2023 Christmas Party!

Hello Ladies,

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I am hosting Ladies to a Christmas Lunch/ Dinner of Jollof Rice+ Chicken and Sparking Alcohol.

Thursday 28th December 2023 2pm – 7pm

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It will be adult themed and there will be breakable glass and TV etc. So sorry No Kids except you have a very young baby who is still in a car seat/pram.

The plan will be:

Sell us your business. Tell us your side Hussle and share your social media, everyone gets a full 10 minutes pitch. If you don’t have a side Hussle you can tell us about yourself with Q and A.

I will be talking about Sickle Cell Awareness.

I have room for just 10 ladies. It’s a first come first on the list. Please indicate only if you can absolutely attend so that we don’t end up with an empty slot that could be used by someone who needs it.

It’s a House Party in the living Room. I am less than 4 minutes’ walk from Kidbrooke Station. There is free parking in nearby streets of about 7 minutes’ walk or you can get parking permit from the concierge (details to be provided).

If you don’t already have my address, I will send the full address to those attending, I will create a temporary WhatsApp group for it for this party. Please feel free to come with your own drinks and food and your own take away pack.  (we can discuss who is bringing what in the WhatsApp to prevent too many of same)

Regards,

Georgia Ugwu

AKA Lil Miss Sunshine

Please Contact us If you are interested or email admin@sicklecellworld.org

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Sade and Chinedu

In the bustling city of Lagos, Nigeria, lived a vibrant teenager named Sade. Sade was a remarkable girl with a zest for life that was infectious. She had an unmistakable charm, a radiant smile, and a personality that could light up even the darkest of days. Yet, Sade carried a secret that only a few close friends and family members knew about – she had sickle cell disease.

Living with sickle cell disease in Nigeria came with its own set of challenges. The disease could bring unpredictable pain crises, fatigue, and other health issues. However, Sade refused to let it define her or limit her dreams, including the pursuit of love.

One sunny afternoon, while at the local library, Sade met a boy named Chinedu. He was tall, had a warm smile, and his laughter was infectious. They struck up a conversation about their favorite books and soon found themselves talking about their dreams and aspirations. Sade had always been open about her condition, and she decided that honesty was the best policy.

“Chinedu,” she began hesitantly, “there’s something I need to tell you. I have sickle cell disease.”

Chinedu looked at her, his expression thoughtful. “Thank you for telling me, Sade. That doesn’t change how I feel about you.”

Their budding romance faced its share of challenges. There were days when Sade felt unwell, and their plans had to be canceled. Chinedu, however, was understanding and supportive. He would bring her ginger tea and tell her stories to make her laugh when the pain was at its worst.

Dating with sickle cell disease meant being mindful of her health. Sade took her medications diligently and made sure Chinedu was aware of the signs of a crisis. Together, they researched and learned how to manage the disease better. Chinedu was always by her side, attending doctor’s appointments and understanding the importance of hydration and rest.

As their relationship deepened, Chinedu and Sade faced another significant milestone – discussing the possibility of a future together. Sade knew that there were higher risks associated with pregnancy for women with sickle cell disease. With a heavy heart, she brought up the topic.

Chinedu listened attentively and then said, “Sade, I love you, and I want a future with you. We can explore adoption or other options. What matters most is that we’re together.”

Their love story continued to flourish. Sade and Chinedu navigated the ups and downs of life in Lagos, supporting each other’s dreams, and building a life together that was filled with love and understanding. Sade’s sickle cell disease was a part of her life, but it did not define her, nor did it limit her capacity to love and be loved.

Their story served as a reminder that love could conquer all obstacles, including the challenges of living with a chronic illness like sickle cell disease, and that true love embraced the person, not just their condition. Sade and Chinedu were living proof that in the colorful tapestry of life, love could be the brightest and most enduring thread of all.

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Kofi’s Story

In a vibrant village in Ghana, lived a young boy named Kofi. Kofi was a bright and determined child, but he faced a unique challenge in his life – he had sickle cell disease. This genetic condition caused his red blood cells to change shape and block blood flow in his body, leading to painful episodes and making him prone to fatigue. However, Kofi was determined to pursue his dreams despite his health condition.

One of Kofi’s biggest challenges was getting to school. Every morning, he woke up with the sun, ready to embark on his journey to the village school. Ghana’s public transport system was a mix of colorful minibusses, crowded tro-tros, and the occasional rickety bicycle. For most children, this daily commute was an adventure, but for Kofi, it was a daunting task.

Kofi’s village was nestled deep in the heart of the Ghanaian countryside, and the nearest school was several miles away. He would begin his journey by walking through narrow dirt paths, surrounded by lush greenery and the sounds of singing birds. He loved these moments of tranquility, but he knew the real challenge lay ahead.

To reach the tro-tro stop, Kofi had to cross a rocky stream, which, during the rainy season, would swell into a rushing river. On more than one occasion, Kofi had slipped and fallen in the water, getting soaked and exacerbating his condition. But he was resilient. He’d learned to use a sturdy stick as a makeshift cane, which helped him navigate the treacherous waters.

Once he reached the tro-tro stop, he had to contend with the notorious unpredictability of public transport in Ghana. The tro-tro drivers were known for their erratic schedules, and sometimes Kofi would wait for hours. On such days, he’d sit under the shade of a large baobab tree and use the time to study his school books, determined not to let the delays affect his education.

When he finally boarded the tro-tro, he’d find a seat by the window to catch the cool breeze. Kofi often felt self-conscious about his condition, but he never let it deter him from his dreams. He knew he couldn’t control the hand he’d been dealt, but he could control how he played it.

At school, Kofi’s classmates and teachers admired his determination. They helped him when he needed it, and he, in turn, became known for his resilience and positive spirit. He excelled academically, proving that nothing could stand in the way of a determined mind.

Despite the daily challenges of living with sickle cell disease and the difficulties of public transport in rural Ghana, Kofi continued to pursue his education with unwavering determination. He knew that education was his ticket to a brighter future, not just for himself but for his family and his village. And so, every day, with a smile on his face, he embarked on his journey, reminding everyone that even in the face of adversity, one could achieve greatness with the right attitude and a little help from friends and family.

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