Friday, March 25, 2016

12 weeks after my 1st Radiation Therapy Treatment for my Ledderhose Disease (Dupuytren's Disease)

On the Monday starting the 12th week after my 1st radiation therapy, I am back in Tampa for my second session of RT with Lawrence Hochman, RO. http://floridacancer.com/physicians/lawrence-hochman-do-facro/   I am feeling none of the anxiousness I felt prior.  I know what to expect.  OR, I should say, I know to expect nothing.  That's a good thing!

I returned with some reservations about getting this second round of RT.  I felt I had enough pain relief that I really considered not having this second session.  It was explained to me that I needed it.  It was explained that round 1 was like taking 1/2 your dose of antibiotics and round 2 was finishing up the antibiotics.  The only reason I had such reservations is because I only get these two sessions of RT for life.  I was wondering if I should "save" this second session for the future if I needed it. Needless to say, I returned and I am so thankful months later that I did!http://www.dupuytrensdiseasesupport.com/


I completed my week of radiation therapy with nothing to report.  It takes appx 45 seconds per foot to administer the RT.  Dr. Hochman's team is an "on-time" group.  My appointment was at 9:30 am and at that time I was already in the room having my treatment and by 9:40 I am out the door.

The team took a look at my fibromas and felt them.  The large one is still there and can be seen and felt with a little less of a pointed stone on the top. The smaller ones are so small they are well under the skin.

I continue my RT-vacation with my water sock, keeping my foot out of the chlorine and sun.  We did take a kayak trip this time and did quiet a bit of vacation looking in Tarpon Springs, Weeki Watchi, Clearwater Beach and any other spot that looked interesting.  Who would want to miss this?
The water is crystal clear!   Image result for weeki wachee springs kayak trip

I cannot stress enough to you how I connected to the Facebook forum DART - Dupuytren's Advocates for Radiation Therapy.  It was this group that got me to where I am and I want to continue to be part of the Dupuytren's and Ledderhose Community and give back.  I wouldn't want anyone to suffer as I did with this disease.  If you do not belong to a Support Group, I strongly suggest you join us at: https://www.facebook.com/groups/1622748151282109/

Below is the DART logo you are looking for: