It has been far too long between posts and for those of you who have written emails of concern for the silence, let there be Joy! I have not written because I have been so busy learning about the biophoton light therapy which is why I am doing so well.  I am not just doing well, I am doing great!  Color is back in my cheeks, I have gaine

Little Bird, Enjoying listening to this beautiful music...Praying for you an encouraging new year...Was recently telling someone the story about your eating my plate of tripe when we were guests at the mayor's home in that tiny Pakistan village. When I had told you I couldn't eat it, after said "I had too," you got me to divert the other's attenti

I have myelofibrosis with JAK2 mutation (JAK2 gene missing).  Because of this, I was afraid the drug Jakafi (a JAK2 inhibitor) would not be effective in reducing the symptoms of myelofibrosis.  I called Incyte, the company manufacturing Jakafi, and was informed the drug is for all patients with myelofibrosis, with and without JAK2 mutatio

Well, the photo below says it all! I am feeling great. Great enough to compete at The Nationals tennis competition in Palm Springs last week with my wonderful team.  I felt well enough to play 2  consecutive days in over 100 degree heat and have two third set super tiebreaks!  Normally I don't brag, here ...I'll brag!   My energ

Medical Update. A joyous one! I had my UCSF appointment 10/27 and it was a “remarkable one” There is a bit of nervousness always as things for 5 months have only been rising (cell counts) and increasing in size - (spleen and liver) and increasing discomfort. However on my appointment before this one my cell count had dropped from 26,000 to 23,000

How I’m Feeling/ What I’m doing – OCTOBER 3 I feel great, lots of energy, eyes clear skin color good and feeling very positive. The problems I am experiencing are my spleen and liver are uncomfortable but perhaps feeling less so and the abdominal swelling seems not as much. Here is the latest in my healing “adventure.” This phase began on the Isl

How and What I am doing. September 24 - Treatments. I’ll speak to how I am doing first. I feel fine actually, just tired earlier at night, so I ‘m getting a lot of great reading done, especially under the Rife machine. My spleen is large and so is my liver, and my abdomen is somewhat distended and quite uncomfortable. However it is not as bad as

Re: "new" diagnosis CMML based upon review of slides and bone marrow study and recent blood work. I don't know enough yet about the current new diagnosis to write a medical update  - CMML - Not to be confused with CML.  For a bit more see the latest post - How Am I Doing - Non Medical. That will update anyone interested in how I am feeli

I haven't written for a while as I have been exploring a very exciting new path of Bio-energetic medicine, and have been waiting until I have the time to write all about it. I have great hope for this physics meets medicine way.  However in that waiting to write all about it, I have been given another diagnosis that is rather disturbing. This

How Am I doing - New York light treatment! I am excited, I am going to New York to get 2 light treatments, (light frequency treatments) similar to the Rife Light principle.  The gentleman who is providing this is 11 years cancer free from bladder and urethra Cancer.  Doctors said they "Had" to operate to save his life, then he would be l