My Medications ... Oh Boy!

I had lost my mother the summer before and didn't have the guidance she would always provide.  I was on my own.  My friends have been a great support system when needed, but I am making major decisions on the fly since the hospitals.  I do my research as well.

I depend on my healthcare professionals to provide the best options for my course of treatment.  Taking Tamoxifen twice daily, plus Zometa treatments monthly to help strengthen my bones and just recently Falsodex (another anti-hormonal drug).  I can remember speaking to an American Cancer Society representative and asked about Zometa.  He gave me a long list of side effects.  I was in for monthly blood draws one week to keep an eye on my kidneys, plus IV infusions the next week.  Blood draws are difficult for me because my veins seem to hide and are deep, sometimes requiring multiple sticks.

Generally, after receiving my Zometa treatment, it drains me for a few days.  But my last treatment along with Falsodex (injections to right and left hips) left me hurting in my hips greater than usual.  I think the doctor hit my bone or possibly a nerve, limiting my ability to walk.  It took a week for me to feel my usual self.

I am walking with a cane these days for short distances and looking forward to warmer pool weather here in Florida for water exercises.  At the turn of 2015, it's a new health insurance year with ObamaCare.   Changing from an HMO to a PPO is the best thing I did for my healthcare.  Thankful that pre-existing conditions were eliminated, I know have an affordable plan.  It is certainly better than not having insurance, learned that the hard way.

March will be my 1st year anniversary of breast cancer and on Tamoxifen.  I still feel the lump in my right breast and will be going for a mammogram.  My Oncologist is suggesting possible radiation treatments based on my results.

I have a GoFundMe page for donations to help with my medical bills.  Your generosity is humbling and appreciated.

Be genuine, share yourself and have a fabulous day!  Susan (aka SuzzzyGal)