illness means to...– Arthur Kleinman, The Illness Narratives (via shanghailil)
To those that have an invisible illness...
colormesmall: is it wrong to wish you looked sick? Just so that you didn’t have to explain all the time?? I’m thankful that I don’t to be honest, but other times I wish I did when I feel most worst?
crystallisedlungs: I just wanna be heathy so I can go out and not feel completely rubbish afterwards, to make worse it’s sunny outside and I’m thinking of all the things I could be doing if I felt well, I feel like an old lady because my legs and back ache, and I feel tired all the time and my eyes hurt due to lack of sleep. I honestly think the last time I properly went outside was two months...
I just want everything to be normal again.
simplicityisbeauty: I want this surgery for my hips to know if it will help with the pain. I want my CFS to go away so I can live life again properly. I want my Nan back to comfort me when I’m sick and to make me feel better. I want some of my old friends back who left me in my moment of need. I want someone to hug me and tell me it’s all going to be okay, that this bad stuff will eventually...
honestly just can’t stop crying
a-mermaid: honestly just can’t stop crying i hate my illness so much. i’m so sick of feeling this ill and this weak all the time. just want to be normal. god. in so much pain and no one even gets it
Smile Stay Strong.: Massive apologies for not... →
smilestaystrong: I’ve been really unwell, i got back to school for the first day back last week and have been off since which sucks :( and yeah it’s not easy to deal with but i’ve finally got an appoitment to see people who can hopefully help me! So there are always positives to look forward too, light at the end…
Heal Kick →
Hey everyone. Check out my friend’s Joey Tuan’s website. It’s called Heal Kick! It’s for people with: Myalgic Encephalomyelitis, Chronic Fatigue Syndrome, Chronic Lyme Disease, Fibromyalgia, Rheumatoid Arthritis, Lupus, Sarcoidosis, Reflex Sympathetic Dystrophy, Multiple Sclerosis, Multiple Chemical Sensitivity, Mold-Related Illness Giving a shout out to Joey Tuan !...
Voices from the Shadows Documentary. If you have ME/CFS or have a friend you has it you should watch it. It’s only available in DVD in the UK and Europe but you can still watch via your computer. http://mubi.com/films/voices-from-the-shadows Pay it Forward for ME/CFS…if you like it ..reblog it !
Voices from the Shadows Documentary →
Is anyone listening? National Institutes of Health... →
National Institutes for Health spending per patient per disease. HIV/AIDS $3059.00 per person CANCER $5448.00 per person ME/CFS $6.00 per person We have to be louder than ever before, we have to be noticed. We are the future remember? Pay It Forward For ME. Take the 10 pledge now to help us get to Washington to speak up for all of us young people. Please Reblog this if you care about...
Seeing Beauty Through Our Pain →
We must remind ourselves again and again that there is more to our life than our pain. We can still find moments to enjoy. Do you enjoy photography? If you are able, look around your house or your street. Find the beauty right outside your front door. Do you enjoy music? How about taking the time to really listen to it– how each instrument blends with the other to create a beautiful melody. Are...
Anonymous asked: Thank you for raising awareness! Thank you for supporting Speak Up About ME! Two thumbs up!!
longlivethegirlinthedress asked: hi! thank you so much for reblogging/liking that post in which whytolovetaylorswift asked you guys to pray for me. it means a lot, thank you! ♥ xoxo
Be not the slave of your own past - plunge into the sublime seas, dive deep, and...– Ralph Waldo Emerson (via jaegerjaques)
SYSTEMPLAYGROUND: trying to see the light, got... →
systemplayground: I would honestly love someone to count the number of knots in my body. I always say “I’m covered in them.” when someone asks about it. I just didn’t feel like going back into Frankenstein mode… really not looking forward to it so I stretch what I can, but it’s not much at all. I can feel my body…
whytolovetaylorswift: please pray for Marishelle (longlivethegirlinthedress) for her Chronic Fatigue Syndrome (CFS) to go away. Thank you. ❤
its-not-a-dreamanymore: The doctor told me today that I’ll get better quicker if I stay positive. Lol. That’ll surely get me better.
Polina rides in pockets.: cfs →
polinaridesinpockets: Some days im good. Some weeks im good. Sometimes i even forget i have this invisible disease. but there are days/weeks/months like today where iv slept for 15 hours, and i want to sleep more. Where my whole body hurts like i been crushed by a load of bricks.Where i can barely get the strength…
Chronic Fatigue Syndrome Specialist from Stanford... →
Twitter & YouTube Information& My Email
Twitter @PayitForward4ME YouTube http://www.youtube.com/user/MyInvisibleIllness Email LizzieFall@aol.com
Change will not come if we wait for some other person or some other time. We are...
Change comes to Washington…not the other way around!
What does CFS mean? by Lynn Jensen →