Bonnie's Journey

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Bonnie says

Posted by norrieds on July 6, 2012 at 9:20 PM

July 6, 2012

I wish I could see better, it was nice going out to eat but now I am really bored. I want to be able to clean and organize things again.

They are treating me like an invalid at the center but I think it's only temporary. They had be go to a wig shop but I have so much hair there doesn't seem like much point right now. The lady said to just wait. They also want me to get a scarf just in case but I have lots of nice scarves at home.

Huggs to Jaz, Thorny, LadiNitro, and DK. Thank you for taking the time to leave me a note. Wanted to let you know that the only pain I have is in my thigh and then only when I move. I think it will go away soon.

I will probably get more energy in time. It's probably the little green pill they give me that throws my sleep pattern off. I don't sleep at night or in the daytime either. I just lay down and zone out. The tireness just seems to take over and I have to lay down and I am gone for a bit. Like is not a series of work like most people it is like living in a series of moments.

We are planning to visit Steven's folks in upper Michigan in August after this set of treatments. My sister-in-law, Jill, is very anxious to see us and my brother-in-law's girl friend is anxious to meet us. The girl friend has brain cancer also and they have given her no hope.


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Reply Jo / Shads
11:36 PM on July 6, 2012 
Big Huggggz RR, I wanted to stop by to say Hello.
I have your blog saved in my bookmarks now, so I will be following along with you in your journey.
You are a very brave woman, and I know you are eager to carry on as always and not let this hold you back if you can help it.
I hope this next set of treatments moves along quickly and effectively so you are able to have a nice visit when you go to visit family.
Sending lots of positive thoughts your way!!!

aka Shads
Reply Terry Wigley aka Tessa
2:36 PM on July 7, 2012 
Hon I'm so sorry you are going through this. I can relate as I have stage 4 non hoskins lymphoma. Have been doing chem since 2009 so I know about your up and down days. If you ever want to talk just email me. Hang in there and stay positive above all else. Hugssssssssss
Reply Dixie
8:24 PM on July 8, 2012 
hugggs sweetie Im praying for you and your hubby. Sure hated to hear what you are having to go thru. Went thru that with my mom. Keep your spirit up girl, I know you are strong and will try your best to be strong, but hey, let them help you for a change, be pampered, Plz dont wear yourself down. You will need every strenght God gives you. Sometimes my mom would even walk faster then us, we actually had to run to keep Also just want you to know, not sure if it happened to Tessa, but my mom's feet after a few treatments started turning purple. They told her it was normal for some to have that. Wanted you to know so you wouldnt freak out. I love you and miss you so, both you and Norrie. Take care of yourself. My prayers are with you and yours. HUGH HUGGGGS