Pinki Kumari

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“I have only one family—The Max Foundation,” and I truly mean it. I was diagnosed with CML in 2012, and for the past 14 years, this program has been my constant support. I make it a point to attend every Patient Support Group meeting because it keeps me connected, informed, and strong. Living on lifelong treatment with donated medicines, I deeply value the guidance I receive on my health, nutrition, and regular monitoring. The no-cost BCR-ABL testing came as a wonderful and reassuring surprise. I am truly grateful for all the care and support, and I always look forward to being part of these meetings.”

Pinki Kumari, diagnosed with CML in 2012, Dhanbad, Jharkhand

Pinki Kumari attended the CML and GIST patient support meeting held in Patna, on 18 April 2026 



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