Support Nek Badu recover from Systemic Lupus Erythematosis! | Milaap
Support Nek Badu recover from Systemic Lupus Erythematosis!
  • JY

    Created by

    Jivish Yadav
  • Nb

    This fundraiser will benefit

    Nek badu

    from New Delhi, Delhi

My name is Jivish Yadav and I am here to fundraise for my friend, Nek badu.

Nek badu is 31 years old and is residing in New Delhi, Delhi. Nek badu has been diagnosed with Systemic lupus erythematosis (sle). But she needs treatment to fully recover. She is being treated at All India Institutes of Medical Sciences. Which will cost around Rs.3,000,000.00.

My friend Badu is suffering from an auto immune disease and happens to only one in a million and there is no cure for the disease yet in the world, it’s a life threatening disease.She had a heart attack more than a month ago , she lost her speeech for some time and in one of the eye she has lost 80% of the vision.
So,3 years back she had a biopsy done. Although the doctor than did not explain to exactly how serious this could be in future.  Since last a year and half she has been having continuous black outs varying from 1 min to 4 min max till now.
She had multiple strokes (three months back to be exact) leading to brain hemorrhage. She was hospitalised for almost 15 days for the same .A month and half back she started complaining about inflammation in her body .  Symptoms like black spots all over her body if she walks more than half an hour. Anxiety attack , heart rate increasing and decreasing simultaneously, unconsciousness etc.
She was then asked to go to AIIMS hospital where currently she is undergoing treatment by doctor Uma Kumar ( rheumotology dept ). She was thought to have PAN ( polyarteritis nodosa) which basically makes the blood in her body flow difficult because of the veins being contrast to each other. PAN also being one in a million case disease she was also asked to go for Viscereal Engeogram which came out to be fine and the doubt of PAN being the problem gone . But now the doctors have detected LUPUS which have almost same symptoms as PAN .
Lupus as you all know is a systematic auto immune disease which has no known cure.
The tests for PAN are very expensive and have a waiting of more than a year in AIIMS. The medicines that she has been prescribed are also very costly.
Please come forward to help me save my friend. Any contribution will immensely help her. I need your support to bring her home. Do contribute and share this campaign link with your friends and family.

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