WantedAlive
Senior Member
- Messages
- 158
Welcome to Phoenix Rising!
Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of and finding treatments for complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia (FM), long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.
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Here's the next series of comics about experiences with 'George and his ME/CFS'. I'm endeavouring to find humour to draw attention to the challenges that patients experience, the absence of appropriate diagnostics and therapy, poor treatment, lack of funding and maybe even a slightly whacky take on the latest research. As mentioned feel free to offer ideas that might fit a 3-window comic for when I get around to another series. Enjoy!
Thanks. I have started sharing them around, e.g.Here's the next series of comics about experiences with 'George and his ME/CFS'. I'm endeavouring to find humour to draw attention to the challenges that patients experience, the absence of appropriate diagnostics and therapy, poor treatment, lack of funding and maybe even a slightly whacky take on the latest research. As mentioned feel free to offer ideas that might fit a 3-window comic for when I get around to another series. Enjoy!
@Pyrrhus @wigglethemouse @Grigor @Tom Kindlon feel free to share the ones you like on your social media channels.
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Also:Thanks. I have started sharing them around, e.g.
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Also here: https://www.facebook.com/TomKindlonMECFS/
I don't know about MEAction, but it wouldn't be terribly hard to make a CafePress or Zazzle store to sell products (t-shirts, mugs, pillows, etc) with graphics you've designed. Maybe that would be something worth looking into @WantedAlive ?Did I already mention I would love to see these on #MEaction t-shirts?
Did I already mention I would love to see these on #MEaction t-shirts? It would be a non-confrontational way to spread awareness and maybe even start a conversation, assuming the person with ME is up to it.
I don't have the energy to do the research on how one gets started though.
Well a sunlamp will brighten your dayLove Acronymitis!
thats definately a REAL disease.
When my doctor finally diagnosed me with SEID (after a series of carefully unexecuted dianostic testing), he lept up and exclaimed to the receptionist: She has SAD She has SAD.
I was thinking he meant, the Seasonal Affective Disorder....I think I'll be cured, I'll get a sunlamp.
Hello there,
I've had a few comics done to capture some of my own experiences and observations during my journey with ME/CFS. Unfortunately, as I've become more severe, my ability to find humour has subsided, and I've run out of ideas. Maybe members can contribute some more ideas? If your ideas work as a comic, I might be able to get some more done. No promises though.
Here are some to get us started. Enjoy! Maybe with enough we can put them into a booklet for fundraising, use them with awareness campaigns, postcards for doctors, or even for new members with early onset ME/CFS. At the very least, I hope you get a laugh.
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