UPDATE: A heartfelt THANK YOU to Teera's well wishers and for your Tremendous help and support. We were able to reach the big milestone. We have raised funds for the Zolgensma gene therapy at this point. We will continue with this fundraising till the end of this month to cover for any shortfalls due to government taxes, fees, duties and hospitalization costs post SMA treatment. These amounts are significant too. Lets pray that our little warrior princess Teera gets better and lives a very happy long life. Again can't thank you all enough.
Hello well-wishers. This is our donation page for 4-month-old baby Teera Kamat, born on August 14, 2020, diagnosed with Spinal Muscular Atrophy Type 1 (SMA1). All she asks is one gene; can you help us get it for her?
I am Rama, Teera’s aunt, who is helping my cousin Mihir and sister in law Priyanka raise the funds required to save our little angel's life. They have very limited financial support in Mumbai, India, where Teera is now located and hospitals are ill equipped to treat such genetic conditions. My family are fundraising in India through their local crowdfunding platforms, but they have tried very hard but have only raised 15% of their total goal. They really need our help, and the clock is running out for Teera as each day passes.
SMA is a terrible disease, a rarest of rare genetic disorder that affects 1 in 10000 kids worldwide. Teera is missing one gene in her body that is required to make a very important protein. That protein keeps her nerve cells active, and without it, they wither away and die. She will have a lifespan of 6 months to 2 years depending on the progression of her condition.
On the surface, she looks like a normal happy child, but inside her condition is killing her nerves and muscles one by one. As the disease progresses she will not be able to move her hands and legs, sit up, crawl, hold her head, or do any of the things normal babies do. Her breathing will be labored; stomach muscles will give way, causing food to go back up to her lungs; and she will choke on her own spit and stomach fluids. Once the disease kills a particular nerve cell, we lose all function in that part of the body and this is irreversible. No amount of treatment given after the nerve cells die will help.
We have some hope. She currently has limited movement in her right leg and has some breathing issues, but is right now breathing and feeding on her own. The 2+ million dollar treatment called Zolgensma is available in the United States. This treatment, given to her now, could be a potential “cure”. As time passes, the effectiveness of the treatment will reduce. So we need to reach our goal within the next 2 months.
We appeal to your human side. You have the opportunity to save this beautiful baby. Please open your heart so we can reach our goal NOW and save her life.
Please help us spread the word. All our social media links and locations are available on Link tree - https://linktr.ee/donatetoteera Every share, donation, encouraging word will help build our campaign up.
The Primary purpose of this fundraiser is to make Zolgensma available to Teera. Payments from gofundme will be made out to the pharmaceutical company or their authorized subsidiary in lieu of purchasing this life saving treatment and making it available to Teera. We may also require to make payments to the hospital for pre and post procedure care, as well as any care required for monitoring Teera as part of the evaluation and treatment.
DonationsSee top donations
- Lakshmanaswamy Atluru
- Sivakumar Pitta Rajagopal
- Roseline Rubanya