Feeling Great

I have had 2 great days. Two days without any ‘anti’ drugs! Ian and I popped out to the shops yesterday and had a lovely lunch outside in sunny Durbanville. Spent the afternoon covering books! Today has been great too, I am still a little bit nauseas, my bones are feeling much better and I have more energy. The only thing that frustrates me is my ‘chemo head’. I know what I want to say and as I start talking I forget some of the words – drives me mad!!! My meditation group have all been asking for us to get together again, which we have not done since Sept last year. I have suggested we do a group meditation this Thursday for one hour… will let you know how it goes!

Schedule 1 completed

My aunt Hennie popped around Sunday to say goodbye as they head back to Singapore after a Christmas break with their children and grandchild. Her son-in-law lost his dad over the week-end due to lung cancer, which was diagnosed 20 weeks ago. Cancer can progress so quickly. Monday I completed my last round of chemo in this session. The operation is set for Monday 11 Feb, late in the afternoon. I still need to get medical approval for the operation and will do this next week, once I feel a bit better. Post the histology of all that will be removed from my abdomen, the next steps will be agreed, but I am preparing myself for another 2 to 3 rounds of chemo as per the original chats with the Docs. The boys went back to school today and I love the ‘normal’ routine. For the first time in my life and their lives I have been a full time mom and a sick one in that. It has been quite a learning experience for all 3 of us. I am experiencing the normal cycle of nausea and the bones are starting to ache along with a dumbness is my fingers.

Chemo Round 4 now on track

Thursday I woke up feeling like a truck had run over me. I had a huge headache and my body was numb. Worse than any hangover that I have had in a long time. After a few paracetamols and an easy day, I felt much better by the evening.
Went for blood tests this morning and the chemo practice phone me around 11 to say that my blood counts are normal and chemo will happen on Monday. We have an easy week-end planned – the norm for the past few months. (Quite boring for most folks).

Neutrophil generators

After 5 phone calls to the oncology unit, I finally got a call back after 14h00 to inform me that the medical aid has approved the injection. Madness really when you think about the time and effort that has gone into processing the approval vs the administration which took seconds! This magic potion is going to kick my bone marrow into action and get them generating cells! And the side effect is sore bones…. Argh again… Chemo causes sore bones and this too!! We are keeping to the schedule of blood test Friday morning and chemo Monday 14th.

I am expecting Dylan home this afternoon, he has spent a week away with friends camping and hiking in the Cederberg. After the initial homecoming I am sure he will be heading straight for the shower and then bed. I missed the bugger. I must thank the parents who took both Dylan and Sean for a holiday during this school break. Really appreciate it!!

Chemo Round 4 rescheduled again

All the emotional preparation for Thursday’s chemo session is again for nothing. The medical aid has as yet not approved the special ‘neutrogen’ that I need (Neutrophils are the white immune fighting cells). This afternoon’s conversation with the chemo practice has now changed the dates again. Assuming I get the generators tomorrow morning, it will only be possible to check my blood late Thursday or early Friday morning, so this has moved chemo to Monday 14 Jan. In the meantime I have been doing lots of resting but still feel permanently tired.

Chemo Round 4 rescheduled

This morning I went for the routine blood tests that are done before chemo to check that the body has recovered enough to allow the next round of chemo to occur. Around lunch time the oncology practice phoned me to say that my white blood cells are way too low for chemo to occur on Monday. Effectively it is my immune fighters that are way below normal. Explains why I have been feeling tired and I was even having a little ‘rest’ when the practice phoned. The oncology nurse reiterated that I must take it easy, must have my rests and keep visitors to a minimum! Nobody with any form of sniffle, cough, temperature, etc may come close to me and crowded places are a no-go zone. Sigh. By this afternoon I had learnt that I need a special once off dosage of white cell generators but this takes 48 hours for the medical aid to approve. The plan is that I get this at the chemo room on Tuesday, more blood tests Wednesday morning and chemo planned for Thurs 10 Jan.

2008 01 02 Welcome 2008

The new me.... (my eyebrows are now finally giving up on me too)

The festive season is behind us and the whole world is focussed on a new year in personal, work and education. The shops are still buzzing but now it is the ‘back to school’ gear for us here in SA. Christmas week was a good week for me. Christmas eve we had a brother in law and brother around and Christmas we lunched with my family at my Dad’s place. I even had a little pony ride Christmas afternoon. All went well until Sunday when I got hit by a terrible tummy bug. Spent most of Sunday evening and night with the face looking down the porcelain pot!! New Years Eve I was still exhausted and not yet 100% so Ian and I did what we both really enjoy. We spent the evening at home with movies and by 22:30 it was lights out for both of us! Sean spent New Years eve with a buddy and the next day came home saying “Oh, happy new year mom… sorry I forgot cos I am not really a new year type of person”. Must admit that Ian and I are the same, we don’t need all the partying, drinking and late nights. Dylan spent new year camping with a friend at a dam and mentioned today that there were an amazing amount of fights new years eve…. Even more reason I don’t need the ‘over done’ bit.