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Currently, Alzheimer's affects over 5 million Americans, and that number is expected to grow to as many as 16 million by 2050.
We think information is one of the most important health tools you can have, and with that in mind I wanted to bring to your attention what I think will be a very important piece tonight on CBS Evening News, WebMD's partner-in-health.
Their senior medical correspondent, Dr. Jon LaPook, has for the last several months been preparing the most extensive segment he's ever been involved with since becoming a medical correspondent for the CBS Evening News with Katie Couric in 2006.
The network will devote six minutes (yes, that's six minutes, incredible for an evening news broadcast) of the 22-minute broadcast to present Dr. LaPook's look at the latest research in Alzheimer's in a segment called "CBS Reports: Where America Stands."
It will air on CBS this evening, January 12th, between 6:30 and 7 pm EST.
If you have concerns about Alzheimer's, or someone in your life is affected by it, I would urge you to tune in.
For more information, click here.View Thread
I just wonder if after this first year of being her primary caretaker if I have done too much and made her too dependent. I also wonder if I can really put in place changes like having her eat at the table rather than most of her meals in bed.
Anyone else dream up the perfect caregiving scenarios for the New Year?View Thread
Dear Members,
Just in time for the holidays:
In anticipation of our soon to launch new upgraded WebMD community, we are happy to announce that we’re starting a monthly sweepstakes to find the faces of WebMD community! This month you could win $500 cash!
You can enter by uploading a new photo via your My Account page between today, Wednesday, December 16, 2009, and Dec. 31, 2009. Be sure to click on the ‘Enter WebMD’s Profile Photo Upload Sweepstakes’ option!
(We’d love to see your faces but if you prefer to share pictures you have taken of your pet or child or scenery, that works too.)
TWO first-prize winners each month will be selected to win!
View Sweepstakes Details and Official Rules.
Please note that any photos you upload on this page will NOT, at this time, show up on your current WebMD profile. You can still share your profile pictures with your WebMD friends here by uploading pictures via your WebMD profile but be aware that photos uploaded via your profile instead of your My Account page are not entered into the sweepstakes.
Also, we are sorry to say that this contest is open only to our members who are legal residents of the United States.
As always, if you have comments, questions, or concerns, please feel free to write to us at webmdcommunity@webmd.net.
Good luck!
Your WebMD Community Management TeamView Thread
Do you have any hints for helping her have some holiday cheer?View Thread
As a Caregiver, the first (and sometimes most important) realization that you must discover is this "Caregiving has an end" . Age has no cure and as sad as it is, death ends the task of caregiving. So much of what we do as caregivers seems to centered around trying to cure or at least change the road of life our loved ones are traveling. May I suggest to you that finding ways to make the journey less anxiety-filled, less painful, less frightening needs to be the overwhelming purpose of our caregiving. Our attempts to hold on to our loved ones often are more for our benefit than theirs.
The Caregiver Foundation of America's latest newsletter focuses four articles on stress and caregivers - you can sign up to receive the newsletter free at www.thecaregiverfoundation.com or please feel free to email me directly and I might be able to help you with some specific advice. But - as others have advised - "hang in there" .
GaryView Thread
Recently, my grandfather passed, and my mother and I have taken my grandma in to our house. She is generally good to have around, and just sits and watches TV. However, she is riddled with dementia, and at times she retreats back to being a teenager or in her twenties, as they so often do. When she gets into those states, she starts to wander around the house looking for the school room or the employment office or wherever it is she thinks she is going.
This is fine and dandy during the day. But once in a while she'll get up at 4am, and try to go outside. That is not a good thing for her to be doing.
My question is: Are there safe and effective ways of blocking the outside (and stair) doors that she can't get through?
We have had to put old, broken, 35lb sewing machines in front of the outer doors. She has figured out all the locks, including the hidden one on the screen, somehow. She gets past child doorknob handles (we thought she wouldn't since she seems so weak). She sees smaller objects and manages to move or unlatch them. We're still not sure she won't get some strange amount of strength and just shove the sewing machines out of the way (perhaps stubbing her toes in the process).
Help would be greatly appreciated with this. We cannot have grandma going outside!
-K Perkins Portland ORView Thread
Three weeks ago today I couldn't get hold of my mom and found her lying on the floor not able to move. She was totally conscious, able to talk just fine and did not want me to call 911, which I did anyway. They were there in a very short time and by then she couldn't talk well, very slurred speech. When they got her to the ER she couldn't be roused. After the labs were ready the ER doctor told me that she had a dangerously low potassium and started a big iv. They ordered a ct scan and the on call doctor came in to talk to my brother and I. He proceeded to tell us that she couldn't breath on her on so he put her on the vent and even tho the ct showed nothing he was convinced she had had a massive stroke and we would have 48 hours to make a big decision. About 4 hours later she was fully awake and once they got her to ICU they had to give her sleeping meds to keep her asleep. For 4 days the doctor kept telling us it was a massive stroke even tho her mouth was drooped, she could move everything and could mouth words that we could understand. After 4 days he said that she might never come off the vent and even tho the second ct showed nothing he was still insisting she had had a massive stroke. I insisted they send her 40 miles away to a larger hospital, the one my husband was in so many times, and as soon as they got her off the helicopter and into ICU that doctor turned off the vent and she was breathing just fine. The numbers were the same with it turned off as it was the whole time in the hospital at home. He said that all signs point to a very small stroke
She improved daily except for some paranoia. The doctor explained that because of the many days in ICU, plus the vent that the paranoia was common.
He sent her back over here to strictly for rehab and she has steadily gained strength but the paranoia is still with her. She thinks the nurses don't know her or where she is. Plus she thinks every time some one talks in the hall they are talking about her. Thursday they put her in a rest home with specialty rehab. Within these 3 days she has gotten able to stand almost completely by herself, walk really well with a walker and her upper body strength is fantastic.
The problem is the paranoia. It is still with her and doesn't show any signs of going away. I am so worried because my Mom has been sharp as a tack, took care of everything on her on and is so smart. She is 77 years old.
Has anyone else known anyone that the lasting side effect is paranoia? There were 2 MRI's done in the larger hospital and all it shows is 1 small spot on one side and 2 small spots on the other.
I would really appreciate any help that any one could give. deeView Thread
I just need help in what to do or how to deal with this?
Thanks, Patty
View Thread
I enumerated several reasons why this is a bad idea. (memory loss, physical condition, inability to understand directions, cost.)
She is furious with me. Now is calling my sister to complain about me. sigh. Any good ideas here?View Thread
This new article has ideas on Dealing with Memory Loss.
What tips do you have for dealing with memory loss in your loved ones? (or yourself?)View Thread
So, I have been taking my Hospice volunteer classes. It has been bitter sweet as the videos we watch are very hard sometimes. But on the flip side, it has helped me heal and I feel I am just about done grieving now thanks to my classes and fellow volunteers. I am really ready to be put to use again and feel this is a great way to help others. My mother was a dialysis patient and I felt like it was a very isolating thing for me and the family. Seemed like no one really understood what we went through with her. I am hearing of more people in my community going on dialysis, so I am hoping to apply what I know and make it easier for someone else.
What we learn as caregivers should never be wasted. We all should take the time to heal, but we also need to share and keep trying to help others. I feel as caregivers and former caregivers we need to keep sharing what we know and hopefully keep perpetually reinventing the wheel so to speak. To make caregiving an easier and less stressful task.
So there you go. Please keep taking care of yourself. You cannot be a good caregiver if you don't take care of you!! Take the break you so desperately need once in a while. Use your resources to make the task less daunting. Enjoy your time with this person. They are taken from us way too quickly. You don't realize it until they are gone! And when the time comes, that you no longer have them, think about turning around and sharing what you know with the next person. You will be amazed at the gift of giving gives you back!
RenaView Thread
This is the first time I've posted on this board, even though I've been a caregiver for my mom for about 6 years. However, over the past 6 weeks her health has declined markedly, resulting in hospital and nursing home care, and I've spent hours and hours and hours on caregiving.
Yesterday I decided to add up all my time and efforts and extra expenses over the past 6 weeks, and I was shocked at the result. I am starting to feel that it is not fair that I take such a financial (and physical, and emotional) "hit" for caregiving without my mom reimbursing me somewhat. (She does have the financial means to easily do so without putting a dent in her savings.) My sister provides absolutely no support, and although my brother has done a few things, the lion's share of work has fallen on me.
Has anyone here had a similar experience? I fear that without some financial reimbursement I will not be able to provide this level of support to my mom as her health declines in the future, because I will simply not be able to pay my bills. I apologize in advance if this sounds selfish of me to merely ask the question.
Thanks all. JudyView Thread
Does anyone else get tired of the social part of caregiving, not just the physical caregiving responsibilities?View Thread
How do you go about setting appointments if you are a caregiver with a full time job and family? What works for you?View Thread
We are happy to announce that your WebMD Community is having a growth spurt in the near future.
This growth will allow members a much more interactive experience as well as provide a new depth to the expert feedback you receive here at WebMD.
Our staff will provide more details as we move closer to the debut of these exciting new offerings.
As always, if you have comments, questions, or concerns, please feel free to write to us at webmdcommunity@webmd.net.
Your WebMD Community Management TeamView Thread
This has led to my mother refusing to ask for any "as needed" meds and a lot of unnecessary pain and discomfort for her. It also leads to things like the other day where she was clearly quite ill and yet refused to go back to bed until I would assure her that I wouldn't note it as a "stayed in bed" day.
When I try to discuss this rationally with her, she gets all upset about how she feels like she is letting us down by not "following the rules" or "not trying hard enough." I try to explain that this isn't a competition and the notes are not about tattling on bad behavior but to help her get the care she needs. I try to explain to her that I love her no matter what and that it isn't our expectations. I am not having much progress.
Any ideas on how to fix this?View Thread
President Obama addressed the nation and congress Wednesday evening, September 9th, regarding health care reform. If you had the chance to ask one question of our president or anyone involved in health care reform issues, what would it be?
Your question may be used in an upcoming article here at WebMD!
The WebMD Staff
For information, click on the links below to read the speech and the Republican response:
http://www.whitehouse.gov/the_press_office/Remarks-by-the-President-to-a-Joint-Session-of-Congress-on-Health-Care/
http://republicanleader.house.gov/News/DocumentSingle.aspx?DocumentID=144009View Thread
So, I am logging it in a notepad for now. The question is whether there is a better way. What information would be useful? What information is too much? So far, I am just including the med, the time, and the amount.View Thread
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