PNH: When blood machinery goes wrong 

No that only thatsunlucky

immune system: sees a cell without a name tag also immune system: ALARM ALARM ALARM

so immune cells to blood cells without tag is like a teacher in kindergarden if you dont wear your tag.

Blood cell: forgets to put on name tag Immune system: THERE IS A RED SPY IN THE BASE

@@sinkrada419 WE NEED TO PROTECT THE BRIEFCASE!

I wish you luck, I'll be praying for you.

You”ll be fine soon .

what did you expect from cells that cannot see/hear/speak in common manner? only chemicals, only hardcore

Immune System when a minor issue happens in your body: "you know when a kid screams? yea that"

Can you please share if you have followed any diet, medication. Also, were you following any treatment? What were your symptoms? Thank you

​@@leilaali7896 I was diagnosed with PNH back in 2004 with an 80% clone size when I was thirteen, back then the only treatment to "cure" PNH was a bone marrow transplant. However, the benefits did not outweigh the risks. the only medication I was put on was iron tablets, warfarin and folic acid. Before my diagnosis I was very active and fit, I played football, went running and trained in martial arts (Judo.) I had to stop after my diagnosis due to being put onto warfarin, contact sports were a risk. I did however, continue to run and started weight training (only light not extreme again due to warfarin.) My diet was manly white meat with the recommend daily intake of fruit/veg. I very rarely ate red meat. My symptoms considering I had 80% abnormality were mild. At times I could feel quite lethargic even with plenty of sleep, this was mostly after being unwell i.e common cold flu etc. Recovery from a cold/flu took longer than most people two three weeks. The main symptom that led to a PNH diagnosis was after a bout of very dark urine (deep brown.) caused by haemolysis. Even with the destruction of red blood cells I did not need to have blood transfusions. I was already being seen by a haematology specialist due to low red blood platelets however, I was about to be discharged from their care due to this returning to normal levels when the PNH symptom occurred. The main treatment for symptomatic PNH is eculizumab (Soliris) with also ravulizumab becoming available on the NHS. The cost on average for both is still exceedingly high so I do not know if it is covered by insurance. luckily I am in the UK so both are covered by the NHS.

I also need this info 😭

How , can you tell please.

Kurzgesagt is kinda like this way,i really recommend kurzgesagt channel!

That's cells

@@drilldoggoboi5618 That's bacterial

A green boi

You cannot inherit PNH. It is an acquired genetic disorder.

@@revan012 thanks!

I was diagnosed two months ago. Which treatment do you follow? How is your general situation? Thanks

My father was diagnosed with this in 2014 he is still doing good with some homeopathic medications but needs blood transfusion once a year