then it'll all come together in one giant luminous burst @jesusonafrickinboat - Tumblr Blog

Charles as Edwin’s dog but in the way that a dog is a captive cheetah’s. Emotional support dog for an animal that could theoretically be a record-setting predator and absolutely has the capacity to bite through your spine but 99% of the time is an anxious mess that will shake itself to death at highway speeds without The Dog

#dead boy detectives

le-freaknasty

version 2.0 bc dnp dont want to be boiled down to clickbait headlines 🫶

#dan and phil #dnp

nebulaedaniel

im so speechless. the way that nothing changes and everything changes. it doesn't matter but it so extremely does matter. it's the most normal thing in the world, and the biggest deal ever. you know.

#dan and phil #dnp

danielhowell

IS PHAN REAL? one of the biggest conspiracies in the history of the internet - we’re gonna talk about it https://youtu.be/Cxe_YMJ4nUs

#anyways no one talk to me for 5-10 business days #I'm just happy for them and wish them all the peace and privacy they deserve #and I will always say thank god the username phantrash was taken on here when I joined in 2016 #jesusonafrickinboat was the much better option here XD #(no offense to whoever had the phantrash username in 2016 lol)

dnphobe

i'm so happy for them. i hope that this leads to an era where they feel fully free and unafraid and have even more fun with us and eachother than ever before

#dan and phil #dnp

plainwheatcereal

“The average frontman dies 3 times on stage” factoid actualy just statistical error. average frontman dies 0 times on stage. Get-Stabbed Gerard, who has strange artistic visions and dies over 10,000 times during the tour, is an outlier adn should not have been counted.

#lltbp #mcr

AHHHHHHHHHH!!!!!!

#mcr #my chemical romance #mcr NJ #mcr metlife #OH MY GOD IT'S HAPPENING!!!!#long live the black parade #lltbp tour

jesusonafrickinboat

May is ME/CFS Awareness Month!

ME/CFS stands for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

Chronic Fatigue (CF), a symptom of many chronic illnesses, is not the same as Chronic Fatigue Syndrome (CFS). There is a push for ME/CFS to be exclusively known as Myalgic Encephalomyelitis (ME) in the future

ME/CFS is a complex, fluctuating, chronic medical condition affecting multiple body systems and symptoms can change unpredictably

Post-exertional malaise (PEM) is the hallmark of ME/CFS

More on symptoms: Symptoms of ME/CFS

ME/CFS affects an estimated 836,000 to 2.5 million Americans, the majority of those diagnosed being AFAB

An estimated 90% of people with ME/CFS are undiagnosed

About 25% of people with ME/CFS are bedbound or housebound for long periods

Most of those diagnosed never regain their pre-disease level of functioning

The root cause of ME/CFS is unknown

Possible triggers include: viral infections (such as mono, the flu, or COVID-19), bacterial infections, physical or psychological stress, and immune system changes. There may also be a genetic component

There is no cure or approved treatment for ME/CFS

However, some symptoms can be treated. For example, PEM is treated by pacing. More on treatments: Treatment of ME/CFS

ME/CFS costs the US economy about $17 to $24 billion annually in medical bills and lost incomes

The ME Association and the CDC have more in-depth articles on ME/CFS for more information

jesusonafrickinboat

May is Celiac Awareness Month!

Celiac is a serious autoimmune disease

It is not a food allergy, diet, or fad

It’s an immune reaction to gluten, a protein found in wheat, barley, and rye

Oats are often cross contaminated, since they are typically grown next to wheat, so only certified gluten free oats are safe

However, oats have a protein that is structurally similar to gluten called avenin, which some people with celiac are triggered by, so they can't eat oats even if they're certified gluten free

Celiac causes physical and sometimes permanent harm to the intestines

Celiac is a genetic disorder

It is also known as "coeliac”

1 in 133 Americans (about 1% of the population) have celiac disease.

83% of people are undiagnosed or misdiagnosed

The average time to get a correct diagnosis is 6-10 years

There is no cure for celiac

The only existing treatment is a strict 100% gluten free diet

Eating gluten free is a life-long, difficult, expensive commitment

Celiac Disease Foundation and Johns Hopkins have more in-depth articles on Celiac for more information

#celiac #celiac awareness month #celiac awareness #autoimmune disease #coeliac #gluten free #celiac disease

genzforbettergenerations

Happy Autism Acceptance Month!

#autism acceptance month #autistic pride #actually autistic #listen to autistic voices #nothing about us without us

mylittleredgirl

i feel like every human should max out at one disability or chronic illness. like when i hit adolescence and my brain chemistry went “bipolar time now?” the response should have been an error message like sorry! this slot can only contain one (1) item and has been filled with childhood asthma. i would even allow the possibility that you can overwrite previous disorders like “you have equipped chronic migraines and so no will no longer display symptoms of bipolar disorder.” i just think it should work that way.