aricept stop taking

D'oh-oh'oh! Evidently I'm not 100% better! I haven't been on Aricept for 70 days - it's only been 40+ days, maybe 50. Dunno what I was thinking. I've never before had to worry about whether I could overdose on a drug. I think I accidentally took two one time - I had a hard time sleeping, and felt a little like everything was in high-resolution. Little hard to explain, but easier if you've ever taken hallucinogens.

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.

If a person has not been diagnosed with alzheimers but is taking aricept, is it okay? will it hurt to be taking it?

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.

t dreaming at all after my relapse, and sleep was just this dark pit I fell into. I started taking Aricept, and started dreaming. At first they were boring filing dreams, but gradually I began dreaming more interesting dreams. I mark it as a sign that your brain is getting better if you're dreaming.

About five months after taking Aricept, I found that my brain was quicker and more adept. I could participate in conversations and follow topics better. I could remember what I was doing from one moment to the next. I could even count change and catch errors at the grocery store! So I stopped taking it. I recommend it for everybody that's having problems with cognitive function.

m momentarily off the Aricept, my work performance has declined. Basically it looks like I have to keep taking Aricept in order to do my job. So my question is, do I tell my employer about my cognitive problems? It sounds like I could lose my job, get a poor performance evaluation, all that that implies, because I'm having cognitive difficulties. My immediate supervisor knows about my diagnosis. Will revealing that I'm having cognitive problems be a bad idea?

my mum was diagnosed with alzaheimer in October 2008, she was prescriped dogmatile fort 200, aricept, trittico and lustral, I wonder if this combination goes well as she is more depessed since she took the medication.

Hi! Thanks for the info on Aricept. I have a few days left until I see the Doctor and I guess Aricept is the front runner. Of course she may not be willing to give me anything, but I am pretty sure that she will once we talk. If anyone has scoop on their experience with Aricept or any other cognition helping drug please take a minute to chime in.

I had the same situation - when I was well-rested, I could think relatively well, but when I was feeling poorly, everything went. I fought this for about a year, then finally opted to push the issue. My neurologist (bless his pointy little head) seems to think that my impairment is so slight that I don't need anything at all. But I pushed for a neuro-psych exam, and got it, which showed moderate cog impairment in a few select areas.

I think you should discuss with your PCP regarding a drug called Aricept. This should be started only on prescription of your treating physician. It is used for treatment of Alzheimer’s, but is helpful for short term memory loss. Aricept is a drug of choice to treat Alzheimer's, but its use is not restricted. It has been observed that Aricept improves cognition and function, which includes effects on memory and performing everyday tasks, hence it would have been prescribed.

After discussion with MS Neuro and my wife , we agreed that I should start Aricept , it is used mostly for Alzheimer, so its off label and he says it has shown great results. I do have a damaged working memory and slower processing speed, cognitive impairment effects every day in some small way. I won't reveal to any other family or friends that I ve stated this med, I just think I would feel self-conscious about people looking for my errors and mistakes.

I think that's exactly what happened to me - I was in a fog for a long time. I asked for a script for Aricept, got it, and was on that for three months. It felt very much like the Aricept gave my brain enough 'power' to jump over the holes. After a while, it was more like the brain knew how to navigate around the holes.

started Lyrica this week, taking 75 mg in the evening...so far it's ok...no changes.

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.

my ex hubby is also dx with graves diease, he was only 23 when his thyroid crashed almost died , they gave him iodine and over dosed him and killed his thyroid so now he knows when hes weak and not coordinated his levels are off hes on 100mcg of levethyroxin and cytomel 15 mg check with your ENDO maybe your levels are off he has since graduated to aricept at 34 cause he was having trouble thinking and talking hes also born hearing impaired so we use sign language when hes not making any sen

The psychiatrist recommended Aricept, so I got a sample and tried it for a month. I have to say, it definitely made a difference. When I ran out, I waited for the cog fog to come back so I could tell whether it was the Aricept - and it did. So I got a prescription, and took it for five months. Each time I ran out, I waited until the fog returned, then got my script refilled. When the fog stayed away, I stopped taking it.

I also brought up the memory issues which are getting very, very bad. I will be starting Aricept. He thinks that it will really help me. I am very encouraged about this. He said that the studies don't show marked improvement for people with MS, but he has seen otherwise in his MS patients and has also heard otherwise. I am very hopeful about this. I know there's others on the forum that have tried it. I would love to hear about that. I also am going to start oral predinisone.

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.

Yeah, all the time. I had so many of those in a row that I began to be concerned - it was hard to function in daily life when I couldn't think straight. I badgered my neuro into giving me Aricept (5mg) which really helped. After three months, I got a little more function back, so I stopped taking it. I still have days when I'm too foggy to be coherent, but I try to rest up so that won't happen as often.

She has moderate to severe short term memory loss and has been started on Aricept. She has also recently had an MRI of the brain. Could you explain: "moderate diffuse cerebral atrophy and chronic white matter small vessel disease"? Thank you!

She also gets up at night and looks for things or wanders around. The consultant has prescribed risperidone, although we were hoping for Aricept. I am very concerned about this as internet research suggests it is for aggressive behaviour and will result in oversedation even drooling. I don't want my mum to be a zombie - I'd just like her to be more like her old self. Does anyone have any experience of this drug at all? I'm not going to give it to her until I learn more.

My doctor switched me over to Actos, which I took for a number of years. Recently, I stopped taking it because of worry about warnings of bladder cancer. Instead, I am taking Gymnema Silvestre and have found it controls my blood sugar very well.

Aricept stop taking

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