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.
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I’ve just written a reply in the box at the bottom of the screen and posted it. But I don’t know where it went.
I guess I didn’t wait long enough !
I do the same. We are only human 🤝
I don’t seem to have a very good memory. I marvel at my friends but I have always been a bit that way about details. I self diagnose myself with mild attention deficit disorder at 65. Something in my mind tells me I don’t need that info especially when people get long winded. A lot has to do with my anxiety and being in the present moment. Of course, it is a part of aging. Hope I don’t sound like a know it all. These are thoughts I have regarding me personally. Maybe it can help others. As always, it pays to have a good sense of humor if your issues aren’t extreme.
I have the exact same issues. Mine was diagnosed as Multiple Sclerosis. Especially the cognitive deficits and the eye issues are hallmark signs of the disease. It took me 10 years to get the correct diagnosis. If I can help you in any way, please feel free to reach out to me. I wish you the very best.
@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