Hi Marcie, it's greenie.  The bar of soap does work, one  thing I might add 
is to each time the soap you take a bath or shower starts to  get to small 
to use exchange the one between the sheets with a new one and you  the old 
one that you were using for the cramps.
 
 
In a message dated 3/10/2013 3:30:00 P.M. Eastern Daylight Time,  
margoo...@aol.com writes:

I was diagnosed March '09 and  put on 400 mg.  One year later, it was 
bumped to 600 which is where I  still stand.  Regretfully, the bone pain and 
charlie horses are part of  the package.  My doctor said it was OK for me to 
try 
salonpas, pain  patches, and they have been helpful for my back, hip and 
knees.  You can  find them in Walgreens and most stores.  The ones I'm 
referring to are  the small patches that come in a 40 count box.
 
As to the charlie horses, I sleep with a bar of Dial soap between my  
bottom and top sheets.  I thought it was an old wives' tale when someone  
suggested it but for 4 years, I have yet to wake up with those awful  cramps.  
I 
still get them other times and they are painful.  You  will find on this site 
really positive, warm and caring people, many who have  been living with CML 
far longer than I.  A positive attitude is so key to  good results.  We 
have an illness that now has numerous drug therapies  and many, many people 
have outlived their original diagnosis by a very long  time.
 
As a new member of a group none of us would have wished to join, I  welcome 
you and please feel free to post any time you have a question.   Some of 
the best advice you will get is here and without question, the  friendship, 
support and love the fellow CML warriors give is priceless.
 
Best wishes to you as you continue on the journey.
 
Marcie
Baltimore


-----Original  Message-----
From: mylissal <mylis...@yahoo.ca>
To: cmlhope  <cmlhope@googlegroups.com>
Sent: Sun, Mar 10, 2013 10:37  am
Subject: [CMLHope] Newly diagnosed with CML


I was diagnosed with CML in Oct 2012.  It was funny, I thought what  I was 
feeling was stress related due to my job and/or perhaps early onset of  the 
change of life.  Symptoms were extreme fatigue, waking up tired after  a 
full nights sleep, night sweats and fever, weight loss and discomfort when  
sitting.  Finally went to a doctor and asked them to check my  hormone levels 
and do a complete physical.  Dr sent me for an ultra sound  too because of a 
hard lump in my side.  Turns out my spleen was twice the  size it should 
have been and my blood test came back with really high white  cells, low red 
cells and high platelets.  Dr referred me to an  Oncologist who has put me on 
Gleevec.  Today, my white cells are  within normal, my red cells are still a 
little low and my platelets remain  higher than they should be.  Had to go 
on a disability leave from work  due to the pain from trying to sit - from 
the enlarged spleen and joint  pain.  Have been off work since late Nov 2012. 
 I currently have  been experiencing pain in my hip and knee joints, as 
well as excruciating pain  in my shin bones.  Is this normal?  Is it the 
Gleevec causing  it, or the leukemia?
 
Also having really weird muscle cramps - charlie horses in my legs that  
hurt bad enough to make me cry and cramping in my fingers and toes.   Feels 
like my hands and feet will never be warm again....am really looking  forward 
to summer.  Anyone else experiencing this?
 
The Oncologist says I might have to try a different drug which is  scaring 
me, as Gleevec has brought down my white counts...what if nothing else  
works?  Has anyone found anything that relieves the pain?  I've  tried A535 and 
hot baths, heating pads etc  Have been told I can't take  aspirin, tylenol 
or advil as they interact with Gleevec.  GP recommended  trying massage 
therapy, but when certain spots on my knees and legs are  touched I can't bear 
it.  Would be really interested to hear if anyone  else has found something 
that helps.... 

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