#m:hppmtm

[eclectic-ways]

Please JOIN in these mission movements

in whichever you care about the most if not all of them

(I have already included above in my masterlist so I post them as screenshots.)

© Eclectic Ways

[eclectic-ways]

Ever heard of a grief kind kicking in much before its cause transpires? Undeterred by the seasoning, it sucks your soul dry and brings your heart to bay.

Time ceases itself whenever it pleases, lurking around the void you’re cornered in. Time both being a forbidding enemy and a useless friend.

A friend, nonetheless.

© Eclectic Ways

Credits for the unedited version of the original images:

- sad black & white face protrait + woman resting her head on her hands + woman with pink eyes & antlers: Jessica Ross Jackson

- last image in the video: Novanoxone

Rest are my image/photos & footages except 3 (1st drawing pic of kissing couple, bat colony & the sigil of power pics) found on pinterest with unknown owners

song: IAMX - Spit It Out

[ M:HPPMTM ]

[eclectic-ways]

Yay! A new research for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) has been initiated by an Australian student, Tina Katsaros. The video is a brief but solid introduction to her thesis essentials.

“Studies have shown that there are a number of defects in how cells from people with me/cfs make energy vs. healthy control cells”, Katsaros claims. In her work, she will focus on trying to specify the causal defect in these energy producing cells (among ones that *Use fats as fuels | *Mitochondria (Powerhouse of cell) | *Proteins that regulate energy)

This research is one of the entries of the annual research competition in LA Trobe University. There are several prizes for different aspects in these researches. This one is “Visualize Your Thesis” by popular vote.

It is extremely important for the fields of medicine and science to be encouraged to pay more attention to chronic illnesses as most anything that is chronic is not taken as seriously as the fatal conditions despite of how debilitating they could be. It’s like how you’re usually approached by most of the ERs: if nothing is life threatening, they won’t rush a bit despite of the screams, moans and cries in agony. As long as you live or are living, “it’s fine” kind of mentality.

We’re living but how we’re living? Through inertia, low life quality, unemployment, shattered dreams, daily distress, frustration, desperation and hopelessness. I personally don’t call that a living. That’s why these (new) researches, thesises and clinical trials are very important. It should be our duty to support them.

Please participate in the voting - Katsaros Entry #4

Give her a like on youtube and perhaps drop a comment while you’re there:

And consider sharing it around.

Thank you.

[m:hppmtm]