#Uterine cancer
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Hi everyone! thought I’d share a local gofundme from my area. Karen doesn’t know I’m sharing it, but she’s been standing outside our grocery store in the blazing sun for hours fundraising and I really hope you’ll consider helping her. She needs help with the pile of medical bills for her ongoing cancer treatment. Please reblog and share even if you can’t donate! Thank you <3
$12.100 / $25.000
https://gofund.me/a8ecb30f
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I'm about to go for my first cervical exam soon. I kind of know what to expect, but i also want to know if there's any way to make it easier?
The doctor I'm having it with has made it VERY clear that if i feel at all like I need to stop, she will and the unrelated appointment I had with her went well. I'm just a little nervous going into it
Also my grandma had uterine cancer (alive and well, don't worry) My mom said we'd all have to get exams more often because of this, but the doctor I went to recently didn't seem to think I did. I've done some very light googling and read that only about 5-10% of cancer cases get passed down genetically, but uterine cancer gets passed down about 10% of the time. Should I be getting tested more often?
Okay.
Honestly, I'm not sure on ways to make it "easier" beyond bringing someone you trust with you. It's a fairly quick exam usually and not associated with pain [unless you have certain conditions that make it painful], so I don't know exactly what else to recommend.
It sounds like you've got a good doctor so far! That's great. It makes sense you'd be nervous, especially for your first time. It can be a little nervewracking, which is why I do suggest bringing someone with you.
I'm assuming if this is your first cervical exam, you're pretty young, so its not likely you need extra exams for uterine cancer even if your grandmother had it.
Uterine cancer usually develops when you're much older and unless you have added risk factors like PCOS and/or diabetes, its very unlikely you need to start extra exams yet.
Though keep in mind, I'm not a medical professional so I could totally be wrong.
Hope this helps, though! Let me know if you have any other questions. <3
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I need to vent about my SIL especially after losing my MIL last week. This might be a lengthy post. Because I'm petty, angry & hurt. I need the catharsis of publicly shaming her sans her name.
My SIL grew up spoiled. She wanted for nothing. What she couldn't get from others, she learned to manipulate from them.
My hubs & his brothers had to beg, plead & steal for all they had.
SIL beat the shit out of my husband when he was around 5yrs old so badly with an extension cord - he still has nerve damage in his back.
Anytime she didn't get her way, she took it out on him because he was the youngest at the time.
SIL was a teen mom & there's no shame in that. But she has always been ashamed of being Hispanic.
She would bleach her son's head as a toddler & when he got older forced him to wear blue contacts until he stood up for himself in middle school.
SIL gloats & brags about ruining lives just because she's practiced enough to do it - careers, families, citizenship, etc
When our girls were smaller we gave SIL a chance hoping she had shed her skin. Nope, SIL was still SIL. She used her own nieces to make herself look good - new SOs, new friends & bosses. Once she seemed wholesome enough & secure, she wanted nothing to do with them.
SIL always lives outside of her means. When hubs Gpa was still alive she forced him to pay her mortgage, auto loan & so much more. Meanwhile vacays, cruises, designer clothes, motorcycles, bought her own cabin, etc
When Gpa cut her off, she bled everyone else within her reach, except us, dry & called it a day.
SIL tried buying our three daughters social security cards from us to get her bio father's family into the USA. When we told her no, she called CPS on us.
SIL treated MIL like shit. Which wasn't a surprise. SIL didn't like MIL was one of the few who didn't spoil her during her life. It was everyone else around her who did. & so SIL made it a point to ice out MIL, including keeping her son, MIL's grandson from her.
SIL tried to convince her son that his own son wasn't his just because she didn't like the girl. SIL made this girl's life a living hell. SIL forced him to terminate his parental rights, which he did. A paternity test proved he was his son, but by then the damage was done. The girl ran from that family & didn't look back.
SIL's son married a girl who had a child with someone else, nothing wrong with that. SIL had an issue with that because he was fresh out of HS. They now have a daughter together. SIL's son rarely interacts with her.
When MIL had her stroke that placed her in a long term nursing home - SIL got POA. SIL embezzled what money SSI gave her outside of paying for the home. We knew this would happen, but SIL was the only one capable of being her POA.
We found out one of my BILs was a child predator who preyed on one of our daughters. SIL who could care less about him before all of this - is suddenly his protector. & said despite what he did, he deserves love & his family. Girl, what? 👁️👄👁️
When Gpa died of Alzheimer's. We were not notified despite being very close with him. We had to find out through Google searching his name here & there. It was a few months after his death.
MIL, her stepsister & all of the grandkids were supposed to get an inheritance when Gpa died. Husband never received his. But he didn't want to take SIL to court. He just said, "She can choke on it."
The nursing home kept calling my husband about MIL because they hadn't heard from SIL in weeks, sometimes months. The only person visiting MIL was her husband she was separated from. We couldn't visit her because SIL told the home we couldn't without her permission.
We found out MIL had been diagnosed with uterine cancer while in the nursing home. We found out through one of the phone calls when they couldn't get a hold of SIL.
More phone calls from nursing home because they can't reach SIL to schedule cancer treatments.
Eventually the calls from nursing home said MILs cancer had progressed to the point of hospice because of the lack of consistent medical intervention.
SIL *finally* contacts us & said we can visit MIL before she's moved to hospice.
MIL was never moved to hospice we found this out because one of hubs paternal cousins got a job at the nursing home.
Last week when MIL died we found out because the nursing home contacted us because guess what? They couldn't get ahold of SIL.
SIL didn't even bother to contact us about her death. She posted about the funeral on her FB page. My aunt told me the details because I have SIL blocked, husband doesn't have her blocked.
I was confused about the funeral home being used because it wasn't the one that side of the family uses. So I called them. SIL went cheap - no embalming (not that I agree with it), no viewing, no open casket, just a graveside service.
I also found out MIL would not be buried next to her dad despite having a plot. She was so proud of that plot before being in the nursing home & comforted that she would be next to him. We still don't know if SIL sold the plot before MIL died because of her POA.
We visited MILs grave a few hours after the service (we didn't attend because predator BIL) & found out she was buried next to her mother, aunt & both maternal grandparents. Which made us glad she was at least next to some family.
There was no headstone at her grave. Which we know isn't placed right away. But knowing SILs behavior - we went in person & spoke to the funeral director. SIL did not purchase one, but said she would be back to place one on a payment plan. We told the funeral director that either SIL will ghost her or meetup & not buy one.
We told the funeral director we would purchase the headstone, but to tell SIL there was an 'anonymous donor'.
SIL did come in for the payment plan appointment, but once she heard there was an 'anonymous donor' - the funeral director said, "SIL had her checkbook out & immediately put it back in her purse when she heard there was a donor. She said she'll pay whatever they (us) don't pay."
We're paying for all of it tomorrow. Out of love for MIL, but also BDE & pettiness at this point.
One last thing. SIL used a free obit service, Echovita, which I'm not mad at. But it was a stock obit that ChatGPT wrote. Echovita has that as a feature. I got on Echovita & wrote one my damn self, that was actually personalized.
End Vent
#vent#petty#mother in law#sister in law#funeral#cemetery#headstone#obituary#evil#cancer#uterine cancer#stroke#nursing home#grief#grieving
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INFERTILITY/CANCER SUCKS.
Sometimes, I just want to delete all socials. I'm happy for them, I am. But knowing I will never get to feel those things just breaks me. Not being able to go to get an ultrasound, being able to hear the heart beat, feel the kicks, have the bump, the things that women are supposed to or are able to feel. I'll never be able to have a tiny human made up of mine and my husband's genes. I'll never get to have a baby shower, maternity photos, I'll never be able to give my parents grandchildren, I'll never be able to make my sister and aunt, my nieces a cousin. I won't be able to wake up at 2 am to comfort my baby to sleep. I'll never be able to make my husband a dad. And boy, would he be the absolute best dad in the whole world.
I could literally go on and on all day about how much this kills me every day.
In 2023 I was diagnosed with uterine cancer. My best friend had the same exact cancer 8 months before me. And honestly if I didn't have her idk what the hell I would've done. She told me girl, this shit sucks and unfortunately, we have to make a hard decision, one of the hardest I've ever had to make.
I don't hate seeing your pregnancy announcements, your baby shower photos, your kids going to school for the first day. All of their milestones. Everything. I love seeing all of this.
There's just a part in me that makes me mad at myself. Why did this have to happen? I've always wanted to be a mom. I've always wanted to have a huge family, be able to do what I was created to do. And in a flash it was all gone. Everything I've ever wanted, gone.
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1/17/24
I’m scared.. I got all my girls out to hold them, then I noticed a smell and saw blood on my hand, then I took each girl back out of the rat robe to look them over.. Noot was bleeding from her privates.
The only other time I’ve seen this in my rats is when they have had uterine cancer.
I don’t have much money left to my name but I want to try my best to help her, and call the vet..
maybe it’s an infection and not cancer.. I hope she has a chance of getting better. I don’t know what will happen.
#my poor baby#Noot#honeycombhank#my pets#rats of tumblr#my rats#dumbo rats#ratblr#sad thoughts#cancer#uterine cancer#tw blood#trigger warning#oh god
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I've not been able to figure out why I've just not felt well enough to do very much (except to binge-play Fallout 76 and now Once Human, but I swear to fuck it's because I get to build bases/houses, which is the most fun thing ever--and we can blame The Sims for getting me into that obsession, thank you very much!!).
But, now I have answers at last.
And that answer is.... endometrial carcinoma. Which is a fancy way of saying uterine cancer.
Fuck cancer.
But, BUT, despite the abnormal bleeding events lasting 3 years, and then becoming especially bad in the past few months, I am very, very, very fucking fortunate that it is 'low grade' and that the surgeons believe it's most likely limited to the uterine lining!
So what's next? First, an MRI to do official "staging" and plotting the best path for the hysterectomy to follow. I knew a hysterectomy would happen anyway based on what they found, but I only found out today the "what" is cancer (again, fuck you cancer).
If all goes as expected (currently), then it will be: MRI, hysterectomy, and finally no more cancer.
Obviously things could change when they get in there. But, I am being optimistic and hopeful that the surgery will be the whole of it, and then I can get on with recovery and feeling more human than I've felt in recent times.
Anyway, I'm going to busy myself with my slow-but-in-progress plans of tidying up some fanfics I want to repost, and doing the equally as slow work on figuring what the fuck I'm doing with my original stories because a lot are blending together and I continually get myself confused - which is no help whatsoever lol
Also I really, really want to get back into gif making as I've been thinking of so many that I want to redo, and others that I've never done and figured could be fun. Mostly it's Sanrion AU's, Rachel/Joey and Rumbelle. And I'm fine with that, as they're my happy space right now!
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I know this probably won't go anywhere but it's worth a try.
Hello!
I'm Shay. I have multiple sclerosis and my mom was diagnosed with stage 4 uterine cancer in November. She is not terminal but she is very sick. She has had to have a hysterectomy at 65 years old and she is undergoing chemo.
Both of us being sick is very expensive and hard. I am not able to work because I have to take care of her and we don't have anyone else that can do it. We only have each other and now we are both very ill. Please help if you can! We are in desperate need of money as we need to buy hats/scarves as she is starting to lose her hair due to the chemo.
My PayPal, if you would like to donate, is https://www.paypal.me/SharayaJ87 Thank you!!!
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I don't know if this is your department but what would happen if a complete hysterectomy was medically necessary (cancer) in the middle of puberty?
Hi Anon,
This is technically not my department - a patient undergoing this would be under the care of a gynecologic oncologist, and a fertility specialist will also probably be a part of the team.
That said, I can discuss the physiology of what would happen:
Uterine cancer in an adolescent is exceedingly rare, and a total hysterectomy would be a treatment only of last resort. The result of a hysterectomy is that the person would become unable to become pregnant.
If the uterus is taken but the ovaries are spared, the person would still go through puberty as normal, developing female secondary sex characteristics, but they would just never menstruate. They would still ovulate, and could theoretically produce a biological child using in vitro fertilization (when eggs are retrieved surgically and fertilized outside the body) and a surrogate to carry the pregnancy.
If both ovaries also had to be removed in addition to the uterus (exceedingly, very very, super rare), the young person would become permanently sterile (no more eggs), and need to receive estrogen hormone replacement therapy to ensure proper growth and health. Estrogen isn't just responsible for the menstrual cycle or for feminizing features - it's also important for bone and cardiovascular health.
For those who are wondering how rare this is:
The annual incidence (how many people per year get a thing) of gynecologic cancers in adolescents (age <18) is 6.7 per MILLION. Of those, 87.5% are of the ovary and only 2.5% are of the uterus. So, out of a MILLION adolescent AFABs, 5.6 people will get ovarian cancer, and 0.2 will get uterine cancer.
That's 2 out of 10 MILLION!
The good news is the survival rates for these cancers is very high!
(Source: Wohlmuth, C., & Wohlmuth-Wieser, I. (2021). Gynecologic Malignancies in Children and Adolescents: How Common is the Uncommon?. Journal of clinical medicine, 10(4), 722. https://doi.org/10.3390/jcm10040722)
---
If this is your situation, Anon, I am very sorry to hear about it. I wish you good health and excellent care!
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So I have an IUD for the past 2 years…
It’s been helpful. I’ve been in remission for a year now, and it’s amazingly unstressful… but it’s not all perfect… and things have been off.
I don’t have periods anymore, but I do get these monthly days where I have lots of mucusy stuff. I call it my ghost period, because cramps too. So like there ya go.
I have the iud because of endometrial neoplasia. My oncologist said the options were taking out the uterus or putting the iud in, and other such things.
So I was trying to explain it to ai but she didn’t get it. She did help me feel a little better though.
#ghost period#iud#liletta#Paraguay’s#uterus#uterus health#endometrial cancer#endometriosis#endometrial neoplasia#ai generated#chat gpt#perioddramacentral#perioddramasonly#women’s health#uterine health#uterine fibroids#uterine cancer
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Official Period Post
fresh, clean no-terf version for reblogs!
Your mom and aunts aren’t on tumblr. Please warn them about this as well.
#womens health#reproductive health#uterus#menopause#menstruation#official period posts#menstrual health#people who menstruate#period#post menopausal bleeding#uterine cancer#tell your friends
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LIVE: TVUP Health Updates
November 8, 2024 (Friday) 12nn
Webinar #216 -- Endometrial Cancer (Kanser sa Matris):
Risk Factors, Prevention, Detection, and Management
#cancer #EndometrialCancer #UterineCancer #EndometrialBiopsy #Hysterectomy #Laparoscopy
https://www.youtube.com/live/f6RJUS-CxaQ?si=F5WPmPeQQKe02hQq
#cancer#endometrial cancer#uterine cancer#endometrial biopsy#hysterectomy#laparoscopy#laparoscopy surgery
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my uterus seems to be actually dying but i can't really tell (hope i can make it til i can actually see a doctor before it's too late)
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https://gofund.me/e4681986
We still need help...please, if you can.
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PLEASE DON'T IGNORE. PLEASE READ.
Mohammeds wife has uterine cancer and needs chemotherapy. She has not received any chemotherapy since the war began.
One of Mohammeds children, Sarah, is now sick and needs medicine
Mohammed suffers from chronic asthma and an extreme allergy in the ear. He needs medicine that is either too expensive or not available.
Mohammed and his whole family need basic necessities like food, water, medicine, clothing, and bedding.
The tent they live in is not adequate for protection from the weather and temperature.
Please donate if you can, share, and reblog.
Mohammed and his families lives depend on it
Every donation, no matter how much is given, is important and helps.
Donations are protected on gofundme for a year. So you can donate in confidence.
PLEASE DON'T IGNORE. PLEASE READ.
My campaign is verified and added to the Gaza Donations page with number 192.
Thank you for documenting my campaign from the following accounts:
@sar-soor @heba-20
@el-shab-hussein
@90-ghost @soon-palestine
@ibtisams @marnota @riding-with-the-wild-hunt @i-am-aprl @northgazaupdates @fallahifag @fairuzfan
I love you all 🙏🙏♥️🌹
I am Mohammed Almanasra, 32 years old, married, and a father of three children: Abdulrahman, 6 years old, Sarah, 4 years old, and Lina, 3 years old.
My story began with the loss of my parents and four of my sisters, who were bombed and lost their lives along with their children after the events of October 7 and the severe war on Gaza. Now, I am facing a severe injury to my leg, which is at risk of amputation if I do not receive the necessary treatment. My wife, children, and I are displaced, without parents or siblings, and my wife is also suffering from uterine cancer.
Recently, I moved to the south of the Gaza Strip, fearing for the lives of my children. We left behind our memories and our new home, for which we had not finished paying the installments, in addition to losing my job. Currently, I live in a tent that does not protect me from the heat of summer or the cold of winter, and without the minimum necessary livinng basics including water, food medical care, clothe and even bedding .
I suffer from a chronic asthma and severe attacks from tightness and an extreme allergy in the ear and I need medicine that are not available, or very expensive .
Under these difficult circumstances, after five attempts at displacement and narrowly escaping death from the bombing, I am trying with all my might to protect my family, the most precious thing I have.
My dreams were shattered, and my house was destroyed, and I found myself living in a tent no larger than 4 square metres. My work turned from a tailor to a street vendor in order to barely buy a few crumbs of bread to feed my children.
Look at what happened to my children because of the intense heat and the insects that thrive in the summer season. Every day, I take them to the hospital to treat them due to poisonous insect bites. I implore every kind-hearted soul to help me protect my children.
My son, Abdul Rahman, has a deep passion for playing football and is a devoted fan of Real Madrid. He always dreamed of playing football at his school, but the war prevented this dream from coming true.
Where are you, Real Madrid fans ?
Help Abdul Rahman achieve his dream.
Every donation will make an enormous difference in helping me save my family.
I feel very sad and embarrassed to ask for help, but I have no other options left. I know that this request is difficult, but I also know that there is still humanity and living consciences and I believe in miracles.
Your support during this extremely difficult time will give us hope in the midst of devastation and despair.
If you have any inquiries or questions, feel free to ask me, please!
To everyone with a compassionate heart,
To all who understand the essence of humanity,
This is a message from my innocent children, who trust that their words will reach everyone who truly understands the meaning of childhood.
We cry out to you, asking you to feel our sorrow and pain, and to extend a helping hand to us in this time when we are in desperate need of your mercy and compassion.
My name is being repeatedly added to many public and private donation campaigns. Please, be a support for me in this difficult situation.
https://docs.google.com/spreadsheets/u/0/d/1yYkNp5U3ANwILl2MknJi9G7ArY4uVTEEQ1CVfzR8Ioo/htmlview
Sincere greetings & thanks
Mohammed & the family
#gaza#free gaza#free palestine#gaza genocide#gofundme#gaza gofundme#palestine gofundme#palestine#gaza go fund me#go fund me#palestine go fund me#gaza fundraiser#palestine fundraiser#cancer#uterine cancer#chronic asthma#sick#ill#donate if possible#donate if you can#please share#please reblog#gaza news#please donate#palestine news#news#donate#don't ignore#don't skip#reblog
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I have GREAT news. So, as of the MRI I had done (two weeks ago), there was no sign of the cancer in my uterus spreading. That is a huge, huge relief.
Alas, I do have a huge fibroid in my uterus, which means a hysterectomy is the only curative action for this cancer.
The op is said to be "very soon", but this is New Zealand's public health sector we're talking about....... my "emergency surgery" to find out why I was bleeding took them over 2 years to do! And yes, yes I do count myself extremely lucky that the cancer I've got is so slow growing and such a low grade that I'm not in a far worse situation than I could have been in, given the circumstances.
What all this means, also, is that the surgery will be "key hole" and so the recovery will be a lot quicker than I was anticipating. I mean obviously things can change when they go in, but I'm being positive!!
I'm just so looking forward to being on the flip side of this cancer so I can recover and get back to geeking out over shit without feeling like the end of the world is approaching (which was the weird foreboding feeling I'd had for over a year now!!).
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A Warning About Post-Menopausal Bleeding
Text Transcription:
I am a Family Doctor and I want to keep a promise made to a patient.
Julie was a healthy, post-menopausal woman in my care who came in for a periodic health examination. One of my routine questions, in what is called the "Review of Systems", was to ask if she had experienced any vaginal bleeding.
She said "No" but then laughed and added, "Other than when my period came back for a few months last year".
All health care professionals are taught early on that 'vaginal bleeding in a post-menopausal woman is Cancer of the Uterus until proven otherwise'. This comment by Julie was, therefore, a red flag (no pun intended) prompting further questions, an examination and an ultrasound of her pelvis.
Julie was surprised to see me so concerned, especially since the symptoms had not recurred over many months.
Sure enough, a pelvic ultrasound and tissue sampling confirmed Cancer of the Uterus.
Julie underwent a hysterectomy and radiation therapy. She is now healthy, cancer-free and is expected to stay that way.
After all this was done, Julie sat ME down for a talk. She told me she'd had no idea a 'short return' of her period after menopause was a danger signal. Furthermore, she addressed the topic with friends over coffee and discovered that, out of 20 women, NONE of them knew this symptom was abnormal! She admonished me to "Tell women this! Don't assume we know it!"
From that day on, I have kept Julie's advice in mind when talking with post-menopausal patients. But recently my wife suggested that I should take this to a wider audience.
So, Julie, this is for you:
If you are a post-menopausal woman and your period 'comes back' or you have even one episode of vaginal bleeding, TELL A HEALTH CARE PROFESSIONAL and insist on having it investigated!
Wishing you all good health and long lives.
— Sheila Toll on Facebook, posted September 2nd of an unknown year.
End Transcription.
I think this may also apply to people whose periods stopped earlier on, pre-menopause. So yeah, if the bleeding stops for years or something, but then 'comes back', you gotta check that out.
Be safe out here.
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