ithelpstodream:

i just watched people blame antifa, BLM and muslims for the mass shooting in las vegas but as soon as it turned out the shooter was white these people all got eerily quiet.

people who were screaming for justice minutes after the news came out, begging that “the threat” will be faced with a “final solution” suddenly keep quiet. why? to defend whiteness? because if a white man is labelled a terrorist, whiteness will be under attack the same way we condemn all muslims for the actions of a few? it’s dispicable.

this is the deadliest mass shooting in US history and you want to tell me the attacker is not a terrorist???

flowury:

please do yourself a favor and date the biggest fckn nerd u can get ur hands on

intoxibella:

intoxibella:

I’m gonna name my daughter Theresa but pronounce it like “there’s a”.

Theresa Snakeinmyboot

weavemama:

IT IS OFFICALLY HALLOTHANKSMAS SEASON

satansfrontlines:

I’m not sure where else to go to get support for this, so I have my hopes here.

My mother was recently diagnosed with Complex Regional Pain Syndrome, also known as the Suicide Disease. It’s known by that name because the suicide rate of the victims is extremely high, higher than any other disease. It is a nervous system disease that attacks the nerves in the body, causing the nerves to send nothing but pain signals to the brain 24 hours a day. There are 4 stages to this disease– it only takes 9 months to get to Stage 4 and when that happens, the disease starts attacking the internal organs. At that point, the pain is so excruciating that many victims will decide to just take their own lives instead of live any longer with that much pain.

My mother is already 3 months in and I have watched her go from a very happy person that got up in the morning every weekend to go hike miles of trails through the mountains to someone who can barely even limp down the stairs in her own house.

But she has recently gotten an amazing opportunity to see a doctor in Arkansas that has successfully put this disease into remission for countless of people. The doctor also wants to professionally document my mother’s experience and treatment in order to help future victims and improve future treatments. But she has to be there by the end of October with $20,000 to pay for the treatment because her insurance won’t even cover a cent of it.

Please, my mother may never get another chance like this again. Even if you can’t donate, a share on Facebook or a reblog would be immensely helpful and so, so appreciated. 

Her gofundme is here: https://www.gofundme.com/help-a-loving-mother-fight-crps

Thank you for any support at all!