If you’ve been watching the noise and paying attention to California, you’ve heard about the Camp Fire.
In a matter of hours, the fire jumped to 20,000 acres. This morning it reached 70,000. My town of Paradise, where I’ve lived my entire life, was consumed entirely. Very little containment has been reached and the situation is absolute hell.
My house was one of the first to go.
My mom and my sisters and I barely got out, in separate cars, and we got separated for 10 hours. My mom and little sister were stuck in Paradise with all my pets in the flames until my stepdad was able to get gas to them so they could get out. My cat was lost, and I personally was only able to grab an extremely small amount of my own belongings because I was helping my mom to grab important documents and photos and to get the pets situated.
We are now homeless, with no clue where to go from here, and desperately in need of help to get food, clothes, supplies, anything. My mom has been disabled for 3 years and we survive on a single income from my stepdad, who is a firefighter. His friends have been hurt trying to fight this. We have a dog with us, and two guinea pigs, and a bearded dragon.
My mom set up a fundraiser, even though we are not at all the type to ask for so much help.
being a female means needing to see 10 different doctors to get a proper diagnosis because they always think you’re exaggerating and/or lying
define proper diagnosis. I mean, does that just mean the diagnosis you want?
no :) it means going to 10 different doctors who disbelieved your symptoms until the 11th found cysts on your ovaries :) which may mean infertility :) sit on a cactus :)
I call bullshit
Of course you do. Like the first 10 doctors. 😒
I call bullshit on the story. If you think you have an issue you should see a specialist not just your PCP.
Like the 4 “specialists” I saw for the crippling numbness in my face and legs I had for over a year while they told me it was “stress”? When it was finally found that I had scars on my brain and spine? Those “specialists” we’re male neurologist who wouldn’t give me an MRI because “women stress too much”. Go fuck yourself.
MY SPINE WAS BROKEN FOR 2 YEARS BECAUSE MY DOCTORS TOLD ME I JUST HAD BAD CRAMPS AND REFUSED TO TAKE XRAYS. FUCK YOU AND YOUR ENTIRE LIFE. WHEN WILL BOYS REALIZE THEIR EXPERIENCES ARENT STANDARD???? I ALSO LOVE THIS IDEA THAT YOU CAN JUST GO TO A SPECIALIST WHENEVER YOU WANT LOL IF OUR PCP DOESNT BELIEVE US WHEN WE TELL THEM OUR SYMPTOMS THEY ARENT GONNA REFER US TO A SPECIALIST YOU FUCKING MOLDY WALNUT
My parents began noticing something large in my throat, saw a specialist….Guess what? Told me to lose some weight..even though I wasn’t overweight. I would have my period for weeks at a time. Was told that it was teenage hormones and stress.
Two fucking years later I attempted suicide they ran a battery of tests as required and bam! They find out that I have untreated Hashimoto’s. The “thing” was a goiter. Possible symptoms of an untreated thyroid disease is the goiter, unexplained weight gain, and depression. All they had to do was test my blood, but they said young people don’t have thyroid problems. 😒
-Allie
Ten years ago, my mother—who is a pretty tough cookie—started feeling both ridiculously wired, anxious, and incredibly emotional. Every doctor she saw told her she was going through early menopause, even though she was still menstruating. Her health declined to point where she was barely sleeping, losing weight, and crying constantly, which was a huge red flag because my mother never cries. Finally, she went to see another doctor 2.5 hours away who referred her to an endocrinologist. And what did the endocrinologist say? He diagnosed her with one of the most advanced cases of Grave’s Disease he had even seen, and said if she had gone just a few more months without being treated, she could have FUCKING DIED.
Also, it turned out that her thyroid levels had been moving out of the normal range in a progressive pattern for years, but nobody bothered to look at her past test results until after the diagnosis. They would just do a test, see that it was “in the normal range” and leave it at that. She could have caught it before she even had symptoms, instead of basically being accused of having hysteria.
i had a brain aneurysm/hemorrhage ten years ago, doctors still tell me im faking my disability BECAUSE YOU CAN TOTALLY FAKE LIMITED MOVEMENT OF THE LEFT SIDE
My sister had intercranial hypertension which was causing headaches, dizzy spells and loss of vision, and you know what the hospital told her? She was being a hysterical girl and making it up. A few weeks later she spent roughly a month in hospital and had several lumbar punctures to relieve her RECORD HIGH spinal pressure that was causing so much strain on her brain and optic nerves she was being sent blind.
Everytime I see this post (and it’s been a good 5/6 times), it has different stories and experiences of women who have been horribly mistreated by doctors and it just blows my mind that this is so big. It’s absolutely disgusting how terribly women are treated in the medical world and something needs to be done about that.
my friend lea had back pain, then pain in her legs and feet, and then numbness. despite seeing 7 different doctors over 2 years, by the time they found the cancer it was inoperable. chemo and radiation didn’t work. the cancer spread. she died and left behind a 5 year old daughter.
A few years ago I would go through spells where I literally could not stand on my own and I couldn’t get out of bed. I would be freezing and too weak to eat. I would keep having heart palpitations as well. I got up the money to go to a clinic and they told me it was just stress and to basically just work on chilling out. I saved up money for a few weeks to do this and I pretty much get a “chill out” from them.
As time went on it got worse, most noticeably the heart palpitations were happening almost constantly. I went again to a different clinic and was told it was normal and that it was probably stress. They did no tests, and they told me it would “just go away”.
Two weeks later I ended up collapsing going down some stairs, and at the hospital it was discovered that I had such severe anemia that my heart could barely keep up with trying to get enough oxygen to my body. I had developed left ventricular hypertrophy (my heart muscle is too big) and because of them ignoring me and dismissing me I’m at a much higher risk of heart attacks and stroke now.
I went to the doctor with severe intermittent pain in my upper right stomach area that was so bad I had to miss school. Despite the fact that my period has been on a regular 3 month cycle for years, and I still had two months left until my period, my doctor told me it was period related cramps and or indigestion. 2 months later I’m in the hospital getting my gallbladder removed. It was so obstructed that there was gangrene developing my my system.
So…everyone who’s given me shit for that one post (about medicine and equal treatment and shit) can just read this because I’m sick of defending my case.
I’m sorry but if I tell you I’m getting violently sick from what you prescribed you better change it not tell me to Try Taking It Again!!!
(I have soo many stories… I’m an NB but I was female at birth so that’s all the doctors see.)
Horror storys are all we have as women.
I thought I had classical (life-threatening) CAH until I called my doctor requesting my exact diagnosis and mutations at age 21. Now I’m going through a temporary (hopefully, fingers crossed) period of mini-Addison’s disease while my adrenal glands regain proper function after the many years in my childhood and adolescence of being on heart-damaging corticosteroids that someone with nonclassical CAH shouldn’t even be using for that long a time. NCAH isn’t inherently life threatening on its own but Addison’s is, and explains why I’ve had severe issues mimicking my childhood declines into hypovolemic shock when I wasn’t able to take the corticosteroids. I should be fine now that I’m six months off of all cortisol replacement therapies, but it shouldn’t have happened in the first place had they read the fucking blood tests on my shock hospitalizations properly to see that they weren’t caused by my adrenal glands.
By the way, go see female doctors exclusively if you can. Sure, there are some terrible female doctors and a few great male ones, but female doctors have statistically much better outcomes and are far better listeners. This is specially true for OB/Gyns.
It took me 6 years to get a proper diagnosis of my ADHD. Doctors dont listen to women, men dont listen to women. Anyone who doesnt believe us is just a reflection of this.
Fuck. Anyone. Who. Says. This. Doesn’t. Happen.
Fucking idiot men damn. All these stories and they’ll still find a way to doubt us. “This is just the anomaly” eat dirt fucker.
Idk how many time I’ve rbgled this post, but every time I see I new addition I need to rb it
Don’t forget to check on your strong Tumblr friends.
Just because someone runs a blog to help others doesn’t mean they shouldn’t be checked on as well.
Sometimes the people who seem like they’re strong and have it all together are actually falling apart but don’t know how to ask for help or they are too scared to—just a friendly reminder 💚
