Lalaland

[whatwhiteswillneverknow]

“Black people did not show up @ the polls -”

TRICK PLEAZE!

Did you not see the chart? Black women went up in droves. There are people who couldn’t vote because of long lines and even then some stood there for a long time to make sure they close it out.

God, I swear, every time when something goes wrong, you blame Black people. How many times do we have to carry things huh?

Civil war, world wars, Reagan, Obama, motherflipping Vine and your style choices. How much more do we have to do?

[aaron2point0]

Tommy Prince Was So Quiet, Sometimes Instead Of Killing Germans He Would Steal Their Shoes

This is the story of Tommy Prince, a Native Indian Canadian soldier who left an indelible mark during World War II due to his Bravery.

Tommy Prince is usually described as a weird yet entertaining character. His colleagues knew that he used to carry a pair of moccasins in his bag, and during the night he would take off his boots and wear the moccasins. He was thus able to creep quietly into the enemy camp, and sometimes he would do crazy things like stealing the Germans’ shoes.

[agnesmontague]

¯\_(ツ)_/¯

[ismileanyway]

[-hope-for-the-hopeless-]

[spoonie-living]

Connect with others fighting cancer, heart disease, diabetes, chronic pain, mental illness (depression, anxiety, PTSD, bipolar disorder, schizophrenia and others), addiction and grieving.

Looks like we’ve got ourselves a new social network in the making! 

This one is app-only, but allows you to pick out which challenges you’re experiencing and see related content and people. It currently has fairly broad categories, but as membership increases we imagine they’ll introduce ways to drill down a little more. 

Give it a whirl here: iOS | Android

[captainevans]

As a white person, I would just like to apologize for what other white people have done tonight. It’s fucking terrifying that this is our reality.

[breakfastautocrat]

This is a decidedly unfriendly reminder that I don’t want you following me or liking/reblogging my posts if you are a Trump supporter, neo-Confederate, TERF, neo-Nazi, or a supporter of any other sort of white supremacist or fascist movement. Get the fuck out. I don’t want you here.

[captainofalltheships]

i can’t believe that 2016 has ruined even my desire for 2016 to be over

[telanu]

oh my god

[hillaryisaboss]

Hillary won the popular vote. Never forget that.

[cleoselene-deactivated20260315]

Trump was right, the system IS rigged.  It’s rigged against the majority of Americans, and here is the proof.

[cleoselene-deactivated20260315]

shawnskaty:

choncegiving:

america gonna have a new president in a week

[buzzfeed]

Ah, yes. 2016. The Great Garbage Fire Year.

[ithelpstodream]

[cleoselene-deactivated20260315]

shirodere:

ithelpstodream:

Representation matters.

Daughter: Mom, why are you crying?

Mom: I got to vote for a woman for President.

Daughter: You’re gonna make me cry.

WHY ARE PEOPLE BEING SO NEGATIVE ON THIS POST PLEASE SHIT ON SOMETHING ELSE

:) my mom is exactly this she even has a little Hillary shrine in her house with a bunch of buttons and a Hillary bobblehead surrounded by her electronic candles lol

it’s amazing how younger generations of women get to breeze by this but I understand why older women have this visceral reaction

it’s a huge deal

[kookalala-blog]

Any MSers tall as a young child?

Any PPMSers or MSers out here in Tumblr land? Was hoping for your feed back. I just need one question answered. Were you tall in grade school?

[cleoselene-deactivated20260315]

very.  was tall all through childhood and reached my max height (6′0″) at age 13.  I have PPMS.

[kookalala-blog]

You ever have throbbing low back pain (kidney area) when something really angers you?

[kookalala-blog]

Any MSers ever wonder why they say MS is a disease of the central nervous system but never mention that the nervous system has a partner in crime, the endocrine system? They are like love and marriage, you can't have one without the other.

[kookalala-blog]

Neurologists Piss Me Off!!!!!!!

I had a Neurologist tell me that my MS related symptoms mean nothing to him. That it was like telling him I had a headache. Boy if that isn’t a slap in the face! My symptoms mean everything to me. So I did some digging. I wanted to know what kind of research has been done that actually involved people with MS and their personal stories. Guess what? Couldn’t find a thing except for the doctor who discovered MS in the 1800’s. They said he did all the research that could be done. Im not buying it. So here we are depending on Neurologists to find a cause and a cure. I say let’s take matters into our own hands and find the cause. Because at the end of the day it is our lives that are affected. If these Neurologists had MS you better believe they would know what caused it by now. So I’m asking all of you that suffer from MS to please share your story with me. I’m not talking about just your MS story, I want your whole story. The answer lies in our stories. I guarantee it. If you are interested in becoming part of the movement please email your story to [email protected]. Together we can find an answer. And for you out there that have no diagnosis, please share your story with me as well. It is probably the most difficult position to be in and your story is valid and should be heard.

[kookalala-blog]

Any MSers tall as a young child?

Any PPMSers or MSers out here in Tumblr land? Was hoping for your feed back. I just need one question answered. Were you tall in grade school?

[thischroniclife]

Discussing treatment plans...

What my doctor says…

What he actually means…