Sunday, September 23, 2012

9/23/12 Sharing My Note from a dear friend pr

This is from a dear friend, whom I have been through "thick and thin".  She knows me well and accepts all my "foibles"...as I do hers.

Hi Sis,

I don't ever write until I catch up on your blog, a joy to read. What do I like most? I love how you push through pain to do that exercise. Not so many would. They could, but it is the would. Why do you push? It is just you, a vital beat in your mind and heart that just won't sit and quit. Lots do sit and don't exercise. I love them too and understand, but I treasure a older people who push on as you do.

Muriel...I cheer you on..Hugs,phyllis05/06/1933     www.women70andover.com

9/23/12 One Two Three? pr


One! Two Three!  You’re out!  Not baseball.  This is the other side of Cancer Radiation of the breast!  What do I mean by that?  My Radiation treatments have taken a turn for the better.  These treatments now consist of the metal block with the special made glass insert with a slant opening in it, just made for my No Boob area.  This is the area across my once breast where the incision now is.  This area is a vulnerable left over of the surgery.  This is the area where the cancer can come back, grow, and show its ugly face.  The block is especially designed for the size of my No Boob area.  The radiation at this point just beams to that part of the No Boob area.  Time wise the time involved is termed “QUICK” I termed it that!  Perhaps it takes a matter of a fast few minutes!  A pleasure.  This is all put in place as all of the Radiation Treatments are for me by Dr. Charles Hechtman, MD/PhD and the large team of doctors and techs of the Radiation Department.  Ms Bernie Boyd and Mariah Millard have been my major techs that I see for most of my treatments.  They are each skilled in their calculations and placement of me on the table.  They have spent many years in school for this procedure.  Most techs in radiation go to school for as many as six years.  They are on their feet all day long running from the radiation room to the patient, getting the table set up for each patient with the patients special made body form on the table and a sheet and roll foam for their legs and a sheet to cover up with, just like a bed.  They want each person to be as comfortable as can be.  They are most kind as they prepare you in the awkward position.  To each of them and Dr. Charles Hechtman MD/PhD I say thank-you, which is very trite.  I say you are all Dear’s for taking the time to come to work on rainy days, for staying until 9 p.m. when needed.  I say I will never forget each of you for being so special and caring and not mentioning it when you got close to my face when I was on the table to see the tears that were sometimes just under my eyelids.  I always wondered if you did see them as you patted my arms when you came in to draw on my No Boob area for your calculations.  You all have added to my quality of life.  You have made me stronger.  If you could hear me, I would say “Whooooo Hooooo!” Thank-you to each of you all wrapped in kindness from me to you  I am glad I choose Halifax Hospital, right here in Daytona Beach, Fl  to lead me on my  Cancer Journey to Wellness I am a lucky duck  at seventy-nine!  Hugs,phyllis 05/06/1933     www.women70andover.com

 

Saturday, September 22, 2012

9/22/12 Good OR Bad? pr


Arimidex (Arimidex 1mg)  I take one pill daily.

This is the medicine I take to prevent the cancer tumors reoccurring in my body. I will be on this medicine for five years. The side effects I have are:

Arthritis, headaches, hot flushes, joint pain and stiffness, bone pain, loss of sleep. Thank heaven these are my only side effects.  I have learned to live with them with style and grace!  When I have joint pain ect. I say, “Phyllis, just walk like you do not hurt! I do and I am able to walk the pain away, like it never bothered me.”  (until the next time!) Trust me!  I know I am very lucky.  I could be sitting in a Chemo chair with I.V. medicene dripping in me, instead I have quality of life.  Walking daily, full of energy, time to volunteer at the Chemo center at Halifax Hospital in Ormond and Daytona Beach, write my blog, draw, bake and cook, read, do research of my writings, enjoy movies and my kind husband, my support center and friends and family and the heavens above.  For me that’s a lot to be thankful for and I think a lot of things are funny, cancer not being one of them, instead my dog Annie makes me laugh and Woody Allan and most of all I laugh at myself! Hugs, phyllis 05/06/1933   www.women70andover.com comments? Send to phyllisreh@aol.com

Side effects

Information specific to: Arimidex 1mg tablets when used in Breast cancers.
Side-effects
A medicine is only made available to the public if the clinical trials have shown that the benefits of taking the medicine outweigh the risks.
Some side-effects may be serious while others may only be a mild inconvenience.
Everyone's reaction to a medicine is different. It is difficult to predict which side-effects you will have from taking a particular medicine, or whether you will have any side-effects at all. The important thing is to tell your prescriber or pharmacist if you are having problems with your medicine.
Very common: More than 1 in 10 people who take Arimidex
  • arthritis
  • headaches
  • hot flushes
  • joint pain or stiffness
  • nausea
  • osteoporosis
  • skin rash or rashes
  • weakness
Common: More than 1 in 100 people who take Arimidex
  • abnormal laboratory test results
  • allergic reactions
  • bone pain
  • carpal tunnel syndrome
  • diarrhoea
  • hair loss
  • high levels of cholesterol in the blood
  • loss of appetite
  • sleepiness
  • vaginal bleeding - seek medical advice if bleeding is persistent
  • vaginal dryness
  • vomiting
Uncommon: More than 1 in 1000 people who take Arimidex
  • liver problems
  • trigger finger
  • urticaria

 

Friday, September 21, 2012

9/21/12 Good Omen? pf

Most everyone has omens of one sort or another.  The day started with Annie, our dog throwing up at 4:30 a.m.  I got up tended to her, calmed her down.  I started the wash machine, took a shower and started the morning with an early a.m. walk.  Left the house at 7 a.m. for my early radiation treatment.  While checking in at the Hospital desk, where I flash my ID card I noticed I also had another appointment in the oncology section across town, so I called Bill and said I would pick him up so he would not feel stuck at home.  All seemed good at that point?  Did I say good?  Soon I was called in for my radiation treatment, got up on the table.  I did my arms up routine and laid there still.  The techs moved me around for the correct reading.  The machine started.  I settled in.  The techs came rushing in.  “The arms of the machine, that take the pictures of me stopped.”  Panic!  “Just do not move”, “We will get things back on track.”  I was so pleased when they cranked the radiation machine back in tune!  Real life gets in the way! Hugs,phyllis 05/06/1933    www.women70andover.com

Thursday, September 20, 2012

9/20/2012 Happy New Year! A time to reflect. pr

This is our Jewish New Year.  A time to reflect!  A time to forgive.  Especially ourselves.  A time for calm.  This is the core of most religions.  For me it is a goal I think of each day and try to do.  I do fail and can humbly be better or try.  I will put that into effect this morning, as I will soon leave for my radiation treatment.  I will lay very still on the table and tell myself calming things.  I will feel the burn that has been left on my chest from past radiation treatments.  I will do good.  I will.  I will. Hugs, phyllis 05/06/1933     www.women70andover.com

Wednesday, September 19, 2012

1/19/12 Your Health Foundation pr


We are the foundations of our own health!  What do I mean by that?  Walk.  Why?  This can be used as a self-gage for you.  How?  If you walk one mile daily, or the same amount everyday at whatever pace you decide then the next day the object is to do the same thing.  Easy you say!  Yes it can be.  On the other hand, your body can also talk to you and say I just cannot do that.  I want to only walk for five minutes.  This is how your body tries to communicate with you.  For the health of it, I encourage you to find your own body gage.  Why?  You must build up some resistance for your body to when major medical events hit you, you will be able to fight back and be stronger than the average non-walker.  I meet a woman last evening at a function.  She had reason to be upset.  At the end of the month, she will have a shunt put in her arm, for dialysis.  She is a dietetic.  She has had open-heart surgery in the past.  She never had a walking program.  Yes, what works for one person does not work for you next you say.  This could be.  On the other hand, you have not put out great amounts of money to find out.  You have not put out great amounts of time to help yourself.  I feel my daily walking is my gage.  Before I was diagnosed with Cancer, I noticed I would tire when I walked.  My legs would hurt.  These were all signs of something is wrong.  Did I act on it and run to the doctor.  NO!  My humanness got in the way, or my stupidity!  My walking has helped me on my journey for recovery from my mastectomy. Enough! Hugs, phyllis 05/06/1933   www.women70andover.com

Tuesday, September 18, 2012

9/18/12 SUGAR HIGH?? pr


Here is the SUGAR HIGH out again and again!  In a large nutshell: in 1966, we ate 113 lbs of sugar.  The last count in 2010 is 132 lbs of sugar.  From 1960, the amount of obese people was 12.8% and in 2010, the amount almost tripled to 35%.  This is not because we are all bad!  It is because there is so much added sugar in foods we think are safe.  We do not thing of all the sugars in coleslaw, low-fat yogurt with fruit, 2 tablespoons of jam or preserves one cup of tomato sauce, even two tablespoons of ketchup.  Perhaps the best thing to do is keep a daily sugar diary or journal.  In plain English, just write it down for your own knowledge and see how you can go from your new knowledge of your sugar high to your well high. Gee! I am going to start that today! Hugs,phyllis 05/06/1933       www.women70andover.com