tanmayfightdmd

tanmayfightdmd Tanmay is fighting a rare disease called "Duchene Muscular Dystrophy". As per the genetic report exon, 46 to 51 deleted from the body.

16/12/2021

डीएमडी बच्चों के हाथ-पैर और पूरा शरीर सामान्य बच्चों की तरह काम नहीं करता। एक्सॉन की कमी के कारण शरीर मांसपेशियों को ताकत देने वाले प्रोटीन नहीं बना पाता है। अभी तन्मय का उल्टा हाथ दाहिने हाथ से कमजोर है, आप इन वीडियो के जरिए देख सकते हैं। तन्मय मुश्किल से हाथ से हैंडल पकड़ पाता है। यह एक जानलेवा बीमारी है जो उम्र के साथ बढ़ती जाती है। इसलिए, इसे रोकने के लिए दवा उपलब्ध है, लेकिन यह हमारी पहुंच से दूर है। सामान्य मध्यमवर्गीय परिवार या भले ही अमीर लोग इसे आसानी से नहीं खरीद सकते।
The arms and legs of DMD children and the whole body do not work like normal children. Due to a lack of exon, the Body is not able to make proteins that give strength to the muscles.
Right now the opposite hand of Tanmay is weaker than the right hand, you can see through these videos.
Tanmay can hardly hold the handle with his hand. It is a life-threatening disease that increases with age. Therefore, medicine is available to stop it, but it is far from our reach. Normal middle-class families or even though rich people can't purchase it easily.
https://www.impactguru.com/fundraiser/help-tanmay-sharma

Hello Friends,जैसा कि आप जानते है कि मेरे बेटे Tanmay का treatment अभी Tamilnadhu मे चल रहा है आप सभी के शहयोग से ओर मदद...
14/12/2021

Hello Friends,

जैसा कि आप जानते है कि मेरे बेटे Tanmay का treatment अभी Tamilnadhu मे चल रहा है आप सभी के शहयोग से ओर मदद से अभी हलका सा सुधार है

मेरी wife अभी अकेले ही उसका उपचार करा रही है ओर हमने वहां पर किराये पर कमरा लिया हुआ है

अभी उसकी बॉडी हाथ पैर सही से काम नहीं करते है लेकिन उसको खडा एंड चलाने की कोसिश चल रही है इंन कुछ उसके latest photos के माध्यम से उसकी current condition को दिखा रहा हूँ

काफी months के बाद वो खडा होने की कौसिस मे है उसके फेस पर डर साफ साफ नज़र आ रहा है.

अभी एक भी step wo खुद् से नहीं रख पाता हम सभी paranets को उस दिन का इंतजार है कब इन kids को medicine उपलब्ध होगी

पांच लाख kids को Muscluer dystrophy है केवल भारत मे .🙏🙏

He is celebrating birthdays with other DMD kids in mayopathy center Tamilnadhu.

I don't have words to define pain of thousands of children and their paranets as well.

It’s that time of the month! Salaries are in and it’s time to ask yourself the question of what you’re going to do with ...
10/12/2021

It’s that time of the month! Salaries are in and it’s time to ask yourself the question of what you’re going to do with that money! Sure, there’s shopping to be done, but you could also help us save a life!
My name is *Manoj Sharma* and I have raised a campaign with ImpactGuru to help save the life of *Tanmay Sharma* he is *Fighting Duchenne Muscular Dystrophy* So far we arranged 6,31,741/- INR, we have goal amount *(2 crores)* and need YOUR help to get us across the finish line so we can save his life. Even if you find yourself unable to donate, you can even help us out by sharing the campaign to all your contacts which will help us to reach more people so we can try and raise funds!
*What you Donate Today Impact Guru Will add 10% extra on it*
*Your generosity is greatly appreciated.*

Friends, if you already donated then please tag this post with your friends.

https://www.impactguru.com/fundraiser/help-tanmay-sharma

Manoj Sharma wants to raise funds for son Tanmay Sharma to fight Duchenne muscular dystrophy. Your donation can guide them to reach their fund goals. Please help.

दोस्तो आपसे अनुरोध है कि इस पोस्ट को आगे अपने सभी मित्रों को भी शेयर कर दे. Please like and share with your all friends ...
25/08/2021

दोस्तो आपसे अनुरोध है कि इस पोस्ट को आगे अपने सभी मित्रों को भी शेयर कर दे.
Please like and share with your all friends for better reach.

Attached is the treatment cost estimation letter provided by doctor Raghawan from Madurai.
14/07/2021

Attached is the treatment cost estimation letter provided by doctor Raghawan from Madurai.

https://youtu.be/iKDOkmud0zQ
26/06/2021

https://youtu.be/iKDOkmud0zQ

The symptoms of Duchenne Muscular Dystrophy (DMD) appear at an early age amongst boys, lucky are the parents who can detect the lethal symptoms early. Tanmay...

16/03/2021

Currently, some physical therapy, exercise and Yoga type of treatment is going on for Tanmay. Doctor says no pain no gain.
This type of treatment is very painful. Muje bhi bahut dard hota hai but kya kare sayed kuch improvement aa jaye in coming months.

Hi Anurag Thakur Sir, My son is suffering from duchene muscluer dystrophy and we don't have fund for his treatment... Ia...
28/02/2021

Hi Anurag Thakur Sir,

My son is suffering from duchene muscluer dystrophy and we don't have fund for his treatment... Iam collecting fund with the help of crowdfunding....
Request you please forward my message to government.. So we can get treatment for him and save his life.
Anurag Thakur

Manoj Sharma wants to raise funds for son Tanmay Sharma to fight Duchenne muscular dystrophy. Your donation can guide them to reach their fund goals. Please help.

Tanmay is looking for your help,  please support him to make your contribution or donate whatever you want. Treatment co...
26/02/2021

Tanmay is looking for your help, please support him to make your contribution or donate whatever you want. Treatment cost is very expensive around 20L every year. So please visit this link... https://www.impactguru.com/fundraiser/help-tanmay-sharma

Manoj Sharma wants to raise funds for son Tanmay Sharma to fight Duchenne muscular dystrophy. Your donation can guide them to reach their fund goals. Please help.

A few days back, We had live Fundraiser account for our lovely son's treatment...Please share, visit and donate through ...
25/02/2021

A few days back, We had live Fundraiser account for our lovely son's treatment...
Please share, visit and donate through this link- https://www.impactguru.com/fundraiser/help-tanmay-sharma

We continuously getting a great support and contribution from our seniors, friends and company. Need to continue further until we can not achieve our goal.

My Son Tanmay was born on the 1st of December 2013 with a severe genetic disorder, called DMD (Ducheme Muscluer Dystrophy).

He started to show signs of the disease at 1.5 years of age and was diagnosed at 2 years of age. Doctor says that Duchene Muscular Dystrophy is a genetic problem but many families don't have any past cases in his generation overall, First of all, DMD affects the legs and move from bottom to upper side. Hands also do not work properly like a normal child.

Tanmay is fighting against muscle wasting with a help of a supportive treatment like Physiotherapy. He is doing physiotherapy for 6 months and it will be continue to him for better health. Attached are his few pics related to exercise.

As I discussed with dartindia.in founder and president Mr. Ravdeep S Anand about the treatment of Tanmay. He said that cost will be approx 20 Lakh every year. For more information, you can visit the new links here - https://www.livemint.com/opinion/columns/new-treatments-for-rare-diseases-need-quick-approval-11601392416338.html

Please share this post with your friends on social media websites and ask them to share spreading the worldwide.

For you it takes only a few seconds or one minute job, For Tanmay, it means healthy long-lasting life.

24/02/2021
24/02/2021
24/02/2021

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