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Lupus - Selena Gomez | Dr Ezgi Ozcan 

Dr Ezgi Ozcan
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#selenagomez #doctorexplains
Welcome back to my new series - Celebrities and the medical conditions you didn't know they had. Today's topic is Selena Gomez and Lupus (SLE)
Timestamps ⏱
00:38 What medical condition does Selena Gomez have?
01:10 The medicine behind it
02:10 Which organs does lupus effect
03:26 Selena gomez & renal transplant
04:02 Why is her hand shaking in her TikTok video?
05:20 Lupus and psychiatric issues
05:30 Selena and psychosis
06:00 How do we diagnose lupus
Last week video:
Gigi Hadid & Hashimoto: • Hashimoto's Disease - ...
Other educational videos:
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Email correspondence: e.ozcan90@gmail.com
Get to know me:
👩🏻‍⚕️ I am a junior doctor working in a North London Practice
🏫 I completed medical school at UCL following my degree in Biomedical Science
👧🏻 I went into GP training following the completion of my foundation years (FY1 & FY2) in London
🕗 I took time out of working as a doctor between 2020-2021 whilst on maternity leave with my daughter Ella
🇬🇧 I am UK born but Turkish by background 🇹🇷
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** Disclaimer **
The information in this video is not intended nor implied to be a substitute for professional medical advice, diagnosis or treatment. All content, including text, graphics, images, and information, contained in this video is for general information purposes only and does not replace a consultation with your own doctor/health professional

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4 мар 2023

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Комментарии : 5   
@steffiu5654
@steffiu5654 Год назад
Thank you for doing this! Maybe you could do a video on MS sometime. I have MS myself and seeing people like Selma Blair and Christina Applegate publicly address their illness has been incredibly inspiring. Selma's documentary is so powerful!
@DrEzgiOzcan
@DrEzgiOzcan Год назад
Of course I can. Thank you so much for watching my video 😊 I hope you’re coping okay with your MS. Its really encouraging when high profile people talk openly about their medical conditions - I hope it’s made you feel less alone with everything you’re going through
@justacrystal567
@justacrystal567 9 месяцев назад
Thank you so much for doing this video. I was diagnosed in 2013. At that time, all they knew about it was about a butterfly rash, and from house M. D., It’s never lupus. I am very very lucky though. My disease was caught with her in a couple of months and it responded very well to Hydroxy chloroquine. The pandemic was very scary for me though. Not only was I concerned about what would happen if I caught it, I was also concerned hearing from other lupus patients that they have been told they could not fill their medication because some people were using it to try and treat Covid. I am a first responder and as such, still on the streets during lockdown and having many interactions with the public. It really frightened me that I could potentially not have my medication to keep my lupus under control and potentially interacting with so done who had Covid. Fortunately, it never happened.
@DrEzgiOzcan
@DrEzgiOzcan 9 месяцев назад
Thank you for watching :) I can imagine how difficult the pandemic must of been, there were so many unknowns and so much misinformation. I'm glad you were safe through it all.
@serdaltatar7629
@serdaltatar7629 Год назад
😮
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