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

22/06/2021

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

Dhara & Chirag Mamania cannot lose their only child. But they 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

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

21/06/2021

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!

Thank You Tisca Chopra for ur Kind Appeal for Mohin 🙏🏻

20/06/2021

Today everyone is celebrating Father's day. Me too, with tears in my eyes. Because I am a helpless and have fear of losing my very special son. I can't afford to lose him only because I am not financially strong to support his treatment. I can't imagine my life without him. He is my reason to smile.
On this auspicious day I request all father's to support me in saving my son's life. Feel the pleasure of saving him by donating just 100 Rs towards Mohin's treatment. SMA children have got wonderful support from India. Now please shower your blessings on Duchenne muscular dystrophy (DMD) child. 🙏

400000 Fathers × 100 Rs = 4 Cr

Donation link in BIO.

20/06/2021

Thank you Bharti ji for your shout out for my son's health. It means a lot to us. You truly have a golden heart too. 🙏
Every contribution is a blessing for my son. Please Donate to save my son's life.

Donation link in BIO

19/06/2021

Aj ek maa ki dil ki baat karna chati hu joh raat ko neend ma siskiya lati .raato ko Darke apna bacha ki dhadkan sunti hai. Kehti kisi kuch nayi par dil ma kitna dard lekhar jee rahe hai .bas bhagwan sa apna bache ki sasa mang rahi hai duwa mai .yeh kahani hai Dhara Mamania ki joh apna bacha ki zindagi bachna ke liya aj crowd funding kar rahi kuch madad karke uska bacha ki zindagi de sakte hai.

Plz donate your little bit and save her child

*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 donate click on the link given below*

*To Donate Via Impact Guru*
https://www.impactguru.com/fundraiser/help-mohin-mamania

*To Donate Via Milap*
https://milaap.org/fundraisers/support-mohin-mamania-1?mlp_referrer_id=4792035&utm_medium=created&utm_source=virtual_bank_account

*For Paytm Payment (for Android users only)* - https://milaap.org/fundraisers/support-mohin-mamania-1/deeplink?deeplink_type=paytm

*For UPI payment:* https://milaap.org/fundraisers/support-mohin-mamania-1/deeplink?deeplink_type=upi

*To Donate In foreign Currency*
https://www.gofundme.com/f/help-mohin-live?utm_source=customer&utm_medium=copy_link&utm_campaign=p_cf+share-flow-1

*Google Pay No*
9664100036
Mamania Dhara

Mohin needs the 4 crore drug Viltepso for his complete recovery

17/06/2021

*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 forever. End our constant fear of losing our child. Please donate.

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

15/06/2021

Somebody said Mother's best friend is her Son. And it's absolutely true. Mohin and I share very secret with eachother. I enjoy every moment with him and hopefully I will till my last breath.

My son needs your support to fight a rare disease called Duchenne muscular dystrophy (DMD). Please donate and share this message to max number of people. Together we can.

Donation link in BIO.

.____

13/06/2021

*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.

Donation link in BIO

11/06/2021

Please Help 10yr old boy.

To donate click on the link given below

To Donate Via Impact Guru
https://www.impactguru.com/fundraiser/help-mohin-mamania

Google Pay No
9664100036
Mamania Dhara

09/06/2021

Thank you Sonu Sood for supporting Mohin. It means a lot to us. 🙏
Follow Mohin_fights_dmd on Instagram

*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.

Donation link in BIO

09/06/2021

Please Please Help and donate 10yr old Boy, Time is going Fast. Every second is counted for Mohin, every second is hope for Mohin.

To donate click on the link given below

To Donate Via Impact Guru
https://www.impactguru.com/fundraiser/help-mohin-mamania

Google Pay No
9664100036
Mamania Dhara

06/06/2021

We are thankful for your blessings and prayers but now with that your bit donation can only make Mohin survival so plz donate your bit and be the part of life savier

Plz Plz donate for Mohin

Donate only bit but plz donate for his life u are only his saviour

05/06/2021

*We need more 3 crores in the next 39 days urgently.*

Reaching this 1 crore amount was never easy for us. All the family members and friends updated us digitally so that we don't miss out on any way of making Mohin's fundraiser reach the masses. But we can't keep calm. We can only have the peaceful sleep after we raise the remaining 3 crores in the next 39 days before his 11th birthday. Once Mohin turns 11 complications for Mohin will also increase gradually. He might also not be able to walk again if don't get the drug on time. Looking at the current health condition of Mohin, this is only possible by getting the Viltepso injected into his body before his 11th birthday.

Mohin looks up to us with hope everyday. He thinks his Mumma & Papa are going to get the magical drug and make him fine. Will it be possible? I pray almost every moment that it be.

Donation link in BIO

03/06/2021

He is Car lover !!!!
Car is his passion !!!
His dream is to become a Car designer !!!
Unfortunately he is suffering from a rare disease called Duchenne muscular dystrophy. But the cost of the drug is out of our reach.

Mohin need your support to fight DMD. Please donate and share as much as possible..

Donation link in BIO

01/06/2021

If you still wondering why to help please hear this mom 🙏🏻🙏🏻

01/06/2021

Please donate , Share and follow to save my son. Every contribution is a blessing for him.

Follow us on Instagram
https://instagram.com/mohin_fights_dmd

Donation link in BIO

31/05/2021

My son Mohin is Fighting a rare disease known as Duchenne muscular dystrophy. Due to this disease he finds lot of difficulty in doing his day to day activities.
We as a parent are very hopeful that one he will get Viltepso drug, which will make his life easy.
We need your support to save him. Please spread this message to maximum number of people.

For donation click the link in BIO

29/05/2021

https://instagram.com/mohin_fights_dmd?utm_medium=copy_link

Please Follow us on Instagram

98 Followers, 81 Following, 45 Posts - See Instagram photos and videos from Mohin Mamania ()

29/05/2021