@tianaparker__
wallacepolsom

@theartofmadeline

JVL
I'd rather be in outer space 🛸
h
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2025 on Tumblr: Trends That Defined the Year
Sweet Seals For You, Always

izzy's playlists!
d e v o n
Not today Justin
Stranger Things

titsay
almost home

Discoholic 🪩

Product Placement
we're not kids anymore.
noise dept.
🩵 avery cochrane 🩵
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@floambitiousgirl
@tianaparker__
I’m so mad because this worked
help me roger
Reblogging myself because
Originally posted by gifs-for-the-masses
Reblogging myself because… what was that? Five minutes?
O_O
………my friend has made me curious
help me roger
Update: after I reblogged this someone messaged me offering me tickets to the sold out Hausu screening with a Q&A and autograph session with the director
let’s do it, roger
Roger helppppp
What’s good, Roger?
bc finals week
Roger…I need you.
Me as fuck man
Foreal
Bruhh what 😧
@guywithamohawk yes bro. The people I went to school with are on some other shit. They are on some need to grow up shit. 😒
Real shit. If we haven’t spoken since high school, 9/10 Idfwu
Dear black parents,
Your black child can be mentally ill. That’s not some shit reserved for white folks and their children.
The power of positive reinforcement. Jonathan Wall shared shared this story on Twitter just a few weeks before his 2016 graduation from Harvard Law. And he’s no ordinary graduate.
sending “I hope you get that job” vibes to the people out here tryna get jobs
reblogging for yall bc the shit worked for me lol
Karma will pop me if I don’t
Clear your mind here
Need a new outfit? YES YOU DO! Check these Jumpsuits out!
THE BEST MEMES !!!!
I’m not even sure which one I’m more like
This is the first time I have heard uptown funk
@someboredloser
@surprisebuttspecks look, it’s come back to my dashboard!!
This is probably the most entertaining Uptown Funk videos I’ve seen in awhile.
I know its kinda long but its def worth the read, i stumbled across it while scrolling down my timeline…
I read this whole thing with my hands on my head. Wow!!
yesterday was a really special and sweet day with my boyfriend we literally cuddled all day, cooked pasta, and watched django and just talked and smoked and made love and i was/am so happy and peaceful and in love. love is such a strong emotion and thing and i am so happy i have it and he’s just so good to me and for me and my best damn friend so i am always forever grateful for this love of mine
Black girl with a Chronic Invisible illness here. The top 2 pictures are what I look like when I am having an okay day, which isn’t often. The rest are a little peek at what my life is actually like. As many of my followers know, I have a brain condition called Chiari Malformation. It is a degenerative disease and there is no cure for it. People are dying from it or are taking their own lives from the excruciating pain it causes because doctors just cannot seem to help us, simply because they are not educated on it, or have never even heard of it! I have wanted to take my own life on many occasions, and still do very often because of what this illness puts me and my body through on a daily basis. There is no escape. It feels hopeless. These pictures were taken in February. Just a few months ago I was going in for my second brain surgery because I was having so many problems again. It was the worst thing in my life to happen. After surgery, I got a CSF leak from ripping the stitches in the back of my neck from throwing up so much because of the anesthesia. I then contracted a strand of meningitis that came from IRAQ. Acinetobacter Baumanni, to be exact. Also known as, Iraqibacter. It is a killer infection. It kills a lot of our troops in Iraq. The mortality rate is high, and there are only 2 antibiotics that can kill it, and they are not even guaranteed to work. So if both antibiotics don’t work, you die. We tried one and it wasn’t working. I ended up unresponsive from it. Almost died from it. I couldn’t even articulate my words or make sense before I became unresponsive. Thank God the only other antibiotic they had was working. They sent me home with a PIC line in my arm, connected to a pole on wheels, with lots of bags of medicine that were to be mailed to my house the next day. My mom was injecting me with the antibiotics weeks after leaving the hospital. Catching the meningitis kept me in the hospital for a month. I thought I was going to die. I lost so much weight and lost all the tone and muscle I had. I had to learn how to walk all over again. It was a terrible experience and I’m glad it’s over. My mom and I do a walk for Chiari every year. We’ve even ended up on the news! We do this walk to raise awareness and money that will be put towards research to find a cure. It would be amazing if everyone could reblog this and spread it around and really get it out there. It’s really important to me and would mean a lot!! We are a little far away from our goal with only 45 days left to donate. Please donate to Team Brianna! ANY amount helps. It all really does add up and it makes me feel good to know it’s all going to research to put a stop to this illness! We desperately need more to be educated on this illness. We desperately need to find a cure. I’m fighting for myself and every other Chiarian out there.
With lots of love, Brianna 💜
Link to donate: http://unitenight.kintera.org/faf/search/searchTeamPart.asp?ievent=1157697&lis=0&kntae1157697=D54108675AB14FF4B94573800F9190BF&supId=0&team=6656316&cj=Y
Invisible illnesses suck. Boost tf out of this. Wishing you love Brianna.
have you ever finished a test in 30 minutes and no one else was even close to being done
i’m either really smart or i fucked up entirely
nailed it or failed it