Saturday, June 1, 2013

My Advice #7 & #8

More Advice (cont.)

#7: Your real friends will shave their heads to show support – I had two people in my life who shaved their head after I lost my hair to cancer.  My husband shaved his head, but he’s bald and has shaved his head for as long as I’ve known him.  My friend Lisa also shaved her head, but she has breast cancer too.  You know what?  Never mind.  Disregard this advice.

#7 Redo: Get used to being confused/chemo brain – Let it be known that your brain will not function properly for a while (I’m hoping it’s temporary.)  It will be most noticeable when you are out with people and you’re trying to talk and do things.  I’m not talking about anything difficult either.  I’m talking about real simple things like putting your shoes on the correct feet, remembering what year it is, opening a door “correctly” (push? pull? slide? automatic? You never even realized there were so many types of doors.  I have stood in front of a door for much longer than I should have before realizing it was not an automatic door), etc.

#8: Don’t worry about taking my advice – everyone handles cancer differently.  Whether you choose to keep your diagnosis, feelings, and experience private or put it all out there for anyone with an internet connection to access, you have to do what’s right for you.  My experience with surgeries, chemo, radiation, and doctor’s might be completely different than yours even with the exact same diagnosis.  So that’s my last piece of advice…you don’t have to listen to me if it’s not right for you.  Good luck!

Looking on the Bright Side…I should also include on my list to try and look on the bright side.  There will be many dark days ahead but try to find something to smile about. 

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