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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@dougjanehaltom Welcome to Mayo Clinic Connect. You have days where you feel depressed because you feel like a burden to others and you are looking for support.
You'll notice that I spelled out MCI and moved your question to a previous discussion. I also added this discussion to the Brain & Nervous System group. I did this so you could connect with members like @helenfrances @emyliander and @artscaping @jimwilson4 that have discussed this topic in the past.
You mentioned that you'd be attending the MCI seminar at Mayo Clinic in January and you needed, "support in this area." Did you mean support in the Rochester area or the topic of MCI?
Hello, @dorty - since you have been informed following your neuropsych testing that you have mild neurocognitive disorder with deficits not severe enough to warrant a diagnosis of dementia but not normal, it makes sense to 1) watch this condition, as you and your doctor are doing and will do when you return for another more detailed MRI and 2) investigate with your doctor any potential causes, like any possible link to your venlafaxine (Effexor) withdrawal.
I'd like you to meet some other Connect members who might have some thoughts and input related to the mild neurocognitive disorder discovered, like @hopeful33250 @debbraw @jenniferhunter @IndianaScott @providence1960 @bonniep. They may also have some insights related to your question about a potential connection to tapering off venlafaxine (Effexor).
Did your doctor have any thoughts for you on any connection between going off the medication and development of cognitive decline, @dorty?
Hi @dorty - Welcome to Connect! I agree with Lisa in terms of watching the condition and investigating causes. My husband was diagnosed with Mild Cognitive Impairment in 2015 and I know from our own experience how frightening that diagnosis can be. It sounds as if your diagnosis was based on the battery of neuropsych tests you just completed. As a follow-up to that, I would encourage you to look at the information and articles on Mayo's website under Mild Cognitive Impairment. Some of the articles and resources were helpful to us. Also, I'm wondering if your neurologist and/or neuropsychologist recommended anything beyond the "wait/re-test" approach? You may consider contacting Mayo to see about your eligibility for participation in their HABIT (Healthy Actions to Benefit Independence & Thinking) program. Here are a couple of links you might find helpful.
https://connect.mayoclinic.org/page/living-with-mild-cognitive-impairment-mci/newsfeed/what-is-habit-healthy-action-to-benefit-independence-thinking/https://www.mayoclinic.org/diseases-conditions/mild-cognitive-impairment/multimedia/vid-20088028
Lisa, he didn't think that was the reason, I guess due to other withdrawal symptoms somewhat improving and cognitive not improving. Thanks, Barb
Thank you Debbra.
I have Mild Cognitive Impairment from a Stroke in 2001! I am 58 years young and am very worried about my future, regardless of how and what the information documents reflect, for a person in my age bracket! I would hope, that relearning my skills and engaging in many different projects, classes, Volunteer Work, online Brain Games, etcetera, will help! However, no-one can predict the future, so I am staying busy and doing my part to stave off Dementia later in life!
Hello, @dorty - just wanted to check in with you and see how things are going with the cognitive decline you mentioned noticing? Has imaging provided any further information?
@rachelanne - also thinking of you today and wondering how the symptoms are recently that you talked about experiencing related to your mild cognitive impairment diagnosis?
Hello - I also wanted to invite a few Mayo Clinic Connect members who were discussing mild cognitive impairment (MCI) on one of the Mayo Clinic Connect pages, the Living with Mild Cognitive Impairment page https://connect.mayoclinic.org/page/living-with-mild-cognitive-impairment-mci/, to join in this discussion.
Please meet @lindaburdett @kingstonian @emyliander. Wondering if each of you three might introduce yourselves and talk about whether you have an MCI diagnosis or are wondering about it, and any symptoms you've been experiencing?
Hello all- I was diagnosed with MCI at age 62 after beginning to realize I was misplacing things, repeating myself, getting frustrated with my husband when he would way 'you already told me that', not wanting to socialize with friends for fear they would think 'what is wrong with her'. My PCP referred me to a Neurologist who did a battery of tests and she advised me I had MCI. Actually, she called it early onset memory loss. Symptoms that I have are walking into a room to get something and not remembering what I wanted to get. Later I remember and go get it. I have been repeating things to my husband and he gets frustrated and says 'you already told me that'. I then get frustrated and leave the room. I enjoy reading books but can't recall what I read so I go back a few pages and then pick up where I left off. I was also able to retire at 62. I had been an Administrator for a large medical practice so I was very happy to take an early retirement before signs started showing up. To make a long story short, when I feel myself getting frustrated I go to a quite spot and do deep breathing exercises and I calm down. I do enjoy reading the articles on MCI as they give me encouragement and know that I am not alone. So that is MCI in a nutshell for me.
Hi @lindaburdett, I can relate with what you are experiencing. I am having problems with my memory. I get so frustrated and want to give up. I have had 2 MRI and there was not a big change. I have a genetic disease called Adrenaleukodystrophy. This could be attributed to my disease. They have no cure for this disease. I take alot of supplements. I try to take natural products if I can. My Dr recommended Meloxicam 15 mg and Hy hydrocortisone 10 mg. He also prescribed Vitamin D 50,000 mg. I see my memory getting worse. My anxiety level is not good. I was thinking of asking my Dr about a Hyperbaric chamber. I dont like drugs. If you seen o the movie Lorenzo's oil that is the disease. It has affected my walking and balance. As I explore my disease I will let you know. Hope you find answers. God Bless.