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Several years direct experience as caregiver for family member who died of end stage AD. Did lots of research and dealt with a lot of health care professionals and caregivers over the 7 years from diagnosis to the end. Used various care options from community based resources to increasing levels of institutional. Mother of three, two born during our loved one's decline, so I know what it is to be the ham in the sandwich, taking care of the older generation and the younger at the same time and trying to balance everyone`s needs. Ask me, I`ve probably been there, done that. We made lost of mistakes and learned everything the hard way - but you don`t have to! If I can`t answer your question, I`ll steer you to a place or person who can.
Currently a program manager for a large utility company. My Alzheimers experience comes from having the illness in our family. Out of necessity, we did a lot of research in order to understand the disease, plan for what might come next, and make the right decisions to help and support our loved one. Please note, I am a Canadian living in Toronto, and therefore am not the best person to ask about US regulations and insurance rules!
Absolutely nothing. This is a horrible disease and has a terrible impact on families. The positive that comes out of it is being able to help other people who need support and information.
To be helpful - to give accurate, timely, useful information and advice, in a compassionate and supportive manner.
Many families do not realize that "senility" is not a normal part of aging. It always has a cause, and it should never be accepted without a thorough medical exploration. There are treatable causes of confusion, and new drugs to help slow down the progress for incurable causes.
Personal peeve: Doctors who do not take confusion and forgetfulness reported by family members seriously or who do not adequately explain or suggest supports or resources. Caregivers need information, so they can understand what is likely to happen as dementia progresses,and make informed plans for future care with all the financial, legal, emotional and practical issues that go with it.
| User | Date | K | C | T | P | Comments |
|---|---|---|---|---|---|---|
| Cindy | 11/21/09 | 10 | 10 | 10 | 10 | Mary, Thank you so much that really ..... |
| sehee | 11/20/09 | 10 | 10 | 10 | 10 | Thankyou sooooooo much! This really helped me ..... |
| Cindy | 11/14/09 | 10 | 10 | 10 | 10 | Mary, Thank you for your prompt response ..... |
| Tenita | 11/12/09 | 10 | 10 | 10 | 10 | Thank you for answering all my questions ..... |
| Mica | 11/11/09 | 10 | 10 | 10 | 10 |
Hi Gay - There is only one airline as far as I know that offers any meaningful travel assistance for the unaccompanied traveller with a cognitive impairment. It's Northwestern. http://www.smartertravel
Hi Cindy, I know this is a tough one for many people - and I do agree this is a much more difficult struggle than dealing with other illnesses. I can just give you my perspective - and it is very
1. Parkinson's Disease and Alzheimer's Disease are very different illnesses. There is no known cure for either. 2. Both of these diseases are relentlessly progressive. There are some medications that
Hi Kathi - a lot depends on what they think her cognitive impairment is from. What you are describing is certainly not typical of a progressive dementia such as Alzheimer's, which tends to have a slow
Hi Mica, my goodness, how absolutely touching and wonderful - I think these were moments you will remember and treasure forever. I'm sure what happened must give you a lot of comfort. It's what most of
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