Thank you very much but I'm not an english speaker, so could you please provide us captions or english text about the content? because captions are not available!
It’s cool & bizarre even. However it’s torment & so painful to live with. I have Porphyria. Just diagnosed at 32 despite looking for answers my entire life. Bedridden, wheelchair bound when leaving home, paralyzed organs. Burning pain. Every part of me hurts. It was bearable when I was younger compared to now. I wish doctors would go more into the deadly & extreme symptoms experience later in life if doctors misdiagnose so long. Depo provera nearly killed me & it destroyed by body & my life. The more I learn about it I do find it very fascinating. Especially the stories of royal family members with it & vampire legends. Just wish I knew sooner. Way more drs need to be aware of this. I seen over 200 before I found an answer. I’m lucky it didn’t kill me. You may be a doctor though & know way more than me. I’m just wanting others to know there’s way more to it than this. This video does help people remember key terms though in an interesting way. Thank you to the creator of the video
@@samanthaellingsworthshows7921 I was diagnosed with this condition as well after suffering with pains for 5 yrs. I'm 40 now and I can honestly say this disease has turned my life upside down. I was recently hospitalized for nearly 2 weeks for what has been the most severe attack I've experienced with this. I received my first Panhematin infusion during that hospitalization which seems to have helped with ending the acute phase. This is only my second day of not feeling that godawful burning pain that you described so I'm holding onto hope that this attack is finally over. I'm scheduled for consultation with a hematologist in Philadelphia in October and I'm hoping to get preventative treatment that could improve my quality of life. I do hope you have found treatment and people close to you that support you. I'm so sorry that you are suffering with this miserable disease but don't lose hope and you're not alone 💔
Sketchy style biochem? you have my attention
As someone with porphyria (vp) this is awesome and spot on. Thanks for making it! :)
This is so freaking awesome!
damn docs can be hot too
Oh my god this is a gem.I am from india.i have struggled my entire medical student life to remember porphyria.this was a genius way to remember
We're so happy to hear this! Thanks for watching!
Pls make more videos on biochemistry topics .. Your videos are really helpful for pg preparation.
Thank you very much but I'm not an english speaker, so could you please provide us captions or english text about the content? because captions are not available!
very nice thank youuu
amazing!!!!!!!!
Thank you!
Great job!!! I love it
thank you !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
Thanks for watching!!
Superb
love love love ur vids,, thanks alot
I tend to get confused between Acute Intermittent Porphyria and Conversion disorder
Makes absolute sense ty x
this is the only way i can remember longer because i'm visualise learner
please do more video for other disease
What is the long turn
thank u!
Best
This disease is so cool
It’s cool & bizarre even. However it’s torment & so painful to live with. I have Porphyria. Just diagnosed at 32 despite looking for answers my entire life. Bedridden, wheelchair bound when leaving home, paralyzed organs. Burning pain. Every part of me hurts. It was bearable when I was younger compared to now. I wish doctors would go more into the deadly & extreme symptoms experience later in life if doctors misdiagnose so long. Depo provera nearly killed me & it destroyed by body & my life.
The more I learn about it I do find it very fascinating. Especially the stories of royal family members with it & vampire legends.
Just wish I knew sooner. Way more drs need to be aware of this. I seen over 200 before I found an answer. I’m lucky it didn’t kill me.
You may be a doctor though & know way more than me. I’m just wanting others to know there’s way more to it than this. This video does help people remember key terms though in an interesting way.
Thank you to the creator of the video
@@samanthaellingsworthshows7921 I was diagnosed with this condition as well after suffering with pains for 5 yrs. I'm 40 now and I can honestly say this disease has turned my life upside down. I was recently hospitalized for nearly 2 weeks for what has been the most severe attack I've experienced with this. I received my first Panhematin infusion during that hospitalization which seems to have helped with ending the acute phase. This is only my second day of not feeling that godawful burning pain that you described so I'm holding onto hope that this attack is finally over. I'm scheduled for consultation with a hematologist in Philadelphia in October and I'm hoping to get preventative treatment that could improve my quality of life. I do hope you have found treatment and people close to you that support you. I'm so sorry that you are suffering with this miserable disease but don't lose hope and you're not alone 💔
Thought the Bill Murray was Bill Maher before you got to him
Sounds like a complicated condition 😕
My profile pic tells u the appreciation of this bad nemonic
Wow
Waaw
Bill Murray NEVER had that much hair.
damnnnnn girlllll
I was really liking your videos until you took God’s name in vain :/ Very disappointing...
thank you!