Jemima M.D

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Jemima M.D

Jemima M.D

@_JemimaB

Mastering Unagi #TeamGP

Central Perk Katılım Aralık 2011
1.2K Takip Edilen1.7K Takipçiler
Jemima M.D retweetledi
Chivalry 💫
Chivalry 💫@UncleFemi_·
All of you are saying “I might skip this year” to Harrods advent calendar are the first to order when it comes out next month. I know your tricks 😂🫵
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Smellgood Queen
Smellgood Queen@mowaGLINT·
I hope you are readyyyyyy! 🙊
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Moboluwaduro okan-mi-bale
Got my first birthday gift of the day from the amazing crew aboard @KLM 692. It was so unexpected but it has made me feel so valued. Thank you @KLM
Moboluwaduro okan-mi-bale tweet media
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Dr Dean
Dr Dean@DeanEggitt·
I start work as a GP at 7:30am. My first appointment is 8:30. In that first hour, I am working on tasks, prescriptions, letters and test results. Some of these are urgent - meaning I can start my first appointment late form time to time. There's a reason for everything.
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mel
mel@MEHholdings·
@loneliest_star I’m gonna need every billionaire to assign themselves one poorly understood medical condition affecting primarily women please
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ella 🕸
ella 🕸@loneliest_star·
okay he can be crazy in peace forever if he keeps this up
Bryan Johnson@bryan_johnson

🚨Kate officially diagnosed with endometriosis > done without surgery > across three modalities: imaging, blood, and AI > all non-invasive > in 42 days For context, average time to diagnosis is 6.6 years. And, we found 2 other diagnoses at the same time. Over the past 6 weeks, we’ve sprinted to confirm or deny Kate’s suspected endometriosis. Endo is notoriously challenging to diagnose. It’s one of the most gnarly diseases and affects 15% of women. Men, to get you on the same page, having endo is akin to an alien growing in your guts and balls, self replicating, and glueing everything together. Causing you constant pain and discomfort. We got to work. > got an MRI > got a transvaginal ultrasound > both results came back negative At this point, Kate’s patient journey had followed the archetype precisely. Most women don’t get diagnosed for 7-10 years. For Kate, it’s been 7 years. And, like most women, her imaging came back clear even though now we know that she has endo. This is why diagnosis has traditionally happened via surgery. There has been no other way than to open her up and look inside. We wanted to avoid surgery so we went back to the drawing board. We searched the world over. On our second go, we did: > endo-specific ultrasound > an endo blood test > AI MRI > saliva test This was successful. We were able to confirm her endo via ultrasound, blood test, and MRI. Confirmed simultaneously by three unique modalities, as far as we know, a world-first approach. The extensive measurement allowed us to find additional things. Her ultrasound showed: > endometriosis > PMOS (formerly PCOS) (needs confirmation) > adenomyosis 30-40% of women have at least one of these conditions. That’s intimidating especially when the path to diagnosis is fraught with so many challenges. Phase I was getting a diagnosis. Phase II is curing endometriosis. We’ve already started working. If you’re a female with suspected endo, here’s what you can do to accelerate your diagnosis. — 1. Endo-Specific Ultrasound You want an endo-specific ultrasound. As we saw with Kate, a standard pelvic/transvaginal ultrasound failed to identify her endo. You want the ultrasound to be performed by a physician or sonographer specifically trained. They follow a special protocol to hunt for endometriosis by mapping the ovaries and uterus, and testing whether organs can slide freely, or are tethered by endometriosis lesions. It’s best timed just after ovulation, when a small amount of peritoneal fluid aids visualization. It can detect superficial endometriosis, lesions, and adenomyosis that general imaging misses. We went to Dr. Kacey Hamilton at Cedar Sinai. 2. AI MRI / MatricesAI Radiologists miss lesions in up to 60% of cases. We worked with @MatricesAI which leverages AI and a unique dataset to detect endometriosis lesions on pelvic MRI. This model is still new, its first pilot study with 200 participants began in April this year. Here is how you can work with them: They’re opening their diagnosis program at the Geneviève Institute to give early access to their AI model in a clinical trial. They will take you through a state-of-the-art clinical intake questionnaire. Help you advocate for your symptoms with your gynecologist, based on your intake or connect you to a new center where their AI is being piloted and the clinical trial conducted. 3. Blood test / HerResolve Kate had two small tubes of blood drawn for a test built by @Heranovalifesci. The test measures seven biological markers (three microRNAs, three proteins, and one hormone) and uses an AI model to help detect endo. It was highly accurate in its validation study at confirming endo and caught most cases that ultrasound and MRI had missed. Their technology has been validated in a peer reviewed study (298 women, 11 sites across US/Europe/Hong Kong, published in the Journal of Minimally Invasive Gynecology): specificity 97.5%, sensitivity 80%, with strong diagnostic performance (94.4%), demonstrating it was highly effective at distinguishing women with endometriosis from those without the disease. A positive result is a strong signal, since only 2.5% of women without endometriosis test positive, though final confirmation is still clinical. A negative is less conclusive, because the test misses about 20% of true cases. The test identified 61.5% of histologically confirmed cases that transvaginal ultrasound and/or MRI missed. # We did one more saliva based test and will report back on that when results are returned.

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Jemima M.D retweetledi
Olúwatósìn Olaseinde
Olúwatósìn Olaseinde@tosinolaseinde·
WOWWWWW
Bryan Johnson@bryan_johnson

🚨Kate officially diagnosed with endometriosis > done without surgery > across three modalities: imaging, blood, and AI > all non-invasive > in 42 days For context, average time to diagnosis is 6.6 years. And, we found 2 other diagnoses at the same time. Over the past 6 weeks, we’ve sprinted to confirm or deny Kate’s suspected endometriosis. Endo is notoriously challenging to diagnose. It’s one of the most gnarly diseases and affects 15% of women. Men, to get you on the same page, having endo is akin to an alien growing in your guts and balls, self replicating, and glueing everything together. Causing you constant pain and discomfort. We got to work. > got an MRI > got a transvaginal ultrasound > both results came back negative At this point, Kate’s patient journey had followed the archetype precisely. Most women don’t get diagnosed for 7-10 years. For Kate, it’s been 7 years. And, like most women, her imaging came back clear even though now we know that she has endo. This is why diagnosis has traditionally happened via surgery. There has been no other way than to open her up and look inside. We wanted to avoid surgery so we went back to the drawing board. We searched the world over. On our second go, we did: > endo-specific ultrasound > an endo blood test > AI MRI > saliva test This was successful. We were able to confirm her endo via ultrasound, blood test, and MRI. Confirmed simultaneously by three unique modalities, as far as we know, a world-first approach. The extensive measurement allowed us to find additional things. Her ultrasound showed: > endometriosis > PMOS (formerly PCOS) (needs confirmation) > adenomyosis 30-40% of women have at least one of these conditions. That’s intimidating especially when the path to diagnosis is fraught with so many challenges. Phase I was getting a diagnosis. Phase II is curing endometriosis. We’ve already started working. If you’re a female with suspected endo, here’s what you can do to accelerate your diagnosis. — 1. Endo-Specific Ultrasound You want an endo-specific ultrasound. As we saw with Kate, a standard pelvic/transvaginal ultrasound failed to identify her endo. You want the ultrasound to be performed by a physician or sonographer specifically trained. They follow a special protocol to hunt for endometriosis by mapping the ovaries and uterus, and testing whether organs can slide freely, or are tethered by endometriosis lesions. It’s best timed just after ovulation, when a small amount of peritoneal fluid aids visualization. It can detect superficial endometriosis, lesions, and adenomyosis that general imaging misses. We went to Dr. Kacey Hamilton at Cedar Sinai. 2. AI MRI / MatricesAI Radiologists miss lesions in up to 60% of cases. We worked with @MatricesAI which leverages AI and a unique dataset to detect endometriosis lesions on pelvic MRI. This model is still new, its first pilot study with 200 participants began in April this year. Here is how you can work with them: They’re opening their diagnosis program at the Geneviève Institute to give early access to their AI model in a clinical trial. They will take you through a state-of-the-art clinical intake questionnaire. Help you advocate for your symptoms with your gynecologist, based on your intake or connect you to a new center where their AI is being piloted and the clinical trial conducted. 3. Blood test / HerResolve Kate had two small tubes of blood drawn for a test built by @Heranovalifesci. The test measures seven biological markers (three microRNAs, three proteins, and one hormone) and uses an AI model to help detect endo. It was highly accurate in its validation study at confirming endo and caught most cases that ultrasound and MRI had missed. Their technology has been validated in a peer reviewed study (298 women, 11 sites across US/Europe/Hong Kong, published in the Journal of Minimally Invasive Gynecology): specificity 97.5%, sensitivity 80%, with strong diagnostic performance (94.4%), demonstrating it was highly effective at distinguishing women with endometriosis from those without the disease. A positive result is a strong signal, since only 2.5% of women without endometriosis test positive, though final confirmation is still clinical. A negative is less conclusive, because the test misses about 20% of true cases. The test identified 61.5% of histologically confirmed cases that transvaginal ultrasound and/or MRI missed. # We did one more saliva based test and will report back on that when results are returned.

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Bryan Johnson
Bryan Johnson@bryan_johnson·
Men, to get you on the same page, having endo is akin to an alien growing in your guts and balls, self replicating, and glueing everything together. Causing you constant pain and discomfort.
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Sai Ishaya
Sai Ishaya@Sai_Ishaya_·
Today Lord, I lay my hands on this account. You said in John 14: 14 that if we ask anything in Your name, You will do it. You are the Author & the Finisher, the One who knows the end from the beginning. You are Jagun Jagun Ode Orun! Father, You said in Matthew 18: 18 that whatever we bind on earth will be bound in heaven, & in Luke 10: 19, You gave us authority to trample on serpents and scorpions and to overcome all the power of the enemy. So, Lord, I stand on this authority to CAST and BIND this demonic spirit of monetisation that has possessed this account! I rebuke every spirit of engagement-farming! I say GO! I say LEAVE! Return to the abyss and never look back! This account will not act possessed again! It shall be a vessel of honour. He will start anew, spirit-filled and sane. Cabash... Rakata... Makososa... Lebo-lebo-lebo...! Thank you, Father. In Jesus' mighty name we have prayed. Amen!
Friendly Neighborhood Nurse@friendlynurse22

A trauma patient needs blood urgently. The only available donor is HIV-positive. Do you transfuse?

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DEDE!
DEDE!@minutesimal_·
This baby never sabi wetin she Dan enter
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Sleepwalker
Sleepwalker@Amatey_·
Dermatology, na only them know wetin them dey do oh
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Sleepwalker
Sleepwalker@Amatey_·
@goodgirltolani I saw the same rash 3 times today, they told me 3 different diagnoses
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Sai Ishaya
Sai Ishaya@Sai_Ishaya_·
Is he a Consultant Nephrologist? If he is, then let me start writing my paper 😅 My position about this has evolved. I see nothing but upsides to the move. It can be seen as temporary step down, & in 3 years, you get to be earning upwards of $250-300k yearly, minus other avenues to top up. He will always be a Professor, and that can't be taken away from him; he can utilise that even in the US & internationally. He gets access to a better healthcare system at a time in his life when he needs it most. He has spent donkey years seeing many of his colleagues resort to online GoFundMe campaigns to afford their treatments, even after donkey years in the Nigerian civil service. It is no different (dare I say, even better in the long run, as higher earnings and an actual CCT) than many consultants from Nigeria who come to the UK to do ST3+ jobs as a pathway to getting on in the UK. You get to use it to deepen already established connections in Nigeria (who says you can't do both? Work in Nigeria, run a private practice, etc). You get a new challenge to keep you going in your middle age. All of this compared to the only "downside" of one of your students being shocked about it on Twitter.
Sai Ishaya tweet media
Timmy turner™🐐@itz_Alaybee

News of the day in 3 pictures God abegg😂😂😂

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Olanipekun Olamide Omonovha
Only by His grace and mercies. I desired it and He did it.
Olanipekun Olamide Omonovha tweet media
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Sandalilli²
Sandalilli²@MotoyosiAwosusi·
The hiholization of these Dove bar soaps are a joke man. Can't be dudu osun
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Sai Ishaya
Sai Ishaya@Sai_Ishaya_·
I discuss this almost every week here, and I wonder how many deaths will occur before something is done. If an ED clinician can't assess a neurodivergent child without a GP letter instructing them what to do, they shouldn't be seeing patients in the ED in the first place. There were at least 20 red flags in this case: no blood tests, no urine dip, no senior review before discharge, giving an enema for 10/10 abdominal pain, no proper history taking about fevers, etc. This isn't a "systemic error"—it's a direct result of doctor substitution in emergency paediatrics. We need to start documenting these preventable deaths and calling them what they are. My heart goes out to Ethan's parents, who will be utterly devastated by all this and may blame themselves for a very preventable death. Even the coroner's report seems to point at the GP, when a child was seen for at two levels (triage & eventual ANP review) in a Paeds ED with failures at almost every stage of his review and treatment. We must actively push to end this farce of doctor substitution and ensure that the correct pathways and systems are re-established. Only doctors should be on doctor rotas; this shouldn't be controversial. Anyone who wants to be on one should return to medical school.
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