Support Kamlesh Singh To Recover From Chronic Kidney Failure
- Support Kamlesh Singh To Recover From Chronic Kidney Failure
87%RaisedUSD3,948 of Rs.4,00,000174 supporters
87%
Raised
USD3,948
of Rs.4,00,000
174 supporters
ShareStory :
My name is Priya Singh and I am here to raise funds for my husband Kamlesh Singh who is 38 years old. Kamlesh Singh lives in Bengaluru, Karnataka with me & our 3 years old son.
Kamlesh Singh is working as a private employee.
Kamlesh Singh is suffering from Chronic Kidney Failure for the past few months and undergoing treatment for the last 6 years. Currently, he is receiving Dialysis at Apollo Hospital. Also, he was in ICU for a week and was hospitalized for 20 days.
Until now, we've spent about USD 50000. we've arranged the amount from savings & insurance and we are completely out of savings.
Kamlesh would get the transplant from his mother In law in the next few days and we need Rs.20,00,000.00 urgently for further treatment. Please come forward to support my cause and save my husband and my family. Any contribution will be of immense help. Do contribute and share this crowdfunding fundraiser link with your friends and family.
The poverty in Bangladesh is an ongoing issue that needs to be addressed. This is a cause that should be taken seriously. There are many organizations that are doing their part to help, but they need more support. The poverty in Bangladesh has been ongoing for decades. It has been estimated that over one-third of the population is living below the poverty line. This is because of a lack of resources, opportunities, and basic human rights. There are many children who are suffering from the effects of poverty. They are suffering from malnutrition, lack of education, and have no access to medical care. Poverty is an issue that should be taken seriously. There are many organizations that are doing their part to help, but they need more support...
_Logo_(2018-2020).svg/768px-Google_Pay_(GPay)_Logo_(2018-2020).svg.png){kind=logo}
Bangladeshi Supporters
BKash + Nagad Personal: 01628600429
Supporters From
The Help Foundation focuses on creating a just world by empowering the most marginalized.
regardless of background.
The foundation seeks to benefit them through various welfare projects such as education, child care, healthcare, employment, empowerment of women etc.
Helping to equip needy with the skills they need to earn for the betterment of their socio-economic status.
The Help Foundation is a registered non-profit organization that has been working for the welfare of the poor in the society for over a decade now.
It aims to provide basic needs to the underprivileged people of the country and to educate children in slums, suburbs or remote rural areas where access to education is not easy.
Supporting Documents
),o_10,w_$h/a_-55/c_pad,h_$h,w_$w/fl_layer_apply/c_fit,w_603/v1643081642/production/images/campaign/448952/WhatsApp_Image_2022-01-24_at_20.57.37_1643081641.jpg)
),o_10,w_$h/a_-55/c_pad,h_$h,w_$w/fl_layer_apply/c_fit,w_603/v1643038098/production/images/campaign/448952/WhatsApp_Image_2022-01-24_at_20.55.28__1__1643038097.jpg)
),o_10,w_$h/a_-55/c_pad,h_$h,w_$w/fl_layer_apply/c_fit,w_603/v1643038076/production/images/campaign/448952/WhatsApp_Image_2022-01-24_at_20.55.28_1643038075.jpg)
This is an additional fundraiser page for Baby Khyati. I am Raman NVSL, raising funds for my 10 months old daughter Khyati. My daughter Khyati has been diagnosed with Spinal Muscular Atrophy (SMA) Type 1 at an age of 4 months. It’s a rare genetic disease.
Baby Khyati is suffering from symptoms like difficulty in holding her neck, labored breathing, difficulty in swallowing, and inability to move her legs like any other normal infant of the same age. She is currently assisted with a BiPAP machine for breathing. If not treated, the life span of infants with SMA Type 1 varies up to 1 or 2 years depending on the progression. Day by day Khyati’s condition is worsening due to reduced muscle activity.
Treatment Options:
Zolgensma Gene Therapy is a potential cure for SMA for children below two years of age and it has to be imported from the USA. Baby Khyati needs Zolgensma gene therapy as soon as possible to save her life. Zolgensma comes at an extortionate price of INR 16 crores (USD $2.125 million) approximately excluding taxes and duties. The price of medicine is beyond my reach considering my annual income.
Fundraising Activities:
We also started crowdfunding two months back on various platforms. We still need Rs.14-crore for the purchase of medicine. This is an additional effort we are making using Milaap Org. to enhance our fundraising effort and expedite the gene therapy availability to Baby Khyati to save her life.
Funds raised through all charity organizations will be combined and utilized for making payments to pharmaceutical companies or their authorized subsidiaries and hospital for purchasing the medicine including pre and post-treatment care.
Crowdfunding for similar medical causes was successful in India in recent instances for such a huge amount. On this note, we seek your strong heartfelt support in fundraising to save our Khyati’s life.
Donate:
Donate whatever you can with your kind heart to save Baby Khyati’s life. Please follow and share Khyati’s story on social media handles.
Spread the word:
Recently, we have been observing more and more SMA cases are visible due to developments in life-saving therapies and medicines. Spreading the word on diagnoses and about the disease could save a few more lives.
Baby Khyati is suffering from symptoms like difficulty in holding her neck, labored breathing, difficulty in swallowing, and inability to move her legs like any other normal infant of the same age. She is currently assisted with a BiPAP machine for breathing. If not treated, the life span of infants with SMA Type 1 varies up to 1 or 2 years depending on the progression. Day by day Khyati’s condition is worsening due to reduced muscle activity.
Treatment Options:
Zolgensma Gene Therapy is a potential cure for SMA for children below two years of age and it has to be imported from the USA. Baby Khyati needs Zolgensma gene therapy as soon as possible to save her life. Zolgensma comes at an extortionate price of INR 16 crores (USD $2.125 million) approximately excluding taxes and duties. The price of medicine is beyond my reach considering my annual income.
Fundraising Activities:
We also started crowdfunding two months back on various platforms. We still need Rs.14-crore for the purchase of medicine. This is an additional effort we are making using Milaap Org. to enhance our fundraising effort and expedite the gene therapy availability to Baby Khyati to save her life.
Funds raised through all charity organizations will be combined and utilized for making payments to pharmaceutical companies or their authorized subsidiaries and hospital for purchasing the medicine including pre and post-treatment care.
Crowdfunding for similar medical causes was successful in India in recent instances for such a huge amount. On this note, we seek your strong heartfelt support in fundraising to save our Khyati’s life.
Donate:
Donate whatever you can with your kind heart to save Baby Khyati’s life. Please follow and share Khyati’s story on social media handles.
Spread the word:
Recently, we have been observing more and more SMA cases are visible due to developments in life-saving therapies and medicines. Spreading the word on diagnoses and about the disease could save a few more lives.
Story
My name is Syed Asma Parveen and I am here to raise funds for my son Mohammed Umer who is 1.7 years old. Mohammed Umer lives with their family, in Hyderabad, Telangana.
Mohammed Umer is suffering from multiple health issues ( IPT, Very low pallet count, haemoglobin 6). He is under treatment and medications at a Pvt Hospital in Hyderabad, Telangana. Currently, he is admitted to the ICU ward and the treating doctor says he is critical. Until now, we have spent about Rs. 400,000/- we have arranged the amount from loans. But now we need Rs.10,00,000/- more for further treatments.
Mohammed Umer is suffering from multiple health issues ( IPT, Very low pallet count, haemoglobin 6). He is under treatment and medications at a Pvt Hospital in Hyderabad, Telangana. Currently, he is admitted to the ICU ward and the treating doctor says he is critical. Until now, we have spent about Rs. 400,000/- we have arranged the amount from loans. But now we need Rs.10,00,000/- more for further treatments.
Please come forward to support my cause. Any contribution will be of immense help. Do contribute and share this crowdfunding fundraiser link with your friends and family.
It advises parents and adolescents to stop child marriage and dowry.
In fact seeks to meet the goal of helping the poor to break the cycle of poverty by integrating education.
This is because of a lack of resources, opportunities, and basic human rights. There are many children who are suffering from the effects of poverty. They are suffering from malnutrition, lack of education, and have no access to medical care. Poverty is an issue that should be taken seriously.
In fact seeks to meet the goal of helping the poor to break the cycle of poverty by integrating education.
This is because of a lack of resources, opportunities, and basic human rights. There are many children who are suffering from the effects of poverty. They are suffering from malnutrition, lack of education, and have no access to medical care. Poverty is an issue that should be taken seriously.
Indian office address
Milaap Social Ventures India Pvt. Ltd.
ClayWorks Create - building,11th KM Create Campus,Arakere Bannerghatta Rd,
Bangalore, Karnataka, India 560076
Comments
Post a Comment