Gratitude: Perfect, Peaceful Surroundings
As I re-read my last entry I realized that some of you may be picturing me in one of those giant, 40 ft long monster RVs with all modern conveniences.
No. My RV is a 1991, 25 ft long (and I would like to go smaller still). I spend most of my time outside, sitting under an awning over a concrete patio beside the RV or taking walks on the beach or finding the perfect palm tree to sit beneath. Sometimes I even sleep outside on the patio (it's where I'm sitting to write this!).
There are virtually no flying insects here, which is part of what makes sleeping outside possible. So that's another thing to appreciate. There is something sort of delicious about being outside when everyone else has gone inside and closed their doors. I'm only about 50 yards from the ocean and sometimes (if the moonlight is just right), I walk down to the beach late at night to watch the phosphoresence of the waves. They really do glow and sparkle in the night. Not always, though, which makes it a special treat to see.
I am also thankful for my dog. He is my traveling companion, my confidant, my guard (he's trained to get help if I fall). Cody (well, actually Kody, I guess -- he got the name because everyone thought he looked like a tiny
Kodiac bear as a puppy) is a 15 year old herding dog mix. Heavy on the border collie, lighter on the blue heeler and kelpie.
I didn't want a dog. But somehow, I let myself be talked into it. I had only had MS for a couple of years, was still in the phase of expecting major disability at any moment. Everyone thought I needed a dog; I'm not quite
sure why. But they were right and so I have something else to be grateful for.
Related Topics: Success Over Stress (Video), Work and Multiple Sclerosis
Technorati Tags: MS, pets, gratitude
No. My RV is a 1991, 25 ft long (and I would like to go smaller still). I spend most of my time outside, sitting under an awning over a concrete patio beside the RV or taking walks on the beach or finding the perfect palm tree to sit beneath. Sometimes I even sleep outside on the patio (it's where I'm sitting to write this!).
There are virtually no flying insects here, which is part of what makes sleeping outside possible. So that's another thing to appreciate. There is something sort of delicious about being outside when everyone else has gone inside and closed their doors. I'm only about 50 yards from the ocean and sometimes (if the moonlight is just right), I walk down to the beach late at night to watch the phosphoresence of the waves. They really do glow and sparkle in the night. Not always, though, which makes it a special treat to see.
I am also thankful for my dog. He is my traveling companion, my confidant, my guard (he's trained to get help if I fall). Cody (well, actually Kody, I guess -- he got the name because everyone thought he looked like a tiny
Kodiac bear as a puppy) is a 15 year old herding dog mix. Heavy on the border collie, lighter on the blue heeler and kelpie.
I didn't want a dog. But somehow, I let myself be talked into it. I had only had MS for a couple of years, was still in the phase of expecting major disability at any moment. Everyone thought I needed a dog; I'm not quite
sure why. But they were right and so I have something else to be grateful for.
Related Topics: Success Over Stress (Video), Work and Multiple Sclerosis
Technorati Tags: MS, pets, gratitude



5 Comments:
Please can anyone tell me is there any yoga type of thing for MS. I just desperately want something that can help.I don't have this disease but when i heard that someone near to me had this disease, i couldn't bear that. It really hurt me when she told about the problem she was having presently. When i saw her kids i couldn't even sleep the whole night. So guys, please help me to get some effective way to get through this disease and live for some more year. Please, please.....
I have been dx'd w/ MS for the past 14 years or so and have suffered cognitive problems from the get go. I could not get 2+2 to equal 4. I started on Cylert (ADHD stimulant) that burned off the fog almost instantly. When Cylert was taken off the market 5 years ago, I shifted over to Ritalin. Same effect. I take 20 mg @ 6A, 1030A & 3P. It helps with my physical as well as cognitive fatigue that plagues so many of us.
Ben
HELLO ABOUT THE YOGA EXERCISE. I DO BODY RECALL 3 TIMES A WEEK. IT COST $40 FOR FOR 10 SESSIONS AND THERE IS BREAKS IN BETWEEN. IT IS YOGA AND STRECHING ON EACH AREA OF THE BODY. I ALSO DO PHYSICAL THERAPY TWICE A WEEK AND TRY TO WALK. I CAN NOT WALK VERY FAR AND IT IS GETTING SHORTER. I HAVE ALL OF THE SYPTOMS AND HAVE BEEN DIAGNOISED WITH MS. I AM GOING TO START ON COPAXONE IN APRIL. I AM GOING ON A CRUISE TO HAWAII FOR 16 DAYS. I SOCIALIZE EACH DAY EITHER WITH A GROUP OF PEAPLE FROM BODY RECALL OR A CHURCH GROUP. DO NOT GIVE UP GIVE IT YOUR ALL FOR AS LONG AS YOU CAN UNTIL YOU CAN NO LONGER WALK OR DO OTHER MOVEMENTS.
Hi I'm 29yrs old in aug.2007 my bladder stopped working and three months after that I was having problems walking some days I'm so bad I just can do it I know I have 4 disks out none of them are hitting my nerves. I get a pain in my left leg (thight)it stabs,burns.aches. I can't handle it but then there days where my leg is fine no pain.There are days I can't put any pressure on my left side my right let is going to take a vacation LOL most of the days my legs feel like their 9 millions pounds I'm working on losing some weight but I really can't walk or move on some days. so in about 1 month I'm getting a box put in my back to give that feeling to go to the bathroom. I just want to feel a little normal again!! my greatgrandmom had ms so thats what the dr's are looking at but 1dr doesn't think its that but how can the other two think it if anyone have any info you could give me I would love it. please email butterflygirl2179@verizon.net I need help!! thanks
I am currently going thru a MS diagnosis. I only have one lesion on my upper spine and my symptoms are fairly mild, only numbeness on one side of my torso and arm and it is getting better. I have had fatigue, bladder & bowel issues and dysphasia and the shocking feeling all through my torso for 4 months but my doctors jumped on this very quickly and for that I am thankful. It sounds like so many people start off really bad and dont seem to get the help they need or a quick diagnosis. i didnt think I would want to do any drug therapy as it all sounded too scary but after reading these blogs I have changed my mind and am trying to research them. I am so thankful I stumbled across this website and I will pray for everyone and do what I can to help fight this disease.
Debi
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