#meawareness

[memyselfandianimation]

I'm making a film!! :D

Hello, My name is Jamie, and I am so excited to announce my animated short film 'M.E, Myself and I', which is currently in production! As it is International ME Awareness week, I thought it would be the perfect time to announce this project to the world, and start to share its production with you all.

The film focuses on our main character 'MJ' as they live their life, and come to terms with their new diagnosis, and how to find joy in the world despite it. This film has been a concept of mine that I have had for many years, and is a story that is close to my heart, as I was diagnosed with M.E. in early 2017. I have previously worked with various studios in the North of England, and have completed work for the BBC, but this project was always on the back of my mind since then! It will be an entirely paper-based animation, like the animation shown below, and will then be hand colour with alcohol markers, mirroring the previous personal projects I have done in watercolour.

Our main character MJ ages throughout the film, and so the design reflect them growing up, aging and adapting as they adjust to using different mobility aids and travelling the world. Here is the concept art we have for our character at various ages throughout the film, as well as an animation test for the character.

I will be updating this blog regularly as production continues, sharing where we are up to and anything exciting that happens along the way.

If you would like to help support the production of the film, we have a Kofi, which will go towards supplies and sound design, and also keeping me hydrated! :D Please see the links below for my Kofi, and my Instagram where I will also be posting updates if you would like to see things there! I leave you with this little piece of concept art for one shot of the film, as well as some storyboard frames to give you a little insight into the story of the film.

Thank you for reading! \o/ Kofi - https://ko-fi.com/jamieisanimating Instagram - www.instagram.com/jamimation

#2d animation #me/cfs #MEAwareness #short film

[belog-grada-crna-princeza]

S obzirom da se 12. maja obeležava Svetski dan svesti o Sindromu hroničnog umora stavljam u nastavku spisak mogućih simptoma.

Sindrom hroničnog umora ili mijalgični encefalomijelitis je neuroimunološko oboljenje koje se javlja najčešće kod mladih osoba i češći je kod žena.

Uzrok je najčešće neka virusna ili bakterijska infekcija, može se javiti i u sklopu lajmske bolesti, nakon porođaja, nakon povreda glave i vrata ili nakon težih trauma. Okidač je uglavnom stres. Lek zvanično ne postoji, ali je terapija usmerena na poboljšanje simptoma i kvaliteta života.

Smatra se da do 1/3 ljudi nakon preležanog C0V1DA ulazi u ovo stanje, tako da je ova bolest nakon pandemije postala veoma česta i globalno se sada sprovode ozbiljna istraživanja o uzrocima i mogućim terapijama. Uprkos svemu tome, mnogi lekari i dalje nisu upoznati sa dijagnozom i greškom simptome pripisuju psihičkim bolestima, čime se nanosi ozbiljna šteta obolelima i dolazi do pogoršanja. Depresija i anksioznost jesu česti komorbiditeti, ali se javljaju kao sekundarni odnosno u sklopu sindroma, a ne nezavisno od njega. Bolest je ozbiljna, u najtežim slučajevima vodi u invaliditet, a s obzirom da je multisistemska i da zahvata celo telo mogu se kao posledica javiti i druge životno ugrožavajuće komplikacije kao što su miokarditis, oboljenja jetre, pankreasa i slično. Može izazvati i druga autoimuna oboljenja poput multiple skleroze, dijabetesa, lupusa itd jer je imuni sistem u disbalansu.

Ako se prepoznajete u ovim simptomima i oni vam traju duže od 6 meseci, a po nekim novijim kriterijumima je dovoljno i da traju 3 meseca, kod dece i 1.5 mesec, važno je što pre reagovati jer su šanse za izlečenje bolje ukoliko se ranije krene sa lečenjem.

U Srbiji i regionu se jedini ovim dijagnozama bavi profesor doktor Branislav Milovanović koji državno radi na Institutu za kardiovaskularne bolesti Dedinje, a privatno radi u okviru ordinacije Neurokard na Novom Beogradu. Ja mogu da kažem da je mene bukvalno spasio i da ću mu biti večito zahvalna jer je ne samo vrhunski stručnjak i izuzetno posvećen lekar, već je pre svega čovek <3

#MeAwareness #myalgic encephalomyelitis #chronic fatigue syndrome #Chronic fatigue syndrome awareness day #Sindrom hroničnog umora #Mijalgični encefalomijelitis #SHU #Depresija #Anksioznost #Beloggradacrnaprinceza

[brokeassstylus]

May12th is ME/CFS awareness day, im a little late and clumsy with the suppport

#MEAwareness #goblueformecfs #MEday #goblueforacure #late

[risingphoenix87]

🤣🤣🤣 Step back satan! - 📸 Via 📷Unknown, tag to credit! - Tag someone who needs to see this💙 - Follow 👉 @sick_gone for more content💓🌼🥰 ======================= Follow 👉 @sick_gone for more content💓🌼🥰 - - - - #spoonielife#potssyndrome#mecfs#raisingawareness#chronicmigraines#spooniesupport#chroniclyme#chronicillnessmemes#notalldisabilitiesarevisible#chronicpainsurvivor#meawareness#spooniesunite#fibromyalgiaproblems#chronicpainlife#costochondritis#spoontheory#chronicpainmanagement Reposted from @spooniesaw https://www.instagram.com/p/Ci8jB-UOobv/?igshid=NGJjMDIxMWI=

#spoonielife #potssyndrome #mecfs #raisingawareness #chronicmigraines #spooniesupport #chroniclyme #chronicillnessmemes #notalldisabilitiesarevisible #chronicpainsurvivor #meawareness #spooniesunite #fibromyalgiaproblems #chronicpainlife #costochondritis #spoontheory #chronicpainmanagement

[myalgicencephalomyelitiscfstom]

Sharon Tiday said on Twitter: For a while now people have told me that I should get this short story/poem published so I sent it off and Edge of Humanity Magazine has now published it please share it for #MEAwareness

#myalgic encephalomyelitis #mecfs #pwmes #pwme #myalgicencephalomyelitis

[aureliacetinn]

happy first #disability pride month post

its the pathfinder 2e and dnd backgrounds optional rules for my condition

m.e/c.f.s

inside other than info on my condition is info on background notes for gms

and 3 tables covering mild to severe m.e

and an optional variant where the tables only give you flavour instead of mechinal issues

the idea is to roll once every day or as much as you like after picking what version feels right for you

this was done for me awareness as well as a personal desire to see if my condition can work in these universe and it can

ofc!

its pay what you wants so enjoy!

#disabled representation #disability aids #disability inclusion #ttrpg stuff #dnd homebrew #pathfinder #delicious in dungeon #m.e/cfs

[pt-hq-xl]

#meawareness #cfsme #cfsawareness #millionsmissing https://www.instagram.com/p/CdcjOI8tq6B/?igshid=NGJjMDIxMWI=

#meawareness #cfsme #cfsawareness #millionsmissing

[alishawhittam]

New blog up now 🤬 https://alishawhittam.com/ #me #myalgicencephalomyelitis #anxiety #meawareness #mecfs #mecfsawareness https://www.instagram.com/p/CdTA-xuMgQ9/?igshid=NGJjMDIxMWI=

#me #myalgicencephalomyelitis #anxiety #meawareness #mecfs #mecfsawareness

[theshoegirldiaries]

For #TeaPartyForME2021 See Tea Party For M.E. for how to participate and donate to M.E. charities to raise funds into the research we so desperately need and do not get.  Post viral illnesses are on topic these days, but they are not new.  I’ve suffered for almost 2 decades after a bout of glandular fever and my life has been devastated by it.  We’re not faking being ill, we’re not exaggerating, most of the time we’re downplaying it and pretending to be well.  See us. Listen to us.  Understand us.  Help us.   

#teapartyforme2021 #bluesunday2021 #irregularchoice #irregular choice #meawareness #meawarenessmonth #shoes #shoeblogger

[metapefilm-blog]

Drama web series based on the experiences of real life M.E sufferers, which hopes to shine a spotlight on the issues sufferers face. Please share.

#myalgicencephalomyelitis #m.e #cfs #meaction #spoonie #meawareness #chronic fatigue #chronic illness #web series #indie film #arts #disability #awareness

[cherylbenson]

#Repost @meactnet with @get_repost ・・・ #Repost @myillnessmythoughts with @insta.save.repost • • • How amazing would it be if that apology came via education & biomedical M.E research in these communities. Now that would effect change. * It’s time for change 🙌🏻 it’s time for #understanding #awareness the end of #neglect & for governments to allocate adequate funding for this life destroying disease known as ‘the living death’ #facts #meawarenessmonth #meawareness #millionsmissing #missingbutnolongersilent #endcfs #mecfs #meadvocacy #maymomentum #openmed #actionforme #endtheneglect #cfsme #thetruthoflifewithME #canyouseeMEnow

#awareness #neglect #canyouseemenow #meawareness #millionsmissing #endtheneglect #missingbutnolongersilent #openmed #repost #thetruthoflifewithme #endcfs #understanding #meadvocacy #maymomentum #actionforme #meawarenessmonth #mecfs #facts #cfsme

[jenicorn88]

THIS! 15 years of struggling, I have got a little bit better at knowing my energy limits but it doesn’t stop me feeling the effects, I’ve just lessened the severity of the crash. I still have some days when I will purposely push myself too far because you only get one life and I don’t want to miss out on everything, but I’ll plan for a couple of days rest after. #meawareness #cfsme #spoonie #PEM #postexertionalmalaise #fatigue https://www.instagram.com/p/CPGqTRthgGFmhLLQFD3lmxOIRtUjaLiToSyYeg0/?utm_medium=tumblr

#meawareness #cfsme #spoonie #pem #postexertionalmalaise #fatigue

[bloomingmindfulness]

New YouTube video: Lets talk about ME/Chronic Fatigue Syndrome [CC] I really hope this video helps spread awareness and don't forget to share & subscribe xx https://youtu.be/tMJY9_d5dR8

#chronic fatigue #meawareness #millionsmissing #chronic illness #youtube

[myalgicencephalomyelitiscfstom]

A wonderfully illustrated comic to explain Myalgic Encephalomyelitis/Encephalopathy (M.E) also known as Chronic Fatigue Syndrome (CFS) to other people. ---

Mahli Quinn Art "But... you did it before" in video form The ME Association asked if they could make the comic into a video in part to help those people with ME who struggle with reading/cognition in those areas and those who are so severely affected that they cannot read at all. I was keen to give narration a go, and, well... here we are! Many thanks to my partner, Nick, for co-narrating and doing all the sound editing and mixing (I would have been hopeless!). Many thanks to Emma and all at the MEA for putting the video together, too. May your batteries be good to you, today https://youtu.be/G4Rijt8jtZg

#meawareness #livingwithme #myalgicencephalomyelitis #mecfs #chronicfatiguesyndrome

[stephiewoodcock]

Today is ME/CFS and Fibromyalgia Awareness Day. . These debilitating conditions are poorly understood, despite hundreds of thousands suffering from ME and 1 in 20 having Fibromyalgia. . More research into causes and treatment for both conditions is badly needed. . #MEAwareness #CFS #Fibromyalgia https://www.instagram.com/p/COxo7t0pnVA/?igshid=k6etu5kmlmtk

#meawareness #cfs #fibromyalgia

[pt-hq-xl]

Quick cross stitch started on ME/CFS awareness day this week #meawareness #cfsawareness #crossstitch https://www.instagram.com/p/CdicUlRticx/?igshid=NGJjMDIxMWI=

#meawareness #cfsawareness #crossstitch