shaudo:

amerigoilluminatusx:

officialfist:

amerigoilluminatusx:

What???

3 people died and 7 became ill after eating blue bell due to the bacteria listeria being found in several machines. Most people’s immune systems shrugged it off but people with compromised immune systems (birth defects or diseases such as HIV) could become seriously ill or in this case die as a result of it.

Damn, that’s crazy that it happened, I’m glad I know not to buy them now.

@amerigoilluminatusx Hello! Texas native, here with more information that you should have the opportunity to know.

The second it became clear that Blue Bell was the source, they voluntarily shut down their facilities and recalled EVERYTHING they currently had on the market, around 8 million gallons of ice cream.

They tested, disassembled and thoroughly sterilized, then retested their manufacturing equipment. At least one major piece of equipment was thrown away, presumably because they couldn’t guarantee it was safe.

They tracked down the source of the “outbreak” and submitted a root cause analysis (with some info redacted here) to the FDA. And then they slowly started manufacturing again, releasing a few flavors at a time, testing each shipment before sending them out.

This happened over a year ago. They’re still recovering.

They threw away MILLIONS OF DOLLARS to keep people safe instead of, you know, trying to keep everything under wraps. (Honestly the tagline here should be “We Scare Because We Care” or somethin.) Blue Bell is a fricken solid and honest company.

So, yeah, enjoy your ice cream! ALL OF BLUE BELL IS DOING EVERYTHING PHYSICALLY POSSIBLE TO KEEP IT SAFE AND DELICIOUS.

That is all.

Please help me escape my abusive relationship for good

indigenousmess:

indigenousmess:

indigenousmess:

indigenousmess:

thefingerfuckingfemalefury:

indigenousmess:

indigenousmess:

If you’ve been following me for a while, you more than likely know what’s going on, but for those who don’t know: I’ve been in an extremely toxic, abusive relationship for the past 6 ½ years with my son’s father. We have a 3 year old together. While I did leave him last year, I (stupidly) came back in March under the promises of “things would change” etc etc. He has been emotionally, verbally, physically, sexually, and financially abusive. I am cooperating with the state in applying for all kinds of state assistance I am eligible for. I have an apartment and have our most basic needs covered. I need help with covering rent at the end of the month as I can’t do it by myself (my rent is $936), I have no consistent means of transportation (there is no bus/public transit in the city I live in) and I really realllyyy don’t want to have to allow my abuser into my home just to help cover these bills. I can manage on my own, but I need help getting on my feet and establishing my independence in the time being.

Any resources, encouraging words (I have virtually no support system), or other help is so much appreciated.

My PayPal is c.newago@yahoo.com, or PayPal.me/bizaanideewin

Please please don’t send anon hate or criticism, I cannot stress how hard I am struggling with my own guilt and self-blaming right now

Miigwech

I’m having a sale on my website, if donating isn’t your jam.

www.bizaanideewin.com

BOOOOOOST

Bringing this back, with an update: I wasn’t able to survive on my own so I had to let him in. Lo and behold the abuse continues. Today he punched a hole in the bedroom door. My dad is going to cosign for a new apartment for me back in my hometown, as long as I cover the costs he is going to help me move. I’ve already got a rental application submitted. I’m done I’m leaving I’m OUT. I have tangible proof and I can break the lease without repercussions through the domestic violence clause in the lease.

I just need help with the intial moving costs and initial housing costs- the apartment I applied for is $645 a month, security deposit same amount. First months rent and security deposit due at lease signing. Moving costs are around $400 (it’s a 300 mile move so it gets expensive fast)

PLEASE PLEASE PLEASE REBLOG

I’m almost 15% of the way there!! Please boost!

UPDATE: before my best friend came to get me to visit her, he and I got into a huge fight. He was screaming at me at the top of his lungs calling me a selfish bitch and a slut. He then proceeded to tell me Makoons won’t have any parents anymore if I call the cops.

Please boost!! I want to leave BEFORE this escalates!!!!

UPDATE: so it escalated last night. He’s in jail. He’s getting charged for domestic disorderly conduct or some shit like that. Once he’s released from jail he’s legally able to come back, if I take him off the lease I’ll be evicted unless I have a cosigner (which I do not have.) so my options are essentially continue dealing with this or move.

I also have venmo: @binesiikwens

eatingcroutons:

black-to-the-bones:

Each one of these women has an amazing story to tell, but we know nothing about them. This history is hidden from us, because they are women of color. 

Their names are Dr Anandibai Joshi, class of 1886; Dr Kei Okami, class of 1889; and Dr Sabat Islambooly, class of 1890. 

Dr Joshi was the first Indian woman to earn an MD; her Wikipedia page has the broad details of her life story. She argued that she should go to medical school due to “a growing need for Hindu lady doctors in India”, and was apparently the only student with the stomach to last through a demonstration autopsy of an infant. She died of tuberculosis in 1887, aged just 21 years old, but was such a remarkable figure that her first biography was published in 1888; since then there have been multiple biographies, a novel, a play, and a Hindi serial about her life. Drexel University has quite a few more documents about her in their archives.

Dr Okami was the first Japanese woman to earn a degree in Western medicine from a Western university; she also has a Wikipedia page which gives an overview of her life. Among other things she was appointed to head the gynaecology unit at Jikei Hospital in Tokyo, but resigned after Emperor Meiji visited the hospital and refused to receive her because she was a woman.

Dr Islambooly is the least well-known; her life was mostly undocumented after she returned home to Syria as the country’s first female physician. She was apparently a Kurdish Jewish woman who later moved to Cairo, where she died in 1941.

Here’s an article about their medical school, mentioning some of the other pioneering women who attended it.

fullyarticulatedgoldskeleton:

fullyarticulatedgoldskeleton:

I don’t get why people think they can catch you out on something like

“You said you couldn’t do X, but then you did Y!”

Like, one of the main things disabled people are trying to explain to the abled world is that our experiences are nuanced. We can do some things and not other things. We can do some things some of the time but not all of the time. Sometimes our abilities change over time. Sometimes we have the same diagnosis as someone else but not the same abilities and limitations. Sometimes we were misdiagnosed and we get correctly diagnosed later on in life. None of this is contradictory, none of this should be controversial to talk about.

Trying to call someone fake because they don’t fit a stereotype and don’t stay exactly the same their whole lives is antithetical to what disability activism is striving for, and it holds disabled people to a much higher standard than abled people to have our lives “make sense” to people who are biased and willfully uninformed.

Abled people are allowed to grow and change without it calling into question their entire life history.

Basically, being a disabled person speaking about disability in a public space means getting constantly subjected to “last year you said you were thirty, this year you said you were thirty-one, WHICH IS IT OBAMA?” type scrutiny. This is garden variety ableism, it’s not new, it’s not original, and it’s not any different when people think they’re harassing fakers for the good of “REAL” disabled people.

If people weren’t so suspicious of disabled people categorically they might actually learn something about disability.

All this does is make disabled people afraid to speak at all. After all, what if they see themselves in the latest victim of the faker hunt? Doesn’t that mean if they don’t talk about their disability very carefully- try very hard not to upset anyone’s preconceived notions of what their disability “should” look like- that they’ll be next? And when we have fewer voices in our community, less people sharing information about the nuances of disability, then we lose something important. There is nothing about trying to oust someone as a “faker” that isn’t toxic for disabled people as a community.