Welcome! This blog contains research & information on lifestyle, nutrition and health for those with MS, as well as continuing information on the understanding of CCSVI and cerebral hypoperfusion. This blog is informative only--all medical decisions should be discussed with your own physicians.The posts are searchable---simply type in your topic of interest in the search box at the top left.Almost all of MS research is initiated and funded by pharmaceutical companies. This maintains the EAE mouse model and the immune paradigm of MS, and continues the 20 billion dollar a year MS treatment industry. But as we learn more about slowed blood flow, gray matter atrophy, and environmental links to MS progression and disability--all things the current drugs do not address--we're discovering more about how to help those with MS.To learn how this journey began, read my first post from August, 2009. Be well! Joan
Tuesday, May 15, 2012
Just keep swimming
May 15, 2012 at 9:51am
In Finding Nemo, Dory the fish has a little song she sings, to keep Nemo from becoming too despondent...
When life gets you down, you know what you gotta do?
Just keep swimming, just keep swimming.
I had an interesting conversation with Dr. John Cooke at the Hubbard Foundation conference. It was good to catch up with him. We hadn't seen him in two years, since Jeff was up to Stanford for his one year testing. He asked how Jeff was doing, and to what did I credit his health after venoplasty. I told him that Jeff was much more fit now, then he was at his MS diagnosis. He was down 15 pounds, and his aerobic capabilities were great. He out paces me up the hills when we hike and bike, and is much more active in his daily life.
"That's great!" said Dr. Cooke. "He's keeping the blood flowing."
Later that day, in his presentation, Dr. Cooke discussed how the endothelium likes fast blood flow. Shear stress, or the stress caused by fast moving blood through our body, is good for our blood vessels. It keeps them open, and flowing.
You see, the body and brain respond to aerobic exercise in many ways that are being studied in the MS population. I know I don't have to tell you this---the terrible tragedy in MS is that as the disease progresses, your ability to move is shut down. It becomes a vicious cycle. Your disabilities increase, your ability to move decreases, your blood flow slows down, your pain and fatigue increase, your MS progresses.
I want to encourage you, like Dory, to find ways to just keep swimming. Find ways to move, everyday. It may not be pretty, but your heart and circulatory system need this. When Jeff was first diagnosed with MS, he had trouble walking. He started with an elliptical machine. He couldn't do very much, and his legs hurt...but he did it, as best he could. After venoplasty, he was able to get back on his bike. He started slowly, with street rides, and then progressed to mountain biking, as his balance and endurance increased. Every single day, he gets his heart pumping. And his veins are staying open, and his gray matter looks normal on MRI.
Here's some research to encourage you: