Help Noha fight Pancreatic cancer

Medical

Help Noha fight Pancreatic cancer
Help Noha fight Pancreatic cancer With the permission of Noha’s family, we are setting up this Medical fund as she fights for her life. Nine years ago, Noha was diagnosed with pancreatic cancer, and today, what Noha needs for a 90% chance of becoming cancer-free are 4 courses of Nuclear treatment “177 Lutetium Dotatate” for her Metastatic Neuroendocrine Tumor. Each shot should be given to Noha once every 2 months. The government and the Ministry of Health in Lebanon have failed to provide basic needs to their people, including cancer medicine. So now we have one chance to raise 16.000 USD to get these courses for Noha, who has neared the end of her treatment and is about to get better, but now suddenly there are no more drugs left. For now, she has spent money to buy drugs at a much higher price on the black market. But she will not be able to afford to do this for long. On 26 Aug 2021, cancer patients rallied in front of a United Nations agency in Lebanon, in protest against a severe medicine shortage plaguing the country. Raising the slogan “We want cancer treatment,” families of cancer patients staged a sit-in near the Grand Serail on Thursday evening, “to protest the genocide of cancer patients,” demanding that medication for their treatment be secured. Can you believe it? In Lebanon, cancer patients -- with all their worries -- are forced to go down into the street and protest to demand medicine. So today, Noha’s friends and family, all together, we have decided to step up to help this dedicated mother fight the toughest battle of her life. We need your generous help to make that possible and reach people all over the world. YOUR SUPPORT, REGARDLESS OF THE AMOUNT, CAN MAKE A HUGE DIFFERENCE!

$0 raised Of $16,000

Nadim SMA baby needs your help

Medical

Nadim SMA baby needs your help
Hi, My name is Nadim Chuaib . i am 7 months old. 2 months ago i was diagnosed with a rare disease which is SMA ( SPINAL MUSCULAR ATORPHY ) type 1. The disease is a genetic disorder that weakens the nerves responsible for the movement of the muscles in the body and especially type 1 is very dangerous if the treatment is not taken ASAP. The only treatment is a medicine called ( zolgensma ) which costs around 2125000 dollars. The full cost including zolgensma and the hospital's cost at aljalila children's hospital in dubai is 2180000$. It's too expensive and we need your support. every dollar could help. this fund raise will help me get cured from this disease and give me a new chance in life. with each coming day the disease grows stronger and it's complications might lead to death. thank you for your donation, please share as much as possible to reach my goal and live a normal life like any other child . مرحبا اسمي نديم شعيب. عمري 7 أشهر. منذ شهرين ، تم تشخيصي بمرض نادر وهو SMA (ضمور عضلي شوكي) من النوع الأول. هذا المرض هو عبارة عن طفرة جينية تؤدي الى نقص في البروتين SMN بالتالي مع الوقت تضمر الأعصاب المسؤولة عن حركة العضلات في الجسم،وخاصة النوع الأول يكون خطيرًا جدًا إذا لا يتم أخذ العلاج في أسرع وقت ممكن. العلاج الوحيد هو عبارة عن حقنة و هو (zolgensma) وتبلغ تكلفته حوالي 2125000 دولار. التكلفة الكاملة هي 2180000 دولار و تشمل zolgensma وتكلفة المستشفى في مستشفى الجليلة للأطفال في دبي. هذا العلاج مكلف للغاية و يفوق قدرتنا لذلك نحتاج إلى دعمكم لتحقيق الهدف. كل دولار يمكن أن يساعد. سيساعدني هذا المبلغ المالي على الشفاء من هذا المرض ويمنحني فرصة جديدة في الحياة. مع كل يوم قادم يزداد المرض قوة وقد تؤدي مضاعفاته إلى الوفاة. شكرا لتبرعكم ، يرجى مشاركة أكبر قدر ممكن للوصول إلى هدفي والعيش حياة طبيعية مثل أي طفل آخر.

$49,848 raised Of $2,180,000