New Treatment For Kawasaki Disease

[@neetrab]

I can't believe I'm JUST looking this up on youtube. Thank you Dr. Kawasaki for discovering this and finding a cure. I thank those that also found another new treatment for the disease. I'd like to make this disease more aware to people....especially since I'm a survivor of it.

[@liamsairplanes24]

I cant believe the parents are just smiling while they see their child suffering from Kawasaki Disease (KD)

[@shiva5749]

is there any article someone can direct me to about potential re-occuring Kawasaki's disease... in short it was recognised that I had Kawasaki's disease at the age of 7-8 weeks ( now turning 18) and it's come to my attention through family members that in total I have taken a large quantity of aspirin with the worry that it may have damaged my heart as I get chest pains which are sharp but don't last long... Does anyone know if this is a potential sign or am I over worrying? I would have contacted the professor who looked after me for all those years until dischcarge but he has since retired... Thanks

[@neetrab]

@1enzeder - This is video comforts me. This is VERY interesting because I am a survivor of this disease. I had it when I was 12 (I'm 32 now). My brother had it when he was 2 (He's 34 now). We both have led normal lives. I am almost shocked to hear someone else had a sister/brother that had it like in my family. I'm wondering if that only happens in Afro-American families because that is my ethnicity just like those in this video. I wish I could talk to that family.

[@zachkemp6535]

Hey how is you and your brother doing nowadays? I had this when i was 6 now 25

[@calystavelvet5526]

It’s East Asian origin, the guy who found it named it Kawasaki after himself because he noticed it in Asian children. You can get it in other cultures but East Asian and Arab are more prevalent. I also have the gene variant for it despite being white but the gene whats never been activated.

[@LoonieMommy]

@jessiefajardo I just read today on another post that it is possible for it to come back. The best thing to do is to go to the doctor and have her checked out. This is the post where I saw it. It did not reoccur in my son but I get him checked out ever time I suspect anything. God bless you and I will pray for you and your daughter!!!! Posted video where I hear about it reoccurring will be posted for you above. Hope it helps.

[@1enzeder]

@jessiefajardo My Son was diagnosed with complete certainty about 9 years ago, exhibiting every known symptom in typical order. As you can see from my videos, he is in perfect health, just short of his 12th birthday. So much so, that we began receiving letters from our doctors asking if we had changed family doctors. As he entered the fever stage, we began feeding him organic carrot juice... he was completely rid of the disease in 12 hours. I am convinced Kawasaki's is a deficiency...cont.

[@DresdonAcacinTheOriginal]

is it true that this is a form of lukemia-or if not worse than lukemia?

[@JACKATTACK9206]

No its much easier to treat than lukemia

[@liamsairplanes24]

It is worse then lukemia but its treated more easily.

[@jessiefajardo]

My daughter was diagnose with kawasaki. Im leaving in the philippines, Is there any chance that kawasaki might came back. I see a while a go on her tongue a little form of rediness. pls some one answer me.

[@dhanunjayabl8623]

Iam DHANUNJAYA my sister son is Kawasaki patients is also treet the SJ hospital is not quar so please give me solution iam an Indian

[@liamsairplanes24]

Well yeah, theres a chance Kawasaki Disease can come back when treated but its very rare and very not likely

[@LoonieMommy]

It won't let me post the video but look up "Kawasaki Disease.wmv"

[@1enzeder]

.... disease, possibly triggered by soy products. I tried to tell other parents on online forums but was ridiculed and dismissed as a lunatic. If parents are too weak and cowardly to take responsibility for the health of their children instead of entrusting the lives of their children to medical professionals who haven't got a clue what they're doing, I am no longer bothered by it or the suffering they bring upon themselves. I have done everything I can.

[@calystavelvet5526]

It is a genetic variant… that interferes with the body’s ability to produce T cells.I had my genes tested and I have the gene for it, so this is false lol. Also I can bring in my geneticist bf to show you how this is true if you still don’t believe it.