May 23, 2016

Still slow

The anti seizure meds still make me feel slow. I hardly have energy to shower and dress so spend several days in my pajamas in a row if I don't have to go out. Dr G may have something to recommend to me re chemo. He doesn't want me to take a break although that's what that's what the past two weeks have given me (without more energy).

No more to say now.


  1. Hugs! Hang in there!

  2. Ick. I am curious what you are in, probably stronger than the Zometa I take (makes me forget words). Have you looked at energy meds? I have to take them in days I am super active and need to be productive.

  3. Anonymous11:30 AM

    Hi Mandi,
    I follow your blog also. I have stage 4 bone mets (it's been a year now). What "energy meds" do you take? Many prayers, Sue

  4. I was dx Sept 2003 with stage IV bc de novo (no prior bc dx). It's a long road and you are just a bit ahead of me. If I didn't have to walk my dog 3 times a day I would be staying in too. The lack of energy is so frustrating. In my case I think people look at me and think but you still look good. So hard to explain. I want to be comforted. Maybe you do too...can you ask your support system for that? So hard to ask. May this post comfort you! Accompanied by virtual hugs. I hope things improve for you. {{{hugs}}}