Excellent information. I am a male, 65 and have SLE. My current rheumatologist and others I have tried, never take the time to explain anything. They just push drugs without explanation. I give up on their so called help. I quit all meds and only go in once a year for the regimen of blood work. Once again the doctor never comments on the results. Doctors....to hell with them!
I have to give it to you: You taught that lesson. I do telephonic nursing for SLE. I wish all my different trainings had been put in a concise but complete nutshell like you did. Amazing
I can't believe you just gave me more information than my rheumatologist and all the medical doctor videos I have watched! I'm so grateful for you taking your time to make this video. Thank you!
Thank you for such an informative video! I was diagnosed in 1985, at that time I was told average lifespan after diagnosis was 10 years. I am now 72 still dealing with this extremely frustrating unpredictable illness.
This was such a informative video, she did such an amazing job explaining Lupus so anyone can understand it. They definitely need her to do more videos, because most of them leave you more confused than when you started. Thank you for all the great information, I was diagnosed with lupus 4/14/22. So I’m trying to learn all I can.
I am wondering if I have lupus, but because I have Hashimoto's disease, my symptoms overlap. I had a distinct butterfly rash for a long time which I didn't know what it was so went to the doctor. He did the ANA test (or whatever it is called) and other tests, and he said, just because I had a negative ANA test, doesn't mean I don't have lupus. Fasttrack to a couple years later and I have new symptoms now. I have issues with my red blood cells count a lot, despite eating a healthy diet which includes red meat for iron. I now have Raynaud's. I have weird rashes that pop up on my body which I have never had. Etc. It just makes me wonder. I worked for a doctor (I supported her father as a home care worker) and she was telling me I probably have lupus that will come forward in the future. She told me usually people with one autoimmune disease will also get a secondary autoimmune disease, so it really makes me wonder about Lupus. I guess I will continue living with all these symptoms until one day I get more answers.
I keep fighting my GP, My hair is falling out, my joint are deteriorating , and had 2 surgeries this year, but getting worse, I have the rash on my face, my hair is falling out, I keep having thrush, I am exhausted, my gums are bleeding and teeth are breaking, I hurt so bad in every joint. I have shown macro anemia for 5 years, Fever for 5 months, brain fog so bad I forget my dr appointment, congestion in my lungs for months, and alot of chest pain ! I think I need a new gp. My ortho dr believes I have a CSF leak, I am testing positive for glucose from my nasal secretion for 6 month! I cant move from pain, I dont want pain meds nor have asked for them, I just want a dr to diagnose me! Its so aggravating!
Is understandable that your rheumatologist don't give al the details of lupus, is more patients waiting for their time, I'm a 65 year's mail, I have 10 years suffering with lupus, us you must know is more severe in males, thanks to my medical team I'm managing, As a provider's, males ad the most elevated deprecion and suicidal thoughts, not being able to soporte your family is terrible, No one had talked about that because the concentration is more in women's than man, Please be patient you doctors are in your side, it may not have the time to explain so detailed like we see it in this video, but your doctor is doing the best for you, Refer to your rheumatologists to prescribe you Benlysta, is working great with me, it stop the increased damage to my keadny's, also the damage to my heart, Thanks for making this video you not only illuminated my soul, also helps to make family and friends to understand that we may looks healthy but no one no the suffering a lupus patients passing day by day🙏
Great presentation! No one has ever explained to me HOW this attack is happening, and what each test looks for and why. Thank you so much, great eye opener!! Oh and I love the little faces on the diagram of the invader cells LOL so cute and helpful!
Thanks your explanation about Lupus very helpful.I know about this diseases but this is the first I understand what's lupus? I wanna ask you about sweating while you work out if sweating was very big amount is it sign that our body have water retention?
Hi Sara Thanx for Very informative and interesting video. My wife is also a lupus patient, she is 29 years old and has been fighting this disease for the past 9 years. I am from Pakistan and I want to know if there is any proper medicine for this disease which can eliminate this disease completely.
I suffer from SLE effecting my liver and kidneys..my kidneys has too much protein in my urine and chronic arthritis pain...what causes too much protein..and I also have autoimmune hepatitis in my DNA
Ayeeeeee I'm super early! How have you been? You helped me so much! I love nursing as a career I've been with you at the start at your channel so it's amazing you have a million followers 🙌
My sister is suffering from SLE and mysthenia gravice from last 2 months. She is now bed ridden please help to understand how much time she will take to get better?
my name is Michael Do you happen to know anything about osteogenesis Imperfecta I got it as I aged I didn't break much bones as a child but when I got older thats when I started fracturing a lot of bones luckily not a leg or arm yet I am 29 years old was told from a recent dexa scan I have Z score of -3.8 which means I also have osteoporosis and osteopenia I have been experiencing a lot of chest pain that goes into my back I am in constant pain I am taking forteo but i don't notice a change in the strength of the bones because I recently injured my spine again. Do you know if ppl with osteogenesis imperfecta live a long time I am actually walking with a cane because it hurts to walk I feel weak and it hurts to breath I have to sleep with two pillows because I can't lay flat I also have trouble swallowing I have the blue sclera
Hey, everyone! Thanks for watching this systemic lupus erythematosus (SLE) review. Don't forget:
Quiz: www.registerednursern.com/systemic-lupus-erythematosus-nursing-nclex-questions-quiz/
Notes: www.registerednursern.com/systemic-lupus-erythematosus/
*Pharm Series*: ruclips.net/p/PLQrdx7rRsKfWpel1Ymwd9IQe0noyzAjeS
*NCLEX Reviews*: ruclips.net/video/nyBV18sHNSg/видео.html
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Oh yeah, how's your baby doing? 👶 🤩😍
legitimate question, mycrophenalate (cellcept) have they used this to combat lupus?
@@iwantmyfriescrispynotburnt3981 that baby is so cute! is the man that does these videos the father?
@@iwantmyfriescrispynotburnt3981 that kid is so cute.
Could you make a video on ADHD?
I am suffering from SLE...since 2013...m on medicatiin..... from this video i learn more deeply.. about my condition..so thnkew so much.... 🙏
God bless you ❤️❤️
how r u
Excellent information. I am a male, 65 and have SLE. My current rheumatologist and others I have tried, never take the time to explain anything. They just push drugs without explanation. I give up on their so called help. I quit all meds and only go in once a year for the regimen of blood work. Once again the doctor never comments on the results. Doctors....to hell with them!
I have to give it to you: You taught that lesson. I do telephonic nursing for SLE. I wish all my different trainings had been put in a concise but complete nutshell like you did. Amazing
I can't believe you just gave me more information than my rheumatologist and all the medical doctor videos I have watched! I'm so grateful for you taking your time to make this video. Thank you!
Seriously though. This video is amazing
Thank you for such an informative video! I was diagnosed in 1985, at that time I was told average lifespan after diagnosis was 10 years. I am now 72 still dealing with this extremely frustrating unpredictable illness.
Thank you! I have had sle since I was 15 and I’m 20 now going into nursing school next year
This was such a informative video, she did such an amazing job explaining Lupus so anyone can understand it. They definitely need her to do more videos, because most of them leave you more confused than when you started. Thank you for all the great information, I was diagnosed with lupus 4/14/22. So I’m trying to learn all I can.
Two days in the ER, extreme hives rash day1 and swelling of the lips and face day 2.
I am wondering if I have lupus, but because I have Hashimoto's disease, my symptoms overlap. I had a distinct butterfly rash for a long time which I didn't know what it was so went to the doctor. He did the ANA test (or whatever it is called) and other tests, and he said, just because I had a negative ANA test, doesn't mean I don't have lupus. Fasttrack to a couple years later and I have new symptoms now. I have issues with my red blood cells count a lot, despite eating a healthy diet which includes red meat for iron. I now have Raynaud's. I have weird rashes that pop up on my body which I have never had. Etc. It just makes me wonder. I worked for a doctor (I supported her father as a home care worker) and she was telling me I probably have lupus that will come forward in the future. She told me usually people with one autoimmune disease will also get a secondary autoimmune disease, so it really makes me wonder about Lupus. I guess I will continue living with all these symptoms until one day I get more answers.
Get a new doctor. My doctors SUCK
You described this perfectly, I’m newly diagnosed and wanted to understand it better, thank you so much.
Hi Sara,thank u for the amazing vids you put in here.I just passed my NCLEX.Thank you very much
I keep fighting my GP, My hair is falling out, my joint are deteriorating , and had 2 surgeries this year, but getting worse, I have the rash on my face, my hair is falling out, I keep having thrush, I am exhausted, my gums are bleeding and teeth are breaking, I hurt so bad in every joint. I have shown macro anemia for 5 years, Fever for 5 months, brain fog so bad I forget my dr appointment, congestion in my lungs for months, and alot of chest pain ! I think I need a new gp. My ortho dr believes I have a CSF leak, I am testing positive for glucose from my nasal secretion for 6 month! I cant move from pain, I dont want pain meds nor have asked for them, I just want a dr to diagnose me! Its so aggravating!
You are the best teacher I ever had ❤️... Thanks a lot ❤️
This is amazing and right on time. We are about to have an exam tomorrow, 10/02/202. Prayers are gladly appreciated.
🙏🏼
Great explanation..Just diagnosed..Autoimmune ailments are no joke..The medications are serious too..Depleting your B cells
Nurse Sarah you helped me pass nclex. Thank you
Is understandable that your rheumatologist don't give al the details of lupus, is more patients waiting for their time, I'm a 65 year's mail, I have 10 years suffering with lupus, us you must know is more severe in males, thanks to my medical team I'm managing,
As a provider's, males ad the most elevated deprecion and suicidal thoughts, not being able to soporte your family is terrible,
No one had talked about that because the concentration is more in women's than man,
Please be patient you doctors are in your side, it may not have the time to explain so detailed like we see it in this video, but your doctor is doing the best for you,
Refer to your rheumatologists to prescribe you Benlysta, is working great with me, it stop the increased damage to my keadny's, also the damage to my heart,
Thanks for making this video you not only illuminated my soul, also helps to make family and friends to understand that we may looks healthy but no one no the suffering a lupus patients passing day by day🙏
Nurse Sarah you are my go to youtube channel when it comes to learning pathophysiology for my oral revalida!
Thank you, i've been waiting for Lupus to be covered by you. I'm a survivor of SLE.
Very good explanation even for non-nurses. Huge thanks.
I will be reporting about SLE today and this is really helpful!!
Thank you I have two sisters with lupus.
You gave me more information than my text book! Thank you Sarah!
Wooooooooow, I miss these videos....a nurse from Iraq
California!
love you Sarah!
@Ali94 If I understand you correctly, you're basically saying sincerely a nurse from Iraq👍. Clearly you're not saying Sarah is from Iraq😳
I am so thankful that you made this video! It was just in time for my Lupus lecture last week. You are amazing!
Wow! This explains a lot, more then my Doctor ever did. Thank you.
Excellent training!! You are a gift to the profession and to the patients.
Can you do videos on safety? Like standard precautions and restraints
Great presentation! No one has ever explained to me HOW this attack is happening, and what each test looks for and why. Thank you so much, great eye opener!! Oh and I love the little faces on the diagram of the invader cells LOL so cute and helpful!
A great video...much more helpful than lots of hours in auditors...
The diary method is good for all kinds of health problems. 👍👍
Thank you for presenting the information in an easy to understand format! Great job!
I improve my nursing and my English skills in ur videos 😊😊😊😊😊😊😊😊❤
Thanks your explanation about Lupus very helpful.I know about this diseases but this is the first I understand what's lupus?
I wanna ask you about sweating while you work out if sweating was very big amount is it sign that our body have water retention?
Hi Sara
Thanx for Very informative and interesting video.
My wife is also a lupus patient, she is 29 years old and has been fighting this disease for the past 9 years. I am from Pakistan and I want to know if there is any proper medicine for this disease which can eliminate this disease completely.
Thank you so much, you’re much more better than my teacher😂 so easy to understand ❤
Over my life I have experience all of these symptoms. Lupus sucks! My daughter has it too.
You are amazing girl! Please make more free videoa for premed and med students❤ Thank you so much🙏🥰
You are a great teacher.
I suffer from SLE effecting my liver and kidneys..my kidneys has too much protein in my urine and chronic arthritis pain...what causes too much protein..and I also have autoimmune hepatitis in my DNA
Ayeeeeee I'm super early!
How have you been? You helped me so much! I love nursing as a career I've been with you at the start at your channel so it's amazing you have a million followers 🙌
Thank you!. You are smart and more knowledgeable that my doctor. You look like Kate Del Castillo.
First to comment...longtime follower and subscriber. Thanks RN Sarah for reminding us nursing knowledge!!!!
Good programme
Thanks you for amazing video 🇮🇳
The quizzes are very helpful ❤️
Thank you this was a great presentation
Definitely has similar symptoms to Photo dermatitis.
Thank you Sarah, you’re amazing 👍❤️
Thank you very much sister .l am from Pakistan .God bless you.
Thank you a lot! This video has helped and informed me a lot! I'm for ever great full❤
Mine all of them. I also have Cvid primary immunodeficiency. Yay me.
Love from India 🇮🇳 ♥ ❤ 💕 💗 💖 🇮🇳 ♥ ❤ 💕 💗 💖 🇮🇳 ♥ ❤ 💕
My sister is suffering from SLE and mysthenia gravice from last 2 months. She is now bed ridden please help to understand how much time she will take to get better?
God bless you
Thank you so much for this video. Medsurg is killing me
It's very hard
AlhamduliAllah,
Thank you so much ❤️💛🧡
just got diagnosed 65 Female
Here is someone from Egypt ?❤
Can u do lupus nephritis?
Thank you!
❤️ Very informative.ThankYou
You love purple like me :)👚 Thank you for this amazing video❤🙏
thank you so much
Love your hair
You are great 👏👏❤
I love this ♥️
Thank you so much 😻💘
my name is Michael Do you happen to know anything about osteogenesis Imperfecta I got it as I aged I didn't break much bones as a child but when I got older thats when I started fracturing a lot of bones luckily not a leg or arm yet I am 29 years old was told from a recent dexa scan I have Z score of -3.8 which means I also have osteoporosis and osteopenia I have been experiencing a lot of chest pain that goes into my back I am in constant pain I am taking forteo but i don't notice a change in the strength of the bones because I recently injured my spine again. Do you know if ppl with osteogenesis imperfecta live a long time I am actually walking with a cane because it hurts to walk I feel weak and it hurts to breath I have to sleep with two pillows because I can't lay flat I also have trouble swallowing I have the blue sclera
Sounds like Ehlers Danlos Syndrome to me. Especially with the blue schlera
Good
❤️
I suddenly had brain attack and blockge I'm in brain and diagnosed as SLE.
👏🏿
😍
🙏💖
Hii
Thank you!