When Dealing with Illness; Knowledge is Key!
Looking back two and a half years, I can still remember
hearing the words, “You have leukemia.” And the number one thing that comes
back to me now, was me thinking, “Crap, I don’t know a thing about leukemia.”
Well, let me tell you, I now know a TON about leukemia,
particularly chronic myelogenous leukemia, also known as CML, and I truly
believe that no matter what illness or condition that you may face; knowledge, about that subject is the
key.
Every single day, new people join our CML boards and groups;
more and more people are living with CML. Our numbers are rising at a rate of
about 6,000 new cases per year. I recently read that there are an estimated 44,000
people, living with CML.
This shocks me; it feels as though we are a drop in the
bucket!
However, since people are now LIVING with CML, and more
and more are being diagnosed daily; this number will continue to grow. It has
really only been during the past twelve-ish years, that people, who are diagnosed
with this type of leukemia, are no longer issued a death sentence; we now will
be given the chance to live, to share our knowledge and hope for a cure.
Anyway, back to my main topic; Knowledge is Strength. Here are some links to help newly diagnosed
CML patients learn the ropes! Many of these suggestions will be helpful to others,
as well.
- Signs
and Symptoms of Leukemia
- Tips
for a More Comfortable Hospital Stay
- When
Choosing a Doctor; Choose Wisely
- Understanding
CML
- Sprycel
vs Tasigna vs Gleevec: In My Words
- So,
Just What is a Philadelphia Chromosome?
- Treatment
of CML
- Living
with CML
- CML;
Measuring It’s Response
- Measuring
It’s Response Part 2
- CML:
Finding Information
- CML;
The First Phase Chronic
- CML;
The Second Phase; Accelerated
- CML;
The Third Phase: Blast Crisis
- Important
Questions for CML Patients
- One
Thing that All Cancer Patients Have in Common
- Sprycel;
Financial Help
- Patients
vs Medical Professionals: Do Your Homework!
- Be
Your Own Self Advocate
- Questions
You May Not Have Though to Ask
These are some of the highlights and most important articles
on my blog; things that I wish I had had at my fingertips when I was diagnosed
with CML. I hope they are of some help, to you!
FaceBook: CML: A Place for Hope and Humor
Instagram: https://www.instagram.com/cmlmichele
Email: CMLMichele59@gmail.com
#chronicillness #bebrave #chronicmyelogenousleukemia #Bosulif #leukemia #lovemylife #cml #travellingwithcancer #hopesanddreams #cmlspecialist #specialist #thrivingwithleukemia #livingwithcancer
FaceBook: CML: A Place for Hope and Humor
Instagram: https://www.instagram.com/cmlmichele
Email: CMLMichele59@gmail.com
#chronicillness #bebrave #chronicmyelogenousleukemia #Bosulif #leukemia #lovemylife #cml #travellingwithcancer #hopesanddreams #cmlspecialist #specialist #thrivingwithleukemia #livingwithcancer
Really excellent work Michele. I would never have eligible because of Medicare but still this is invaluable to younger patients. Maybe a charitable foundation would help lower my co pay. Have to figure out if my insurance is paying too but I think they are so maybe not but all us older folk may need this help if Medicare is cut and insurance cuts too.
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