Monday, February 15, 2016

Scamming People With Dementia- Very Wrong but Very Common!

Today I want to talk about something that has really bothered me since I started taking care of my father, and that is the amount of people and businesses who willingly and purposely seek out people like my father to take advantage of them. I want to share a few examples of the things I have seen. 

My father has the tendency to purchase anything that is suggested to him and I am dealing with a horrible problem with his mail right now. He has signed up to receive so much junk it is ridiculous and the worst part is that companies are willing to invoice him so that when the junk arrives so does a bill. Many of these companies are quite skilled at getting the elderly and people with dementia to buy from them and are also quite good at scamming them. If you are a care giver please be aware of this and work to control and go through the mail of your loved one before they can to get rid of the potential scams and junk mail. 

Another issue I dealt with that was near impossible to get stopped was Internet fraud. Two different “woman”,  convinced my father to send them money through Western Union to a few different African nations. They did this by sending horribly created nudes with a “perfect” body with a “perfect” head photo-shopped on and sent it to him through text and email. They also told him tons of sob stories.  These “women” are actually mostly computer generated and my father was unable to get that. Getting rid of “Candy” was horrible. We had to change his email and cell phone number 3 times. He still to this day believes that "she" is a beautiful woman who is in love with him. 

Examples like these are all to common in our world today and it is up to us as care givers to do all we can to protect those we love. The world is very unsafe for those with dementia because they can be scammed so easy. I am working on totally taking the Internet away from my father to try to combat all types of scam that I can.

Please share anything you have found helpful to protect your loved ones from scams.

Attached are a few resources regarding how easy it is to scam someone with dementia:


Saturday, February 6, 2016

Balloon Day!

Today was the day that Craig was sponsored to go up in the hot air balloon by St. Croix Electric. The day started off early with me picking up Craig at 6:10 AM. We were to the Hudson House by the designated 6:30 AM time and sadly found out that the winds were way to high to go up. Craig was disappointed by this news so I agreed that we should all go on a balloon ride as a family this summer. He likes that idea and we are planning on doing that. And agreed to meet back at 2:15 PM.

At 2:15 we arrived at the Hudson House again and sadly found out it was even more windy then before. Craig took this news well and we agreed to accompany Nancy to pass out fliers at the Hudson Hot Air  Affair grounds. We passed out fliers for about a half hour before my dad started to look really tired. He stated he was ready to go and I brought him home.

While we were waiting for Nancy to meet us we did see some cool things and I snapped this awesome picture of my dad with an ice sculpture.

 I would also encourage anyone with an elderly parent or a family member with dementia to check out First Call by St. Croix Electric. I wish I had known about this before I got my dad into assisted living.

Parade Pictures

I want to start including more things on the blog so I decided to start with pictures. These are pictures from the parade last night.

Nancy had this wonderful sign printed out that got many people's attention. Hudson Fire Department did a wonderful job of attaching the banner. It was great for the ADRC and Hudson Fire Department to partner together. 




Here is my dad with the banner and with the brush truck. This is the fire truck used to fight grass fires. I would like to thank our wonderful sponsor St. Croix Electric. 

Friday, February 5, 2016

Parade day!

Tomorrow is the big day that we go up in a hot air balloon and today was the parade. I remember going to the parade for the Hot Air Fair as a child and remembered how cool it was to have glow sticks. Seeing as I have found out how great the dollar store is for having parties and showers at my home, I thought I would check it out for glow sticks and I found quite the abundance of options. I ended up getting my dad a "fire fighter ax" glow stick and I got a princess wand for myself (pink!). I also found some awesome necklaces. If you are ever having a party and need glow sticks the dollar store is the way to go! 

After work today I headed to happy hour at Red Cedar which was wonderful as always. I had time to to run to the dollar store and to Target then headed back to pick my dad up. At 6:30 we showed up at the fire station and everything was all ready to go. I got our glow sticks ready and we were off to the night-time parade! We rode in a fire truck with a wonderful banner on it that talked about dementia. One of the fire fighters drove and when we got to the announcer booth the announcer gave the most wonderful recognition to my father. He mentioned my dads years of service to the Hudson Fire Department and talked about his dementia. It was very moving. As we got to the end of the parade I noticed a little girl who looked cold and tired. I hopped out and gave her my princess wand. She was so happy! 

After the parade I dropped my dad off and now am getting ready for bed. Tomorrow is the big day and we have to be at the pick up location at 6:30 AM. 

I will update about the balloon ride tomorrow afternoon. 

Wednesday, February 3, 2016

Self-Care

Today after work I took a self-care day. Self-care days are important for caregivers. They allow us to take care of our self and good self-care allows us to take better care of those we love. I thought today would be a good day to focus on the ways that we can practice good self-care. 

1. Exercise
2. Call a friend
3. Pamper yourself
4. Watch a TV show you love
5. Read a book (or part of one, use caregivers are busy people) 
6. Do another activity you enjoy
7. Paint your nails, or trim them
8. Plan a meal for tomorrow
9. Meditate
10. Color, write, paint or do a craft 

These are just a few ideas for good self care but I am also going to attach resources below. 

This is an interesting article about self-compassion, I think I am going to go more into Self-Compassion later but it is a good time to present this article. 
Self-Compassion

These are good resources about self-care
Self Care for Everyone
Self Care from Caregiver.org

Good Information about Caregiver Stress from the Mayo Clinic
Caregiver Stress


When I first started caring for my father I forgot to take care of me. I was so overwhelmed, stressed and tired. I gained a lot of weight during that time and developed eating habits that were not normal for me.  I also did not have time to exercise. I later found out that these are common things to happen when we begin to care for a loved one.  My adventure into self care started when a wonderful friend of mine introduced me to a group of women who are all very focused on taking good care of themselves after a discussion about my struggles with gaining weight and my newly developed poor eating habits. The woman in the group are supportive and they motivate me to stay on track. These women are very important for my journey into good self-care. 

How you are able to find time to participate in self care is up to you, but I would encourage all care givers to try to practice good self care. Try doing something for you. You will feel better afterwards and have renewed energy to get things done.

I would like for others to post what they do in regards to self care in the comments section. 

Tuesday, February 2, 2016

Good Communication

This week is turning out to be much busier than I was thinking it was going to be. The finishing details for the Hudson Hot Air Fair are being figured out, and I am awaiting finding out the final schedule. I will keep you updated on those as soon as I know more. Hopefully, the snowstorm today doesn’t isn’t too big!
Today, I thought it would be really important to discuss some of the best communication techniques for talking to someone with dementia. I have learned many of these through communicating with my father but there are also resources that can help you learn more about communication.

Communicating with someone with dementia- My Top Ten:
 1.     Ask clear questions
 2.    Give them plenty of time to answer
 3.    Be understanding
 4.    If you can tell that they are struggling it is ok to help
 5.    It is OK if they forget
 6.    Show them love and compassion
 7.    Ask them questions that will help build their confidence
 8.    Express that you are there for them
 9.    If an answer doesn’t make sense, try to clarify but if you still can’t make sense of it, move on.
 10.  Be honest, someone who has dementia can tell if you are telling a lie to them.

Everyone with dementia is different and it will take time to develop good communication with different dementia patients, but it is important to remember that their doing their best to communicate with you.
Please share if you have developed good communication skills with someone you love who has been diagnosed with dementia.

Here are some resources for communicating with dementia patients:


Thursday, January 28, 2016

Neurologist Appt. And Get to Know FTD


Today Craig and I went to the Neurologist. It was the first time I had accompanied him to the Neurologist. I didn't learn much new because I have worked very hard to become very well informed about FTD and to have a good understanding of how the dementia will affect Craig and his actions. I also learned that we will not loose my dad as soon as we thought so yippee! But it did make me realize I have not shared very much information about what FTD is. In the next few days I plan on introducing FTD, FTD research and unveiling resources for families.

This was my first resource I looked at when my dad was diagnosed and it has helped me greatly. 

Frontal Temporal General Information

If you are unable to get the link to work please go to: 
http://www.alz.org/dementia/fronto-temporal-dementia-ftd-symptoms.asp


Emily

Friday, January 15, 2016

New Year Update


Happy New Year!

It’s been a long time since I have posted in this blog and some very big changes have occurred. On Christmas Eve all of our issues with giving my dad adequate and medically competent care came crashing to an end when my Grandfather passed away. See, he had durable power of attorney documents and the only way us kids were going to be able to get power over my dad’s medical care was with guardianship. Now my grandfather was not the best person around, he had a history of abuse. He also was down right in denial about my father’s diagnosis and what it meant for a long term prognosis. His death came as a relief to my siblings and I, and thankfully we will no longer have to go through such difficult family situations in order to help my father in the necessary way.
Some other very big changes are that I have been working with the county dementia care specialist to bring awareness to that young people can get dementia. Many doctors fail to realize that memory loss is abnormal at any age and that is one of the issues we are working on. To bring awareness to that young people suffer from dementia my father and I will be doing a news interview with a big metropolitan news station and will also be being part of the Hudson Hot Air Fair! We will be going up in a balloon to educate people about dementia!
I feel very happy with how our lives are going, but I still realize that there is much work to be done, both with helping my father, and with education of the public

Wednesday, December 30, 2015

Part 2

The Second part of our story is much different from the first:
After a long and very difficult battle over what was best for my father with my grandfather we moved my father into assisted living in the middle of October 2015. The move was very difficult because my grandfather did everything he could think of to block the move, including going as far to have the police bar me from going to “his house” to help my father move out. It all ended up working out in the end because of a few useful steps, first I scheduled the move and made it clear there would be a list of items to be moved and no other items were needed. I gave that list to my father and he was to give a copy to the movers. After he gave a copy to the movers, they would get the stuff and he would drive to the assisted living facility in his car. Once he arrived at the assisted living facility the movers would move things in and I would help direct them as to where things need to go. A few items that were not welcome made it, but it all ended up working out. The next thing we did was bring a lot of stuff to Goodwill. After this, we got a laundry sorter from Amazon and a mattress pad from Target. Then we just started to get him settled in. The first few weeks my dad was in assisted living I was very nervous and went there frequently but after a while I started to be able to prioritize what needed to be done and started to set a three visit a week limit unless something important needed to be done. I also made it clear that our Fridays were to be spent having fun. His assisted living facility does a very fun happy hour with food and music on Friday afternoon and I make sure to go every week. Our focus has now shifted from getting things done to creating good systems that can minimize the time we spend doing “jobs” so that we can spend time together. I know that he will continue to loose cognitive function and I want to spend the time with him now before the dementia gets worse. I want for him to remember me.

Saturday, September 26, 2015

Moving Forward and our Story Part 1

After deciding on a place, our next steps are to put money down on the assisted living facility that we like and then my father will have to meet with the nurse at the facility.  After that we will need to get a recommendation from his physician that assisted living will be a good fit for him.

I started on this journey about a month and a half ago after a wicked situation I learned about involving my grandfather waking my dad up, pulling him out of bed and screaming at him at 1:00 in the morning. Talk about abuse! It hadn't been my first time calling adult protection, and he had already been on their radar but this time my siblings and I felt that it was time for us to step in. We had been misled that my grandfather was taking wonderful care of my father, when in fact throughout the last few weeks we have found quite the opposite was taking place. My dad had total freedom and was getting himself into trouble all over the place.

Now, I will introduce my siblings and I and let you know more about the situation. I am Emily. I am 26, have a beautiful home with my loving and very smart boyfriend, and am very caring and compassionate. My brother is 22, he has a wife and a baby on the way. My sister is 16 and is a junior in high school. She lives with our mother. My mother is a wonderful woman who divorced my father because his actions were erratic and my sister did not feel safe around him. We all love my father very much and work hard to be there for him. Everyone, including my mother, work hard to get him the best care and work to entertain him.

About two and a half years ago my father began acting very strange. We had reports of him telling random women he loved them, getting in trouble at work, driving erratically, poor bladder control, and many other things. We brought him to a local clinic and started the initial testing for factors that we knew could cause these problems in a 50 year old male. He tested negative for diabetes, so we thought harder and he ultimately tested negative for things like syphilis. Not being able to find any answers, we went to the Mayo in Rochester, MN. After many appointments, we found out my father had fungus growing in his sinus cavity and that that could have been causing all of his issues. After surgery, it was clear he was acting weirder than ever. He continued care at the mayo where one day he got a horrible diagnosis of FTD. We were in shock and after reading about FTD it didn't seem right to us at the time, now we know it is the correct diagnosis.

I moved out shortly after the diagnosis into my new home and started my own life, my mother continued to work full time and try to babysit my father (a chore I had shared with her while living with them). I could tell things were bad at home and that my siblings were starting to be scared of my father and my mom was stressed beyond imagine. Then one horrible day, my father asked my mom's friend out on a date in front of her and she kicked him out. She thought of taking him back very quickly but couldn't because my sister expressed her fear of my father. That is where things started to get good for him, but also bad for him.

My father moved into a home owned by my grandfather and also lived in by my uncle and was continue with the divorce. About a month after him moving out, he landed in the ER after collapsing at work. We learned later it was because he had not ate almost anything for over a month. He ended up staying the night because he developed a different issue that caused the collapse. I knew this was all somehow related to the weird behavior and so I started to advocate and ask questions about the FTD. He ended up getting discharged but I had advocated enough to get him started with a neurologist. This was also the horrible day I had to explain to my father he wasn't going to be aloud to work anymore. He cried and cried, it was horrible. We had meetings at the union hall to explain his behavior and learned that many of his co-workers we covering for him when he would make mistakes. I thank these men and women because they did a very kind thing for him and for our family.

Somewhere in the divorce he stopped talking to his kids, which I later learned was a result of comments made by my grandfather. During this time my uncle moved out and got a new home after. After the divorce was over, we would occasionally go out with our father and would see a drastic reduction in his mental function and weight. This is how he originally got the adult protection worker (I would call on him). But after the last incident, I went to his meeting with her and that is when things started to change.

I am getting ready to relax for the night and will share the second part of this long story tomorrow. This is a painful thing to talk about so it takes some time to get through it and process it well.

To all those who have a parent with Frontal Temporal Dementia, I am sure you have a story too, please feel free to share.

Emily