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We’ve interviewed doctors, researchers, social workers and other experts on care for people with Alzheimer’s and related dementia in order to get answers to some of the most important questions members have about Alzheimer’s disease and caregiving. We update the Ask an Expert section several times a year; if you’d like to submit a question click here.

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94
Chris Wynn
29-Jan-2010
Votes: +0

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Dwight, please write to me at

This e-mail address is being protected from spambots. You need JavaScript enabled to view it

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Dwight Norrena
18-Jan-2010
Votes: +0

CEO

I am the innovator of four non-medical assistive devices that would assist those with mild to moderate demenia (Alzheimer's), our aging population, those who are hearing impaired and those who are medically ill needing vital statistics while at home.
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I am attempting to bring these producs to market readiness with the assistance of a university in Ontario, Canada.
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The University is requesting that I obtain an evaluation of these products from a qualified source. Alzheimer's associations in Canada will not provide an evaluation but do comment that, "the products would be of grate value" to those with Alzheimer's and other forms of dementia.
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Can you give me direction on how I might obtain some sort of evaluation from a qualified source?
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Dwight Norrena

94
Chris Wynn
01-Nov-2009
Votes: +0

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Hello All

I know this has been a bit confusing and we are trying to correct this problem, but if you have a specific question for an expert, please post it here and I will get an answer from one of our experts ASAP!!!

Thanks to everyone for their posts!

Chris

289
Marcus Bennett
13-Aug-2009
Votes: +1

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Susan You should write a book. I have heard this story too many times from too many wronged caregivers.You should make an educational movie.Expose the out of touch family that talks to moma on the phone and decides that she is fine and you are the bad guy. The hell that it causes you on top of dealing with everything else.Hang in there kid. I know how you feel.
Vickey
I love the supplements and use them myself.Instead of butter or margerine I use coconut oil.Only thing I see missing is the olive oil.
You all have this part right
Ebixa * (Namenda in the States)
Namenda + Aricept
The results of a clinical trial published in the Journal of the American Medical Association showed Alzheimer's patients taking Namenda in combination with Aricept (donepezil) experienced a slower rate of decline in thinking, function and behavior compared to those taking Aricept alone.
To read more about this go to
http://www.simplesite.com/Marcus/8714683
Chrissy You learn all you can about your disease.So you can learn coping skills to deal with it.Come chat with others facing some of the same problems on Alztalk.org
Check out the Alzheimer's Association nearest you. http://www.alz.org/index.asp
Get involved in finding the cure. We are closer now than we have ever been.

0
Vickie
27-Jul-2009
Votes: +0

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My husband Chet was diagnosed with Alzheimer's at age 62 now 64. He is in the early stages 4. I feel he is doing OK. stutters and sometime can't get the words out. He takes the following:

RX Namenda 10 mg morning
Rx Folbic B vitamin for brain
Rx Citalopram HBR 20 mg for depression
Flex seed afternoon
Omega 3 Fish Oil
B12 sublingual tablets over counter
coconut Oil in oatmeal with cinnamon
Centrum Vitamin
Vitamin E
Aspirin 81 mg occasonally takes
niacin 400 mg -- vitamin --- occasinaly takes
Vitamin D 400 units good for brain
Rx Namenda 10 mg -SUPPER TIME
Rx Aricept 10 mg - Bedtime
Rx Pravastatin 40 mg- cholesterol

Vickie

0
chrissy
24-Jul-2009
Votes: +0

Alzheimer's

Hi my name is christine mackie and i am 62 years old and married.I was diagnosed with early alzhimer's march of 2009 and also white matter disease.I am on 10 mg. of aricept once a day and 5 mg. of ebixa once a day.When I had the spect test done they found alzheimers was only affecting my left side of the brain.why would this be?It usually affects both sides.They are going to try and find out why but boy it is taking awhile.

0
susie
03-Mar-2009
Votes: +2

sibling fighting

how do u get siblings to understand that dad has alzheimers,and to accept the desease and everything that comes with it, my dad was diagnosed over 2 years ago,after leaving one sister's house to go to the other sisters house for supper which is only a 10 minit ride, he ended being lost for over 17 hours. we had police over i dont know how many city's looking for him, after countless falls in his own home,it was best to have him panneled for a care facility,while we were waiting for placement he moved in with me and my family ,who happen to live in the same small town as my dad,he stayed here for 2 months with frequent trips to hospital, after one nite tryed to go out his bedroom window .when asked where he was going ,he said to the resteraunt, keep in mind it was 4.30 a.m. i worked full time and attended school,1 nite a week still have one child at home and my husband does not live with us mon. to friday as he works in the city,all week we were here by ourselves ,one nite dad even thru a knife at my sons hand, thankfully it didnt cut him,and also threw a ceramic cup at my son,again he wasnt hurt.it was not safe for my dad in a family home no more, he was getting up all thru the nite ,erregular sleeping patterns,anyways there r 11 siblings,and not one other than me can axccept the fact dad is sick. i have been accused of so many things , there is not enough paper to write them all down on. i was the primary caregiver{my mom passed away 3 years ago} and because i was living here everything got pushed on me,there is a power of attorney assigned to myself and two younger siblings,but i was appointed primary caregiver, again because i live here,my dad is living in the facility but when one of the siblings come to visit dad starts to cry and says he wants to go home,and then the phone deesnt stop ringing, how come i am leaving him locked up in there, i dont know how to deal with this anymore, some of them have even tryed to get a lawyer,to remove him from the facility, {keep in mind out of 11 siblings there is only 4 that even come to see my dad, the rest just aurgue amongst themselves making there own decitions,one is the trouble maker ,who lives 1 hour away, and only comes ,maybe 2 fridays out of each month and makes the visit so bad for my dad he crys, the facility even had to call police because she was trying to take him out,that is nice visit 2 hours of nothing except seeing him cry, and telling him it was me who wont let he leave.he is very angry with me right now,but i still go everyday to visit and make the most out of it, i know it is the desease. but it still makes it hard,i dont know how to force these kids to come to terms with this,,,any ideas,please.

100
Michael Wynn
02-Mar-2009
Votes: +0

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Hi Tom, sorry to hear about your diagnosis, our father was on Aricept but I don't believe he ever took Namenda or the other oils you've mentioned.

0
Tom
23-Jan-2009
Votes: +0

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Hello, my name is Tom. I have been diagnosed with Alz related dementia. Pleaser tell me, was your father taking any of the new meds to slow the disease? I'm taking Aricept and Namenda plus suplimenting with Fish Oil and Coconut Oil.

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