Some worry they will be treated differently if they tell their friends or family they have Sickle Cell. Others fear their friends will “feel sorry” for them or be afraid to be around them. Being open and honest with loved ones is the key to preventing this from happening. Communicate with people about your illness in a patient and polite manner. Help them understand how Sickle Cell impacts your life. This will resolve any concerns they may have. Take heart. Be courageous enough to be upfront with people to ensure any fears you may have don’t become reality.
I can honestly say that I’ve never had anybody treat me differently after they learned I live with Sickle Cell Disease. Typically, people want to know more about the illness and are curious how it impacts my daily life. Mostly, they are amazed at the things I endure and how well I cope with it.
This blog is intended to help people of all ages cope with many of the challenges that come with Sickle Cell Disease. When first launched, my target audience was teens and parents. Over the years, however, the scope of my content has expanded to help people of all ages who may struggle with similar complications as I. Whether you’re reading this for yourself or to help a loved one cope with Sickle Cell, I believe there is something here for everybody affected by this disease and other illnesses.
- Home
- About Me
- Dedication
- Introduction
- Contents of Topic 1
- Contents of Topics 2-5
- Contents of Topic 6
- Contents of Topics 7-9
- Contents of Topics 10-13
- Contents of Topics 14-16
- Contents of Topics 17-19
- Coping with Sickle Cell
- Health and Nutrition
- Leg Ulcers - My Experiences
- Leg Ulcers - Treatments
- More on Meditation
- My Artwork
- My Hip Problems
- My Music
- My Poetry
- My Sushi
- Red Light Therapy
- Thoughts / Experiences
No comments:
Post a Comment