Living Archives - Page 3 of 5 - Sickle Cell Warriors Inc

Brrrr! Bundle Up Warriors!

Its cold, freezing, and snowing in most parts of the United States and North America right now. Here are some tips to keep you from going into crisis.

It’s so easy to sit back, complain, and expect things to change, but if we are not a part of the change, solution, and activism; then we are a part of the problem. Tamera eloquently addresses several issues plaguing the sickle cell community.

Sickle Cell Scholarships

Wondering about scholarships for sickle cell patients? SC Mom Kristina did the research for you. Click here for a list of active scholarships for sickle cell students.

Constipation and Sickle Cell

Pain meds can lead to constipation. Keep your bowels running smoothly with a few tips from other warriors just like you.

1st Annual Sickle Cell Warriors Cruise

Have you ever wanted to get together with a group of Sickle Cell Warriors, your family, and friends on a vacation where you got to share your life experiences? Well then, this cruise is specifically designed just for you.

Sickle Cell and Tattoos

Ever thought of getting a tattoo but sickle cell has you a tad worried about it? Well then, this one is for you.

Making the Team

Tamara details the importance of screening all members of your healthcare team— especially your doctors. Tryouts and Probation is mandatory, not optional.

From the Heart of a Warriors’ Caregiver

Tamara is an independent, strong, beautiful woman who is head over heels and happily married to her own true Sickle cell warrior. Read about her journey from a wide-eyed novice to his staunchest advocate and expert at the bedside.