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JOAN’S WEEKEND BLOG – August 2/3, 2008 - UPDATE ON INFORMATION FOR THE NEWLY DIAGNOSED AND THOSE NEW TO THIS SITE There have been so many new members to our Alzheimer Spouse family in just the past two months, that I thought I would take this opportunity to update the Blog I wrote last February on the resources available to help you through this AD journey. Below is the February Blog with better organized reading material, and more informative resources. To those of you who have written on the Message Boards and filled my E-mail Inbox with cries of despair upon recently receiving the diagnosis – Alzheimer’s Disease – please take some deep breaths to calm yourself, and know that with knowledge, medications, and support, it can get better for you for an indeterminate amount of time. If you are not new to the disease, but are new to this website, you can also benefit from this information. Oh, yes, I and all of our readers and writers here understand the shock, fear, and panic upon first hearing those stunning words – Alzheimer’s Disease. I was overcome with shock – “No, it can’t be. It can’t. The other neurologist said it wasn’t; the other neuropsychologist said it wasn’t. Never mind they had no idea what it was. They SAID IT WASN’T ALZHEIMER’S DISEASE.” But it was. The diagnosis was as definitive as it could get, after ruling out everything else. 1. Call the Alzheimer’s Association (1-800-272-3900) and ask for a support group in your area. Our support group friends have literally saved our lives. Ask to meet with a social worker – explain ALL of your concerns to her/him, and take whatever advice is offered. If needed, ask for a social worker to come to your house as often as needed to guide you through the first tough months. 2. Read and learn about the disease, its stages, what to expect, and the best ways to handle what comes along. CLICK ON EACH BOOK’S NAME FOR MORE INFORMATION: When The Doctor Says "Alzheimer's": Your Caregiver's Guide to Alzheimer's & Dementia (Paperback) A Caregiver's Guide and Sourcebook - Howard Gruetzner Alzheimer's Disease - 300 Tips by Callone, Kudlacek, Vasiloff, Manternach, and Brumback The 36-Hour Day by Nancy L. Mace,M.A. and Peter V. Rabins, M.D., M.P.H The Alzheimer’s Action Plan By P. Murali Doraiswamy, Lisa P. Gwyther, Tina Adler Alzheimer's Early Stages: First Steps for Family, Friends, and Caregivers – Daniel Kuhn A Dignified Life: The Best Friend's Approach to Alzheimer's Care by Virginia Bell and David Troxel When Someone You Love Has Alzheimer's-by Marilynn Larkin Learning to Speak Alzheimer’s by Joanne Koenig Coste
5.. Seek out and accept emotional support from support group friends and Message Board friends. 6.. If you need more emotional help, ask your spouse’s neurologist to recommend a therapist who specializes in helping caregivers cope with the stresses of Alzheimer’s Disease. 7. Seek treatment from the best Alzheimer’s Disease Research Center or Memory Disorders Clinic in your area. Our Message Board writer and author, Betty, sent us this link for a guide to AD Research Centers. In Florida, in the Palm Beach County area, contact Premiere Research Institute at Palm Beach Neurology 561-845-0500. 8. Click this link to find out about research trials in your area. 9.. Finances – CLICK HERE for information on taking care of those legal matters. 10.. Click this link to listen to my radio interview on Jacqueline Marcel’s “Coping With Caregiving” show. 11. Click this link to listen to my CBS radio interview with Tracey Morgan on Pittsburgh Stations, WBSW/WDSY/WZPT. This is a long journey. You will not learn all about Alzheimer’s Disease in a day; you will not get all of the support you need in a day; your spouse will not get all of the correct medications in a day. It is a process. Every day you will learn something new about the disease and how to handle it; you will meet new counselors, social workers, support group friends – in person and here on the Message Boards; you will accept the advice and medications from your spouse’s doctor. You will have some smooth sailings; you will hit many storms; you will stumble and fall, but there will always be someone there to pick you up and help you along. There is no denying that this journey stinks (that’s the more polite word for the one I really wanted to use), and you surely did not volunteer for it. But you’re stuck with it, and the only way to get through it is to remember that you CANNOT DO IT ALONE. LEARN all you can, and ACCEPT HELP. POST COMMENTS UNDER MESSAGE BOARD TOPIC: JOAN'S WEEKEND BLOG - INFORMATION FOR NEWLY DIAGNOSED AND NEW MEMBERS
The material included on this website contains general information intended as information only. This site is not intended to provide personal, professional, medical, or psychological advice, and should not be relied upon to govern behavior in any certain or particular circumstances. The opinions in the blogs are solely those of the owner of the website. The opinions on the message boards are not necessarily endorsed by the owner of this website, and are the opinions of those persons writing the messages. All material on this web site is for demonstration and informational purposes only.
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