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The Long and Winding Road…

~ An Alzheimer's Journey and Beyond

The Long and Winding Road…

Category Archives: Technology

Dementia Mentors Site Launches June 1st!

24 Saturday May 2014

Posted by Ann Napoletan in Activities for Your Loved One, Advocacy and Awareness, Caregivers, Early Onset, Events, Helpful Resources, Inspiration, Support system, Technology, The Early Years

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alzheimers, dementia, dementia activities, dementia awareness, dementia mentors

Where there’s hope, there’s life. –Norman McNamara

Many of us have had a mentor at one time or another during our lives. They guide us, offer words of wisdom, and provide feedback on our ideas or problems. A teacher may serve as a student’s mentor, or someone in a more senior position at work may mentor a less experienced associate. The role might be formal or informal. There are no set rules, but generally the relationship involves trust, counsel, and mutual respect.

No Longer Alone

Imagine receiving a diagnosis of Alzheimer’s or another form of dementia. Few things would be as frightening; few things would elicit such a strong sense of being alone. But what if, upon diagnosis, you were introduced to a dementia mentor? How might that change things?

Well, Gary LeBlanc, along with Norman McNamara (UK), Harry Urban (US), Barry Pankhurst (Indonesia), Chris Roberts (Wales), Richard Taylor (US), and others are preparing to launch a project that has been almost six months in the making. This collaboration between friends and advocates around the world is groundbreaking. Nothing like it has ever been done, but it promises to change the way people deal with the diagnosis and the fear, uncertainty, and loneliness that comes with it.

On June 1st, the Dementia Mentors website will be unveiled. The site was designed and built by Harry Urban, founder of Forget-Me-Not. Harry is living with dementia so he knew exactly what was needed to make the site dementia friendly. The goal is simple: to provide newly diagnosed individuals with the tools they need to start this journey on the right track, from the moment the diagnosis is received.

Those Dreaded Words – And Then What?

Those involved in this project know firsthand how frightening it is to hear the words, “You have dementia.” Imagine hearing those words, then being handed a prescription and told to “come back in six months.” In many cases, that’s exactly what happens. Chris Roberts of Wales describes being stunned and in shock, head spinning such that he didn’t know where to turn.

My personal experience with Mom was similar. Although I absolutely loved the family physician we were seeing at the time, we essentially left the office after each visit knowing things had gotten a little worse but with no resources to help us understand what was happening or connect us with those who could. That was a while ago, and fortunately, I think things have begun to change a bit; at least people are talking about it more now. But, that being said, we have a long way to go.

Renewed Hope

Dementia Mentors is about helping newly diagnosed patients understand their lives aren’t over. In fact, quite the contrary! When one looks at everything people like Norrms McNamara and Harry Urban have accomplished since their diagnosis, it’s nothing short of incredible. These men are true pioneers and are inspiring hope around the globe.

Chris Roberts says, “It’s about what you can do, not what you can’t,” and that’s the message the founders of Dementia Mentors want to convey.

the journey beginsHarry is quick to encourage people not to give up, assuring them they do have a meaningful life ahead of them. In this digital world where Google has become our best friend, it’s vital for folks to realize that when they hit the Internet for information, they will likely be bombarded with material about the later stages of the disease. The disease isn’t JUST the later stages! Yet, there tends to be very little information out there about the earlier stages. This is where Dementia Mentors comes in.

  • Imagine a website created by dementia patients, for dementia patients. That means simple navigation, pleasing to the eyes, clear, and concise presentation. Someone having problems reading the text can simply click a button to hear the passage read aloud.
  • Imagine being able to listen to people who are actually living with dementia discuss a wide variety of topics – all from their own unique point of view and based on real life experience. At launch, the site will have approximately 30 pre-recorded videos, no more than three minutes in length. Additional videos will be added in the coming months.
  • Imagine having a face-to-face video chat with someone who has walked/is walking in your shoes. Patients will be able to schedule an appointment to talk one-on-one with a mentor. Keeping to the dementia friendly theme, a simple mouse click is all it will take to be connected with a mentor via both audio and video. Of course, all discussions will be completely confidential.
  • Imagine one-stop access to over 70 puzzles and activities, all designed with dementia patients in mind. The activity page will be updated with new material regularly to keep it fresh and interesting.
  • Imagine quick, easy access to virtual memory cafés where patients can enjoy socializing with one another. People like Harry, Chris, and Norrms credit keeping busy, maintaining social connections, and staying engaged with helping them keep progression at bay. The beauty of social media – no one ever needs to feel alone.

The Vision

Gary and his team envision today’s mentees becoming tomorrow’s mentors. The value of helping others can’t be overstated. We all feel more energized, hopeful, and positive when we know we’ve made a difference to another person. That’s what Dementia Mentors is all about – people helping people. Everyone involved benefits from the program; each life is enriched along the way.

This project is innovative and 100% grassroots-based. All participants are donating their time and the team is seeking additional mentors. They would like to have every corner of the world covered, so that people can be connected 24 hours per day, seven days per week. According to Gary, there are 15 mentors on board as of this writing, with many others expressing interest already.

Friends Helping Friends

friends helping friendsThe Dementia Mentors tagline says it best, “Mentoring, Motivation, and More. We Help You Rule Your Dementia.” I truly believe that is the key – rule it, don’t let it rule you. We didn’t do that with my mom. At that time, we didn’t even talk about it let alone think there might be a way to connect her with others who could understand her fears so much more than we could. What a blessing that would have been…

You can help by spreading the word about the June 1st launch and directing people to http://www.dementiamentors.org. By doing so, you, too, will truly be making a difference! If you or someone you know would like more information about the project, please send a message via the “Contact Me” link at the top of the page and I’ll put you in touch with Gary!

____

Gary LeBlanc is an author, columnist with the Tampa Tribune, founder of the Alzheimer’s/Dementia Hospital Wristband Project, a Purple Angel Ambassador, and former caregiver to his father who lived with dementia. You can visit him at Common Sense Caregiving.

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Walk, Run, Bike, and Earn!!

28 Tuesday Jan 2014

Posted by Ann Napoletan in Advocacy and Awareness, ALZ Assn - National, Fundraising, Technology, Tips

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alzheimers, alzheimers association, alzheimers fundraising, charity miles, dementia

charity miles“I’m just one person. In the grand scheme of things, how much of a difference can I really make?”

Common sentiment. I’m sure most of us have asked ourselves that question a time or two.

The fact is, we CAN make a difference; there are all kinds of ways to help and not all of them involve a huge financial or time commitment!

Have you heard about Charity Miles? You can download this great little app for your iPhone or Android device, and it’s FREE!

With Charity Miles, you can earn money for the Alzheimer’s Association when you take a walk, go for a run, or hop on your bicycle! Before you head out, just launch the app and choose the Alzheimer’s Association as your charity. As you walk/run/ride, you’ll earn 10 cents/mile for biking and 25 cents/mile for walking or running! It’s THAT easy! (See Terms of Service for complete details.)

snowybikeThose of us in the midwest and east are currently mired in the latest arctic blast, while some folks are posting “selfies” as they sip margaritas on the beach!! But that’s okay!!

Whether you’re living in a climate that affords you the opportunity to enjoy those walks and rides year ’round or you’re like me and dreaming of spring – download Charity Miles and let’s earn some easy money for the Alzheimer’s Association!  (And tell all your friends, too!!)


Addendum to original post:  Note that in order to complete the donation process, users must accept sponsorship and share via either Twitter or Facebook. Thanks to Lynda Everman for this important piece of information!

Excerpt from Charity Miles Terms of Service

Earning Sponsorships.  You can earn sponsorships for a different Charity (or the same Charity) each time that you use the Application.  To begin earning a sponsorship, simply swipe the Application’s home screen to select your desired Charity.  Once you have selected your Charity, please choose whether you want to walk, run or bike… And then press the “START” button to commence a session.  

Once you commence a session, the Application will track your distance and, subject to the amount of the Purse, you can earn 25¢ per mile for your chosen Charity while walking or running, and 10¢ per mile while biking.  The Application will convey your achievements both in terms of: (i) the miles you complete; and (ii) the real world impact that you can help your Charity fund.  Please note that our expressions of your real world impact are good faith approximations and may not be exact in each case.

When you finish a session, the Application will summarize your achievements and offer you a sponsorship for your Charity.  To accept the sponsorship, you will be asked to share your achievements, raise awareness for your Charity and (please) thank your Sponsor on Facebook and/or Twitter.  In each instance, we will present you with a proposed but editable message to share.  Subject to the User Content Rules (described below) you can say anything you want in these messages.  However, as we discuss below, we encourage you to thank your Sponsors.

Also, please note: if you do not accept the sponsorship, then your achievements will not accrue on behalf of your Charity.  We have instituted this policy for two reasons.  First, walking, running and biking for charity is not just about raising money—it is also about raising awareness.  Therefore, we want to encourage you to use Charity Miles to promote your Charities as much as possible.  

Second, while our Sponsors are genuinely grateful for the opportunity to support you, we are just as grateful for their support.  So, if you are grateful for your Sponsor’s support, then we encourage you to promote them too.  It’s not required.  But the point of Charity Miles is to turn amateur walkers, runners and bikers into sponsored athletes.  And just like professionally sponsored athletes, we should try to do right by our Sponsors.  Remember: the more we support our sponsors, the more they will support us.  And the more they support us, the bigger the Purse will be for the Charities!

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Party at Harry’s Place!

31 Tuesday Dec 2013

Posted by Ann Napoletan in Advocacy and Awareness, Caregivers, Events, Helpful Resources, Holidays, Inspiration, Ruminations, Smiles, Support system, Technology, Tips

≈ 2 Comments

Tags

alzheimers, alzheimers awareness, alzheimers support, caregiving, dementia, life with alzheimers

2014I’ve never been big on all the hoopla that surrounds New Year’s Eve. As a serious introvert, my perfect celebration involves enjoying a nice quiet evening with a fire and a couple of glasses of wine. If I’m feeling really adventurous, I’ll break out the DVD player and pop in When Harry Met Sally (my favorite feel good movie of all time)!!

This year will be a little different, but that’s another post for another day and probably another website. I may or may not title it “Family Circus” – draw your own conclusions from that. ((( Smile )))

A Huge Dose of Inspiration

But back to the topic at hand! What I really want to do is introduce you to Harry Urban, founder of the Forget Me Not community on Facebook. It just so happens that he and his wife, Hazel, are hosting a virtual New Year’s Eve bash to ring in 2014! What’s that, you ask? Well, read on for more information!

I had a chance to talk with Harry for the first time during a video chat over the weekend and really enjoyed the conversation. It’s one thing to hear from care partners and other advocates, but getting input from the people who are living with this disease day in and day out is particularly enlightening.

I have immense respect for people like Harry and Norrms McNamara who are so open and honest about what it’s like to receive that diagnosis and live with dementia. How I wish I’d been able to talk to one of these gentlemen years ago in the early stages of my mom’s illness.

After Sunday’s call, I was inspired to do a post on Harry and asked if I could email him a few questions. Of course, he was more than willing to oblige and I’m happy to be able to share this insightful Q&A with you.

Q&A with Harry

AN:  So many people who are diagnosed fall into denial and/or depression, and they commonly withdraw more and more as the disease progresses. You have managed to do the opposite so beautifully. To what do you attribute your positive attitude, desire to raise awareness, and ability to inspire thousands of people?

HU: Like so many others, I fell into denial and depression when I was first diagnosed. I was scared and didn’t know what my future was going to be like. I explained my diagnosis to my family and friends and was quickly abandoned by most. They just didn’t know how to deal with what I told them. This only added to my depression, and I realized this should never happen to anybody. I started to pick up the pieces and made a vow I would try to help others so they would never have to go through the hurt and pain I did.

I spent a considerable amount of time trying to figure out why patients with dementia are treated like this. I came to the conclusion that people are not in general nasty, but rather, they don’t understand the disease. The same goes for someone that was diagnosed; they don’t know what the future holds so they assume the worst.

It appeared to me that education was what is needed to better understand what our lives are like. The myths and stigmas associated with dementia had to be broken. The person who was diagnosed had to believe their life is not over but many fruitful years lie ahead. Over the past several years I have been telling my stories with amazing results. I don’t get pity, but the ideas of dementia are changing. I like to think I am spreading the word of HOPE, not a cure, but a better quality of life for us suffering from dementia.

fmnAN: Who is your greatest inspiration?

HU: I have so many. All of them suffer from some form of dementia. I have a friend, Kenneth Teaspoon Overcast who suffers with dementia. What an amazing man; he realizes that he lost most of his skills but still manages to live a wonderful life. He is surrounded by family and friends that simply adore him. The support his family showers him with cannot be beat. Every bump in the road that comes along, he handles with grace.

Ken suffers greatly but never lets his disease control his life. I want others to enjoy the happiness Ken has living with dementia. Ken inspires me to speak out so others can also be happy.

AN: What was the inspiration for Forget Me Not, and how long has the group been in existence?

I struggled with my emotions when I was first diagnosed and join several support groups. I found out that all of them just did not fill the void I had. Prayers and hugs are nice but I needed more. I wanted to talk about my disease without being judged. I wanted a safe, comfortable place that I could vent about my disease and explain why I do the things I do. I wanted a group that raises awareness, where members share their stories in order to help others.

My friends knew I was unhappy and convinced me to create a group that offered love and support but also gave members the opportunity to discuss their disease. February of 2013, I did that by creating Forget Me Not.

I soon realized you cannot have a successful group if it was all doom and gloom so we created “sister” groups so we could escape the frustrations of Dementia. We also started a Spanish group called No me olvides for the Spanish community. This group is a mirror image of Forget Me Not with the same ideals.

Happy New Year!

Click to Enlarge

AN: Can you share a little bit about your virtual New Year’s Eve party? What is it? What made you decide to do this? How can folks join the fun?

HU: One of the worst feelings for those living with dementia is the feeling of loneliness, especially around the holidays. On Christmas Eve, my wife and I were talking about how many people are spending the evening alone so we started a Zoom video chat and invited anybody on Forget Me Not to join us to simply say hello or spend the evening with us. It was a huge success and many laughs were shared that night.

That is when we thought why can’t we have a virtual New Year’s Eve party? Many care partners can only celebrate bringing in the New Year at home, so why not stop in to visit us!

I plan on starting a Zoom video chat at around 8:00 EST so anyone can stop in to wish each other a Happy New Year or stay and party with us to bring in the New Year.

Everyone is welcome and the instructions for joining are as follows:

Please click this URL to join:  https://zoom.us/j/499150272

Or, go to:  https://zoom.us/join and enter meeting ID: 499 150 272

 

To join from dial-in phone line:

Dial: +1 (424) 203-8450 or +1 (209) 255-1200
Meeting ID: 499 150 272
Participant ID: Shown after joining the meeting

Life Is Meant To Be Lived

As you can see based on Harry’s comments, there’s so much we can learn if we’re just willing to listen. I think what inspires me so profoundly is his grace and wonderful attitude despite being dealt what we can all agree is such an unfair hand.

Harry reminds us that while research is vital, it’s equally important to give today’s dementia patients the absolute best quality of life possible. He serves as a role model to those who have been and will be diagnosed – life does go on, and it can be a great life.

If the day should come that I walk in Harry’s shoes, I can only pray to do so with half as much poise, courage, and sense of humor.  Thank you for all you do, Harry, and most of all, thanks for being you!

Are you a patient or care partner? If so, I would recommend joining Harry’s Facebook group, Forget Me Not. Not only will you find a wealth of helpful tips and information, you’ll also meet some fantastic people who understand what you’re going through and “speak your language.”

Harry also hosts the Forget Me Not Memory Cafe, as well as a weekly video chat support group.

Be safe everyone, and Happy New Year!

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