Vic is very restless and agitated. Hospice says that at this stage they normally sedate the patients to make the passing easier. It would be a wonderful solution. Vic’s mind is mostly crystal clear and busier than ever. She continuously asks for photos to be taken, not necessarily of herself but of the boys, her friends and family. Last night I actually said to her (after her insisting on photos being taken of me – on my own) “Sweetie, you cannot take your cell phone to heaven with you.”
“Oh…” she said. “Why not? I think I will…”
We laughed.
In her desperate attempts to cling to life she is trying to capture images on her phone…I do know that she is imbedding the images on her heart and she will take the images of her loved ones with her.
Last night was very difficult. The Pethidine makes her hyper. She fights sleep at night! Vic is scared she will close her eyes and never open them again.
Vic clung to Danie’s hands when he came to say goodnight. “Don’t leave me Daddy! Please don’t leave me!!! I am so scared!” Poor Danie was totally distraught!
“I am so tired” Vic cries and seconds later she will try and get out of bed, so she can stay awake!
In the early hours of the morning I was exhausted when I eventually got inpatient with Vic and told her to get into bed. She looked at me and said “I sometimes think you love me to death but other times I think you hate me…”
I know she is confused at times. I will not allow these words to haunt me later. She “sees” people. She babbles non-stop.
The weight is falling off her. Her trembling fingers are bony, almost skeleton like. Her eyes are sunken and reflect her pain and anguish. My poor baby is starving to death! She has absolutely no appetite. I don’t know when last she was hungry or able to eat.
Esther and Leon came to visit today. Esther was very emotional when she saw Vic. I know she said her goodbyes today. I could see that they had spoken to their boys. Both Henk and Yuri kissed Vic whilst she was sleeping.
Jared asked me today why I don’t sedate Vic. I explained to him that she refuses to be sedated. “I think it will be better for Mom to sleep all the time now Oumie. It is too hard for her now and she is too scared…Ask Sr Siza to give her some sedation…”
Oh Lord how do I make this easier for my family? How do I spare the boys the pain of seeing their mother dying bit by bit? Do I send them to their father and have them hate me for it or do I subject them to the horror of what’s happening?
I wish Vic was in a hospital where the decisions weren’t mine. But I promised Vic “no more hospitals”. I will never go back on my word.
I am babbling.
Vic is very restless and agitated. Hospice says that at this stage they normally sedate the patients to make the passing easier. It would be a wonderful solution. Vic’s mind is mostly crystal clear and busier than ever. She continuously asks for photos to be taken, not necessarily of herself but of the boys, her friends and family. Last night I actually said to her (after her insisting on photos being taken of me – on my own) “Sweetie, you cannot take your cell phone to heaven with you.”
“Oh…” she said. “Why not? I think I will…”
We laughed.
In her desperate attempts to cling to life she is trying to capture images on her phone…I do know that she is imbedding the images on her heart and she will take the images of her loved ones with her.
Last night was very difficult. The Pethidine makes her hyper. She fights sleep at night! Vic is scared she will close her eyes and never open them again.
Vic clung to Danie’s hands when he came to say goodnight. “Don’t leave me Daddy! Please don’t leave me!!! I am so scared!” Poor Danie was totally distraught!
“I am so tired” Vic cries and seconds later she will try to get out of bed so she can stay awake!
In the early hours of the morning I was exhausted when I eventually got inpatient with Vic and told her to get into bed. She looked at me and said “I sometimes think you love me to death but other times I think you hate me…”
I know she is confused at times. I will not allow these words to haunt me later. She “sees” people. She babbles non-stop.
The weight is falling off her. Her trembling fingers are bony, almost skeleton like. Her eyes are sunken and reflect her pain and anguish. My poor baby is starving to death! She has absolutely no appetite. I don’t know when last she was hungry or able to eat.
Esther and Leon came to visit today. Esther was very emotional when she saw Vic. I know she said her goodbyes today. I could see that they had spoken to their boys. Both Henk and Yuri kissed Vic whilst she was sleeping.
Jared asked me today why I don’t sedate Vic. I explained to him that she refuses to be sedated. “I think it will be better for Mom to sleep all the time now Oumie. It is too hard for her now and she is too scared…Ask Sr Siza to give her some sedation…”
Oh Lord how do I make this easier for my family? How do I spare the boys the pain of seeing their mother dying bit by bit? Do I send them to their father and have them hate me for it or do I subject them to the horror of what’s happening?
I wish Vic was in a hospital where the decisions weren’t mine. But I promised Vic “no more hospitals”. I will never go back on my word.
I am babbling.
” Sometimes the pain’s too strong to bear…and life gets so hard you just don’t care. You feel so alone you just sit and cry…every second you wish you could die.”
Vic is rapidly deteriorating. Last night the nausea was absolutely relentless. With no food in her stomach Vic vomited blood. Old blood and new blood….. Her vitals are very unstable and I thought that she would not survive the night. I cried and slept in her bed with her.
Today Sr Siza tried to put up an IV drip. Vic has absolutely no veins left that are suitable for a drip. The sub-cutaneous driver is back up. At this stage of the game the risk of cellulitis is less than the need for pain and symptom control. We will reposition the subcutaneous driver as and when we need to.
Dr Sue has prescribed Cyklokapron. “Tranexamic acid (commonly marketed in tablet form as Lysteda and in IV form as Cyklokapron in the U.S. and Australia and asTransamin,Transcam in Asia, and Espercil in South America. Also marketed as TRAXYL (Nuvista Pharma) in Bangladesh,Cyclo-F and Femstrual in UK.) is a synthetic derivative of the amino acid lysine. It is used to treat or prevent excessive blood loss during surgery and in various other medical conditions. It is an antifibrinolytic that competitively inhibits the activation of plasminogen to plasmin, by binding to specific sites of both plasminogen and plasmin, a molecule responsible for the degradation of fibrin. Fibrin is a protein that forms the framework of blood clots. It has roughly eight times the antifibrinolytic activity of an older analogue, ε-aminocaproic acid.” http://en.wikipedia.org/wiki/Tranexamic_acid
She suggested that Vic be admitted to hospital. Vic refused.
On the 1st of January 2013 Stepping Stone Hospice and Palliative Care started operating. It is pretty ironic that Vic may well be our first death.
But then again, tomorrow may be better than yesterday….Today was better than last night.
Vic lost the Christmas gift she bought Esther. It is not the first time this has happened – Vic previously bought Esther a “Sister” fridge magnet and mislaid it somewhere…
Vic has spent a lot of time sorting out some last things – double checking her insurance policies, photo albums, writing cards for the boys to be read on the first Christmas, first anniversary, final school exam… She has been going tick, tick, tick…Oops Outstanding item: Esther’s gift!
I have searched the house and not found the sentimental nick-nacks Vic bought Esther for Christmas. I have driven around and looked for replacement gifts, but to no avail. So yesterday Vic said to Esther “Sis, I have to replace your Christmas gift… I cannot move on before I do that…Mommy is taking me to Eastgate tomorrow. I know I will find it there.”
Esther, who has a superb sense of humour, said “I won’t let you die before I get my present…What time are we leaving tomorrow?”
Early this morning Vic was dressed and ready for the excursion. At about 11am we set off shopping (after a hefty pain and nausea injection…) At the second shop we struck gold! (I actually found the gift she was looking for.) Vic had the salesperson wrap it with Christmas gift wrap. She is a stickler for “attention to detail”
Mission accomplished we went to a restaurant for lunch. As usual Vic agonised over the menu. She wanted a salmon dish with cream cheese – No salmon…. Arghhh! She settled for a sandwich and coffee.
The gift Vic bought was a Willow Tree figurine set of two girls holding hands. “Just like we lay and chatted last night Sis…”
Sisters by Heart
Celebrating a treasured friendship of sharing and understanding
Vic and Esther are step sisters. There is no blood bond, but they are bound by their deep love for one another. Esther has been an absolute pillar of strength to Vic and the rest of the family. Daily Esther sends Vic beautiful text messages. She brings Vic flowers from her garden. She lies next to Vic and listens to her babbling. Esther is the sister Vic never had.
Needless to say, Vic did not handle her lunch well and after a visit to the toilet we left. I could see her heart beating like crazy in her neck. People looked at us as far as we walked. I realized with a shock that it is because Vic obviously looks ill and shuffles like an old person. I look at her and I only see a beautiful young woman; my baby girl and the mother of my grandsons.
Vic is having a strange day… Her blood pressure is all over; her heart races and then slows down.
“Something is wrong mommy.”
This evening Vic double checked with me whether I remembered which hymns had to be sung at her memorial service. She cried when she (again) named her pallbearers. “Please don’t let me lie in a refrigerator for a long time Mommy…Let them cremate me as quickly as possible”
Vic asked that I get her minister to come and administer Holy Communion to her this week.
The whole situation is so surreal. I find it impossible to believe that Vic may actually be dying. She is so beautiful and her mind is crystal clear! I think Vic is just caught up in the Hospice talk. Maybe I am in denial. She has not vomited blood for two days. That is a good sign. Google says her heart rate can go up to 250 and Vic’s HR is only at 120 and occasionally at 155.
Oh dear God please grant my child peace. Please grant us all peace.
Celebrating a treasured friendship of sharing and understanding
I hardly received any 2013 New Year’s wishes. Normally I would receive so many beautiful wishes but this year I received messages for a” peaceful New Year’s Eve filled with laughter and good memories…”
Last night my sister said in a text message “what tears do 2013 hold for you? Maybe it should stay 2012”…
Jared went a friend’s home; Danie went to bed early – he is coming down with flu; Vic was asleep so that left Jon-Daniel and I. We watched Comedy Central and had some good laughs waiting for 2012 to end.
Jon-Daniel loves making his Mommy laugh. In a way I suppose he uses humour as a coping mechanism.
“I think we should wake Mom up at 12” I said
“Okay…Let’s sing Happy Birthday to Mom….” He said with a twinkle in his eyes.
As the hooters and sirens started going Jon-Daniel and I sneaked into Vic’s room and sang “Happy Birthday to you…” Vic opened her eyes and said “What is happening?” and immediately fell asleep again.
The joke was on us.
Today was a quiet day. The boys spend some wonderful quality time with their Mom. Danie remained in bed until almost 4pm as he is feeling lousy from the flu. We all drifted in and out Vic’s room. In the afternoon Jared went for a swim. Vic went outside and spoke to him.
Jared had some questions and she patiently explained to him what an “Executor’s” duties are. She explained why Leon and I were the Executors of her will and the Trustees of their Trust. (I got some lovely photos of Vic chatting to the boys!) Vic tried to show Jared that she could whistle through an acorn… Jon-Daniel taught her! As much as she tried she could not get a sound out of the acorn. To everybody’s laughter she said “But I can do it!”
We convinced her that she should get onto the inflated lilo. The cold water would reduce her body temperature and the sun would be good for the jaundice. Very reluctantly she got onto the “non- life-saving inflatable device”. I got into the pool with Vic.
Esther and Yuri arrived and she made a dash for her camera… later Leon and Henk arrived. The boys swam and laughed and played…
It was a wonderful day filled with glorious memories. We laughed and joked and eventually ate. Esther lay with Vic and they spoke about where Vic was in her journey.
It was a special day.
I think friends and family don’t know what to wish us…How do you say “Happy New Year” to a household where death is knocking on the door? I would not know what to say to us if I wasn’t me…
But from our home to yours: We wish you a great 2013. We hope that 2013 is filled with laughter, good health, abundance and time to do some good every day. We thank you for your love and support. Thank you for your prayers and words of encouragement. You have been such an amazing source of comfort to us.
Thank you Hospice for giving us the means to have these special memories! Thank you to the manufacturers of Morphine, Pethidine, Stemitil and Buscopan…
Sue came in this morning and managed to find a vein. The vein held for the Perfalgan and she also managed to get a bag of saline into Vic. This will hopefully rehydrate her. It has been a rough 24 hours with so much vomiting. The poor child…
We hooked the saline onto a hanger and it now hangs from her ceiling. Leon, SiL, put a hook into her ceiling and we have suspended the drip from it. I have to keep the drip flowing until 12pm tonight when I can run another lot of Perfalgan. Tomorrow Sue will try to find another vein.
I suggested that Vic is mainlined or a stent is fitted. Sue agreed that it would certainly make life a lot easier. It would be easier to administer all Vic’s IV medication. Vic said “Sorry Mommy, no hospitals…”
Her heart rate, even whilst she is sleeping, is constantly above 110.
The IV medication immediately helped. Vic’s breathing is better. Vic has not vomited since 11 am this morning! She even managed to have a bit to eat tonight.
When Sue left today she asked me what is holding Vic back. Medically and clinically speaking there is no explanation why Vic is still alive…. She said that she has never seen anybody fight death the way Vic does… She asked me whether we have given Vic permission to die…
Sue says that Vic still says we are going to Italy next year…. Her kidneys and liver have failed. That is what the blood tests show.
What is holding Vic back? Sue says death happens when one relaxes completely and deeply! Vic’s adrenaline levels are preventing her from relaxing and dying.
All I want is for my little girl to find peace and her suffering to end.
Esther and Leon brought dinner tonight and just visited. Vic even got out of bed for a while and had a laugh. It was great being surrounded by the love of the family.
I wish I knew what to do to make Vic accept the inevitable. I wish with every fibre of my body Vic will find peace. That she will find the strength to let go…
Vic has been ill for such a long time. Maybe she just thinks this is how life is. Maybe she cannot remember what it is like to feel good, go out, be carefree, move without pain. To play with her kids, go out for drinks or a movie with a friend.
On Christmas Eve Siza said to Vic “I read in the Bible that Heaven is a great place”….
Here On Earth …, There In Heaven…
Here on earth imperfection, there in heaven perfection
Here on earth discontent, there in heaven content
Here on earth disgrace, there in heaven grace
Here on earth disease, there in heaven ease
Here on earth hatred, there in heaven love
Here on earth war, there in heaven peace
Here on earth decay, there in heaven freshness
Here on earth selfish, there in heaven selfless
Here on earth oppression, there in heaven liberty
Here on earth agonize, there in heaven relax
It’s either on earth, or in heaven
The decision, all yours
Obed Akuma
Baby Girl it is time for Heaven… You have to let go!
Today was an horrible day. Dr Sue spent a lot of time with Vic. Siza (Hospice Nurse) was here too.
Vic’s BP is elevated and her heart rate fluctuates between 115 and 120. Her breathing is laboured. She appears to be a little jaundiced. Sue says the vomiting is due to the kidney failure.
Tomorrow we will try and run some Perfalgan intravenously. If only her veins were strong enough to tolerate an IV drip…
I am scared.
On the 26th of December 1996 Jared Colin Sadie was born. He was a beautiful, healthy baby boy. I cried with joy when I first saw him and that first “rush of love” hit me.
Vic fell pregnant 6 weeks after she got married. When the kids asked us whether they could get married I had a LONG talk to them about NOT having babies. They both said “We know…” I explained the dangers of passing the Osteogenesis gene onto a next generation of innocent children.
I will never forget that dreadful Sunday night when they told us that Vic was pregnant. My heart stopped. I sobbed in the shower. For the first time in her life I feared for Vic’s life.
Vicky refused flat out to have an abortion. She said the baby a gift from God. And so he was….
Jared is an amazing young man. According to our government he is now old enough to vote, get his learners licence for a motor bike and work… I look at him and I see a little boy who was going to be a stuntman; a young child helping his Mommy cook; get out of bed; walk down stairs…
Both Jared and Jon-Daniel are loving, compassionate monuments of Vic love and mothering.
Jared is a “computer nerd” with a wonderful personality. He has a keen sense of humour and wise beyond his years. He is fiercely protective of his mother. A very dear Saudi friend of mine says Jared has a “white heart”. (Albak Abyad” an Egyptian expression that indicates a person with a good heart. It’s literal translation to English is “You have a white heart” as opposed to being a bad person with a black heart).
Vic, once again, managed to get out of bed. She was falling asleep in her chair, but managed to visit with most of the guests who came, ate something and left. Laughter and joy reverberated through the house. Vic was the proud mother. It was a happy home for the day…
The boys have a hard time coming to terms with the stage that Vic’s illness is at. Jared’s first words when he comes back into the house after Siza leaves is “What did Hospice say?”. He researches every symptom and sends me links on liver and renal failure. He is an expert on Osteogenesis Imperfecta and was 9 years old when he spoke about his Mommy at a Public Speaking lesson at school. The subject was “My Hero“. We all expected him to speak of Nelson Mandela, but he chose to speak about his Mom. (His brother followed suit two years later)
He said that his mom is his hero because despite the fact that she is so ill she still looks after them…
Jared had a wonderful 16th birthday. He was absolutely thrilled with the Docking Station Vic had bought for him. As soon as he gets his license we will buy him a motorbike.
Yesterday was a milestone in Vic’s life. I fear it may be the last she will reach. It is clear that Italy will not be possible.
I was so tired last night that I slept through Vic’s 23:31 and 03:00 “Vomiting” text messages…. Vic refuses to use the intercom! She feels it is “disrespectful”.
As much as Vic resents the fact I may have to bring in a night nurse.
I remember Vic’s 16th as if it was yesterday. Now she is a grown woman with two teenage sons – nearing the end of her tenure on earth
https://tersiaburger.com/2012/08/27/kidney-stones-on-the-move/
https://tersiaburger.com/2012/10/10/i-am-taking-a-break-from-your-blog/ https://tersiaburger.com/2012/07/07/chronic-illness-versus-terminal-illness/ https://tersiaburger.com/2012/05/28/22-2-2002-to-28-5-2012/ https://tersiaburger.com/2012/06/09/9-6-2012/ https://tersiaburger.com/2012/10/16/and-the-winner-is/
December 24, 2012 by Dr Bill
“I salute you. I am your friend, and my love for you goes deep.
There is nothing I can give you which you have not. But there is much,
very much, that, while I cannot give it, you can take. No heaven can
come to us unless our hearts find rest in it today. Take heaven!
No peace lies in the future which is not hidden in this present little instant.
Take peace! The gloom of the world is but a shadow. Behind it, yet within
our reach, is joy. There is radiance and glory in darkness, could we but see.
And to see, we have only to look. I beseech you to look!
Life is so generous a giver. But we, judging its gifts by their covering,
cast them away as ugly or heavy or hard. Remove the covering, and you
will find beneath it a living splendor, woven of love by wisdom, with power.
Welcome it, grasp it, and you touch the angel’s hand that brings it to you.
Everything we call a trial, a sorrow or a duty, believe me, that angel’s hand is there.
The gift is there and the wonder of an overshadowing presence. Your joys, too,
be not content with them as joys. They, too, conceal diviner gifts.
Life is so full of meaning and purpose, so full of beauty beneath its covering,
that you will find earth but cloaks your heaven. Courage then to claim it; that is all!
But courage you have, and the knowledge that we are pilgrims together,
wending through unknown country home.
And so, at this time, I greet you, not quite as the world sends greetings,
but with profound esteem and with the prayer that for you, now and
forever, the day breaks and shadows flee away.”
~ Fra Giovanni
It is Christmas. It is a warm, and sunny-day, and my heart is cold.
This is our last Christmas as a complete family.
Vic has been vomiting non-stop. The acid has burnt the inside of her mouth. Her derriere is so lumpy, black and blue from the constant injections. Sr Siza popped in. She examined Vic and started drawing up a Clopamon and Morphine injection.
“Please Sister, not my bum. Please do it on my thigh.”
Vic no longer has an appetite. She is sleeping at least 20 out of 24 hours. Vic is very warm to the touch and appears flushed. The thermometer reflects a temperature of 37 degrees C.
“Do you understand what your body is telling you Vic?” Siza asked
Vic nodded and whispered “I do not want to die…”
“Nobody wants to die, Vicky. We all will walk this path. Some sooner than others… You have a degenerative illness and your body is tired…”
“You must surrender your body to God. It is time for your brain to make peace with what is happening in your body.” Siza said. “Where is your Bible?”
Siza read from Ecclesiastes 3 – New International Version (NIV)
3 There is a time for everything,
and a season for every activity under the heavens:2 a time to be born and a time to die,
a time to plant and a time to uproot,
3 a time to kill and a time to heal,
a time to tear down and a time to build,
4 a time to weep and a time to laugh,
a time to mourn and a time to dance,
5 a time to scatter stones and a time to gather them,
a time to embrace and a time to refrain from embracing,
6 a time to search and a time to give up,
a time to keep and a time to throw away,
7 a time to tear and a time to mend,
a time to be silent and a time to speak,
8 a time to love and a time to hate,
a time for war and a time for peace.
Siza prayed for Vic and the family for peace and grace in this time. Vic cried and Danie gently held her.
Danie, and I walked with Siza. Her eyes were sad when she said “Her body is shutting down. It could be quick or it could be a few weeks.”
The rest of Christmas Eve passed as if I was in a daze. Lani and the kids arrived, my dear friend Judy arrived after a marathon charity event and the smell of gammon and roast lamb permeated the house. The tables looked festive and there were tons of gifts under the tree.
Vic handed out the gifts. The kids shrieked with delight. A lot of thought went into the gifts. The gifts were truly gifts of love.
3 There is a time for everything,
and a season for every activity under the heavens:
a time to be born and a time to die,
Today has been a very, very bad day. Sr Siza was here when Vic had a violent vomiting spell. Yesterday Vic fractured a vertebra again. Her pain is out of control. Her breathing was shallow.
“I don’t want Jon-Daniel to see me now Mommy. It freaks him out when I can’t breathe” Vic pleaded
I lay behind her back, gently holding her whilst the tears wracked through her little body.
“I don’t want to die Mommy. If only I can live for another year….. But I am so tired!” Vic softly cried
“Do you think we will be able to do Italy Mommy?” she asked after a long silence
“I hope so Baby. I think we must take the boys with us…” I replied
“Oh Mommy, can we? We don’t have to go for a long time…” Vic said
We lay quietly for a while. Vic trying to breathe through her nausea and pain and I contemplating how I am going to pull off this Italy thing… Just imagine flying with a caseload of injections and a litre of morphine syrup…
“Mommy, I don’t care what you do with my ashes… It was so hard putting my father’s ashes into that wall of remembrance! Are you going to be okay Mommy?” Vic cried
My heart stopped. This was so out of the blue… “You will always be with me. I will not put you into any wall” I said
“I will be your guardian angel.” Vic said
“I know but remember I will need some privacy… “I said
“Don’t worry Mommy! I will make sure my father doesn’t peep as well” Vic laughed through her tears
“I am scared Mommy…”
“I am scared too Vic…”
I just read two very insightful posts that Andrew of http://lymphomajourney.wordpress.com posted/reblogged. The first was under the heading “Why not choose death” http://lymphomajourney.wordpress.com/2012/12/04/why-not-choose-death-sunrise-rounds-sunrise-rounds/ and the second “Morphine too little or to much?” http://sunriserounds.com/morphine-too-much-or-too-little/
I read the articles through the eyes of a primary caregiver who has prayed for her child’s death many, many days. https://tersiaburger.wordpress.com/wp-admin/post.php?post=3&action=edit . BH, (Before Hospice), I often blogged about The Right to Die with Dignity…..
Over the past 10 years I have seen my child suffer so much indignity and indescribable pain. I have seen the despair in her eyes, the helplessness in the eyes of her boys….I have stood next to her bed and physically pulled my hair in frustration – tears pouring down my cheeks. I have wept before God and prayed for Vic to die. I begged God to take away her suffering.
I advocated the right to die with dignity.
Vic has been in the care of Hospice for the past 3 months. In this time Vic has been given a new lease on life. Hospice cannot change the prognosis but they have given Vic quality of Life. For the past three months Vic has been able to occasionally get out of bed, go for milkshakes with her boys, she went to Jared’s confirmation and Jon-Daniel’s honours evening. She completed her photo albums.
Vic is in renal and hepatic failure. Her tissue is horrendous. Her pain is under control! As and when symptoms surface, Vic’s medication is adjusted. She is treated with compassion and respect. Her wish is the teams command….
As the situation is now I am so grateful that my child is alive. I treasure every breath that she takes. We chat, laugh and cry. We dream of going to Italy in 2013.
So given the situation now what would I advocate – The right to die with dignity or the right to live?
I have no doubt that if Vic’s pain and symptoms got worse, I would want her suffering to end. If it remains as great as it is now of course I want her to live. But it is key that Vic is allowed to live with Dignity!
As much as I advocate the right to die with dignity I believe that the final decision lies with the sick person. It is not for family or physicians to play God. The patient has to be the only decision maker.
I must admit that if the decision was mine to make, my child’s suffering would have ended a long time ago.
We all have the right to Live with Dignity. There is a huge difference between breathing and living…
BH (before Hospice) Vic breathed. Now she lives. She may not live for a long time but she has the right to live with dignity!
https://tersiaburger.com/2012/06/04/5-6-2012/ No one will love me ever again
https://tersiaburger.com/2012/06/12/12-6-2012/ (Eat, sleep, Vomit)
https://tersiaburger.com/2012/08/17/the-right-to-die/
https://tersiaburger.com/2012/09/14/palliative-care/
https://tersiaburger.com/2012/08/22/rest-in-peace-tony-nicklinson-brave-warrior/
https://tersiaburger.com/2012/08/20/768/ (How to die in Oregan)
There is a Sacredness in tears. They are not the mark of weakness, but of power. They speak more eloquently than ten thousand tongues. They are messengers of overwhelming grief and unspeakable Love. ~Washington Irving
I have been quite busy album-making for Christmas. Over the past month I have gone through thousands of photos!
One of the most touching photos I came across, was a photo of Vic where she is crying. She was not crying from pain or fear. She was crying from pride and happiness…
Then I saw this “Status” of an old schoolfriend and I knew I had to post about the sacredness of tears. I posted the quote earlier but after going through the photographs I decided to actually write about Vic’s tears.
Vic was a little girl of about 7 years of age. We were driving home from the school sports day. I looked in the mirror and saw the tears running down her cheeks….
What’s wrong angel? I asked
“I also want to run Mommy….” She said
I have seen tears of pain in her eyes more times than I wish to remember.
I have seen tears of fear shimmering in her eyes many, many times.
I have seen tears of sadness roll down her cheeks…tears of despair…
I have seen tears of resignation
I have also seen tears in the eyes of her Gastrointestinal Surgeon when he said “No More”
But the tears that I will always want to remember are the tears of pride that Vic has cried. She has cried at Jon-Daniel’s Prize Giving’s, school concerts and when Jared plays guitar in Church and at recitals, Jared’s confirmation…
Vic’s tears are sacred. They are like rain on the windows to her soul. In the words of Eileen Mayhew” “Let your tears come. Let them water your soul.”
I love you angel child! Maybe you will cry tears of happiness again one day…
It has been a crazy week. Between Vic, final 2012 business meetings, a brochure photo shoot, visiting grandchildren, Jared’s birthday party and Hospice meetings I have run around in circles. I have not had time to blog or read all the blogs I am following.
Vic has had a reasonable week. I can see her getting weaker every day. At night I give Vic a Pethidine, Zantac and Buscopan injection. The Pethidine makes her sleepy. During the day she is able to tell me she needs an anti-nausea injection. At night the drug-induced sleep does not allow her the luxury of early warning. Vic projectile vomits every day of her life!
Vic has also had a couple of uncontrolled sneezing attacks and lots of hiccups. I fear she will fracture ribs and vertebrae if we are not able to control this quickly. I have started giving her antihistamine tablets. Hospice tells me it is a symptom of the kidney and liver failure and will get much worse.
Her arm is still very inflamed and painful. We are now on the 3rd round of antibiotics. The tissue in her derriere is very poor. It is lumpy and bruised. It is becoming more and more difficult finding good tissue where I can inject her.
Emotionally it is really a difficult time. Vic is spending as much time with the boys as possible. She is doing a lot of what appears to be “lasts”….
It is 11 days to Christmas, and we are looking forward to a quiet Christmas Eve with the family. Our gifts are not as extravagant as other years. Our priorities are simply different this year. This year Christmas will be a time of love and togetherness.
It is 10 days to Christmas Eve…
Vic's Final Journey 