Wednesday 20 May 2009

20 May Update



20 May 2009


Dear family and friends

Yesterday, Luna had investigative surgery - a video camera up her urethra into the bladder and biopsies taken around any area close to the tumour that could have been affected.

We now know that the tumour is about the size of a small plum (less than 5% by volume of the original size), and some of the remaining cells are either dying or dead. We also know that the stem of the tumour is attached to about one quarter of the bladder wall, just to the side of the urethra. The surgeons are very hopeful therefore that Luna can be left with enough of a bladder for it to remain functional (albeit she will probably need to go to the toilet more often than a 'normal' person), and that her urethra should be safe from surgery.

For us, and the surgical team, this is the best possible outcome! We had been very concerned that they would have to remove her urethra (as the tumour is so close) and possibly part of her vagina wall. We had also been extremely concerned about the need for radiotherapy (with serious long term side effects) post surgery. Whilst the exact procedure will not be confirmed until we have the results of the biopsies and, even then, not until they actually open her up to do the surgery, we are extremely happy with the outcome of yesterday.

For the first time, we saw the doctors smile and finally got them to admit that Luna's prognosis was now greatly improved (we have believed that for a long time - ever since she pro-lapsed so much of her tumour).

The main surgery is now scheduled for June 23rd.

We still have a long and hard road ahead. Luna is back in hospital on Friday for her next round of chemo. The effects of chemo are cumulative, so even though she did so well after her first two rounds of chemo, she is taking longer to recover now. We will continue to go into hospital between chemo sessions, as she gets temperature spikes (suspected infections) that have to be treated. We will continue to struggle to feed her and rely on feeding through a nasogastric tube / pump. And even after the chemo is finished (towards the end of the year), we will have to go into hospital for repeat investigative surgery every three months to monitor the affected site. All of this is very challenging and tiring. However, the difference now is that we feel we have a goal that together we can attain.

Thank you everyone for all your support. We have appreciated it immensely. It has kept us going.

With much love Monica, David, Luna ('our little warrior') and Leo (our attention-lacking dog)