Monday, February 21, 2011

Roni's Service

In Loving Memory of

VERONICA LOUISE (nee McMullen) McILVEEN

Born

November 24, 1953

Vancouver, B.C.

Passed Away

Friday, February 18, 2011

at home in

Port Coquitlam, B.C.

Celebration of Life

February 27, 2011

1:30 PM

Old Orchard Hall

646 Bentley Road

Port Moody, B.C.

Celebrant

Matt Wade

As Roni requested her ashes will be placed in the gardens at her home in Port Coquitlam

I Believe...
That heroes are the people
who do what has to be done,
when it needs to be done,

regardless of the consequences.

Friday, February 18, 2011

AND GRACE WILL LEAD ME HOME

On this bright and sunny February day at just after noon, with her usual grace and courage Roni broke free from her war torn body and took the next step on the journey. I will miss here terribly but I am relieved that her pain is over. She was one amazing woman; though we knew from the start that the journey would end she battled on, complained very little and inspired so many, she is my hero. I will never forget her.

I want to extend a very heartfelt Thank-you to Dr Joan Eddy and the palliative team; Catherine and Kia. You girls have been just great and we could not have gotten by without you. Thank you so very much.

Thank you to all who made it out to see Roni in final days and to all who posted, email or delivered their thought and prayers. These have all been a great comfort to us. We will let everyone know about her celebration of life in the near future but right now we just need a little down time.

Brian

Saturday, February 12, 2011

OUR WARRIOR WEARRIES

Our beautiful Pink Chemo Warrior has surrendered the battlefield, but continues to fight. Over the last few weeks Roni’s condition has deteriorated, but she soldiered on. She is now too weak to stand and spends most of her time with her eyes closed, but not necessarily asleep. She does join conversations but is very tired, it has been a tough two and half year, 24 hour per day, 7 day a week struggle. With courage, dignity, and honor she waged a very personal war against this unrelenting killer. Our country does not award medals to these types of heroes, but Roni often commented that the love and admiration of her friends and family were compensation enough. She is an inspiration to so many.

Modern medicine does not have the tools to save our hero.

Last week when the palliative care doctor came to visit she suggested that Roni’s body was shutting down and it was time. I thought she was off her nut. She asked Roni if she was ready to quit chemo and received an adamant NO in reply. A day or so latter Shannon led me to a cancer website where Roni’s symptoms were laid out in the section about the final stage of cancer. My beautiful, loving, always sassy Irish lass is losing the battle.

I recall back when it was my mother’s time; I was the only sibling nearby. I went to hospital where Mom had lived for 12 years. Her mind had left years ago, her eyes no longer functioned and her hearing was likewise impaired. She had wasted away to about 60 lbs. Mom was a few months short of turning 90. I sat with her and held her hand for several hours and as the sun was setting I mustered up the courage to tell her it was ok for her to go on, we would be ok. I kissed her cheek and a single tear slipped from her eye. I was at peace with the situation. One evening last week after the house was quiet and we watch TV in bedroom I turned down the volume and told Roni, “It is OK for you to go, I will be fine. I will miss you terribly, but I’ll be OK.” Roni looked back at me with a little smile and said, “I love you.”

Roni had a close friend, Rae, visit Wednesday’s night but mostly kept her eyes closed, she occasionally struggled to ‘wake-up’ but each attempt was short-lived. At bedtime Roni struggled to swallow her evening pills and Thursday morning was worse. The palliative care doctor, nurse and a social worker arrived Thursday morning and switched her meds to injections.

Roni and I both have Living Wills and had discussed in depth what our personal choices are. At the onset of the metastasised cancer, having been told that there is no cure, Roni also completed and sign a Do Not Resuscitate Order. She asked to be allowed to die at home and so the doctor has also signed Intent to Die at Home Form. Her intent and desires are clear to me…no heroics. After a short discussion with the palliative care team I decided to cease chemo therapy and continue on with only end of life care. I thought my heart was being torn from my chest, but I am comfortable with the decision and her children agree with me, it is Roni’s time. Nature will be allowed to run it course.

Roni’s pain is well controlled and she is resting comfortably. She is capable of having visitors, in fact we would like people to come and talk with Roni. She can hear and understand and responds both verbally and with body language. She likes to hold hands. Perhaps you can share a memory, certainly a hug and even tears. These will all be a comfort to both Roni and us. Please, at this point if you have a cold, cough, etc. stay away. Finally, as Megz posted previously, this may not be the Roni you knew. This is a woman with final stage cancer, prepare yourself. Please phone first and we’ll tell a good time.

I want to thank all of Team Roni, you have all been so supportive of Roni and her loved ones. I also express my gratitude to Dr. Paul Klimo and the oncology team at Lions Gate Hospital, you gave my beloved more quality time, and I can’t thank-you enough. A very special thank-you to Roni’s children. Megz, Pat and Shanny; your love and support have kept us soldiering on, your all have your Mom’s fortitude. A super special thanks to Shannon; you have been a Godsend.

Your thoughts and prayers, visits, phone calls, cards and flowers are all appreciated. As Roni requested we will be doing a small memorial garden in the backyard, complete with bench should anyone wish to visit, so you may choose to sends seeds or plants for that. I believe we are a hardiness zone 8a.

Brian

Wednesday, February 9, 2011

Small update

Hey Everyone,

Just a quick update here... I've been wondering what to write on here, as nothing quite seems right....

Mom is continuing to fight and hang in there. She has her good days and her bad days. Mom is not in any pain and is comfortable.

She is still up for visitors, although we do ask that you call first to make sure that Mom is up to a visit that day or that they are home-they may be at an appointment. For those that don't have her phone number and would like to call, please send me an email- mghan.mckay@gmail.com .

One other thing, for those who are coming to visit, we do want to give a bit of a warning that Mom is not the same mentally or physically from what you remember her as. We want you to know this, so as to not be surprised.

Tuesday, February 1, 2011

Health Update

Hello All,

This is Shannon, Roni's daughter. We just wanted to send out a note to her most contacted folks with a little update, since we have been getting a number of inquiries about her health.

The main reason you haven't heard from Mom is that 1. she doesn't have the energy to spend time at the computer and 2. she has forgotten all of her passwords to gmail, facebook, banking, etc. We have an interesting time trying to source info from her, it is like a combo between 20 questions, charades, and reading minds. She says "I forgot my passwords, but I didn't forget who you are." We have recently cracked her code to get into Facebook.

Her health has declined. She continues chemo, but since the brain surgery there has been a decline in her lucidity and her general health. She sleeps about 18-20 hours a day and when she is awake, she is at varying degrees of lucidity-the mouth is not cooperating with the brain.

She does have her spirits up for the most part, and will enjoy a joke of course. She will eat when she finds something she likes, but that can be a challenge at times.

Her kids along with Brian are sitting down this week to organize things like a full time care schedule, getting home supports in place, and looking forward, what needs to happen when she passes-when that comes to be. But for right now, we just want to make sure she has someone around as she is so easily winded and wobbly and that she is comfortable and has what she needs.

Any of you wishing to call and speak with her, she is usually awake during lunch and dinnertime and would love to hear all your kind words. We have passed on your messages of support facebook and email so far.

Thanks for your thoughts, and please keep her in your prayers.

Roni

(via Shannon and family)

Wednesday, January 26, 2011

It's been a while....

Hey everyone,

It's Meghan here, I've been meaning to get an update on here for a while and but ran into some troubles logging in. I hope you are all comfortable 'cause there is A LOT to update everyone on....

I know a lot of you have sent me messages on facebook, asking me if Mom is ok, as she hasn't been online for a while. She has been fighting a cold for a while now and it is just starting to finally go away. With her not feeling well, she has been laying low-thus the reason she hasn't been online.

Shortly after having the radiation in early December, Mom also had a round of chemo. She ended up having an odd reaction to both of them combined (swelling/redness in the face). Since then Mom has not had any more radiation-but for a good reason, the radiation on her brain did what it was supposed to-stop the tumors from growing.

Unfortunately, the news isn't so good for Mom's lungs. As there was an almost 2 month gap between having the radiation and chemo, the tumors in her lungs have had a chance to grow-A LOT! So as of right now, we are waiting for Dr. Klimo to come up with a new set of chemo drugs for Mom to take.

Mom had a good Christmas, spent with some family and friends. We had a family Christmas dinner on Boxing Day, filled with presents, turkey (and fixings), roast beef, pumpkin cheese cake and pie.

Mom would love phone calls and visitors, as she gets lonely being at home all day.

I know there is more to be updated here, but I will have to cut it short for a few reasons... First, I've lost the piece of paper that had everything on it to be updated. And second, I have a sick, little boy sitting on my lap at the moment... I will update more tomorrow....

Friday, December 10, 2010

Radiation, Surprise Visitors and more

Hello everyone,

Christmas is just around the corner and I figure I should update the blog! – It has been a while, hasn’t it!

Last week, Brian and got to go to the 2010 Grant Recipient Reception for the CBCF for doctors who are doing various type of research with respect to breast cancer. It was a nice short and sweet event. No long speeches – just two and they were done within 45 minutes including handing out the monies and plaques. Was fun chatting with various staff from the foundation – all different levels. It was held at the Bill Reid Art Gallery and standing amongst his artwork as amazing – just wish I could afford some of it – but you could feel his spirit within the building. For those of you who do not know who he is, he is a renowned Haida Gwaii artist and is known all over the world. I also got my letter which is going out to over 100,000 people as one of the foundations big fundraiser and I proud to have my name attached to it.

Things at the BCCA have not changed from when I left them in March. As mentioned in the previous update, Dr. Sasha sent an email to Dr. Kwan at the agency for my appointment. Nothing. I had to call the agency and ask if there was an appointment to meet with him – and yes there was, they just hadn’t phoned me to let me know. So Brian and I met with him and a young student doctor. The appointment took almost 3 hours – long – never had so many questions asked!! They said I would get a call for my first appointment – they would do the brain first. Guess what – I had to call them to get the appointment – they were too busy to call patients with their appointment times. But I did get my times slowly but surely and radiation began. It was an interesting experience for sure. I felt like I was under the “K-Mart” blue light special! And it was warm. There were five treatments for the brain and then he decided he was not going to map neither the spine nor the hip. He told me to tell Dr. Klimo to order a bone scan!! Let’s just say, Dr. Klimo is not impressed – he knows there is something in the spine and hip! So, I have a bone scan on Monday afternoon. If I had to wait for the BCCA to book one it would be at least one or two months. Klimo orders and it is done! He had wanted it done yesterday but they were booked – and I am glad!

Chemo has started again and I am so glad. Gotta fight the dang tumours in my body. And also the extra drugs to keep the red and white counts where they should be – and that means bonus Airmiles at Safeway – wahooo!! Chemo starts today and then the next session is Christmas Eve – that will be the 3rd one that has landed on that day! At least it is being done!!!

Went out to Club Colour the other day with my neighbor and painted a few pieces of ceramics for gifts for some of the staff at the clinic – will pick them up next week – and yes, will take pictures of them and post here. It is always so relaxing doing the painting and a lot of fun.

I finally applied for my handicap parking pass – now just have to take it into the office which I will do today on way home from chemo, if my driver had time! Will make things a lot easier when going out and not having to worry about running out of steam within a few feet – there are lots of spots where I grocery shop and at the mall.

The tree is up with the lights on – no decorations as of yet – will have to get on that. The lights are in the windows and on the pony wall. Just need to move the decorations from the boxes to the tree! Maybe I can get some volunteers!!! Patrick and Brian put the lights on the tree! And then get started on my Xmas baking. Have started making some chocolates and think tomorrow will be mincemeat and butter tarts. Then lots of little cookies with my Mom’s really old cookie press – can do lots of shapes for the shortbread and make some other cookies from the recipe book that I remember as a child. Then into the freezer they go.

We have another birthday party for one of our granddaughter’s. Ayla turns 2 on the 17th, but her party is tomorrow, so will be lots of fun – a whole bunch of little kids running around!! Noise level should be interesting in the building they hold it in, but it is warm and that is good!

Christmas will be a little different this year. Brian has to work on Christmas Dad, but it is an afternoon shift so really not that bad. I am going to my former neighbor’s for dinner that evening – her daughter and son-in-law live a few blocks from here so they will take me. My kids will be at their father’s house. I will be hosting our Christmas dinner on Boxing Day – pot luck and can’t wait. Always fun to have the family over for dinner, especially when there are little kids around.

We had surprise visitors yesterday afternoon. My neice Elaine and her husband Jim had driven down from Clearwater to do some shoping and visit with his son who just lives up a few blocks from us. They were headed back home today so was just a short visit with us but tha tis ok. We don't get to see each other very often so the time we had was special.

Well, guess I should sign off for now, need to make a few phone calls before I go out and go out onto the deck and clean up the mess the Gloria made – she managed to knock over the recycle can and plastic is everywhere – silly cat. Write some cards and mail a gift.

So, if I am not on before Christmas – A Very Merry Christmas to everyone and lot of a peace and love. Looking forward to comments – they really do brighten my day when I read them.

Roni