Showing posts with label pictures. Show all posts
Showing posts with label pictures. Show all posts

Monday, November 1, 2010

An Email From a Friend.......

As many of you know from time to time I share emails with permission. This is one I got just recently. You all seem to be amazed that even advancing in this fricken disease I can still communicate. I want you to know that all of us with AD or other forms of dementia are not always stumbling, bumbling and drooling people. Some to the end, not many still reamin mentally strong, maybe not physically but one cannot have everything. Also this email may give you a hint of why I take no meds for AD, just mood stabilizers, the shit does not work if that helps.**************
Dear Joe and Lynn,

Thank you again for your response...these letters and blogs must keep you both very busy...I don't know how Joe still does it, but thank you from the bottom of my heart. My father suffered from AD silently...we did not know what he was thinking or feeling...he tried to live life as if he didn't have the disease, including not talking about it. The only glimpses we had were his physical struggles, his hallucinations, and listening to his frustrations...we had to try to fill in ourselves what was going on in his head. Joe, you have no idea how much your shared words help us understand what you are feeling or experiencing or thinking...more than you know. I wish my father could have expressed what he was experiencing, but he didn't, so I am learning from you.

I just checked into your blog...I am sorry to say that I haven't been able to keep up with it regularly (due to restricted internet access), but every time I visit your page, it brings tears to my eyes...I am just filled up with sentimental emotion on how much you share, and your struggles doing it, and your struggles with the disease...thank you for all the work you put in. I am amazed at how articulate you still are at this stage.

I am so happy you published a book!!!! That's great.

I unfortunately could not find the memorial link on your page...I must be overlooking it. But I would love to send you the information on my father, and a photo. I will let my mother know.

I was also thrilled to hear that you are doing the Memory walk in Oceanside. Before I knew that, I was going to e-mail and ask if you and/or your family if you and they might be interested because I want to do it too. But I have to get my butt in gear to sign up and send out the e-mails. My mother did the walk in Florida about a week or two ago. I'll honor my father with a team bearing his name; however, I do not have family here, so unless friends join me (and they might), I might be a team of one. I would be honored to walk with you and Lynn if you like. It sounds like you might not have many walking with you, so if you and Lynn need any help at all, I would be happy and honored to help. I helped give care to my father until he passed.

This is getting long for you to read, so I will sign off. If you want to put any of this last response on your blog, you have my permission.

God bless you all (and my father would have agreed with Joe on "...and this great country of ours")

Cheryl

________________________________
God Bless & Keep You & This Country of Ours!!!
joe
PS Cheryl has no real idea what emails and comments from you folks really mean to me. They keep me wanting to post, even though I feel no one really gives a shit.

Wednesday, September 16, 2009

An Email Identity Secret

Message = Hello
I work at a local Alzheimer Society .......... My co-workers and I have been watching the HBO series over our lunch hour. I wanted to stop by and visit your blog.

Thank you for having the courage to share your story so publically. You have made such a huge difference for other people with ADRD because you have put a face behind this disease. Your story is particularly important because it shows that anyone can get Alzheimer's disease...even someone as accomplished as you.

Not everyone is interested in being the "poster child" for Alzheimer's disease (for lack of a better phrase). It is such a personal journey. Thank you for the courage and commitment to do this.

Our chapter is marking it's .... Anniversary this year. In fact we are having a ... on ....... with over 150 people attending it (i.e., to honour the occasion). There are so many people who have touched the chapter...be it person's with Dementia, their family, volunteers and staff.

There are so many people who are working towards improving the quality of life all of those affected by Alzheimer's disease. I know that each of them would send you and your family their well-wishes.

I have worked at the chapter for about half that time. During that time, there have been incredible strides in research and public awareness about Alzheimer's disease. It is encouraging to see this but we all know that there is so much more that needs to be done. Your story will bring much needed awareness to this disease and will help to move things one step further in search of a cure.

Anyway, I just wanted to say hello and THANK YOU!

Sending you and your family warm thoughts...

I have removeed info that would id this person to keep them anoynomous. I am using this email because I have received countless numebers that call me the face of alhzeimers and the voice. I am neither. Just a person with this fricken disease who wants to share our side of the story with you.

I have asked all of you for pics and dates of you loved ones that passted from this disease, as all of us with it do. I received one. So I will be posting it. You see those before me are the face and voice of this disease and should be remmembered and I want this blog to pay tribute to their fight for life. I get tired of hearing about all the big people who have survived this and that, big fuckin deal. We all die period. I am tired of all the crap about cures and how to stop this disease, well prove it to me with a survivor of it. No matter the advancements the real cause and any real treatment exscapes the med prof., maybe someday, I wonder.

I hope Bill's daughter does not take offense at the pic that I have because hers did not come through so I took one from his site. To me it shows the real heart of the man and how he felt about this disease and inate love of life.

God Bless You & This Country of Ours!!!!!!!
Joe

PS: I received a very sad email of the passing of one in my World, but it is sad for the daughter, for mom she is free now. The whole left of years of caregiving will be difficult I believe at best to deal with. To you my love and prayers.

Friday, August 14, 2009

A Special Request.

I would like to add a slide show to the side of my blog. I want to make this a memorial to those who have passed from this disease. So I am asking you to email me a picture of a friend or loved one with their name and birth and deceased years so I can make the slide show. I would like to honor those that have gone before me and paid the final price of this disease. Maybe their faces will prompt those who visit this blog to take some type of action or get involved some way to get those needed to help out (government????). I hope this is not offensive to anyone, if it is well then.

Thank you in advance. jolynn1@cox.net is the email to send to.

God Bless You & This Country of Ours!
Joe