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Autoimmune Hemolytic Anemia | Rare Disease
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810 Views • Feb 26, 2023 • Click to toggle off description
February is Rare Disease Month. It only makes sense that I raise some awareness for hemolytic anemia, a rare type of anemia.

Hemolytic anemia is a sub-type of anemia where the low red blood cell count is caused by the destruction — rather than the underproduction of red blood cells.

Do you have hemolytic anemia?

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[Video Description: A video of Samantha speaking to the camera. Samantha is wearing a blue t-shirt with a crescent moon on it and her hair is tied back.]

#HemolyticAnemia #ChronicIllness #Lupus #LupusAwareness #ChronicIllnessAdvocate #AIHA
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Views : 810
Genre: People & Blogs
Uploaded At Feb 26, 2023 ^^


warning: returnyoutubedislikes may not be accurate, this is just an estiment ehe :3
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User score: 100.00- Masterpiece Video

RYD date created : 2023-04-25T13:02:08.288549Z
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YouTube Comments - 14 Comments

Top Comments of this video!! :3

@chaelxi6823

1 year ago

Thank you so much for sharing , I'm 19 y'o and i was diagnosed with AIHA , SLE last year when I was 18 y'o and i liked it that I'm rare

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@Cycling-n-Stuff

9 months ago

I've had this blood disorder for many many years and it was detected many many years ago but never disclosed to me until recently so I have been living with a extremely deadly blood disorder that nearly cost me my life once and required emergency life-saving surgery

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@banglamarvel4649

8 months ago

I was diagnosed with GBS in 2022 February which led me to be fully body Paralyzed. It was one of the most horrific events in my life.I can still remember i had to pee and do poop on my bed. I even dropped my college for 2 years for this disease. Even some of my relatives thought i might not live.Btw doctors are told me My GBS caused by the over dose of prednisolone .

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@SillyCheeseGrater

11 months ago

BRO THE FACT I WAS BORN IN FEBRUARY AND I HAD THAT DISEASE MAKES THIS SHOCKING.

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@citizen9021

8 months ago

I am 18 and recently got diagnosed with AIHA .... i am on medications which are mostly steroidal ..I am rare 😃😃😃...Lots of love from India

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@ladyJustis

1 year ago

Hi! I Was just diagnosed with this and waiting on more test. Hope you and all are feeling good 💜

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@rosac2833

1 year ago

I'm 68 and at this point of my life the rheumatologist have been telling " I don't know what to do with you"

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@Informativeboys

4 months ago

My mother is suffering from AIHA from past 2 years. She is under treatment @ appolo hospital kolkata under hematoalogist Dr Soumya Bhattacjarya. She was on steroid for around 1 year but it did not work , so now 4 rituximab injection is advised and 1 is already given but now found infection in her body after this. Is there a permanent treatment for this AIHA other than suppressing immune system.

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@simoneb3070

1 month ago

Hi! I too have Hemolytic Anemia. I’ve had it for about the past 9years. I was told that it could disappear just as quickly as it came. Has anyone had a full recovery?

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@PallaviKumari-qj6yi

10 months ago

I too have this rare disease

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@catl3885

1 year ago

hey I've been watching you for awhile. I have SLE (diagnosed 2005 at 19 yrs old). I also have raynauds, anti-phospholipid syndrome, kidney and skin involvement. I have been anemic forever. how do you get tested for this? what are signs of this?

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