Patiently waiting and resting......Its my Job...

Good Morning Sweet Community

I hope you are all having a good morning, or afternoon, depending on where you are. No matter what, I hope your day is full of hope and cheer and sunshine or even a cozy rainstorm. Whatever, I hope you are smiling.

All is about the same here. I have had a strange cough for about a week now. Nothing the docs are too concerned about, no infection, just tons and tons of phlegm. Uck. But one nurse mentioned I could be coughing up mucus plugs that were in my bronchioles, now does that mean my lungs are becoming unblocked. I don’t really know.

I do know that oddly enough this cough is not limiting my breathing more. So I guess that’s a good thing. I don’t like vagueness. So I am not completely clear but will be.

Tomorrow is clinic and hopeful I can get some clarity. I will most certainly ask for it, that’s for sure.

Till then I am resting, coughing, spitting, painting a little and resting more.

I move in and out of impatience and just plain boredom. Noah has been away all week again and that is difficult, but he will be back on Friday PM and here for about 7 days instead of 1.5 days like it have been the past couple of weeks.

What can ya do? We are doing all we can to make it easy on me and him, but still it is a challenge.

Good thing I am resting so much. There is so much going on this month

A week from today Oct 18th is Light the Night, I cant believe it. I am very excited. I will be speaking at this event AND they gave our team (we have 18 people now) our own tent.

They will come to us to register us and bring us our tee shirts and balloons and give us a case of water and a place to meet before and after the event.

Usually they give this to teams that have reached $10,000 in donations, we are getting close at $8,875 (remember our goal was $5,000), and I am considered the Honored Hero of San Francisco. I’m the one who is honored and humbled that they are being so generous with us. Who knows we still could make it to $10,000, the donations are still coming in. Thank you to everyone who have given so generously.

Oct 16th I have my one year bone marrow biopsy. Lots of prayers sent that way for continued Remission and Complete and Unlimited Health and healing.

Oct 18th is not only the walk but I am getting my first Pulmonary Function Test in several months, to see the improvement in my lungs. I’m sure there is improvement it certainly feels that way.

Oct 24th will mark one year since the Stem Cell transplant and they call that your New Birthday. That’s what I’d call it because I got my life back.

Then Oct 28th Noah and I are having a Remission celebration, we wish everyone near and far could be there. But if you are in the area and for some reason didn’t get an invite let me know and I will send an evite out to you.

It is a combo 1 year Remission, 1 year "New" bday party.

Then Nov 2 to the 4th I am going away to a little cabin in northern Cal with a group of 10 girlfriends. It will be nice to be away with my women friends for a that connection and play and rest and being in nature.

So there is a lot going on when I step back and look at it all, so rest is important.

I patiently wait for the day when I begin to feel my strength come back and a little more energy and no cough. I may not fully be the Victoria I was before but I am looking forward to some vital vibrant energy so I can be out in the world more actively.

This is part of my Complete and Unlimited Health and Healing I pray for. Always honoring the slow process and doing what I can to participate in aiding the process as well.

To all of you be well, take care during this flu season, eat healthy nourishing foods, get rest, be joyful, laugh a lot, and always carry a positive loving thought for yourself.

Love Love and Nothing more then Love.


Namaste
Victoria