This past October marked by 13th "official" year with myeloma. I had plenty of back pain prior to 1996, so I have been carrying this around for at least two years before diagnosis. Finally, the right doctors brought me on the right path, and they are still with me. However, we have to expect this disease to make its progression, and I have experienced some uncomfortable changes. I seem to pick up colds and laryngitis very frequently. Because I have been a broadcaster and TV weather anchor, this is turning into a problem which could lead to my "on air" retirement. I will turn 65 this year, so maybe it is time, but I still feel, as long as I don't embarass anyone, my presence gives hope to others, and that is exactly what these pages are about. I am hopeful to become part of a patient to patient program where old veterans like myself  can help newly diagnosed patients overcome the anxiety and fear of myeloma.

 There is more reason for hope now than ever before. The targeted treatments are working well...and it all started with Thalidomide, and then advanced into newer medications. The old rules still apply. Find a cancer center that has a specialty in this disease, experience needed. I can help you with that. Also beware of interractions with these drugs. There are many, worthy of a column in itself.

Sure there are serious side effects, but we can navigate around them. If Beethoven could write symphonies while deaf, I can play my piano with neuropathy. I walk two miles each day, then go off to work, even with a heavy dose of Immodium. Revlimid and antibiotics do some number on your gastro system, but it all diminishes and I pray each day for one more. If I had 10,000 more days, I would still pray for another. Who can ever have enough life?

So, keep up with the latest developments, especially from this year's ASH meeting. New doors continue to be opened.