Here's a website where Palestine GoFundMes are vetted and shared that you can send out to people. The url is gazafunds.com
Easy to use and simple. Just share the site whenever someone asks for GFMs for Palestine.
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Here's a website where Palestine GoFundMes are vetted and shared that you can send out to people. The url is gazafunds.com
Easy to use and simple. Just share the site whenever someone asks for GFMs for Palestine.

Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
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ive had so much improvement to my ME im wondering if I should start calling myself moderate-severe instead of severe. maybe I should wait to see if this improvement sticks first but god im excited at the thought that it might
went camping this week which was nuts. didnât think iâd be able to do that again after my last decline but Iâve improved enough thatâs itâs become possible. i did spend most of my time on the airbed and now im crashing but stilllll for a brief beautiful time i was in a field connected with nature meeting wonderful people
itâs severe myalgic encephalomyelitis awareness day. đ i got ME when i was 9 after a flu. it turned severe when i was 15. ive spent the decade since then largely bedbound with debilitating symptoms. meanwhile ME is one of the least researched and funded conditions compared to its significant disease burden. there are 0 approved treatments. i rarely bother to see doctors because thereâs nothing they can do for me. half of them have never even heard of severe ME.
ME is common and affects millions. you can get it from covid so cases are increasing. it can make anyone bedbound, you or your loved ones. you canât hope or believe or exercise you way out of it. it crushes lives, and without funding thereâs no way to stop it. we need funding.
ME association keeps doctors informed and supports patients. invest in ME finds, facilitates, and funds research. the open medicine foundation also does research and searches for treatments. if you canât donate, please take a moment to reblog!
hey, itâs severe myalgic encephalomyelitis awareness day. iâm hopeful that things will change. iâm hopeful that people will learn about us.
infographic credit; see more here
please hold us in your heart. ME itself is not rare (itâs over 5x more common than MS), but itâs really rare to find someone who actually knows what severe ME is! ME has been misrepresented as a vague fatigue syndrome. it is not. itâs a complex multisystem illness with a predictable pattern of neuroimmune crashes that come 24-72 hrs after physical or sensory exertion. it can become progressive and fatal. millions of people with severe ME are isolated and neglected by doctors whose knowledge of ME is based on outdated research.
it seems as though long covid can sometimes progress into ME, so cases are increasing, but many of us have had it for decades already. it crushed my life when i was a kid. but iâm still hopeful.

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facts about myalgic encephalomyelitis (ME/CFS) to combat the disinformation campaigns going on:
what does the name mean? my = muscle. algic = pain. encephalo = brain. myel = spinal cord. itis = inflammation.
ME is classed by the WHO as a neurological disease. the Decode ME study found immune and neurological genetic markers in its analysis of 15,000 subjects.
ME is more complex than just fatigue. many experts and patients dislike the old name âchronic fatigue syndromeâ because fatigue is only one part of the condition, and itâs the least unique trait.
the most unique trait is post exertional malaise, where, 24-72 hours after any exertion outside the patientâs limits, thereâs a peak of worsening and new symptoms affecting multiple bodily systems. PEM often involves immune activation, such as sore throat and a low fever, and a loss of muscle recovery after exertion, measurable through CPET testing. (normal muscle recovery takes 200 mins, but muscle recovery in ME takes days, with some patients taking longer than a year to recover from a single exertion.)
ME can range from mild to profoundly severe. these severity levels are only within the context of ME, not general illness; âmildâ ME is still a severe illness as it includes a 50% loss of functioning. âmildâ ME can feature debilitating pain and complex symptoms and can turn basic activities of daily living into a marathon.
severe ME is (naturally) even more physically limiting than mild ME. people with severe ME are largely bedbound and only rarely able to leave their room in a wheelchair, and usually canât perform their own care tasks, needing help dressing, washing, and eating.
in very severe ME, the person may be unable to leave bed at all and may not be able to speak, swallow, roll over, sit up, read, or be exposed to light or noise, for years or decades.
ME has a measurably lower quality of life than any other illness studied, including cancer and stroke.
finally, many of us can attest that exertion can cause years of deterioration and loss of functioning in ME patients. ive been 95% bedbound for the last decade bc of ONE WEEKEND where i walked too much when i was 15. im 26 now. and ive known so many people who went through something similar. do with this info what you will.
today, 8th august, is severe & very severe ME awareness day. it was chosen to honour sophia mirza who died of severe ME. please consider and remember us today đ
youâre not a bad person if you struggle with hygiene because of disability or mental illness. hygiene is not morality.
when i use the word âdisabledâ in my posts iâm always including people disabled by autism, mental illness, adhd, or any kind of invisible condition btw. recently had a couple people rb my posts and say âim not disabled but i relate to this bcâŚâ then describe down to a tee being disabled by their condition. if you feel kinship with disabled people due to a condition that makes it hard for you to get by, there may be a reason for that
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said it before and iâll say it again. deconditioning is a side effect of ME, not a cause. and deconditioning is way less harmful to an ME patientâs prognosis than repeated overexertion.
thinking about that quote from a researcher(?) who said theyâd never come across an ME patient who rested too much, only numerous patients who overexerted themselves outside their safe capabilities and paid a terrible price for it
said it before and iâll say it again. deconditioning is a side effect of ME, not a cause. and deconditioning is way less harmful to an ME patientâs prognosis than repeated overexertion.
I made that awareness post then only remembered afterwards that severe ME awareness day is on the 8th of aug!! serendipity. i will rb again on the 8th <3
are any of you guys doing anything for severe ME awareness day? reading thru my ME tag can be the Thing You Do, if you like
facts about myalgic encephalomyelitis (ME/CFS) to combat the disinformation campaigns going on:
what does the name mean? my = muscle. algic = pain. encephalo = brain. myel = spinal cord. itis = inflammation.
ME is classed by the WHO as a neurological disease. the Decode ME study found immune and neurological genetic markers in its analysis of 15,000 subjects.
ME is more complex than just fatigue. many experts and patients dislike the old name âchronic fatigue syndromeâ because fatigue is only one part of the condition, and itâs the least unique trait.
the most unique trait is post exertional malaise, where, 24-72 hours after any exertion outside the patientâs limits, thereâs a peak of worsening and new symptoms affecting multiple bodily systems. PEM often involves immune activation, such as sore throat and a low fever, and a loss of muscle recovery after exertion, measurable through CPET testing. (normal muscle recovery takes 200 mins, but muscle recovery in ME takes days, with some patients taking longer than a year to recover from a single exertion.)
ME can range from mild to profoundly severe. these severity levels are only within the context of ME, not general illness; âmildâ ME is still a severe illness as it includes a 50% loss of functioning. âmildâ ME can feature debilitating pain and complex symptoms and can turn basic activities of daily living into a marathon.
severe ME is (naturally) even more physically limiting than mild ME. people with severe ME are largely bedbound and only rarely able to leave their room in a wheelchair, and usually canât perform their own care tasks, needing help dressing, washing, and eating.
in very severe ME, the person may be unable to leave bed at all and may not be able to speak, swallow, roll over, sit up, read, or be exposed to light or noise, for years or decades.
ME has a measurably lower quality of life than any other illness studied, including cancer and stroke.
finally, many of us can attest that exertion can cause years of deterioration and loss of functioning in ME patients. ive been 95% bedbound for the last decade bc of ONE WEEKEND where i walked too much when i was 15. im 26 now. and ive known so many people who went through something similar. do with this info what you will.
there are hate campaigns happening against creators with ME on tiktok rn and itâs making my heart sink i feel terrible for the people affected. there are numerous huge videos getting like millions of views just purely making vitriolic fun of a person with ME talking about how they canât work. the trend of these vids has made ME into a buzzword thing to mock and now random creators with ME are getting tons of hate comments. please send kindness to anyone you know with ME especially if theyâre active on tiktok

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i get the sentiment behind the whole âwhat if people treated mental illness like physical illness!â thing but itâs a huge miss for me. disrespectful and misrepresentative of the lived reality of those with physical disabilities.. people with invisible physical disabilities get treated pretty similarly to people w mental illnesses, and people with visible physical disabilities just receive another flavour of garbage treatment, theyâre no better off. this widely-held assumption that physical (especially visible) disabilities are generally respected and accommodated is complete fantasy.
âpeople wouldnât tell a crutch user to stop using their crutches as a crutchâ yes they absolutely would
âpeople wouldnât tell a non-ambulatory wheelchair user to just get up and try walkingâ yes they would
âpeople wouldnât tell someone with cancer to just believe that theyâll get betterâ yes they woulddd
you underestimate ableism!! and you yourself are participating in lateral ableism by being facetious about the reality of physically/visibly disabled people
rest isnât something you should have to earn or suffer for or feel guilty for. rest is free. rest is morally neutral. you donât have to have been productive or busy in order to âdeserveâ rest. you can cram in a quick rest anytime you have time for it, free of charge, without having pushed yourself to the brink of death first. you can rest when you feel normal to build up energy for later. you can rest when you already feel awesome, to maximise the awesomeness. you can rest after a day where you achieved nothing. thereâs no need to feel shame for wanting to rest. in case you need any more convincing, hereâs a coupon for 4 million guilt free rests