However, I personally know about Aricept because I tried it for tardive dyskinesia and had a pretty poor response. My grandfather was prescribed Aricept for age related memory loss after a cardiovascular impairment. He couldn't tolerate it either. That doesn't mean at all its the wrong medication generally. Its just it has a fair amount of side effects for some people. But as anti-Parkinsonian medications can cause depression and other personality alterations that might be the one.
t know anything about that - all I know is that before Aricept, I was in a gray mist, and after five months of Aricept, everything seemed to make more sense. Before Aricept, it was as if I had low water pressure - I just couldn't get enough juice in my brain to put thoughts together. On Aricept, suddenly my brain could make connections.
The only trippy thing I noticed was an almost hi-def moire behind my eyeballs when I went to sleep.
If a person has not been diagnosed with alzheimers but is taking aricept, is it okay? will it hurt to be taking it?
My husband has been taking 10mg of Aricept for 2 years now and I have not noticed any significant difference in his memory. Actually, my observation is his memory is becoming worse. I'm struggling with whether I should discontinue the medication since I don't see improvement and because it is quite costly. I also know Aricept is designed to slow down the dementia so if I discontinue it I'm wondering if he will become worse much faster.
I have been taking aricept for about 9 months. It is hard to tell if there is an improvement. It has been a while since I forgot my way home but I still forget a lot of little stuff. I keep taking it because I am convinced it cant hurt anything and it just might help a little.
s due to also having EDS. However I have been suffering terribly for over 5 years with severe short term memory loss & was even put on Aricept (usually used for Alzheimer's) about 5 years ago & have become increasingly severly depressed. I seem to be resistant to all or most anit-depressants, years of therapy & more.
My husband was diagnosed with Graved Disease and has had radio iodine therapy in March. He has since fallen severely hypothyroid and has slurred speech as well as fatigue, weight gain, and irritability. His MD has put him on Synthroid, but my question is will his speech go back to normal and if so, how long? It's very disturbing to hear because it sounds as if he has been drinking (he doesn't at all), and I'm worried how this may affect him long term.
I am confused as to which is the most important issue and how I approach each. I see a neurologist this week and have been placed on Aricept. Yet still the confusion lingers. Please give me some directive on which is the most imperative issue.
When I was having some serious cog fog, I asked my neurologist for a sample of Aricept. Had to argue with him, actually. It worked! I got back some of my cognitive function - not all, but enough that I felt confident about my decisions.
I took it for four months, total. I still have one month left over on the scrip, so if I really need it, I'll have it.
fast weight loss is most of the time lost water and muscles. Fat takes ages to go away.
Third: Think of a diet as something permanent. Crash diets just help you gain weight faster once they are over. So, pick some simple rules of a balanced and healthy diet, and follow them. Don't sweat it if you crave for something "bad", to a balanced diet belongs the bad side, too. If you give in now to a small piece of chocolate, it is much better than to eat two whole packages later.
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