For those who are caring for a loved one with dementia or Alzheimer's disease, what are you looking for from an online community like this?
We want to create a helpful, supportive, and meaningful space for you. Please share what you would find most helpful in an online community. Are there particular things you'd like to talk about or learn? What kind of support or information would make a difference in your daily life?
Thank you for this. I do need support. My husband has Lewi Bodi and Alzheimer's. Diagnosed in 2021. I thought I could help him on my own. But I'm falling way short. We're moving to a one level home. He's been here for 50 years.
I Need advice please.
Hello. Thank you for being here with us. Our community is always here, so we are glad you found us. I am sorry things are hard and you feel that things are falling short. What is the most challenging to you right now? When is the move to the new home occurring, and do you have support to help pack and move? I know a move is a big project, so if you haven't already, please get in touch with family and friends to help. Moving can also bring changes to you and your loved ones when establishing your new place. Remember to allow yourself grace and patience with the move. ♥️
When you ask for advice, is there a particular area in which you need tips/suggestions, information, or support? Please let our team know so we can help to support you and get you the information you need. Our site has many articles and stories about Alzheimer's. I located a few articles that I feel will help you as you search for resources within your community and with your husband's healthcare team.
https://alzheimersdisease.net/clinical/types-of-dementia https://alzheimersdisease.net/answers/resources
https://alzheimersdisease.net/living/tips-for-solo-caregiverI am thinking of you and sending along a comforting hug. Warmly, Nancy Alzheimersdisease.net Team Member 💜
We just got a diagnosis of severe cerebral microvascular disease and Alzheimer’s. DH has no recollection of what the doctor said. He is late stage MIld Cognitive Decline. I lost my Mom to AD 29 years ago and was her caretaker. My DH is 75. I dread going through this again. At least this time, I can get information and support. I am looking for practical ways to manage what is ahead and how to handle the stress of it all.
, we're so glad you're here, and we are surely here to share support, or listen when you need a friendly ear. You're not alone. - Warm (((hugs))), Donna (Team Member)
