Announcement

Collapse
No announcement yet.

A Sad News Documentary Piece about our families

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

    A Sad News Documentary Piece about our families

    This was Part 1 of a CBC documentary news piece on aging parents of children with disabilities:
    Only registered and activated users can see links., Click Here To Register... Pretty sad and pretty dire.
    Donna, Mum to Natalie (22), ablebodied, kind and beautiful and Nicholas(26), severe CP, non-verbal, tube fed, multiple surgeries, chronic pain, happy kid except when the Liverpool football club or the Ottawa Senators Hockey Team are losing!
    Check out my blog: http://www.donnathomson.com


    #2
    ((((((Donna))))))

    Hmmm ... not sure that I can manage watching this one. Will have to ponder it awhile ...

    Love & Light,

    Rose
    Mom to Jon, 49, & Michael, 32, born with an undiagnosed progressive neuromuscular disease. Angel Michael received his wings in 2003. Angel Jon received his wings in 2019. In 2020, Jim, their Dad, joined them.

    Comment


      #3
      Hi!

      I watched it yesterday, very sad piece. Glad that she has a great supportive husband to help her, but wish they didn't have to wait so long for placement...20 yrs?? Wow. I feel so bad how she talked about giving up doing things for herself. Personally, I always try to sneak in time for me when I can...yes I've had to cut back on the amount of time but I refuse to completely give up and give in! But Caitlin does not require as intensive care as the lady's son does. With Caitlin, I can put in a movie and be in a different room in the house if I need to be. I know all situations are so different....it is such a shame that society sweeps these problems under the rug. I admit, that before I had Caitlin I didn't really think about it either. It's scary to wonder what services will be available when she is an adult. I do think about it quite a bit, but am usually too busy putting out the fires of today to look into anything in depth for future placement/services. I 'liked' a thing on facebook, I think it was called Wisconsin Familes Forward, so I do get updates on what my state is doing politically for and against the disabled population. That was around the time my state froze FamilyCare (how services are provided to adults for inhome care)...the freeze would have forced families to only be able to put elderly/disabled into costly nursing homes even if they didn't need that level of care. Glad that the feds forced the state to lift the freeze. That is about as much as I know though. C will have a home visit this yr for Katie beckett renewal so I am planning to use my time with the caseworker to ask about future care/services. Can't wait to see part 2, hoping there is a happier ending for that family...

      Lisa O.
      sigpicLisa O: mom to Caitlin (14-CP, VA shunt, seizures), Brandon (12), Tyler (10), Logan (7)...my babies are all getting so old!!

      Comment


        #4
        Hi guys, well, the only thing I can say is that the earlier you plan, the better. And that means financially, emotionally, spiritually, physically.... for both our children and ourselves. Scenario planning is the key - it's the 'what if' principle. But it's so hard when you are in the thick of looking after kids every day - there's no time to IMAGINE the future! But still, it is necessary. I'll post part 2 of the series now. Love to all my dearest friends here on CN2 xoxoD
        Donna, Mum to Natalie (22), ablebodied, kind and beautiful and Nicholas(26), severe CP, non-verbal, tube fed, multiple surgeries, chronic pain, happy kid except when the Liverpool football club or the Ottawa Senators Hockey Team are losing!
        Check out my blog: http://www.donnathomson.com

        Comment


          #5
          This is so sad...
          Mild Spastic Diplegia Cerebral Palsy and bad proprioception.
          My website for my original short films! http://cripvideoproductions.com/astrokeofendurance.php

          Comment


            #6
            ((((((Donna))))))

            Jim and I watched the video twice. I have written two lengthy responses, but I'm sitting on my hands.

            My reaction might be misconstrued.

            So, I will just say this:

            Appropriate in home and out of home supports should be in place for all families~those, who choose and are able to provide care at home, and those, who do not choose or cannot provide care in the home. The number one priority of all involved agencies, parents, families, friends, and medical providers should be the best interests of the adult child with a disabling condition.

            The first question is always: what is best for my child?

            Love & Light,

            Rose
            Mom to Jon, 49, & Michael, 32, born with an undiagnosed progressive neuromuscular disease. Angel Michael received his wings in 2003. Angel Jon received his wings in 2019. In 2020, Jim, their Dad, joined them.

            Comment


              #7
              Didn't get to watch it this morning the sound on my computer wasn't working. I'll try tomorrow.
              Mary Grace

              Comment


                #8
                Rose, I completely agree. I'll post Part 2 now so you can see that too. In Canada, there is a generation of baby boomers who did not plan financially or otherwise for the future of their child with a disability because a) there was no expectation for children to survive their parents - that situation is unprecedented and so everyone is unprepared and b) we have a tradition in this country of full national health care which families believed extended to social care of their adult sons and daughters with disabilities. Now, children with disabilities are surviving and we have an ageing population. Governments cannot afford to offer social care to adults so families are left holding the bag, unprepared. What this documentary does not represent though, are the success stories of families who have banded together to create innovative solutions for their kids. Lots of families have pooled their money to buy a property then created a micro board to run the home with the disability pension benefits pooled to buy home help. Home shares are another wonderful example of what works for many, especially in the UK where it's really taken off. I think though, that this FIRST generation of families just suddenly find themselves in this situation without having planned for it and that is proving to be catastrophic for many. That aside though, I thought the people in the news item were just awful to their son. I felt so sorry for that lovely young man. Sending lots of love to you, Jim and Jon on this Thanksgiving! xo
                Donna, Mum to Natalie (22), ablebodied, kind and beautiful and Nicholas(26), severe CP, non-verbal, tube fed, multiple surgeries, chronic pain, happy kid except when the Liverpool football club or the Ottawa Senators Hockey Team are losing!
                Check out my blog: http://www.donnathomson.com

                Comment


                  #9
                  Oops, just realized that I already posted it the other day!
                  Donna, Mum to Natalie (22), ablebodied, kind and beautiful and Nicholas(26), severe CP, non-verbal, tube fed, multiple surgeries, chronic pain, happy kid except when the Liverpool football club or the Ottawa Senators Hockey Team are losing!
                  Check out my blog: http://www.donnathomson.com

                  Comment


                    #10
                    ((((((Donna))))))

                    Okay. You said what I wanted to say. Thank you.

                    Jim and I both felt that these parents viewed their son as a burden and with tremendous resentment. They demonstrated no affection toward him. It was all about how miserable their lives are because of the drudgery of his care, how they've lost friends, and how they have given up their own lives.

                    The narrator opened with, "His home is his retreat, but it's his parents' prison." That said it all to us.

                    The narrator mentioned that this young man attends an adult day program, and that they have respite care for him. So, if they are in a prison, it is of their own making, because they have those opportunities to be free to do what they want to do.

                    Additionally, this young man's level of care seems pretty basic to me. He's ambulatory, he self-feeds (although not fast enough to suit his mom), and he has comprehension and communication skills. No Gtube, no special diet, no respiratory problems ...

                    The purpose of the story is valid, and attention needs to be drawn to the lack of options for aging parents of adult children with special needs. In my opinion, they chose the wrong family to showcase that need, because these parents did not draw any empathy from me or Jim. My heart goes out to the young man, because I don't see any love or joy in his life with his parents. They've been looking to place him out of home for 20 years.

                    What this documentary does is reinforce the stereotype that children with special needs are a burden, and that parents of special needs children are bitter.

                    As you said, a better way to convey the magnitude of the crisis of aging parents and their adult children would be to focus on the innovative networking of parents, and families like yours, who found the perfect solution to meet Nick's needs, when in home care was removed as an option for him.

                    Whew! There. I said it.

                    Thanks for your Thanksgiving wishes! I'll be tossing the Tofurkey in the oven in a few hours. We watched the parade together this morning. We're thankful that Jon is well today, as yesterday, he had one of his mysterious fevers and lethargy. It came down with cooling baths, and it's normal today. I'm thinking hypothalamus or hypothyroid. Or both. He had no symptoms of anything. Just a temp of 100.7, which is high for him.

                    I give thanks for all of our wonderful CN and BT family and wish everyone a blessed Thanksgiving and holiday season.

                    Love & Light,

                    Rose
                    Mom to Jon, 49, & Michael, 32, born with an undiagnosed progressive neuromuscular disease. Angel Michael received his wings in 2003. Angel Jon received his wings in 2019. In 2020, Jim, their Dad, joined them.

                    Comment


                      #11
                      Oh, thank goodness that Jon's temp is normal today. That's a great reason to be Thankful! I agree with you completely about this family - I found it so awful that he kept asking for something and she kept saying 'sure, in a minute' (but never intending to make any effort to give him something he wants. Did you see the state of the basement which is the only oasis for this poor young man (in this huge house on this huge property). Honestly, some people just should never be parents period. Anyway, that is really beside the point that our children need flexible options for making a future good life that gives a decent old age to parents and where love can abound in families. Happy Thanksgiving, my dear friend.
                      Donna, Mum to Natalie (22), ablebodied, kind and beautiful and Nicholas(26), severe CP, non-verbal, tube fed, multiple surgeries, chronic pain, happy kid except when the Liverpool football club or the Ottawa Senators Hockey Team are losing!
                      Check out my blog: http://www.donnathomson.com

                      Comment


                        #12
                        ((((((Donna))))))

                        Yes, the state of that basement was horrible. It just reflected the neglect that young man suffers.

                        To me the parents' attitude toward their son is and yet it isn't beside the point that society needs to address living situations for aging parents and their adult children. As I said, this documentary reinforces a negative stereotype about adult children with disabilities and their parents. That has an overarching impact on viewers.

                        These people aren't desperate. They just don't care and don't want to be bothered. Families, who are really in dire need of assistance, should be featured to generate the compassion and advocacy of others, who aren't in this situation.

                        To garner the attention of the general public, which is necessary to implement change, we need to show loving families, who are truly struggling with 24 hour care for their child, or parents, who have their own medical issues, as well as their child's care, or parents, who were denied the supports for in home care, so that their child could remain at home, and are forced to find out of home placement, where none exists. And the parent cooperative, which you mentioned.

                        Choosing the wrong family to represent the cause hurts the cause. And this was undoubtedly the wrong family for this cause.

                        I weep for that young man. I just want to wrap my arms around him, take him in, love him, make him smile and laugh, and take him everywhere he wants to go. I can think of a million ways to have a joyful life with him. It's tragic that his parents can't find a single one.

                        Love & Light,

                        Rose
                        Mom to Jon, 49, & Michael, 32, born with an undiagnosed progressive neuromuscular disease. Angel Michael received his wings in 2003. Angel Jon received his wings in 2019. In 2020, Jim, their Dad, joined them.

                        Comment


                          #13
                          Happy Thanksgiving everyone! :)

                          I did wonder that too, why the mom didn't do things for herself while their son was at the day program. I thought as nice as the house looked, they didn't have a better room for him to hang out in other than the basement? That, to me, was weird. I have my boys' toys in our basement which is still unfinished, but I at least painted the cement walls white (with drylok paint so I still need to put a coat of color on it...someday!) but it doesn't look 'basementy' at least and I put rugs down too and our old loveseat and recliner. His room looked very lonely. I agree with Rose, it would be nice if they did a part 3 with creative solutions that are working good for familes.

                          Lisa O.
                          sigpicLisa O: mom to Caitlin (14-CP, VA shunt, seizures), Brandon (12), Tyler (10), Logan (7)...my babies are all getting so old!!

                          Comment


                            #14
                            Rose and Lisa, we three could figure out a million ways to give that young man a good life. My heart broke for him. xD
                            Donna, Mum to Natalie (22), ablebodied, kind and beautiful and Nicholas(26), severe CP, non-verbal, tube fed, multiple surgeries, chronic pain, happy kid except when the Liverpool football club or the Ottawa Senators Hockey Team are losing!
                            Check out my blog: http://www.donnathomson.com

                            Comment

                            Working...
                            X