New to this disease
My husband was diagnosed with dementia about 6 months ago and I feel so lost. We've been married for 23 years, this is a second marriage for both of us. All of my family is halfway across the country, so I feel very much alone in this journey. He has one daughter who is very caring and concerned but she lives a ways from us, his other daughter has been incarcerated for over a year and has taken advantage of her father all of her life. His exwife is bipolar, so as you can see, not much support going on.
I am very lucky that my DH is very loving and sweet. We used to share all the chores around the house and he would help with anything I would ask of him. Now, I find myself taking care of everything, even things that I don't have a clue about. It's been a real learning experience and I keep telling myself, see, you can do things you never knew you could do. The downside is that I am exhausted every day.
This isn't the picture that I had in my mind of our "golden" years. It makes me so sad. I just wanted to reach out, to become a part of a "community" and hopefully as time goes on, I can "give back" with words of encouragement and tips and tricks that I find helpful in our journey.
Any helpful advice would be much appreciated.
Comments
-
My story is similar. My DH is a second marriage of only 13 years. He has no children and I have 2. They are both a distance away. My DH has MCI secondary to Alzheimer's and was diagnosed about 5 months ago. I am also new to this site and this journey. This site has given me a lot of information and support. I know others will have some specific information, books to read such as The 36 Hour Day. Come here often and read and post as much as you can.
3 -
I just got The 36 Hour Day and the first few chapters I have read certainly struck a chord with me! Thank you for responding.
1 -
Welcome, @Andi C Glad you found us and sorry it has to be under these circumstances.
@Dusty217 gave you a recommendation for a good book that will help you get started. I still refer to The 36-Hour Day often. Some good health professionals online are Tam Cummings, Teepa Snow, Natalie Edmonds, and Camille Sinclair. All have different tools and good videos to help you get a better understanding of this awful disease and how to handle certain situations/behaviors. I am going to attach an assessment tool from Tam Cummings’ website. I find it invaluable in determining what stage my DH is in and what to expect down the road. (Not a pretty picture)
If you and your DH haven’t done so already, you must get your legal affairs in order. Hire an Elder Care attorney to assist you with durable powers of attorney, wills/trusts, healthcare surrogate, and HIPPA forms. (Do not list your husband as your DPOA - rather a trusted family member. You will be his DPOA) This attorney can help protect your assets in case your DH needs placement in memory care or skilled nursing home. I met with ours alone the first visit so we could talk openly.
I know others will chime in with other good advice. They are my lifeline! I am so very thankful I found this site.
Let us know how you are doing. We care.
2 -
Hi Andi.
Welcome to this site. This has been a good place for me. My DH, passed away 8 years ago, he spent his last year in a MC, facility. I got a lot of good aswers to my questions, and lot of lovjng support going through this horrible journey. Please share anything you like to with us and ask any question you need answer to.
You are not alone, someone's here 24/7, please let us help you. Please make sure your resting and taking care of yourself. Hugs Zetta
6 -
Thank you!!
0 -
Thank you so much!
0 -
💝
0 -
I just want to say Jgreen's comment about the legal papers is very important, even if you have them reviewing them for this situation is a good idea.
5 -
You have come to the right place for a feeling of community! This site is a godsend for us because we all can understand what you’re going through. The advice and moral support here is invaluable. My DH passed away 3 months ago and I recently looked at my first post and was surprised to see it was almost 3 years ago. In those 3 years I learned so much - some from books but mostly from the good people that take the time to read and respond here. You’ll get through this and we’re here to help!
8 -
You are not alone! We are ALL here for you. Our "golden" years are also gone but I try to make the best of it.
8 -
Can you share what the attorney did to protect your assets? I’ve read comments from others saying to do this, but I’ve wondered what they can do. Thank you.
1 -
While Medicaid is a federal program, it is up to each state to determine how it is administered which means what is shared here may not be applicable to you. Available trusts can also vary.
A local CELA is best for this sort of information. Often the first consultation is free. Sometimes local attorneys will offer free talks for area seniors. Your area agency on aging may have more information.
HB3 -
Welcome. There are many of us on this site in the same situation. We were thrown into deep water with no life raft. I am going to share with you what I learned and have done in this situation. Taking action to keep us both safe and secure gave me peace.
To this immediately:
Keep all information in one notebook including symptoms you see as the disease progresses. Share these symptoms with his doctors privately. Contact an elder law attorney and get your financials in order while he can still sign legal documents. Get HIPPA forms signed by your husband giving you access to doctors and medical records. If your husband is on social security, contact them and become his designated payee.
You will have to take over all finances. Get accounts, account numbers, log in and passwords for all accounts, banking, brokerage accounts, computer, phone. Most insurance companies will not cover an accident if your husband is in one- even if he was not at fault because he should not have been driving. You can get sued for everything you own. The neurologist should be able to tell you if he can still drive. There are companies that offer a three hour extensive driving test to determine if someone is capable of driving.
You will need a plan b in place in the event you can no longer care for your husband. This will involve touring assisted living/memory care facilities and placing him on a waitlist with a refundable deposit. If there is an Oasis Senior Services in your area, they offer free assistance with in home care and out of home placement. Call in home care agencies and find one or two you like. Call your local Council on Aging and ask what services are available including adult day care. Don’t wait until you need these services. By then, your stress level will be too high to deal with all of this. Have your plan in place to execute to take the stress of of you. You can’t do this alone. You are going to need help in the home and later outside the home.
Put TILE gps trackers on wallets, phones, keys. These track the item and person through the Life 360 app. You will also need to put a wearable gps tracker on him as the disease progresses. Your local police or sheriff’s department has a program called Project Lifesaver that offers gps tracking watches. They will place your husband’s picture and information in a central database to allow him to be tracked anywhere in the country if lost. 100 percent recovery rate.
Read The 36 Hour Day. It will help you prepare for what will come.
Do not argue with your husband. His brain is broken and he won’t understand that he is wrong. Accept the blame and apologize for what you never did! Try and live in his world and understand that his reality is not yours and never will be again. Structure and routine will keep him calmer.
Travel and live everyday to its fullest after this list is completed. You might have years before you cannot travel anymore.
Come back here for help and support. The people here are extremely helpful and knowledgeable.7 -
Thank you for all the wonderful advice.
0 -
My pleasure. Take care of yourself.
1 -
As hb said each state is different, so check with a lawyer in your state. Mom didn’t have much money. We were told a trust was not worth it for her. The lawyer did suggest a prepaid funeral, which we did. Moms house had some very serious issues and the lawyer suggested we put some money into necessary repairs (not home improvements). I tried to make sure she had everything she might need before applying to medicaid. Just basic personal things, an extra set of pjs, a nice lap blanket, a new bath robe, a couple of bottles of her favorite hand lotion, a new pair of shoes…. These things really didn’t amount to much, but it will save me having to pay for them out of my pocket. In my state mom is only allowed to keep $50 a month out of her income for personal things.
5 -
It is a brutal disease. It isn’t exactly the same for everyone but most of the symptoms are not unique. I like to come to this site and search. I always find someone who is having or who has had a similar experience. Also I have kept a journal and I find that helpful. Time seems to fly by and when I am asked by a health care professional when a symptom showed up I can usually figure it out.
I can’t think of any words of comfort but know that there are many people who are caring for loved ones who have dementia. You are not alone.
4 -
Thank you……it's so nice to have a place to ask questions, get suggestions.
2 -
I also miss my helpful, handy husband. But, like you, I'm surprised what I can do on my own. You tube is my friend. I've learned how to install a toilet, jump my car, repair the lawnmower, etc. I may even try changing the oil….
2 -
Dang, you've learned a lot!! That's wonderful! My next feat is to drive on the beltway which I am terrified of. We have a home at the beach and I so want us to get down there because there is much more stimulation than just watching TV for my husband. You Tube is also my best friend!
3 -
I also am new and I am overwhelmed. He just got out of the hospital after 4 days to rule out stroke. Turns out to be moderate to severe dementia. He gets very delusional in the evenings. Short term memory gone. He also has ataxia and is a high fall risk. I am basically alone without much support except for a wonderful daughter but she has 2 small children and is busy. Like many I have to all chores now. My husband is 82, I am 73 and have hip and back issues. I go in my closet and cry a lot. I am so depressed as it seems his symptoms got worse fast. Nobody understands what we are going through unless they are going through it. Thank God for sites like this. 🙏7
-
Yep, I so relate to your situation, I also hide and cry at times, not that it helps, but sometime just to get the emotions calmed down and then move on. I too am glad to have found this message board, any tips to help is appreciated.
Have any of you done a virtual group that this site offers? Did you feel that it was a benefit to you?
2 -
I also keep a journal of how the days go. Some days are better than others, so it's nice to go back and see that I need to be thankful for those good ones.
2 -
I hate the belt way and try and find anyway to travel to avoid it. I get that. My husband has done most of the driving until now but that is coming to an end. My Neurologist said he can still drive, South Carolina doesn't pull his license for dementia, and he is just MCI at this point. But it will be soon. I hate to take that away from him and most everyone on this site will tell you, you should.
4 -
Protect is a very broad term. This is how I think of this.
Make sure you are aware of all assets which are in the name of the PWD, get joint access, or move them to your name. Monitor the state of the assets closely. In the early/mid stages, PWD are susceptible to fraud and poor judgement. PWD cannot be trusted to protect their financial interests. You need to take over.
If your income and assets are such that you see yourself potentially needing the support of Medicaid, then there are things that can be done to protect certain assets from having to be sold or spent down before obtaining Medicaid eligibility. This is where you really need the insight of a CELA in your state. If you are fortunate enough to have assets such that you do not see Medicaid support needed in your 5 to 10 year future, then this is a less critical step at this time.
Finally if you put together an estate plan pre-ALZ, it is worth getting that reviewed to ensure the intent of the plan in not compromised by having a spouse with ALZ.
0
Commonly Used Abbreviations
DH = Dear Husband
DW= Dear Wife, Darling Wife
LO = Loved One
ES = Early Stage
EO = Early Onset
FTD = Frontotemporal Dementia
VD = Vascular Dementia
MC = Memory Care
AL = Assisted Living
POA = Power of Attorney
Read more
Categories
- All Categories
- 634 Living With Alzheimer's or Dementia
- 350 I Am Living With Alzheimer's or Other Dementia
- 284 I Am Living With Younger Onset Alzheimer's
- 17.7K Supporting Someone Living with Dementia
- 5.7K I Am a Caregiver (General Topics)
- 8.7K Caring For a Spouse or Partner
- 2.9K Caring for a Parent
- 227 Caring Long Distance
- 177 Supporting Those Who Have Lost Someone
- 12 Discusiones en Español
- 1 Vivir con Alzheimer u Otra Demencia
- 1 Vivo con Alzheimer u Otra Demencia
- Vivo con Alzheimer de Inicio Más Joven
- 11 Prestación de Cuidado
- 2 Soy Cuidador (Temas Generales)
- 8 Cuidar de un Padre
- 23 ALZConnected Resources
- View Discussions For People Living with Dementia
- View Discussions for Caregivers
- Discusiones en Español
- Browse All Discussions
- Dementia Resources
- 8 Account Assistance
- 15 Help



