Kidney stones on the move….


Another Hospital Passage – Different Day

On the 23rd of July, we found out that Jared had kidney stones.  (https://tersiaburger.com/2012/07/23/deje-vu-7/).  At the time the kidney stones were  not obstructing the urinary track so the decision was made, by the Urologist, to leave it and reassess the situation in 6 months.   On Friday night, at a Youth Meeting, Jared’s kidney stones gave notice that they had started to move!

I was petrified that if we took him to Casualty we would end up with a bum Urologist (https://tersiaburger.com/2012/07/27/vic-olympic-champion) so after researching “Kidney Stones” on Google we (I) decided to monitor and control his pain, let him drink lots of water, anti-inflammatory tablets and a urinary track antacid…  In the event of him “vomiting from pain” or “passing blood” we would be forced to be at the mercy of the On Call Urologist!

By Sunday night the poor soul was quite pale and said his pain was at an “8”.  There was no sign of bleeding and an insignificant level of protein in his urine (I kept testing his urine) and the Leucocytes, Nitrate, UrobilinogenpH, Blood, Specific Gravity, Ketone, Bilirubin and Glucose levels were all within the correct limits….

I managed to get an appointment with the Urologist for 10:00 this morning.  He did a scan and low and behold there was this large (6.6mm) kidney stone stuck in the  urethra…. At 15:00 this afternoon Jared was wheeled into the operating theater for the 2nd time this year.  Thirty minutes later the urologist came through and told us that Jared had passed 5 of the original 6 kidney stones – including the one that showed up as causing an obstruction at 10:00 this morning!  The child did not whimper or moan!  He was stoic in his pain!  The 6th kidney stone was dissolved with a  procedure called lithotripsy. In this procedure, shock waves are used to break up a large stone into smaller pieces that can then pass through the urinary system.

In the passage of the hospital Vic said to me “Mommy, I am so grateful.  Jared got through the operation like a real trooper.  ”  I was immediately filled with an all-consuming anger.  The operation went well, Jared did get through it like a trooper but what has started happening in his young body?  Adhesions people!!  Flippen adhesions!!!!

I said nothing but she saw my face.

As soon as we had Jared settled and comfortable I brought Vic home.  She was totally exhausted and in absolute agony!

In the car Vic said to me “Mommy, you seem so angry with me?  What have I done?”

“I am angry that an innocent child is going through the same hell that you went through as a child”

Vic’s father and I were not aware of the Osteogenesis Imperfecta gene on her Dad’s side of the family.  We made the decision not to have more children after Vic was diagnosed.  We were determined to never subject another child to OI.

From a young age, we told Vic that OI was a genetic disorder.  She KNEW that she should not have children.  She fell pregnant TWICE.  I know she was on  the Pill, suffered from SEVERE endometriosis and that she fell pregnant against all odds.  Yet, she chose to carry the babies and risk them being born with the OI gene…. Despite the Dept of Genealogy at Wits University, her gynecologist and doctors strongly advising against it!

I love the boys with every fiber in my body!  I am so grateful that they are in my life.  They have enriched my life in every way.  I cannot imagine my life without them.  I don’t want to live without them.    But, almost every day of my life I counsel at least one of the boys that, only if the OI gene can be isolated, should they consider having children one day…  They see their mother’s suffering.  They live her suffering!  Jared is starting to live his own suffering.

We are seeing Jared regress into Osteogenesis.  It has been obvious for a long time that Jared’s ligaments and tissue are affected.  He has only had a couple of mild fractures but he is always hurting somewhere.

Today Vic said that I have become “hard”.  I suppose I have.   Vic thinks I am hard because I believe in death with dignity.  Because I stopped all aggressive treatment for Alzheimers Pneumonia after my Dad no longer had any control over his body functions and had forgotten how to swallow or walk!  Vic cannot believe that I want to talk to the boys about considering vasectomies when they become sexually active (or earlier).

I cannot do this again.  I am venting.  I am so angry!!  I am angry with a debilitating disease and yes, I am angry with Vicky for allowing this dreadful gene to be passed on to an innocent child.

This vicious cycle has to stop!

Sunshine award!


Whoopee!!!!  I have been nominated for a Sunshine Award by brave Katie Mitchell whose blog I follow slavishly!  Katie suffers from a Connective Tissue Disorder, Marfan’s Disease.  I have learned so much of this talented young person’s journey with pain and how it has affected her life.  Katie’s mother also suffers from chronic pain so she knows both sides of the pain story…  Thank you Katie for the nomination and for sharing your journey with us!

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When I started my blog is was because I needed an outlet for all my pent-up emotions.  It is difficult for me to articulate my emotions because I am scared that if I started crying I would not stop.  It also bears my soul to the world so it was difficult at first.  Every time, before I  linked my post to FB, I would sit for a long time and wonder if I should allow family, friends and acquaintances to see my soul or whether I should remain anonymous in WordPress….  I am now comfortable with my FB link as it that I have received the most amazing support from old school friends, family and strangers.  I have a new network of people, that care, that surrounds me.

I no longer feel embarrassed about posting – people have the choice to read my blog or ignore it.  Thank you for your caring and support!  This blog has become a dear friend and confidant!

But allow me to be brutally honest – I am thrilled about this nomination.  I don’t know how it works but I mailed Katie and she gave me instructions…Thank you again brave Katie!

So according to Katie – here are the rules:

If you are nominated you must include the link in a blog, linking to the person/blog that nominated you.
You must answer some questions and nominate 10 fellow bloggers and link their blogs in your post.
Let the people you have nominated know that you have nominated them!

Here are the questions:

1. Who is your favorite philosopher?

Confucius without a shadow of a doubt!

2. What is your favorite number?

9 – I believe in the science of numerology the qualities of the number 9 are those of leadership, the ability to see clearly, integration, personal integrity, unity, truth, perfection and concord.

9 represents wisdom and responsibility, and the ultimate goal of the number 9 is to serve humanity.

9 represents human’s ‘earthly lesson’, which is ‘forgiveness’.  Number 9 learns selflessness and compassion.  People with the 9 energy work without motive.  Their purpose is for the greatest good of all.  They have a protective energy and they have great power and love in their soul.  They will grow and learn throughout their lifetime tolerance, compassion, selflessness and generosity.  There is a great strength of character within the 9 person, as well as wisdom, intuition and high idealism.  There is also a great deal of warmth of feeling and love of home, family and friends.

3. What is your favorite animal?

Eagles!

Did you know that an eagle knows when a storm is approaching long before it breaks?

The eagle will fly to some high spot and wait for the winds to come. When the storm hits, the eagle sets its wings so that the wind will pick it up and lift it above the storm. While the storm rages below, the eagle is soaring above it.

The eagle does not escape the storm. It simply uses the storm to lift it higher. It rises on the winds that bring the storm.

We are all faced with the winds of the storm that bring sickness, tragedy, failure, and disappointment in our lives. It is not the burdens of life that weigh us down, it is how we handle them.

The Bible says:  “Those who hope in the Lord will renew their strength.  They will soar on wings like eagles.” Isaiah 40;31.

4. What are your facebook and twitter ?
https://www.facebook.com/tersia.m.burger

Twitter @Tersia912

5. What is your favorite time of day?

I am a night owl.  I am not a morning person!

6. What was your favorite vacation (or ‘holiday’ as we say where I’m from)?

My honeymoon in Switserland and Germany in 1990.  Everything was so magical.

7. What is your favorite physical activity?

Walking barefoot on the beach.

8. What is your favorite non-alcoholic drink?

Tea!  I must have 15 cups of tea a day!

9. What is your favorite flower?                                                                                                             For the life of me I cannot remember the name of my favorite flowers.  

10. What is your passion?

My family,  my work and the downtrodden.

My Ten Nominees:

I actually don’t know if I can only nominate 10 bloggers.  All these bloggers have meant a lot to me.  I have learnt from them.  Some of them have given me great insight into Vic’s journey and http://ourlonggoodbye.wordpress.com transports me into an Assisted Living Facility and brings back memories of my Dad’s Alzheimers journey….  Trazy of ohwhatpain has given me great insight in pain.  Here goes!

  1. http://connectivetissuedisorders.wordpress.com
  2. http://ohwhatapain.wordpress.com
  3. http://thedrsays.org
  4. http://ourlonggoodbye.wordpress.com
  5. http://ramblinsofagrievingmom.wordpress.com/
  6. http://made4victory.wordpress.com/
  7. http://smilescavenger.wordpress.com
  8. http://onewomansperspective02.wordpress.com/
  9. http://allthatmakesyou.wordpress.com/
  10. http://walkingthroughpain.wordpress.com

If you click on any of the links above, you will enter a different world that will enrich your life.  Thank you to everyone who reads my blogs and puts up with my rambling, self centred emosions.

God’s Megaphone…….


C.S. Lewis says “Pain insists upon being attended to. God whispers to us in our pleasures, speaks in our consciences, but shouts in our pains. It is his megaphone to rouse a deaf world.”

For 37 years I have bargained with God.  He alone knows of all my anguish, tears, pleading, my fears and pain.  I am strong.  I don’t cry easily or often.   I have cried before God.  Pleaded with Him for mercy.

He chose to ignore my pleas for mercy.

I have not been to Church in more than two years.  I attended Marlene and then my Dad’s funeral.  I went to one service at Reuben church.  I have been angry with God….. Disappointed that the God of Mercy I learnt about from my parents’ knees does not exist.  I have only experienced a God who has sentenced my child, and now my grandson, to a life of pain and suffering.

Today I attended the annual church fete.  The arms that I have missed for more than 2 years enveloped me.  Kisses rained on my cheeks.  “I have missed you”, “We still pray for you and Vicky everyday of our lives”….. “It is so good to see you!”

The minister, Martin, hugged me and said “I think of you every day.  We are always here for you….

I cried.  I miss my church friends but I cannot go back for the wrong reasons.

I wondered tonight why the friendships did not last outside the confines of the church?  I realized that our pain is too much for people to cope with.  They hurt for me…..

But in the  silence in our everyday lives is deafening…God’s megaphone has obviously not roused the deaf in our world…….

The final battle


Vic and JD watching a movie on the laptop
Vic and JD watching a movie on the laptop

For the past couple of days JD has not eaten well and lost control over her bowels a couple of times.  This morning she looked at me with her beautiful, soulful brown eyes and whimpered….

A couple of times we have had her paloured for her final journey and then my courage forsook me.  I kept finding excuses why she should not go for an injection.  Her cough was better, “she has a sparkle in her eye”,” she “bounced” around her snack”….  Yesterday I gave her some of her all time favorite treats i.e. dried sausage (droëwors) and she did not touch it!

Last night she sat upright – I think it was too difficult to breathe.  JD had congenital heart failure.

Today Danie came home from a business appointment and I said “It is time”.  He knew exactly what I was saying.  Vic came through and sat on the carpet with JD.  She said goodbye.   I picked JD up and walked to the car.  Danie drove.

We took JD to our local SPCA.  A young, sympathetic, female veterinarian asked me if I wanted to leave.  I said “No.”  She battled to find a vein.  “It’s the congenital heart failure” she said.

“She is almost 16 years old” I said.

“Wow, she is really very old.  She is a pretty little dog” she said

“Have you ever had a dog euthanized?”  she asked

“No” I said

“I will inject an anesthetic into her veins and she will fall asleep.  She may have a muscle contraction or a bowel movement.  It will be unpleasant for you but not for JD.  She would have passed on.”

“Okay” I said

She found a vein and JD slipped away whilst my tears fell on her coat.

At 12:05 on the 24th of August 2012 JD went to Doggie Heaven.