New to living with Mild Cognitive Impairment (MCI)
I have recently been diagnosed with MCI and I'll be attending Mayo Clinic group on this. Each day just seems to bring me challenges. I have days when I get depressed because I feel like I'm being a burden to others. I will be attending MCI seminar at Mayo Clinic in January. I need help and support in this area.
Interested in more discussions like this? Go to the Brain & Nervous System Support Group.
I have taken Clonazapam for years: diagnosis of cervical dystonia. I never knew! that you could develop a dependency on this pharmaceutical!!
AND it affects your mood and MEMORY!
I have never sued anyone in my life BUT I am tempted.
I too have taken Klonopin 0.5mg daily for many years, it is a small dose but it’s the only way I can keep my emotions in control without crying at any unexpected time of the day. I also have memory problems as I’ve written about before.
What will you do, stop the Klonopin? It’s not a choice I have made so far.
I tried taking Buspar, it didn’t help me.
Have you been formally tested for your memory problems? COVID 19 delayed my appointment for testing and now I have moved to NY and have to start over again.
I hope you can find an answer to this dilemma and would be interested to know what it will be.
If I had known( famous last words?) I would have asked for a smaller less frequent script (of Clon)for my head tremor.
After taking Clonazepam for several years, I began to have a memory problem.
Recently I was evaluated by a neurologist ( mild cognitive impairment). He was not the prescriber, was retiring. ..and took me to the office of two new neurologists.
He assured me that I did not have Alzheimer’s and one of these two new neurologists would help me.
My research: MCI(mild cognitive impairment)can lead to AD. I hope I can delay it!
I will let you know about my evaluation.
Please do not see anyone who is not a neurologist (who can answer ALL your questions or calls him self a rehab doctor). I am tritrating from Clonazepam half a tablet decrease each week.
I thank God for my gastroenterologist. She told me that I would have ab pain when I began decreasing this pharmaceutical. I do. The prescriber denies this and says that it is caused by GI issues which are wonderfully under control!! ( I have celiac disease. A diet corrects that!)
Please let me know if you have questions. If I can help anyone titrating off of Clonazapam
I will. I am praying that these new neurologists know of a support group... or perhaps start one!
Look first for research based information on the Mayo website.
All the best!
Ellen
(Write any time)
@helenfrancis . You are so right . Research is most important with any problems . I look it up if the Dr doesn't give me a satisfactory answer . I use the pharmacist for med information and interactions since they have all my meds. Very good source also . Drugs.com is a good one online
Thank you, lioness. I never heard of drugs.com
I usually ask the pharmacist but that is not always convenient for me or them.
@helenfrances Yes I found it as we can't get out now so I use it every time I get a new med .
Many thanks!
I also have Celiac disease controlled by diet. When I asked my family Dr. For a referral to a neurologist she told me that first I should see a Geriatrician and referred me to one. I moved before I saw anyone. Now I am looking for a family Dr. near Albany NY. And then will ask for a referral.
My Psychiatrist who I liked, and prescribed my psych meds knew I had trouble with my memory but never suggested it could be from the Klonopin, I also have trouble with day time sleepiness for which I take Provigil.
Oh what a tangled webb we weave when we practice psych meds !!
Hi @emyliander, how are you? It's been awhile since we heard from you.
@helenfrances, I'm so glad you got the technical issues worked out and were able to log back in. Happy to have you back.
@artscaping, let's get this discussion going again. I miss your posts and conversation here.
Greetings...welcome to our first reunion, Sarah, @emyliander, and Ellen @helenfrances. It certainly does seem like it has been a long time since we had an update and a timely conversation? Sara, @emyliander, how is your new home? Are you all moved in? I have to ask.....do you have a garden for your flowers? And I hope your daughter is tucked away at her special school or is COVID19 still mandating that she remain with you.
And how about you Ellen, @helenfrances? You, in June, were waiting to complete a withdrawal from Clonazepam and continuing to do research and some shared decision making about your road ahead with your neurologist.
I think in June, we were all talking about how cognitive impairment at the mild stage was affecting our lives. Do our life partners and families recognize our somewhat staggering memories? I think you were looking at a shared support group or class with your husband Sarah. And I was asking you to get a medicine review to make sure those stomach issues were being taken care of.
I will share with you a couple of medical hurdles that I find challenging right now. I found a tiny crunchy nodule on my sternum which ended up being squamous cell carcinoma and was promptly surgically removed. Now I wait like so many others who receive a cancer diagnosis of any kind.
You're not going to believe this one.....I sure didn't until I had spent several days in what I call an itch bomb. It is called neuropathic itch and does its annoying work inside your body. No matter how hard you try you can't scatch it because you can't reach it. So now I am being a guinea pig for different medications to see which might work best without side effects. At the end of two weeks, I make a switch and we see what happens with a new trial.
So...fill me in and fill me up with news and highlights. It seems like things are pretty quiet with the travel restrictions. I must admit I am hungry for a play at the Gutherie. Dinner at Sea Change.....actually sitting in a restaurant might also be nice. Shoot, I would even go to our adopted granddaughter's softball games if I could remember the day. And that is where I will end for tonight. I am noticing greater difficulty with recent memory especially when I am talking and lose my thought. I see people either trying to help me by feeding me the words or looking away as if they haven't noticed.
How are your memories holding up.........do you have any tricks or hacks to share? As Ellen says...write any time. And I say.....do it now or you just might forget. My very best to you both........I would love to hear from you.
May you have peace and ease.
Chris