Sandhya Jariwala

designer

[Sandhya Jariwala @SandhyaJariwala]

@ShivNadarFDN

[Sandhya Jariwala @SandhyaJariwala]

@ShivNadarFDN
My #Artist son is just 11years, born with genetic disorder #duchenne muscular distrophy. We and his school has taken the initiative to put up his first #artexhibition. All proceedings from it will go for his treatment. Please help in sponsoring his event.

[Sandhya Jariwala @SandhyaJariwala]

@Dizz1628 Hey please go through my tweet about my son 'Ayaan' exhibition and fundraising for his treatment.

[Sandhya Jariwala @SandhyaJariwala]

@Dizz1628 We spoke last year about Ayaan my son who is now 11years. Need funds for his treatment (gene therapy 53 exon skipping) which is just arrived. Ayaan is coming up with his first solo ART exhibition. Need funds to organise it. All the proceedings will go for his treatment.

[Sandhya Jariwala @SandhyaJariwala]

@CureDuchenne @ParentProjectMD @Sarepta

[Sandhya Jariwala @SandhyaJariwala]

@CureRareDisease My son Ayaan is 11 years having @DMD . He is coming up with his first solo ART exhibition in #India . All the proceedings of this exhibition with go for his treatment @53exonskipping @genetherapy. I need help please raise funds for this your Artist. @Sarepta

[Sandhya Jariwala @SandhyaJariwala]

@Dizz1628 @ParentProjectMD @Sarepta

[Sandhya Jariwala @SandhyaJariwala]

@ParentProjectMD

[Sandhya Jariwala @SandhyaJariwala]

Hello, @priyankachopra @nickjonas Please be Santa for my son Ayaan. Ayaan is an 11 years and an artist. We are putting his first art exhibition this Dec. To raise funds for his treatment (gene therapy) as he has DMD(Duchhenn Muscular Distrophy). Attaching few of his arts.

[Sandhya Jariwala @SandhyaJariwala]

@BeingSalmanKhan @tweetbeinghuman @ParentProjectMD

[Sandhya Jariwala @SandhyaJariwala]

@BeingSalmanKhan Can you pls be Santa for my son Ayaan. Ayaan is an 11years and an artist. We are putting his first art exhibition this Dec. To raise funds for his treatment (gene therapy) as he has DMD(Duchhenn Muscular Distrophy). Attaching few of his arts.
@ParentProjectMD

[Sandhya Jariwala @SandhyaJariwala]

@Sarepta @Sarepta how can I get the life saving drug @53exonskipping @dmd for my son in India. He is 11year and came on wheelchair since a year. He is an artist , will be going for his first solo exhibition this Christmas. Please help.
@BeingSalmanKhan @priyankachopra @ParentProjectMD

[Parent Project Muscular Dystrophy (PPMD) @ParentProjectMD]

Episode 2 of PPMD's Living Duchenne podcast, "When Milestones Look a Little Different," is live! https://t.co/qk5sVcO9zI

[Sandhya Jariwala @SandhyaJariwala]

@SaveOurSons Congratulations:) wow what a inspiration to the society and world.

[Sandhya Jariwala @SandhyaJariwala]

@cvmxn4 @ParentProjectMD @NSPharmaInc I would like to reach out for your help @ParentProjectMD @NSPharmaInc for my son's treatment @dmd @53exonskipping . We are from India.

[Sandhya Jariwala @SandhyaJariwala]

@ParentProjectMD I need to know more about CAP-1002. Can someone help please. @ParentProjectMD @DuchenneXchange @CureDuchenne @FDA_Drug_Info

[Sandhya Jariwala @SandhyaJariwala]

@ParentProjectMD @ParentProjectMD iam from India and my son is #Duchenne #dmd boy. He is 11year old. Can you pls provide me the contact details or email id to whom I can write to at @ParentProjectMD . I need @Viltepso in India for my son's treatment.
My email id is [email protected].

[Sandhya Jariwala @SandhyaJariwala]

@AzmiShabana Om Shanti.

[Sandhya Jariwala @SandhyaJariwala]

@duchennecentrum Can you pls send me the links live of recorded. Iam from India and my son is 11year with @DMD

[Sandhya Jariwala @SandhyaJariwala]

@worldduchenne @drjarodwong How can I watch @drjarodwong session on bone density. Iam from India and my son has @DMD