Mohin_fights_dmd

29/10/2021

Mohin got his first dose of Viltepso on 21st of October. Thank you everyone for your kind donation and support.

09/08/2021

He is a happy boy. But his disease is affecting his happiness. Let's all come together and help him to fight a rare genetic disorder known as Duchenne muscular dystrophy.

Donation link
https://www.impactguru.com/fundraiser/help-mohin-mamania

03/08/2021

Mohin is fighting a Rare Genetic disorder called Duchenne muscular dystrophy (DMD). Which will soon make him wheelchair bond and slowly will affect all his organs. Let's all come together and help him fight a deadly disease with a treatment name Viltepso.
Donate generously to save him and once again show the power of common man to save a RARE Child.

Donation link below
https://www.impactguru.com/fundraiser/help-mohin-mamania

29/07/2021

Every contribution is a blessing for him. The way India supported SMA , request you all to please show your love and affection for a DMD child too. 🙏

Donation link below
https://www.impactguru.com/fundraiser/help-mohin-mamania

For more updates follow mohin_fights _dmd on Instagram.
https://instagram.com/mohin_fights_dmd?igshid=7g1i9060p5yy

23/07/2021

India please come forward and donate to support a Rare Genetic disease called Duchenne muscular dystrophy DMD.

Your generous support for SMA has saved more than 4 children. This time a child suffering from DMD needs your support.

We need your love and support to save our child. Donation link below.

https://www.impactguru.com/fundraiser/help-mohin-mamania

22/07/2021

*Your Donations Can Save My Son Mohin's Life, Please Support !*

My name is *Dhara Mamania* I am raising funds for *my 10-years-old son Mohin Mamania*. Who is suffering from *Duchenne Muscular Dystrophy(DMD)* an irreversible muscle wasting disease. In which Mohin suffer frequent falls, trouble getting up or running, wadding gait, and many other problems.

The life-threatening disease with time affects the heart muscle and the respiratory functions. Ending up taking the Patient's life. However, the treatment which we can give Mohin to save his life is called *Viltepso* for his recovery.

The drug costs a massive amount of *4 crore rupees more than (5,50,000 $)*. We can't see our son struggling like this so we have started this fundraiser as our only hope to *save our son's life*. Please show your support by donating on the link given below and sharing the message ahead within your network. Each and every help will be appreciated!

To support please follow us Facebook and Instagram
https://instagram.com/mohin_fights_dmd

Donation link in BIO

17/07/2021

India let's come together to save Mohin's Life. All Indian citizens have shown their love and support for SMA patients, but this time I request you to support and shower your blessings to a DMD patient. DMD is equally life threating like SMA.

Donation link below
https://www.impactguru.com/fundraiser/help-mohin-mamania

Follow us on our Instagram to know more about a deadly disease DMD
https://instagram.com/mohin_fights_dmd

04/07/2021

A rare illness is affecting Mohin’s organs one by one. It will soon affect his lungs and heart.

He takes baby steps when walking. He needs help walking up the stairs. He can barely walk for 10 minutes before getting tired. All this suffering is caused by his rare genetic condition called Duchenne’s Muscular dystrophy, which can cause a slow painful death. His only hope is a drug called Viltepso, which costs Rs. 4 crores. Every day that Mohin spends without getting this critical treatment, is a day his condition worsens to the point of no return.
Your help can ensure that Mohin gets this treatment at the earliest so that he can walk again. End these parents constant fear of losing their child. Please donate.

Please follow to support Mohin
https://instagram.com/mohin_fights_dmd

Donation link in BIO

30/06/2021

*DMD will soon put Mohin in a wheelchair if he doesn't receive timely treatment.*

We cannot lose their only child. But we also don't have Rs. 4 crores to save him from a rare genetic disease called Duchenne Muscular Dystrophy (DMD). Your kindness will give our sweet 10-year-old a fighting chance to survive. Please help us. His muscles are growing weak by the day, and without urgent treatment, we fear his heart and lungs will fail too.

*Every Contribution Matters*

Donation link in BIO

Don't forget to follow Mohin_fights_dmd on Instagram. We strongly need your support. 🙏

Mohin needs the 4 crore drug Viltepso for his complete recovery

26/06/2021

He is playing alone by himself, without any friends. But I am sure one day he will play with his friends. And for this I will need your support. Please donate and spread the message to maximum number of people.

Donation link in BIO