The Disease That Has A Thousand Symptoms

The symptoms vary from one person to another in a wide range of spectrum and change a lot over time. It also mimics many other disorders and so it's not easy to diagnose someone with one.

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CREDITS:
Director: Ramadhan Istabaq
Supervisor: Ibrahim Pyke
Researcher: Hafiz Insan
Storyboard Artist: Bima Bhirawa
Illustrator: Rizki Yurizal
Animator: Dhienno Adhar
Sfx Designer: Rafly Moravia
Subtitler: Wulan Kuswotanti

#FreeMedicalEducation #Lupus

[salemabarker]

I am a female who was diagnosed with SLE in 1998. It hasn’t been a easy journey but i am doing well. Had a kidney transplant in 2016. For all my fellow lupus warriors out there I prayed God will give you strength and endurance to keep going.

[ygjsg]

I was diagnosed with Lupus in 2019, I was doubted by everyone and I'm still being ill treated by people close to me

[EM-rmxh]

Unfortunately getting diagnosed is too expensive for many people.

[Soneca]

A friend of mine got diagnosed with Lupus and this video helped me understand a lot of his struggle. Thank you a lot

[prateekanand]

One of the most underrated channels on YouTube.

[crystalclear]

My doctors think I may have lupus but because it can be so different for everyone they are hesitant on diagnosing me, my symptoms are become debilitating I now have pots so I have a fear of fainting everytime I stand, I tested positive be for ana antibodies, I have constant swelling and aching in my feet and knees and try to take care of my 5 month old daughter while constantly being tired aaaand I just started getting vitiligo patches on my arms so I think it's about time I get that diagnoses

[thefunnerman]

Male 28, I was diagnosed with lupus when I was 12 during the 8th grade.

I flared during my sophomore year in 2010, mainly because I went out in the very hot sun.

after healing, like a dummy, I went out again this whole summer to parks, and now I am flaring up. The sun seems to be my #1 trigger.

[dakotahostermeyer]

Im 99% sure ive had lupus all or nearly all my life. I cant seem to get tested because my doctors just flat out refuse to. This is really getting annoying

[gladyoucame]

This is one of the most accurate animation about medicine ever

[suzanneladue]

Lupus and Fibromyalgia
It sucks
Stay positive
Change your diet
Pray relentlessly 💞🙏

[ThaniusKress]

I was just diagnosed today, I'm glad I found this video, helped me understand this a bit better.

[mama_keikei]

Can’t keep a job due to always being sick but can’t afford to live on disability….how do we live?

[sumitpatel]

Very nice explained. Thank you for these video

[MonkyDollqueen]

Life throws curveballs. And while there might be blockers to success, it's imperative to keep pushing with the knowledge mistakes will be made and failure is inevitable.

[thewingedpotato]

Lupus

House M.D.'s official red herring of choice!
(Suggested in every episode, only actually happened ONCE)

[culturebreath]

Binge watching lupus videos because for a while now results in lab work, suddenly lab work showing signs, and well several sets of lab work later and each have come back with more. Not confirmed diagnosis yet but... Idk how to feel or what to do.

[helenarichard]

I have petichae (point bleeding) that is getting worse, joint pain, Raynauds, rashes, weight gain, random night fevers, swelling of feet, shortness of breath, photosensitivity. I used to suffer from severe iron deficiency, leaky gut, allergies, Tietze, intolerance, fungi, scelorderma, extreme fatigue, depression, anxiety and the worst: adrenal crisis. Do I need a lupus test? My dad has skin lupus and Raynauds.

[sinjinmonsoon]

I got a bleeding disorder that's really messing with me. I pray none of you get it.

[mahirabrar]

It pains me to see this channel only has 366k subs hope yt algorithm gonna push it to everyone just like it did to me

[gabrielas]

I have lupus, sometimes is really hard…