My son detected DIPG looking for treatment, am wondered no treatment for cure , if any one has know about treatment pls advise

what is gdnf? the website looks sketchy.

I wonder if they ever got the money?

Parkinson disease is a very terrible illness, my Dad suffered from it for 19 years until we finally got a help and a medicine from Dr Madida that truly works that helped treat, cure and reversed all his symptoms completely💯…My Dad is well again💫..

doctor RAVI PANERI FROM INDIA HAS THE CURE FOR PARKINSONS YOU CAN TESTIMONIALS ON KZbin

Are we hearing the story of a girl with cancer, or treatment studies?

How old were u when u we’re diagnosed please

Nice

them bastards dont tell you to look for natural remedies, they make you wait until is too late for natural cures to work, they will wait until the tumor is too big just to tell you there is nothing they can do anymore 🖕🖕🖕🖕

that is amazing

Has anyone tried to make a go fund me page to raise the money for the study? I'd rather see families reaching out to strangers to raise money hen what most ppl use it for to raise money for burials instead of having life insurance on your kids.

I’ve come across these videos on KZbin lately, about MND. I live in the United States, and here we know this awful disease as ALS. But what is so intriguing to me, is that mostly every story I’ve seen & read the person is usually so fit & healthy. I mean majority of everyone is a healthy individual that ends up having this disease. I haven’t seen,or read a story yet, about an individual being a drug addict or a unhealthy person that has contracted this disease. I’m honestly beginning to think it’s a correlation to this .

Update please.

Tengo parkinso quiero más información en español

Tengo parkinson quiero más información en español

You’re from Italy so you should know the English way of spelling cancerous lumps is “tumOr”

There no such thing as radio therapy. You mean radiation therapy

Stop wasting NHS money on gender reassignment, correcting botched private plastic surgery, gender neutral toilets in hospitals, £120K jobs for “diversity managers” and instead spend the money on saving children from this horrendous disease.

I am no expert but Dr.'s say there is no known cause for DIPG, which can't completely rule out environmental factors that may be in play. I'm not trying to turn this into a conspiracy but the chemicals and pollution we encounter every day must be taken into consideration

I’m so sorry 😢😢😢😢😢

We have got to do more to save our children, they are our future.

Dbs..deep brain stimulation..

can kymriah help? its very expensive

Evidently what they were touting in this video did not work very well. This was 8 years ago, and children are still dying to this day.

Please god. let there be a cure for pediatric cancer known as DIPG

Please help 😢 a 5 years old baby has DIPG. He just start radio therapy 20 days ago 😢 🙏 🙏 🙏

Have any body recover from dipg tumor ?

Oh God please stop this...

Absent a cure, the only effective course of action is make funeral arrangements and maximize what precious little time remains. Cherish those moments.

lol

I HATE CANCER 😠

WHY ARE SO MANY KIDS DIAGNOSED WITH THIS...

Please God let there be a cure for pediatric DIPG

My child is diagnosed with DIPG 3 months back, completed radiation therapy. Health condition deteriorating.

wow i hope this is going to be the cure. and also that last fact is false. there are survivors

We must find a cure, so all these beautiful kids can go on to enjoy their lives. They deserve to be here, and the day we find a cure..will be the most joyous day 🌞 im praying for every single person effected by this terrible disease

Poor baby

Thanks for your story. i started watching these personal stories a few years ago as i got symptoms that were concerning. Like you i was losing dexterity and found it difficult to eat and put a spoon in my mouth or get it out again. Dropping things and falling over a few times a day. Horrendous fatigue with muscles twitching madly. Saliva turned to jelly and i couldn't spit. strange body sensations that made me feel i was going to die. This for 6 years now and slowly getting better. Only fall over every few days now. I had been exposed to toxic fumes for 3 months which i believe caused all this. That is why my lungs still have a thick jelly coating on them and my body is weak. I drive trucks but have limited strength to lift anything and embarrassingly fall over sometimes in the office or elsewhere. I believe there is a toxin that is responsible for triggering MND. There is a growing concern that Blue Green Algae may be responsible as there are clusters of MND cases near effected waterways. You may already know that but it would be worth trying to detox your body as i have done early on to try to stop the progression of the illness. Steam and sauna rooms are marvellous for flushing out toxins from the body. All the best Ian.