An initiation for Siyona medical fundraiser by Yugal Gurung and his friends from UK, Helles barrack Gurkhas raised Rs 113549.8 for the treatment cost for Siyona.We appreciated their support and contribution for the baby girl.Join TEAM SIYONA-SMA for all updates… Read More ›
babygirl
UPDATES-11 CRORE 60 LAKHS collected .
Siyona’s parents Sandeep Shrestha and Aleena Gurung Shrestha went live today to share the updates of total fund collected for her medical fundraiser along with her health status.Siyona is in Warsaw hospital of Poland and she is doing alright as… Read More ›
Interact Club Of Prativa Pokhara Fishtail for Siyona
Interact Club Of Prativa Pokhara Fishtail supporting Siyona medical fundraiser.We thanks them for helping the parents of Siyona to raise funds and awaring the general public about the disease.Appreciated.https://www.facebook.com/icprativa Post link here.
Tiktoker Raju Dahal asking for support for Siyona
Siyona supporter and Nepali tiktoker @rajudahal8 joins our fight for Siyona and asks for the funding for her medical fundraiser.We thank him for his video on our baby girl Siyona.Join teamsiyona-sma for all updates on Siyona.
Total paypal donation for Siyona till date
https://docs.google.com/spreadsheets/d/19kvSh13YRc4ePvymcjXfydhq4KDsT_j3Sm87hb78ifY/edit#gid=1126100503 The upper link shows the total donation made by supporters via paypal medium.A total of $839.85 have been collected via paypal. Do donate for Siyona who is fighting for her life you can support via this link-https://www.paypal.com/paypalme/anishshrestha4343
Galkot(गलकोट घुम्टे रोधी सांगीतिक समूह) supports Siyona
We thanks Galkot Ghumtey Rodhi group/गलकोट घुम्टे रोधी सांगीतिक समूह for their immense help and support for Siyona.As per the Galkot Updates on Siyona post, गलकोटमा “गलकोट घुम्टे रोधी” सांगीतिक समूह द्वारा सियोना श्रेष्ठ बचाउ अभियान चलाई उपचारार्थ आर्थिक रकम… Read More ›
P2NBGaming donates Rs 1,67,455 for Siyona
A Nepali PUBG gaming channel P2NB_Gaming on facebook donated Rs 1,67,455 for Siyona Shrestha who is battling for her life against a rare form of genetic disease called Spinal Muscular Atrophy Type1(SMA Type 1).We thank K.C. Rossann for contacting us(admins… Read More ›
