Where to Get a Free Pdf Copy of My Friend Jen: A Little Different Book
My Friend Jen: A Little Different Book Pdf
Have you ever wondered what it's like to have a friend who is a little different from you? Have you ever wanted to learn more about a condition that affects millions of people around the world? If so, you might want to check out My Friend Jen: A Little Different, a children's book that tells the story of Jen, a girl who has Sickle Cell Anaemia, a blood disorder that causes her pain and fatigue. In this article, we will give you a summary and a review of this book, as well as some FAQs about Sickle Cell Anaemia. We will also tell you how you can get a free pdf copy of this book online.
My Friend Jen: A Little Different Book Pdf
Introduction
My Friend Jen: A Little Different is a children's book written by Jenica Leah and illustrated by Aditya Permana. It was published in 2016 by Createspace Independent Publishing. It is the first in a series of books that aim to create better understanding and awareness of Sickle Cell Anaemia in a fun and informative way. The book is suitable for children aged 8 to 12 years old, but it can also be enjoyed by adults who want to learn more about this condition.
Sickle Cell Anaemia is a genetic disorder that affects the red blood cells, which carry oxygen around the body. People with this condition have red blood cells that are shaped like sickles or crescents, instead of round and flexible. This makes it harder for them to flow through the blood vessels, causing blockages, pain, infections, organ damage, and other complications. Sickle Cell Anaemia mainly affects people of African, Caribbean, Middle Eastern, Asian, or Mediterranean descent, but it can also affect people from other backgrounds.
The book is important because it helps to educate people about Sickle Cell Anaemia and how it affects people's lives. It also helps to reduce stigma and discrimination that people with this condition may face. It also encourages empathy and friendship among children who may have different experiences and challenges.
Summary of the book
The book is narrated by Jen's friend, who tells us a story about how they met and became friends. The friend does not have Sickle Cell Anaemia, but he learns a lot from Jen about her condition and how she copes with it.
The main characters in the book are:
Jen: A girl who has Sickle Cell Anaemia. She is brave, smart, kind, and fun-loving. She likes to play games, read books, watch movies, and do arts and crafts. She also likes to help others and raise awareness about her condition.
Jen's friend: A boy who does not have Sickle Cell Anaemia. He is curious, friendly, supportive, and loyal. He likes to hang out with Jen and learn new things from her. He also likes to help her when she needs it.
Jen's mom: A woman who takes care of Jen and loves her very much. She is patient, caring, attentive, and protective. She makes sure that Jen takes her medication, drinks enough water, eats healthy food, and rests when she needs to. She also takes her to the hospital when she has a crisis, which is a severe episode of pain caused by Sickle Cell Anaemia.
Jen's teacher: A woman who teaches Jen and her friend at school. She is understanding, respectful, flexible, and encouraging. She makes sure that Jen and her friend have a good learning environment and that they are not left behind or bullied by other students.
The main events and challenges in the book are:
Jen and her friend meet for the first time at school and become friends.
Jen tells her friend about her condition and explains what it means and how it affects her.
Jen and her friend play together, do homework together, and go to the park together.
Jen has a crisis at school and has to go to the hospital. Her friend worries about her and visits her with a gift.
Jen recovers from her crisis and returns to school. Her friend is happy to see her and they hug.
The main message and lessons in the book are:
People with Sickle Cell Anaemia are not different from other people. They have the same hopes, dreams, feelings, and interests as anyone else.
People with Sickle Cell Anaemia can do many things that other people can do, but they may need some adjustments or accommodations to stay well and comfortable.
People with Sickle Cell Anaemia need support and understanding from their family, friends, teachers, and others. They also need to take care of themselves and follow their doctor's advice.
People with Sickle Cell Anaemia are not alone. There are many people who have this condition or know someone who has it. There are also many organizations and resources that can help them.
People with Sickle Cell Anaemia can make a positive difference in the world by sharing their stories, raising awareness, and helping others.
Review of the book
My Friend Jen: A Little Different is a well-written and well-illustrated book that provides a realistic and positive portrayal of Sickle Cell Anaemia. The book has many strengths and few weaknesses.
The strengths of the book are:
The book is easy to read and understand. The language is simple, clear, and engaging. The sentences are short and concise. The vocabulary is appropriate for the age group.
The book is informative and accurate. The book explains what Sickle Cell Anaemia is, how it affects people's lives, and how people can cope with it. The book also provides some tips on how to stay well with Sickle Cell Anaemia, such as drinking enough water, taking medication, avoiding extreme temperatures, and getting enough rest.
The book is relatable and inspiring. The book shows how Jen and her friend have a normal friendship despite their differences. The book also shows how Jen faces her challenges with courage, optimism, and resilience. The book also shows how Jen's friend supports her with compassion, respect, and loyalty.
The book is colorful and attractive. The illustrations are bright, vivid, and expressive. They complement the text and enhance the mood of the story. They also capture the emotions and personalities of the characters.
The weaknesses of the book are:
The book is short and simple. The book only covers one aspect of Sickle Cell Anaemia, which is the pain crisis. The book does not mention other complications or treatments that people with this condition may experience or need. The book also does not explore other aspects of Jen's life, such as her hobbies, interests, goals, or challenges outside of school.
The book is idealistic and optimistic. The book portrays Jen as a happy and confident girl who has a supportive family, friend, teacher, and community. The book does not show any negative or realistic situations that people with Sickle Cell Anaemia may face, such as discrimination, isolation, depression, anxiety, or low self-esteem.
The target audience and age group of the book are children aged 8 to 12 years old who want to learn more about Sickle Cell Anaemia or who have this condition themselves or know someone who has it. The book can also be useful for adults who want to educate themselves or others about this condition.
The rating and recommendation of the book are 4 out of 5 stars. The book is a good introduction to Sickle Cell Anaemia for children who may not be familiar with it or who may have misconceptions about it. The book is also a good source of inspiration and empowerment for children who have this condition or who know Continuing the article: Conclusion
My Friend Jen: A Little Different is a valuable book that can help children and adults learn more about Sickle Cell Anaemia and how it affects people's lives. The book is written in a simple and engaging way, with colorful and expressive illustrations. The book also delivers a positive and empowering message about friendship, diversity, and resilience. The book is a great resource for anyone who wants to increase their knowledge and awareness of this condition, or who wants to support someone who has it.
If you are interested in reading this book, you can get a free pdf copy online by visiting the author's website: https://www.myfriendjen.co.uk/. You can also order a paperback copy from Amazon or other online retailers. You can also check out the second book in the series, My Friend Jen: The Check Up, which follows Jen and her friend as they go to the hospital for a routine check-up.
FAQs
Here are some frequently asked questions about Sickle Cell Anaemia:
What is Sickle Cell Anaemia?
Sickle Cell Anaemia is a genetic disorder that affects the red blood cells, which carry oxygen around the body. People with this condition have red blood cells that are shaped like sickles or crescents, instead of round and flexible. This makes it harder for them to flow through the blood vessels, causing blockages, pain, infections, organ damage, and other complications.
How common is Sickle Cell Anaemia?
Sickle Cell Anaemia is one of the most common inherited blood disorders in the world. It mainly affects people of African, Caribbean, Middle Eastern, Asian, or Mediterranean descent, but it can also affect people from other backgrounds. According to the World Health Organization (WHO), about 300,000 babies are born with Sickle Cell Anaemia each year, mostly in sub-Saharan Africa. About 5% of the world's population carries the gene for Sickle Cell Anaemia.
How can people with Sickle Cell Anaemia stay well?
People with Sickle Cell Anaemia need to take care of themselves and follow their doctor's advice to prevent or treat complications. Some of the things they can do are:
Take medication as prescribed, such as antibiotics, painkillers, hydroxyurea, or blood transfusions.
Drink plenty of water and avoid dehydration.
Eat a balanced diet and take folic acid supplements.
Avoid extreme temperatures and high altitudes.
Get regular check-ups and vaccinations.
Avoid smoking, alcohol, and drugs.
Manage stress and emotions.
Seek help when needed.
Where can people get more information and support about Sickle Cell Anaemia?
People with Sickle Cell Anaemia can get more information and support from various sources, such as:
Their health care providers, such as doctors, nurses, pharmacists, or counsellors.
Their family members, friends, teachers, or co-workers.
Their local or national sickle cell organizations or associations.
Their online communities or forums for people with sickle cell disease.
Their books, magazines, websites, podcasts, or videos about sickle cell disease.
How can people help raise awareness and funds for Sickle Cell Anaemia?
People can help raise awareness and funds for Sickle Cell Anaemia by doing various activities, such as:
Sharing their stories or experiences with sickle cell disease on social media or other platforms.
Wearing red ribbons or clothing on World Sickle Cell Day (June 19) or other occasions.
Organizing or participating in events or campaigns that promote sickle cell awareness or education.
Donating or fundraising for sickle cell research or services.
Volunteering or advocating for sickle cell causes or policies.
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