Thursday, June 14, 2012

Celebrating Young Carers

Over the next week there will events across Niagara and Haldimand County supporting and celebrating Young Carers and their families.  These events will shine a spotlight on Young Carers and raise awareness of the issues and the need for us to support and recognize youth for their contributions.  These events have been arranged through the Powerhouse Project Young Carers Initiative.

I know that having MS impacts not only me but my whole family.  In our area we have started up programs to provide life skills, support and recreational opportunities to children who live in families facing chronic illness, disability, addiction, and language barriers.  These programs have offered my kids an opportunity to meet people in similar situations and have fun.

Do you have Youth Caregiver/ Young Carers programs in your area?  What do you love about the programs?  What would you like to see happen in them?  I'd love to hear about what is happening in your neck of the woods!





Niagara Events
Flag Raising at St.Catharines City Hall with Mayor Brian McMullan
Monday June 18th @ 9:30 am

Information Booth at the St.Catharines Central Library
Wednesday June 20th @ 1:00 – 4:00pm

Powerhouse Project Documentary Debut at the St.Catharines Central Library
Wendesday June 20th @ 6:30-7:30pm

Carer’s Week Celebration at Queenston Heights Memorial Park in Niagara Falls
Friday June 22nd @ 5:00 – 7:30pm
Haldimand County and Norfolk
Meet and Greet BBQ
 Monday June 18th @ 5:00 – 8:00pm

Powerhouse Project 101 Presentation to the Community at the Haldimand Abilities Centre
Wednesday June 20th @ 11:00am – 12:00

Hagersville Scavenger Hunt
Friday June 22nd @ 5:00 – 9:00pm

Thursday, June 7, 2012

Support the Multiple Sclerosis Kidz Klub

Please support my friend in her mission to help out children who care for a parent with Multiple Sclerosis.
Here is her story:

‎13 years ago I was diagnosed with ms, It changed my life forever. I lost alot of things during my struggle. I could no longer teach, marriage, friends, but most important was my kids lost there childhood. They had to take care of me during these times when I lost use of my legs, when I went blind, loss of my hands. 
I Now have a chance to help other kids regain some of there childhood for a short time and after contest. I am by far the best makeover, but it goes according to votes. So I am asking you to go to the link below and vote. Each e-mail can be entered 5 times a day. I am hoping to win the $2500.00 for the MS kids summer camp.
Help me by helping them forget there worries and be kids for the summer.
Thanks
Kim and please pass the word



Here is a link that will allow you to vote for her.  People are permitted 5 votes per day.

 https://www.mkmakeovercontest.com/gallery.jsp?id=201932&lang=en&region=CA

Thursday, May 31, 2012

Caregiving Kids


I am going to share an article published by CNN because it does such a good job of explaining the kinds of challenges faced by children who provide care to a disabled relative, the implications of these responsibilities and how programs can help to support families.  These children are worthy of recognition and support.  Bravo for shining a light on these children in the CNN Hero's story.  Kim

Help for a 'hidden population' of caregiving kids

By Danielle Berger, CNN
updated 6:11 PM EDT, Thu May 17, 2012


Boca Raton, Florida (CNN) -- At 13 years old, Nickolaus Dent is his mother's primary caregiver.
He's responsible for the grocery shopping and cooking. He cleans the house. He does all the laundry.
His mother, Janine Helms, has been battling HIV for as long as Nickolaus can recall, and her health has deteriorated in the last couple of years. Nickolaus makes sure she takes her medication. He often helps her get dressed, and at times, he has helped her bathe.
Nickolaus' father died two years ago. Since then, ensuring Helms' well-being has been a full-time job for Nickolaus, leaving him with little energy to socialize or study.
"It does make it hard to pay attention in class," he said. "Helping her out is a bigger priority than going to school and getting (an) education, because I feel if I don't have her, I don't want to go to school. Whatever happens to her happens to me."
Nickolaus is just one of the estimated 10,000 youth caregivers living in Palm Beach County, Florida, according to the American Association of Caregiving Youth. The nonprofit, founded by county resident Connie Siskowski, was instrumental in bringing this previously unrecognized population to light in 2002, and it has since provided support to more than 500 area youths who are caring for an ill, disabled or aging family member.
Connie Siskowski knows firsthand what it\'s like to be a child and take care of a loved one.
Connie Siskowski knows firsthand what it's like to be a child and take care of a loved one.
"No child in the United States should have to drop out of school because of caregiving," said Siskowski, 65. "These children suffer silently behind closed doors. ... They don't have the help and the support and the recognition that they need."
According to a 2006 study conducted by Civic Enterprises for the Bill and Melinda Gates Foundation, 22% of high school dropouts in the United States leave school to care for a family member (PDF).
It's these children who Siskowski had in mind when her group started the Caregiving Youth Project at Boca Raton Middle School. The project, the first of its kind in the nation, aims to intervene early on in the academic lives of youth caregivers.
Special classes, led by a mental-health professional or social worker, cover topics such as coping with stress and anger, managing finances and setting goals.
Periodic field trips and overnight camps offer recreational, social and educational activities. There are home-care demonstrations and workshops.
The program also makes teachers and school administrators more aware of the children's extenuating circumstances and how they can lead to truancy, absenteeism and dips in academic performance.
The hope is to reduce the negative effects -- anxiety, depression and feelings of isolation -- that caregiving responsibilities can have on a child's mental, physical and emotional health.
CNN Hero helps teen who cares for mom
"We can't change the health condition of the person (receiving care)," Siskowski said. "But what we can do is provide the skills and the resources and the value to the children so that they can have a little more balance in their life. And also so that they know that they're not alone."
Since 2006, the program has been introduced into eight area middle schools and followed hundreds of students into 17 area high schools.
"We stay with them to graduation, and it's amazing," Siskowski said. "We've watched these kids grow up before our eyes. It's nothing that happens overnight, but it's very gratifying. It's like, 'OK, there's one more kid that's going to make it.' "
Nickolaus joined the program last year. The group provided him with a computer, a bed, clothing and tutoring. Now, he has raised his grades and aims to make the honor roll. He was also able to attend the group's overnight camp while a nurse's aide stayed with his mom.
"I found out there are more people that do the things I do, and some do more," he said. "Now I'm getting As and Bs, and I feel more confident in school."
Children in the program are also offered a home study by a medically licensed staff member or contractor who assesses what skills and resources are most needed to support a child. Working with dozens of community partners, Siskowski's group helps families with unique needs.
"We've provided clean-water systems and enlisted the support of community members to build wheelchair ramps or relocate a family from a moldy environment," said Siskowski, whose group relies solely on donations and grants. "We've provided in-home tutoring, light cleaning, translation and transportation support, counseling, access to medical care, financial assistance and food resources.
"We've donated computers and printers. And slow cookers, as we've had several fires in homes where children are cooking for their families."
Siskowski knows the toll that caring for a loved one can take. As an 11-year-old, she cared for her grandfather until his death two years later. She remembers waking up at 2 a.m. to give him his medication and finding that he had died.
"I don't think I realized he was going to die. No one prepared me for that," she said. "It was very traumatic. But way back then, nobody really appreciated the trauma or the impact of losing someone."
Siskowski became a registered nurse in 1967 and has worked in Florida's health-care community for decades. Over the years, she has witnessed how technological advances have affected aging baby boomers and their families.
"People are living longer," she said. "We have much more technology and electronics that are available. ... More and more people who maybe yesterday would've been in a nursing home are being cared for at home. And so that puts a burden on a family.
"The hospital is in a unique situation. ... Technically, they're supposed to be able to give instruction to a caregiver. But sometimes that caregiver is a child."
The tasks can be sophisticated, too, from monitoring respiratory devices to cleaning catheters and preparing syringes. And not all of the children are caring for just one parent like Nickolaus. Others have to care for multiple family members, including siblings.
A report released in 2005 (PDF) by the National Alliance for Caregiving and the United Hospital Fund said there were at least 1.3 million caregiving youths, ages 8 to 18, nationwide. It's a population that has been virtually hidden for several reasons, including the reluctance of many sick parents to go public with their infirmity.
"Parents are embarrassed to tell school members, or the principal, that they have medical problems. ... Their pride goes out the window, and most feel more vulnerable," Helms said.
Children also fear trouble for themselves and for their families. While they might know that too many truancies and absences could land them in court, they're often more fearful that a parent could be deemed incapacitated and the family split up.
"Children are afraid to reach out because they don't want to be taken away from the parent," Helms said. "It's scary. And people don't want to be near you when you have an illness. It's just as hard on the disabled parent as it is the child, to open up. That's why it's kept like under the table."
Siskowski and her group are determined to create other options and provide other solutions. She says the first step is acknowledging youth caregivers and telling them they are not alone.
"We have definitely turned around lives and kept kids in school because they feel valued," she said. "They never knew anyone noticed or cared.
"It can turn their frustration and anger and flip it around to feel valued and supported in the role they are having for the family as well as society. If they weren't doing some of the things they are doing, who would be?"
Want to get involved? Check out the American Association of Caregiving Youth website at www.aacy.org and see how to help.

Wednesday, May 30, 2012

World MS Day

Red lights shone over Niagara Falls for World MS Day






Today is World MS Day!  Today I will be attending a celebration hosted by the MS Society of Canada in Niagara Falls.  There will be a presentation by a radiologist from Buffalo on the topic of CCSVI followed by a lighting of the Niagara Falls.  The falls will be lit up in red the national colour for MS in Canada.

Thursday, May 10, 2012

Bridging the Gaps

                                                           Photo CreditShakeelgilgity
Time has a way of moving forward.  It moves forward even in spite of the events that seem to stop the world for just a moment for those of us in it.  I am sure if you think for a second you can conjure an image of a time when you were so lost in the moment that it seemed like time was standing still.  A few of these moments come to mind for me and they are the richest moments my life has offered me.  


For instance, the moment when my eyes first met my children; when my ears were blessed with the sound of their cry or the moment after learning of a death that I realized I would never see my loved one again.  I imagine that for people who survive natural disasters there is a moment that is a blip in time when the shock of what was and what is to come fractures the past from the future in an cosmic surge. What was, is no longer and there is nothing to do but let time provide a bridge to what will be.

bridge is a structure built to span physical obstacles with the purpose of providing passage over the obstacle.   The bridge is a perfect analogy for the chasm that existed between my illness and my recovery; my life before diagnosis and my life after.  My life before illness and after were starkly different lands and the journey that bridged the two was built with some very important teachings.  The planks laid out for each step to be taken were vitally important so that I didn't fall into the abyss below.  There were many people who acted as stabilizing forces encouraging forward movement like a loud ticking clock leading me and propelling me along my journey.


Embracing fear, and working through the grief process has not been a linear process for me.  I have moved between fear (of my unknown future in terms of health), anger at the loss of my social stature and career, worry about how my mental adjustment and my physical health are impacting my children, and I have learned to relish moments of acceptance that are hard won and don't seem to last nearly as long as I'd like them to.


One thing that has become exceedingly clear to me is that while our experiences are different our individual journeys hold some stark similarities.  We all have a cross to bear in this world and we all struggle to find worth and purpose.  We all love, lose, grieve, triumph and we all have something unique to offer this world.  My work in the Young Carers movement has brought some vibrant, committed people of all ages into my life.  It has given me a place to invest my time, energy and advocacy.  


I look forward to sharing some themes from the recent conference I attended in my next entries and thank you for bridging the gap between what was and what is in my life.



Monday, April 30, 2012

First international young carers conference!


I am so excited!  I completed my conference selections for the first International Young Carers Conference which will be held in Vancouver British Columbia in May.  The conference is called Child and Youth Matters and has combined three conferences in one.  They are the First national Family Mental Health Conference, the Third International World Congress on Children of Parents with Mental Illness and the First International Young Carers Congress.

The number of presentations to choose from made choosing the conferences difficult.  There were so many things that appealed to me from my previous life as a mental health Case Manager and  my new role as an advocate for care-giving children couldn't be a better fit.  The conference will bring together people from many different backgrounds to share and learn.

The Young Carers movement in the UK and Australia is well established.  In England the government has a national strategy for Caregivers.  Our Canadian group will be able to learn a great deal from these established programs.   I am looking forward to the experience and learning opportunities that will shape our Canadian commitment to children who take on important roles in their families and communities.  I will report back in a few weeks after the conference!

Sunday, April 1, 2012

Supporting our Supporters



Caregivers rarely beat their own drums.  As a group they don't see the things they do as heroic they simply plug along giving and providing in response to the needs that present themselves in front of them.  It is expected that families will care for the young, sick and frail.  As a society little value is placed on the tireless advocacy and care provided to those who need it.


I have been an active participant in programs that support caregivers young and old.  Trying to garner support for these groups has been an uphill battle.  People are reluctant to cast themselves as martyrs or to beat their own drums.  They simply meet the tasks before them and wade through one after another out of love, commitment or a sense of responsibility.


What brought me to writing this latest post is reflecting on the role that the local chapter of the MS Society has played in my life since my diagnosis.  I've served on the Board of Directors for the Young Carers Initiative and volunteer at the local chapter of the MS Society where meeting the challenges facing caregivers is a frequent discussion.  What is also difficult is reaching overburdened caregivers both young and old to give them support and replenish them to keep doing what the do.  They too do a poor job at the beating their own drum about the work they do and the significance of the contributions they make.


The local chapter of the MS Society has been a cornerstone in my life since my diagnosis.  At the local chapter I have been an active volunteer as I worked through my own grief cycles.  They allowed me to contribute and be a part of their mission to improve the lives of those living with MS as I dealt with the loss of my career, my image and grappled with my sense of self.  From the early days following my diagnosis they provided me with information, equipment, exposure to modified yoga and exercise programs, support groups and a friendly visitor program for people who can not get out. My children have benefited from the Kidz Klub program where they have had opportunities to attend amusement parks, and engage in activities with other children who live with a parent with MS.  I have participated in creating a newsletter, provided educational in-services to newly trained health professionals, provided office support, and assisted in writing grant proposals.  


The more I reflected on the role they have held in my life for the last six years, the more committed I became to supporting them.  The MS Society of Canada is experiencing some significant growing pains due to decreased revenue.  They receive no government funding and rely solely on public donations to enable continuing research goals and support at the local level to those living with MS.  They are in a position to need to make some serious decisions about where their priorities lie.  I only hope they are able to find a way to keep offering supports "on the ground" and to provided needed dollars to enable research to continue.


I would encourage you to complete this survey to let the MS Society of Canada know what is important to you: (Canadians only)


This 'renewal initiative' outlines the potential priorities.
http://mssociety.ca/en/community/mssc/Renewal.htm

Here is the survey (Click on the survey monkey link)
http://mssociety.ca/en/pdf/RI-Paper-...-Solutions.pdf



And finally to consider making a contribution to the local MS WALK in support of those who support people living with MS.
http://mssoc.convio.net/site/TR/MSWalk/OntarioDivision?px=1256015&pg=personal&fr_id=1296



“There is no greater agony than bearing an untold story inside you.” Maya Angelou