Invisible Illness

This is just something i put together a few days ago when i was bored.. hope you enjoy! xxo!

Postural Orthostatic Tachycardia Syndrome Dysautonomia Late Stage Lyme Disease CFS Chronic Invisible Illness

Category:

People & Blogs

Tags:

• Dysautonomia
• Late Stage Lyme Disease
• CFS
• Chronic
• Invisible
• Illness
• Chronic Fatigue Syndrome

[CrystalFaith100]

AMAZING job! This video truly is outstanding!! If you feel like answering, what was the music? ;D

[radlikemad]

@CrystalFaith100 thanks so much. it's called Everything Changes by Staind :)

[SashaLily11]

I Loove This Video, It Made Me Cry!

To Know Someone Feels The Same Way Is Awesome, And It Is So Creative.

Good Work

[radlikemad]

@SashaLily11 thank you :)

[star382000]

I feel tears coming on. This is beautiful ♥

[radlikemad]

@star382000 thank you <3

[Potsgirl22]

I LOVE this video! It explains EVERYTHING and its very creative! :) keep posting to make a difference! :)

[BlueberrySman]

really awsome video, im so glad i stumbled upon this video. it gave me clarity in a way i cant explain, so thank you.

By the way you are really pretty. :) 

[3DMuse]

Hi, I suffer from Bradbury-Eggleston (a form of Pure autonomic failure/Dysautonomia), FMS, Asthma, and migraine syndrome and have for well over 20 yrs.  I thought this was a great video, there are so many illness that this video speaks out for. Nice job, glad you decided to turn your boredom into something creative.

[mrahodgson1]

i love this video thanks for speaking up for people like you and me HUGZ

[utalice]

You got me with this one...very good. :)

I've lived with FMS for at least 10 yrs now and I feel helpless in conveying my pain and exhaustion to others. It hurts a lot when ...after all of this time (and information I've given), I still hear comments from family members who will tell me to just exercise or something else that I know doesn't help. It's very frustrating and painful.

THANK YOU for making this.

[TheLibra2767]

Great video. My bf of nearly 20yrs,has this 'invisable' disease MECFS and has done now for nearly 9yrs. Knowing him from then,till now,and the difference and suffering that it causes,I applaud you on this video. MECFS is REAL,thks for vid. ;) #MECFS

[GetWellFromME]

Really powerful video, thank you!

[LiveLoveLaugh031]

I'm turning 15 next month and just got diagnosed with POTS last April. For 3 years I had the pleasure of being told it's all in my head or that I'm faking it for attention. I decided to search up POTS Syndrome and found your video. It's nice to know that I'm not the only one that's been through all of the hundreds of doctors appointments and have been told that there's no reason for me to miss any school. I just wanted to say thank you for this video[:

[CheyLovesSoftball]

This Video Was Soooo Good. Made Me Cry. I've Been Told My Some Of My Own Family Members I Was Making All My Symptoms Up For Attention. I Will Defiantly Be Sharing This!