|I dedicate this sunset photo to Hamada|
who, according to Susie, loved them.
It is also a horrible reminder that without aggressive and skilled medical intervention, this disease will show no mercy and will steal life long before that life should have ended. There was a notice on one of the MM sites that some people in the UK are putting forth an extra effort to educate the medical community about the symptoms of Multiple Myeloma since it is often mis-diagnosed, losing valuable time for the disease to gain a stronger position.
Reading other blogs often provides links to new information or theories which may bear fruit, for example "Riding the Wave" or "Margaret's Corner." I would not want to forget Phil Brabb's blog, MM for Dummies, and the efforts to fund-raise with Cancer Kickers, providing an inexpensive way to bring MM more into the public eye.
Education is something that should be happening world-wide since it appears that more and more individuals are facing this fight and at younger years (in MM for Dummies this week there is a story of a young woman in her 30's). I know I will continue to do what I can to educate those I meet about it, encouraging people to be more proactive in their discussions with their doctors and more than that, pushing them to eat healthier, more natural foods. I have also tried to get the message to President Obama that the government Veteran's Administration has not demonstrated compassionate care for our vets and in the U.S. there is a huge population of veterans suffering from MM.
This is no consolation for the wife of a man who loved her and who was well loved in return - nor will it bring him back. But perhaps those who are about to be diagnosed with MM or those who have recently been discovered to have it will take time to read the various blogs and make some educated decisions about their treatment so they can have a better chance at the remission that is sought after.