Sunday, October 18, 2009
Halloween Pumpkin Pictures
I thought you guys might enjoy pics of Chelsea picking out a pumpkin to decorate (no carving here!).
Labels:
decorate pumpkin,
down syndrome,
halloween pumpkin
Sunday, October 11, 2009
Looking for your input
As some of you may be aware, I am building a directory of DS resources. I guess the lack of resources available for my family has driven me to do what I can to keep others from being in a situation similar to ours. Maybe I can learn a thing or two along the way as well. At any rate, one of the directory sections is Down Syndrome blogs. I would like to extend an open invitation to those of you who blog about your experiences as DS caregivers to include your blog in the directory. If you would like your blog included, just leave me a comment with your link and I will see that it is included. Feel free to let me know if there is something particular you would like included in the description, otherwise, I will use the information directly from your blog. If you would like to take a look at the directory to see if you are interested first, it can be found at http://downsyndromehelp.boomja.com/ Some of you may find your blog already there, if so, let me know if you don't want it included.
Saturday, September 26, 2009
Nice blog
Sunday, September 13, 2009
By popular request - Pictures
Another day in paradise
I woke up to a beautiful morning this morning. The sun was streaming in through the window, a pleasant breeze bringing me the scent of fresh air. In my state of not being quite awake, I thought "What a nice morning, maybe we'll go have some breakfast somewhere." Then I woke up. Then I felt the sadness wash over me. I remembered that there are no more pleasant breakfasts with hubby at the local diner, no more mornings spent cuddling and enjoying the sunshine. No more mornings spent planning our future over coffee. This is our future, right here, right now. Do I regret giving up my future to insure that Chelsea has one? Not a bit. Do I desperately wish there was another solution? Absolutely. During the few short weeks my son had Chelsea, he signed her up on the group home waiting list in an adjoining county. The case worker told me that he told her point blank that he would not take care of her until she is 18. What a tragedy that this loving little girl is the subject of so much controversy, that her own father doesn't want to take care of her. It is the one thing that makes me ashamed of my son. I pray daily that some solution that is truly best for all, most of all Chelsea, will come to light. No matter what the cost, I will not abandon her or put her in a bad situation just because I want my life back. I will continue to love her, take care of her, and then cry in private for as long as it takes to find a solution. All of you who pray, please pray for us, for our family, for Chelsea. She deserves the best, and I am not capable of giving her more than mediocre, so please pray for something wonderful for her.
Labels:
coping with disability,
disabled child,
downs,
downs syndrome
Monday, September 7, 2009
Friday, August 28, 2009
Chelsea's Homecoming
Well, on Tuesday evening, Chelsea came home without much fanfare. My son dropped her off at around 7:30 pm and she had school the next day. She sat in her room watching a favorite movie for about an hour, and then asked me what time her dad was coming back. When I explained to her that she was back with us now, that her time with dad had been just a little vacation, she smiled and jumped under the covers. She was asleep in five minutes. I had no idea that he had not explained anything to her. She had not had a bath, and he didn't bring her clothes until 10:30 that night, clean but thrown unfolded in a box. Not my idea of preparing for the first day of school. That's just not how I live. I have everything ready the night before, baths over with, clothing laid out, etc. I like a nice, calm, organized morning. To make matters worse, I overslept the next morning, so it turned into a mad dash to get ready and get out the door. Chelsea took it all in stride, I, on the other hand, was a very unhappy camper.
Thursday, August 20, 2009
The break is over, even if she isn't home yet
We have a few days left, but already I am preparing for school to start, getting her room cleaned, and having anxiety attacks about how I will schedule my doctors' appointments around her school schedule and the absence of anyone to babysit or get her from school if my appointments run over. I have appointments with specialists, and those can be all day events. I am worrying about how I will keep up with her laundry, because our dryer is irreparably broken and we can't afford a new one (or even a good used one). I worry about how I will take care of her if my family doctor's predictions of my final diagnosis come true. I think I am worrying too far ahead, yet I feel like I have to. They say that God never gives us more than we can handle, but I think that being 50 and taking care of a Downs child, being dirt poor, and having a possible diagnosis of MS (and no health insurance) hanging over my head is a bit much.
Monday, August 17, 2009
One more week of freedom
School starts next Tuesday, so Chelsea will be back with us on Monday evening. I have such mixed feelings about it. Already I dread the loss of freedom. Back to begging someone to watch her so hubby and I can go somewhere together for a couple of hours. Back to the morning routine of getting ready for school; gone are the leisurely mornings filled with newspaper reading and coffee drinking. There will be no more uninterrupted conversations with my husband, no more sleeping in on the weekends, no more eating dinner at 9:00 pm just because we want to. But there is also a part of me that is excited to have her back. I miss her, plain and simple. If she's here, I know she's safe. This has been a wonderful few weeks' break for us, no doubt about it. It has given my husband and I a chance to reconnect, to remember who we were as a couple. I only hope we can hold on to that connection when Chelsea comes home again.
Monday, August 3, 2009
Chelsea is 15 today!
I can hardly believe she is 15 years old today. It seems like just yesterday that I held her in my arms just minutes after she was born. Time goes by so fast, and it doesn't seem to matter whether times are good or bad, they still fly past us at the speed of light. When I blink again, she will be 18, then 30. We are celebrating her birthday this coming weekend, it is the only time all the family can get together. I am looking forward to it, it is one of the rare times when no one cares if she smears food all over. Her dad has a fenced yard, so the kids will be able to play and fling cake to their hearts content. In spite of all the bad, I am so grateful that she was spared the night her sister was murdered. I wish all of this had turned out differently, no child should have to be raised by old folks..lol. She should be where she is right now, at her dad's, playing with her brother and sister, being a kid. Not with us; we have no friends with kids, no fenced yard for her, and we're too tired to do much after working all day. She will be at her dad's for three more weeks, then back with us in time for school to start. I will enjoy and make the most of the three weeks of freedom I have left, but I will also miss her every minute of it.
Sunday, August 2, 2009
For those who don't know
I often get get comments pointing out how depressing my blog is at times. I am quite certain that many find it to be a "downer" when perhaps they were looking for something uplifting. I thought maybe this would be a good time to bring to light the reason we have Chelsea in the first place, for those who don't already know. Perhaps knowing how we came to be Chelsea's guardians will explain why our experience is so different from those who are parenting a Down's child by choice. It is a rather long story, but I will summarize it.
On July 13, 1999, Chelsea's baby sister was murdered by her mother and step-father. After much emotional trauma, dealings with Child Protective Services, and two murder trials, my son was given custody of Chelsea by the courts. He was a newlywed at the time, and the combination of the murder itself and having a disabled child placed in their lives with little warning caused their marriage to disintegrate and they divorced. My son tried valiantly to care for Chelsea on his own, but amidst his grief over his murdered child and his divorce, did not cope well. Chelsea was not thriving and learning as she had been before his wife left. In order to protect Chelsea and give her some kind of chance in the world, my husband and I agreed to take her until he could get his life in order. It has been years now, and he still cannot seem to cope with her. I understand this, because I can barely do so myself.
I had only been married about a year when Chelsea came, having been happy and enjoying my life for the first time in years. Being middle-aged and suddenly have a disabled child to care for does not lend itself to happiness. I had always looked forward to that time in life when my boys were on their own and I could once again get to know myself as something other than someones caregiver. One event, on July 13, has had such a ripple effect in all of our lives, but I cannot let go of the thought that Bethanie's murder not only ripped a part of my heart out forever, it also cost me my happiness. If you really take the time to think of the emotional dynamic that takes place every day as a result of these events, you may have a better understanding of why my blog is not all about the wonders and joys of a Down Syndrome child. I will love protect Chelsea until my last breath, but I can't help but mourn the lost years of my life, just when I had started to enjoy them. For more information about Bethanie and her murderers, see my blog "Never Another Child" http://neveranotherchild.blogspot.com/ Thanks for reading.
On July 13, 1999, Chelsea's baby sister was murdered by her mother and step-father. After much emotional trauma, dealings with Child Protective Services, and two murder trials, my son was given custody of Chelsea by the courts. He was a newlywed at the time, and the combination of the murder itself and having a disabled child placed in their lives with little warning caused their marriage to disintegrate and they divorced. My son tried valiantly to care for Chelsea on his own, but amidst his grief over his murdered child and his divorce, did not cope well. Chelsea was not thriving and learning as she had been before his wife left. In order to protect Chelsea and give her some kind of chance in the world, my husband and I agreed to take her until he could get his life in order. It has been years now, and he still cannot seem to cope with her. I understand this, because I can barely do so myself.
I had only been married about a year when Chelsea came, having been happy and enjoying my life for the first time in years. Being middle-aged and suddenly have a disabled child to care for does not lend itself to happiness. I had always looked forward to that time in life when my boys were on their own and I could once again get to know myself as something other than someones caregiver. One event, on July 13, has had such a ripple effect in all of our lives, but I cannot let go of the thought that Bethanie's murder not only ripped a part of my heart out forever, it also cost me my happiness. If you really take the time to think of the emotional dynamic that takes place every day as a result of these events, you may have a better understanding of why my blog is not all about the wonders and joys of a Down Syndrome child. I will love protect Chelsea until my last breath, but I can't help but mourn the lost years of my life, just when I had started to enjoy them. For more information about Bethanie and her murderers, see my blog "Never Another Child" http://neveranotherchild.blogspot.com/ Thanks for reading.
Tuesday, July 28, 2009
The problems with the solution
My son came and got his daughter. Just like that, no fuss, no stalling, no complaining. "Well, that was easy", I thought to myself. I should have known better. It was less than 24 hours before the calls and text messages starting. Pleas for help, tirades of how this is tearing his marriage apart, ruining his finances, etc., etc., and that was just Day One. Day Two arrives, and his wife left, said she couldn't handle it. Day Three, the wife returns and proceeds to spew venomous text messages at me, and I just wait for the rest. Day Four, oh Day Four, she started her period. Frantic calls again. My reply? "Why do you think I sent you the pads and briefs?" Day Five comes with no morning call or text. I feel trepidation, wondering if this is the calm before the storm. Late afternoon, and I hear the peep of my cell phone. It's my son, of course. He now tells me that he never knew what I had done for him for the past five years, and that he can't do it. I tell him he only has to do it for a few more weeks, and she will be back with us for nine months. Today is Day Nine, and no calls at all. Is is possible that the tough love that was so hard to institute is actually working? Could he actually be adjusting to having his daughter and taking responsibility for her? I will be waiting anxiously for tomorrow, but in the meantime I am basking in the glow of having a life again, even if only for a brief interlude.
Monday, July 20, 2009
A solution to the problem...I hope
I think we may have happened upon the solution for the summertime blues. We have told my son (Chelsea's dad) that he WILL keep his daughter through the summer months. He came and picked her up last night. It will be much better for her than sitting around all day with us old folks. She has two siblings to play with, a great big sturdy dog, and a fenced yard. No more sitting in front of the television all day in the summer. It is definitely what is best for her. My son lives just a few blocks away, so I am comfortable that I can drop in any time I feel the need to check on her. The thing is, I feel sad about the whole thing. Sad because I had to force her dad to take her for a few weeks. Sad that she seems to be the child no one wants, other than me, and I can't manage taking care of her with the other responsibilities in my life, all of which are necessary. I wonder what will become of her in the future. Will she be one of those people sitting in an institution, grasping for any little morsel of attention? I will do my best to prevent that from happening, but I am only one person, and one person with a ton of responsibility. It's just all so sad.
Thursday, July 9, 2009
I really hate summer
Yes, this is one of my dark, depressing posts. Sorry, but this is where I vent, and hopefully get some encouragement. School is out for the summer, which means 24/7 Chelsea. It also means my hubby is too depressed to do anything around the house, which in turn means I work all day and then come home to clean up and take care of things, then start my data entry job. Every year I have trudged through the summer, but this one is different. I am sick. I am struggling to get through every day at work, and hoping I won't lose my job, but it is so hard to keep going when I feel like I do. I have to try to stay awake to do the online work at night in spite of meds that make me sleepy. Then there is the stress of wondering how this will all turn out. The doctor suspects MS, and if that is true, what will become of Chelsea? How ironic to have sacrificed so much of my life to keep her safe, only to have to send her somewhere else. I don't know how much longer I can keep this up, folks, I really don't.
Wednesday, July 1, 2009
Vocabulary software - interesting learning tool
I just happened upon this software that helps with learning vocabulary and pronunciation, and who of us wouldn't like help teaching that? It has a free trail trial download link available, so you can try before you buy. I personally think this is pretty cool stuff! If you're interested in checking it out, just click on the post title and you're there.
Saturday, June 6, 2009
Resources
I am working on a new Down Syndrome resource directory that should encompass any and all resources in the US when I am done. I do plan to branch out to resources in other countries as well, but I gotta start somewhere! You can contribute to the directory yourself, or feel free to send me any resources you would like to see included (even if not US based). If you have a DS blog, I will gladly include it in the directory. I will be working on this for many months, if not years,so your input is appreciated. Perhaps I can help someone find the support they need, and you can be a part of that, too. Here's the link:
http://downsyndromehelp.boomja.com/
http://downsyndromehelp.boomja.com/
Wednesday, June 3, 2009
The Phone Call
Yesterday I got a call from the group home. Chelsea has been on the waiting list for about a year. They said they had an opening for her, but it was in a co-ed home. I turned it down. As badly as I want my life back, I couldn't accept the placement knowing she would be housed with grown men. I told them I would just wait for an opening at the all female home. Part of me wants there to be an opening tomorrow, part of me doesn't want there to ever be an opening. Sometimes I think I'm just crazy!
Labels:
coping with disability,
disabled child,
downs,
group home,
respite
Monday, May 18, 2009
Sometimes the stress is just too much
School will be out for the summer in just a couple of weeks and I still have no one to keep Chelsea. There are no day care centers in my area, and any within driving distance won't take her because of her chronological age. Meanwhile, my husband reminds me that he can't take care of her all day anymore, my son (her father) says he would have to adjust his work hours and he just doesn't think he can do that. I "adjusted" my entire life to accommodate this situation but no one else seems to want to budge. I have no idea what to do.
Monday, May 11, 2009
Problem solved....for the moment
The Depo shots failed miserably. What was supposed to solve a problem actually made it ten times worse. Instead of having to deal with the "problem" for five days a month, we had to deal with it every day for six months. God bless her doctor, she put her on birth control pills. Not only has the problem stopped, but Chelsea's mood has greatly improved. She will take the pills continuously for three months, then off one week, then repeat. She is getting an interesting case of acne, but that's easier to deal with than the other problem! Hooray!!!!
Sunday, May 10, 2009
Tuesday, May 5, 2009
A Set-back
The other day I found myself thinking that Chelsea had been pretty well-behaved lately. No episodes of incontinence, no eating of toys, no pulling the hair out of her dolls, nothing out of the ordinary for any kid. I met with her teacher a couple of days ago and she told me how much she had matured and how much better her behavior had been lately. Right about the time I started feeling pretty good about seeing results of our hard work...major backslide! I got some pudding out to put her pill in. After she took her pill, a customer needed taken care of (we own a greenhouse). I left the pudding sitting out on the counter. When I came back, she had eaten it with her hands like some kind of feral creature. She knows that she is not to touch food on the counter without asking. I won't go into the places she puts her hands, but I don't want them in food I'm planning to eat. Well, fairly minor transgression, so I just scolded her and reminded her of the rule. She pouted for a minute, then went back to watching a movie. A little while later, I gave her a plate of ravioli for supper. Another customer wanders in and I go out to tend to them. About 15 minutes later I went back into the house to find my while dog's neck encircled in spaghetti sauce. Chelsea has hurt our dogs before, and we have a solid rule about touching the dogs without an adult in the room. I suppose I needed a rule specific to choking the dogs. Needless to say, I was furious...and Chelsea is grounded. I don't think it will ever really get better, it just abates for awhile and then comes back with a vengeance.
Sunday, April 26, 2009
Grown up stuff
We've had a pretty good couple of days (I think). About six months ago we started her on Depo shots, for obvious reasons. Well, they had the opposite of the intended effect and that which was only a once a month nightmare has been constant since last November. It finally stopped, and she saw the Dr. on Friday, who is putting her on the pill. Not the perfect solution, but anythings better than what we've been through. My mother thinks she should have a hysterectomy, and I am so torn about that. It's true that her monthly cycle is unmanageable. It's true that it would be disastrous if she would become pregnant, but how to I take an innocent such as her and subject her to surgery?
I took her for a haircut and went for a whole new look. It's a cute little short, cool-for-summer 'do, and she loves it. It was a lot of fun watching her reaction to it. It will be a lot easier to deal with in the morning, too!
I took her for a haircut and went for a whole new look. It's a cute little short, cool-for-summer 'do, and she loves it. It was a lot of fun watching her reaction to it. It will be a lot easier to deal with in the morning, too!
Tuesday, April 21, 2009
I hate feeling like this...
Summer is quickly approaching, and with summer comes Chelsea's summer break. Unfortunately Chelsea has reached an age where she is physically an adult and my husband cannot provide her personal care. My husband works our small business 14 hours a day in the summer and can't possibly watch her and do that. We had planned on a summer respite placement and we were so looking forward to it. A whole summer to be "us" again! Well, the bomb dropped...no money in the county budget to pay for her summer respite. So, what am I supposed to do now? It's like having an infant and no day care, only worse. It's worse because I could find a sitter for an infant. I can't find anyone to keep Chelsea. There is no help out there. I don't know what people are supposed to do in these situations. I am at the point where I fear we will have to place her with the state, not because we want to, but because we have no choice. I will send another plaintive email to her case manager and let you know what happens.
Friday, April 17, 2009
And the Easter candy just keeps on coming
This is going to be a very short post because I'm a very tired woman. Although I enjoyed the smile on her face when she got Easter candy, there are only so many times you can tolerate having to hose down a 14 year old every time she eats a piece of candy. How on earth does she manage to look like she rolled in a vat of chocolate when she never left the table?
Sunday, April 12, 2009
Up out of the darkness...for a minute
Since I've been accused of being dark, told that this site is a downer (no pun intended), I thought I would take a minute to tell you some nice stuff. Today is Easter. Since Chelsea will not be joining the ranks of little girls in their Easter finery today, I thought it would be nice to play the Easter bunny thing with her. When she didn't find a basket this morning, I told her that the EB must have stopped at her dad's instead of here. Lo and behold, dad came in with a huge basket, you know, the kind the EB leaves for good little girls. I sat her at the table with her haul and let her eat chocolate, jelly beans and peeps. Clean up was not pretty, but what the heck, she's just a little girl, after all. Happy Easter, everyone!
Tuesday, April 7, 2009
It's been awhile...
Hi all! I'm finally back after a long haul with my hubby. He donated his kidney to a friend and had some complications. I am happy to report that both hubby and friend are now doing great! Can you imagine the stress of trying to take care of a sick hubby for months on end and dealing with Chelsea at the same time? I'm going to guess that you really can't guess. But here's the really sad part...I spent an entire week of days in the hospital and nights in a hotel alone while he was recovering from the initial surgery, and they were the best days I've had in a long, long time. Sounds kinda twisted when I say it out loud, but it was so liberating to eat when I want, sleep when I want, not have to bathe anyone but myself. As much as I love Chelsea, I would be lying if I said I looked forward to coming back to her vortex. Back to cleaning up feces and urine, back to picking food out of her hair, back to the absence of peace. The surgery took place in Florida, which also happens to be my birthplace and my favorite place on earth. I had to leave it behind and come back to Ohio, where I hate the weather and about a million other things I won't bother to go into. I sunk into a deep depression, missing the healthy version of my husband, missing my beautiful ocean, missing the "me" I used to be. It has been months and I am just now starting to acclimate to my forced surroundings again. I keep thinking it will all be over someday and I can resume my life again, but I will be 50 this summer...how much longer must I wait?
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