Support Group for Those of Us Living With Mild Dementia
I know there is a Dementia Caregiver Support Group.
I would like to have a group for people like me. I am entering the Mild Dementia phase from Mild Cognitive Impairment.
It’s frightening to think about my future.
Could a group for Dementia Patients be started?
Interested in more discussions like this? Go to the Aging Well Support Group.
Dear 904dmt,
Slower name recall, such as you describe, is common with aging, and not necessarily a sign of serious cognitive decline. Your neurologist is a good person to ask. If you're an AARP member, they offer free cognitive tests on line.
Meanwhile, it's a good thing for all of us to simplify our lives and get all end-of-life planning and information in order. _Get It Together_ from Nolo Press is a workbook for this. Once you do this, you'll find your worry burden is lighter.
I know it seems overwhelming, but please make time for yourself. Calendar self-care - if it's a walk in nature, shopping, not answering the phone, or turning off social media, just do it. You deserve a break.
Good evening @edsutton, I would like to start my return to Mayo Connect mentoring with a response to a Mayo Connect member and monitor who I have been following.....even when I was unable to respond due to my unstable mind. I do remember appreciating your replies rather frequently. Although I have been listed as a mentor for six years, I have been unable to perform the tasks of a mentor as I struggled to recover from physical restrictions and was quite emotionally challenged for a few months by a temperamental personality. Thanks for your help. I am ready to accept today's challenges.
Chris Trout
My husband and I are both 72 years old. We both have "memory issues."
Mine: Primarily unable to find words, sometimes mid-sentence -- which makes less confident in conversation with others. And I notice I don't spell as well as I used to .
My husband's: Not recollecting recent things he's been told.
We have no children or close relatives. It's frightening to think of cognitive issues worsening.
Neither of us have had testing. I've been frightened to find out that I might have a cognitive impairment, thinking there's no real treatment. I'm thinking I need to face this and talk to an expert.
Please, I've been able to get RECOMMENDATIONS from Mayo Connect folks about GREAT DOCTORS I might connect with. I'm lucky to get my primary care at MAYO CLINIC, ROCHESTER. So, please, would any of you be willing to suggest a name or two of someone here that I might seek to see? Either writing the name(s) in response here or by sending me a private message, if you'd prefer. I would be so grateful!!!
All the Best to You All! Rose
Rose here again. I just read my posting and realize it might sound like I've already gotten recommendations for seeing someone at Mayo about possible MCI. But I haven't, so asking you for possible Rochester May recommendations. (I've gotten great suggestions for providers here for other health issues.) Thanks again for any feedback and/or suggestions. Rose
My handwriting is illegible now. Is it related to MCI?
@lhb09876 yes, it is one of the results of having brain changes.
Shirley, You are so right! I'm 80 and raised in a time when we were told to " work, work, work." Now, when I sit down, my mind keeps going over what I should be doing! I actually mentally list what I've done and think I should be doing something. It's just my husband and me. There's nothing to do in the house, how many times can I dust, do the laundry, etc. It's crazy how we have been mentally programed. It's hard to just do nothing. It is a mind set.
My husband seems to be most
Forgettable when he is engaged in conversation outside the home. He seems to get more excited when he talks to people.
He is also hard of hearing.
@pollyhet I have the same issue. I think it’s because when I am among people and trying to participate in conversation I can’t keep up. At home I don’t have that problem.