My mother, Mary Lou Thompson, was diagnosed with Alzheimer’s disease two years ago at the age of 61. I had seen signs for at least four years prior to her diagnosis and at first my family dismissed my concerns and told me not to worry. After awhile my mother was also noticing these alarming symptoms and she became terrified by what they might mean. You never want to think of your own parents as being scared, but she was; it was a painful to see it.
Although there is currently no cure for Alzheimer’s, I knew that ignoring the problem would not make it go away and that if there were clinical trials available, then we had to get her involved with them as soon as possible. In 2007, we all went to the Memory Disorders Clinic at
It has been most painful to watch my mom’s personality change. My mom was a voracious reader, finishing several books a week alongside her daily newspaper dose. She loved to spend time talking about current events with her many friends. Today, she has trouble reading and conversing in a group setting. She is loosing touch with her friends because she is embarrassed by the diagnosis.
In the last two years, while her condition has continued to deteriorate, our ability to deal with Alzheimer’s as a family has greatly improved. One of the reasons for this is the New York City Chapter of the Alzheimer’s Association. My sister and I have attended the educational meetings and met with the social workers that specialize in helping early onset patients and their families. We learned strategies to cope with the changes while gaining a better understanding of what is physically happening to her brain. I also joined a wonderful support group for daughters of Alzheimer’s patients. It is nice to be able to meet and spend time with people who understand exactly what I am going through.
One of the many terrible things about Alzheimer’s is its impact on the caregiver. Watching my mom’s disease progress at such a young age has been hard on the entire family but seeing the impact on my dad’s life is especially challenging. My dad, a very healthy and active 62 year old, had recently retired in order for them to begin the exciting “Golden Years” that lay in front of them. Instead, he spends these times as the main caregiver, watching after various responsibilities for my mom. She needs help with many daily activities. I know that he would not have it any other way. I hope that when it comes time for me to take care of my husband in our golden years I can do as good of a job as my dad does for my mom. I am running in honor of both of them.
Running has helped me get through the last several years. I feel that the constant, rhythmic motion of my feet hitting the pavement helps to clear my mind, relieve my emotions, focus my thoughts and motivate me to continue being the most supportive and helpful daughter that I can be . I feel that caring for an Alzheimer’s patient is very similar to running a marathon in that it requires a deep level of commitment and discipline, it will be very painful at times and it is a long process that you plug away at both day in, and day out. I am honored to be running my first marathon in the city I love on behalf of my mom and dad and the millions of patients and caregivers who run their own Alzheimer’s
Rachel, I had a lump in my throat reading this article and also the e mail from your Dad which i got only today. I wish you had shared this earlier. Friends can only help. There's no need to keep it within the immediate family only.
ReplyDeleteI understand there is no known cure today however, I do know of a process in yoga that goes a long way in reducing stress and improve the healing process in our bodies.Its called "Yoga Nidra". Will send you a book and CD on the subject in a few days. I felt like jumping on a plane to come and meet Mary Lou but I definitely want to connect ASAP in HK or NY. Please, please keep us informed. Love, Suresh Rajpal
Val and I were devastated to read Doug's message today, but can not begin to know how it feels to have your Mom afflicted. Suresh said as we only wish we would have known earlier to provide any support we could. You can not fight these things with blindfolds, so we are here for you as a family for any support you need. We are thankful for your strength as a family, and Doug's loving care for Mary Lou. She is in the best hands! Love, Val and John
ReplyDeleteI'm so proud of you, Rach and wish you the best of luck in the Marathon and this journey with your Mom and your family. Love to you! -Autumn
ReplyDeleteAs a sign of gratitude for how my son was saved from Alpers' Disease , i decided to reach out to those still suffering from this.
ReplyDeleteMy son was diagnosed of Alpers' Disease in 2013 and it was really tough and heartbreaking for me because he was my all and the symptoms were terrible, he always have seizure , and he always complain of loss of cognitive ability . we tried various therapies prescribed by our neurologist but none could cure him. I searched for a cure and i saw a testimony by someone who was cured and so many other with similar body problem, and he left the contact of the doctor who had the cure to Alpers' Disease . I never imagined Alpers' Disease has a natural cure not until i contacted him and he assured me my son will be fine. I got the herbal medication he recommended and my son used it and in one months he was fully okay even up till this moment he is so full of life. Alpers' Disease has a cure and it is a herbal cure contact the doctor for more info on drwilliams098675@gmail.com on how to get the medication. Thanks admin for such an informative blog.