Showing posts with label tanner. Show all posts
Showing posts with label tanner. Show all posts

Wednesday, March 2, 2011

Talking About The Elephant In The Room

For those of you who read my periodic postings, you know that Catherine - a.k.a. Her Bad Mother - is my daughter and that Tanner is my grandson, and you know them both extremely well. You do not know a whole lot about my younger daughter, Christina - Chrissi - who is Tanner’s mother.

Christina and Tanner’s father separated almost three years ago and since that time she has borne the brunt of the responsibility, financially, physically and emotionally for Tanner. My son-in-law loves Tanner very much but for a very long time he was emotionally incapable of dealing with all of the issues that are involved with caring for a child whose disease is aggressive and terminal.

Chrissi has always been a working mom. Her job is one that is hard on the heart and soul (she deals with the legal side of broken and bitter families). But despite her job, her son’s diagnosis and the breakdown of her marriage, Chrissi has always projected the persona of a confident, totally-in-control, I-can-do-it-myself woman. After Tanner’s diagnosis, Chrissi dealt with the pain of knowing she had to watch her son die slowly, piece by piece, by pushing herself to extreme limits. In her efforts to insulate herself from pain, Chrissi developed a brittle veneer that discouraged any attempt by friends or family to give her the support that she needed. In her mind, Chrissi had to be supermom. She had to be an advocate for Tanner, and for other boys with Muscular Dystrophy. She had to educate the community, the school system. She had to fight for the support and resources that Tanner needed and that she needed. She had to maintain her career. She had to ensure that Tanner’s needs did not interfere too invasively with his siblings' needs.

Somewhere in the constant battles she was fighting, she found an outlet for her pain – running. She became superwoman – a record setting marathon runner (every run was in Tanner’s name and for Duchennes Muscular Dystrophy research). The physical challenges of long distance running masked her emotional challenges.

Every race she ran received extensive local media coverage. She achieved her goal – she ran the Boston Marathon – she was an inspiration! But the higher Chrissi and Tanner’s profile became in their community, the pressure on Chrissi to be supermom correspondingly increased – keep smiling, don’t let anyone know that you can’t be up half the night with a sleepless Tanner and be “perky Chrissi” the next day, don’t let anyone know how frustrated you get when Tanner soils himself just before you are leaving for work, don’t let anyone know that there are times when Tanner's constant screaming makes you want to scream back, don’t let anyone know - don't let anyone know this, especially - that there are times when you wish the end was sooner rather than later because you can’t stand to watch his deterioration, his suffering, his pain.

Supermom Chris – couldn’t let her guard down – couldn’t let the cracks show - what would people think? So she internalized the guilt she had around her “bad mother” feelings and tried harder.

But as Tanner’s care needs increased (he gets heavier and heavier, even as his muscles disintegrate, so that moving him to change a diaper or get comfortable in bed is a challenge, and his bones are becoming fragile and prone to breaking; his leg was broken during that Air Canada mess last year, something Cathy never talked about), Chrissi struggled with her increasing inability to handle his physical needs and the ever-evolving mental health issues that his autism brings.

Nobody could help, not really. She allowed her sister to help, somewhat, from a distance. But she kept me and her friends at bay. Any expression of concern was seen as criticisms of her performance as a mother. She resisted help. She resisted support. She tired, as best she could, to keep her pain to herself. So when Chrissi broke, she broke hard. She had a breakdown last fall and has been on stress leave ever since.

The past months have been difficult for all of us, but they also have been cathartic. The time has brought us closer together, as a family. The conversations Chris and I now have are thoughtful and supportive. The brittle veneer has been shattered and she has let herself be vulnerable. She has opened herself to the love and support of family and friends. More importantly, she now realizes it’s okay to verbalize her negative feelings and her concerns of inadequacy and to accept reassurance that those don;t make her a 'bad mom.'

But it has been a long process and many of our conversations have hurt my heart. When my child sits across from me and says, “Mom, I don't want this – why does everything have to hurt so much?”, I can barely stand the pain. The worst part is that she has been carrying this pain, and especially, this guilt, all by herself for a very long time.

Why do we, as a society, expect so much from those people who face adversity? Why do we expect bravery, sacrifice, stoicism in the face of pain and struggle and loss? Some pains are too great to face stoically. We're only human.

Chrissi still struggles with guilt but she has finally accepted the reality that she can no longer be Tanner’s sole and primary caregiver. She and Tanner’s father are now working together on a plan for Tanny’s care – he'll move into her house and take over the bulk of the physical care; she'll move into the basement that is being renovated, at least part-time - and that in itself is a major breakthrough.

The story is not over, but things are changing and there are no more elephants left in the room.

Friday, June 5, 2009

Injustice Is Another Word For This Sucks And I'm Angry

I am angry, really, really angry.

I visited daughter #2 today (mother of Zachary, Tanner & Sophie.) Chrissy is now on stress leave . She cried as she told me things were getting to be too much for her. The progression of Tanner’s disease and its inevitable outcome is beginning to take its toll.

Chrissy is a brave, strong woman, but today I saw an emotionally drawn, defenseless young woman. She has filled her life and Tanner’s with almost manic-like activity, but the reality of his disease is catching up with her and I am worried. Chrissy is crashing.

Tanner’s father and Chrissy have been separated for almost two years now and he is as useless as tits on a board. He can not now, nor has he ever been, able to deal with Tanner’s Muscular Dystrophy. He has not been paying his share of childcare expenses, he has not been paying child support regularly and he can’t cope with having the children for an extended period of time. Tanner’s father has had no part whatsoever in the house being refitted to wheelchair accessibility, the van being equipped with a lift, the bimonthly trips to Children’s Hospital in Vancouver, the frequent meetings with physiotherapists, occupational therapists, school support staff and so on & so on! He is embarrassed that he has a visibly disabled child. I am surprised Chrissy has held on this long.

My husband and I take the kids when we can and when it works for Chrissy. The distance we live from each other sometimes interferes with visiting. We will have Tanner and Sophie this weekend, so that Chrissy can have some much needed respite.

I guess I am more angry at Tanner’s father than anything. I don’t get how a 45-year old man can be such an irresponsible prick. Why is it that women end up with the short end of the stick. I’ve had a few glasses of wine and I am rambling and I may sound bitter, but when I sit and watch my child weep because she’s had enough it rips my heart out and I want to corner my ex son-in-law and rip his balls off and stuff them in his mouth. I want to say “be a man, love this child, show him and the world that disabilities don’t matter – Tanner’s disabilities are not a reflection of your precious manhood!"

Tanner is the sweetest little man in the world and it tears both me and my husband apart when Tanner wants to play soccer (like his sister) and we have to say “Tanny, you can’t." When Tanner wants to go to the river to walk around and pick rocks (like we used to) and we have to say “Tanner, you can't." What makes it even worse is that Tanner understands what we are saying. Tanner has no friends, he doesn’t have play dates because he’s different and most parents are as cruel as their children. It is fucking killing me and it’s killing my daughter.

Chrissy deals with all of this, alone – yes, she has wonderful, supportive friends and family, but at the end of the day it’s just Chrissy at home, by herself.

I spent twenty years in a profession helping children and families. I advocated and fought for justice for those who could not advocate or fight for themselves. There is nothing in this world that I abhor more than injustice. I always felt that because I was so blessed and my daughters were so privileged that I had a responsibility to advocate for those families and children who were not as fortunate as we were.

But I can’t seem to do anything to alleviate or ameliorate the injustice that is occurring in my family.

I have said my piece, thank you for listening.

Tuesday, April 14, 2009

Why, God?

I haven't been able to write anything for almost a week. I have been emotionally spent. Yesterday I read my daughter's heartrending blog and my heart wept again - for the families of those precious little souls who were taken too soon, and for my family - for what is yet to come.

Every time I read or hear about the death of a child, or the pain and suffering of a child, or of a child who, because of a disease, will never experience the pride of graduating from school, the anticipation of a first date, the excitement of first love, the joy of marriage and children, the contentment of growing old surrounded by family, and dying in peace, I ask God why.

There are millions of people in this world who do not question God – I am not one of them.

I believe in God, in his only Son, in Mary and all the saints , but there are times when I am angry with God. My audacity scares me - but, there are things I can not accept unquestioningly, willingly or with thanks.

I cannot accept unquestioningly that God would give parents the precious gift of a child and then abruptly take His gift away.

I cannot accept it is God 's will that my beautiful, innocent grandson die slowly, piece by piece.

There have been many times during my life that I have felt His presence and been thankful for blessings received.

This is not one of those times.