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Melfre

@melfrewo

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Posted On: July 6th 2026, 02:23 pm
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OUT NOW! “Mahi Wey Menu” is now live! ✨ Watch it now, show your love, and let us know your favourite part in the comments. ❤️▶️ Watch now on The Panther Records Official YouTube Channel & don’t forget to LIKE, COMMENT & SUBSCRIBE! After all the love Chalray Chalray Wal received here and across the border, I’m so excited to share something truly special with you all. ❤️ Presenting “Mahi Wey Menu” — my humble tribute to the legendary Madam Noor Jehan, whose voice and legacy continue to inspire generations. I hope you feel the love behind this one as much as I felt while creating it. 🤍 A huge shoutout to the incredible team at @thepantherrecords for bringing this project to life. CREDITS 🎙️ Singer: Shanzay Sial 🎬 Director & Producers: @realsahibzada @shaheer_asim 🎼 Music Producer: @kitualitafu 💄 Makeup Artist: @khizra_usman 👗 Stylist: @iqramurtazaofficial 🎞️ Edit & Colorist: @thepantherstudios 🎥DOP: @shotbysahibzada @shaheer_asim 🏷️ Presented by: @thepantherrecords This one is for the love of music, the magic of Punjab, and the timeless legacy of Madam Noor Jehan. ✨ I hope you all love Mahi Wey Menu. Do share your thoughts and show us some love! ❤️ #MahiWeyMenu #ShanzaySial #MadamNoorJehan #ThePantherRecords #punjabimusic
Not everyone is ready to be SEEN @_atseen 🐆
For years, I knew something was wrong with my body. I went from doctor to doctor, trying to explain the pain and symptoms that were taking over my life, only to be told that nothing was wrong. Eventually, I was diagnosed with endometriosis and PCOS. Endometriosis meant surgery. I underwent excision surgery in 2023 to remove the disease tissue growing inside my body after years of pain and unanswered questions. It was a major moment in my life, both physically and emotionally. I finally had an explanation for what I had been experiencing, but surgery wasn’t the end of my health journey. Despite treatment, lifestyle changes, and continuing to search for answers, my symptoms persisted. The pain began affecting my entire body. Eventually, I was diagnosed with lupus, a serious autoimmune disease that can affect multiple organs and become life-threatening. Research has found associations between endometriosis and certain autoimmune diseases, including lupus, although we still have much to learn about why these conditions overlap. Living through this has made me think deeply about women’s health, the effects of chronic illness on the body, and how much we still don’t understand. Too many women are taught to normalize debilitating pain instead of being given answers, support, and appropriate care. I know how isolating it feels to fight for answers while trying to keep your life moving. I also know how fortunate I am to have a supportive family and access to medical care. Not everyone has those resources, and that is one of the reasons this matters so much to me. I used to think I’d wait until I had my health figured out before sharing my story. But I don’t want to wait for a perfect ending to start a conversation that needs to be happening now. I’m incredibly grateful to be getting involved with the Endometriosis Foundation and to contribute to the work being done around endometriosis awareness and women’s reproductive health. I’m excited to share more soon. For now, I wanted to start by sharing an overview of my story, because no woman should have to fight this hard to be heard. 💛
26 years of blessings, and this year feels extra special… 🤍✨ عيد ميلاد مختلف، وأنا نعيش أجمل فصول حياتي، فصل الحب والزواج وبداية أحلام جديدة. الحمد لله على نعمة العمر، ونعمة الحب، وعلى كل جميل خبّأه لي القدر. 🎂💍 #عيد_ميلاد #bithday #photography #pic #birthdaygirl
Moja mala velika ljubav. I najbolja ekipa za svaki dan 🖤
Zionnnnn ❤️🦁 Book a tour here at www.Singlevisioninc.org
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