Lucile Nourouzi, nee Cooke, has sadly passed away, leaving behind a legacy of love and resilience. Lucile, who had long struggled with the debilitating effects of Myalgic Encephalomyelitis (ME), is remembered for her strength and determination, despite the overwhelming fatigue that often kept her from engaging in daily activities.
Lucile was first diagnosed with ME in 1997 and again in 2007. The illness significantly impacted her life, limiting her ability to walk and engage in social activities, and leaving her with little energy for even the most basic of tasks. Despite these challenges, Lucile’s passion for raising awareness about the condition never wavered. She found it deeply unfair that so little research was done to understand ME, a condition that affects an estimated 250,000 people in the UK.
In the wake of Lucile’s passing, her family has set up a fundraiser to honor her memory and support the ME Association, a charity dedicated to furthering research on the illness. The fundraiser, organized by her daughter Amelia Wesley, has already raised £540 from generous donors.
Many have shared their support online, including heartfelt messages from those who knew her. Ashley Hushyar expressed her condolences, saying, "I want you to know that I am thinking of you, Nedah and the children, at these difficult times. My heart is there with you. Please don’t hesitate to reach out, stay together as a family, and take care of each other."
Lucile’s family and friends now cherish the time they had with her, holding onto the memories of her love and advocacy. Her memory will continue to inspire those who knew her to raise awareness about ME and the challenges faced by those affected by it.
Our thoughts and prayers are with Lucile’s family during this difficult time.
Short Summary of Lucile Nourouzi (nee Cooke)
| Aspect | Details |
|---|---|
| Name | Lucile Nourouzi (nee Cooke) |
| Date of Passing | Recently |
| Fundraiser Created By | Amelia Wesley |
| Goal Amount | £540 |
| Amount Raised | £540 |
| Location | Not mentioned |
| Purpose | To benefit the ME Association and raise awareness for Myalgic Encephalomyelitis (ME) |
Note:This post was written and edited by Paisley White, based on their expertise and research. It is intended for informational purposes only. It does not constitute legal advice. We welcome your feedback and questions on this content. Please feel free to contact us.