I have a problem with what my post looks like after I click on "Publish Post." The published post looks different visually than what I write. My last post is a good example...
I am a stickler for what I write to "look good." When I look at my published post, the spacing is irregular. Sometimes there is a space between what I wrote and sometimes there is not a space.
I need HELP...do I need to leave Blogspot or is there a magic button I haven't clicked?
Thanks!
I created this blog to record my experiences with Fibromyalgia. To share information with you and I hope you will share your experiences and information with me and other followers.
Monday, January 31, 2011
Friday, January 28, 2011
Grab Happiness
"Grab Happiness In The Passing Moments of Life"
Having a chronic illness or two, it is easy for depression to creep into our lives. We will have days that our self esteem is low. This is because we hurt, our balance is off, our eyes won't focus, etc. When you live with these symptoms, of which I only mentioned a few, you can become depressed. My suggestion is to "grab happiness in the passing moments" of your life. They may be short moments or something you can enjoy for longer periods of time. Here are some ideas:
Watch the sun rise or set
Listen to music you enjoy
Look at a flower. Have you ever looked closely at a Dandelion? It's a weed, but it's beautiful!
Take a walk
Look at a smile
Be aware of birds singing
Watch a small child learning to walk
Ice Cream?
Enjoy pet therapy
A good meal
Read a good book
Be aware and grab happiness where ever you can. You won't regret becoming aware of happy moments!
Monday, January 24, 2011
Need Extra Batteries???
I recently read, "Keep a stash of extra batteries." They were referring to keeping extra batteries in case of an emergency. I often think that "MY" batteries run down.
Fibromyalgia/Chronic Fatigue depleats your energy faster than you can blink. Well, maybe not that fast, but faster than most people could understand. Not only is your energy depleted, but because of a malfunction of the central nervous system, the pain is unbearable. You must learn what works for you to regain your strength and what takes the edge off your pain. For me, rest replenishes my physical and emotional strength. Prescription medication helps with my pain.
So...do you have an endless supply of batteries? When you are run down, exhausted, with no strength to continue, how do you replenish your energy?
Fibromyalgia/Chronic Fatigue depleats your energy faster than you can blink. Well, maybe not that fast, but faster than most people could understand. Not only is your energy depleted, but because of a malfunction of the central nervous system, the pain is unbearable. You must learn what works for you to regain your strength and what takes the edge off your pain. For me, rest replenishes my physical and emotional strength. Prescription medication helps with my pain.
So...do you have an endless supply of batteries? When you are run down, exhausted, with no strength to continue, how do you replenish your energy?
Sunday, January 16, 2011
We Are In The Same Boat
"We may live on separate shores, but in the end, we're all in the same boat"
Author Unknown
Isn't this the truth? I enjoy communicating on Facebook. I keep up with my friends and family. Part of my friends group, are those with chronic diseases like Fibromyalgia, Chronic Fatigue, Lupus, Lime Disease, Sjogrens and Rheumatoid Arthritis, just to name a few. These friends are scattered throughout the world! I talk with people from South Africa, England, Japan and all over the United States. We live on "separate shores" but we're all in the same boat." We share the unimaginable life of chronic pain. No one understands our pain and the obstacles we face daily as well as another. We become a family. I thank God every day for my computer and the ability to communicate with my brothers and sisters in the same boat.
Author Unknown
Isn't this the truth? I enjoy communicating on Facebook. I keep up with my friends and family. Part of my friends group, are those with chronic diseases like Fibromyalgia, Chronic Fatigue, Lupus, Lime Disease, Sjogrens and Rheumatoid Arthritis, just to name a few. These friends are scattered throughout the world! I talk with people from South Africa, England, Japan and all over the United States. We live on "separate shores" but we're all in the same boat." We share the unimaginable life of chronic pain. No one understands our pain and the obstacles we face daily as well as another. We become a family. I thank God every day for my computer and the ability to communicate with my brothers and sisters in the same boat.
Tuesday, January 4, 2011
Got My Venlafaxine! (Sort of)
I need to make a correction to my last blog post. I DON'T take 325 mg of Venlafaxine. I take 225 mg.
Went to the pharmacy yesterday. The doctor had ok'd my refill of Venlafaxine. However, the pharmacy didn't have enough to fill my prescription. They gave me ten tablets and said I can pick of the remainder in two days. That's ok with me.
I did notice the instructions on the prescription bottle states to take one tablet in the morning and two tablets in the evening. I looked at the just emptied bottle and it had the same direction. I have been taking this medication for nearly ten years and my doctor's verbal instructions were for one a day, taken in the morning. I have been taking this prescription bottle out of my medicine cabinet everyone morning for nearly a year and I did not notice the additional two at night. I must call my doctor for clarification. We are not in an area where our telephones work so will call tomorrow when we go to town.
Two questions arise for me. One, if I had seen and accepted the additional two pills a day and took them would I have had a reaction? The second question is if I had taken the two additional pills, could I have felt much better starting a year ago? Guess I will wait until Wednesday to find out and will only take my usual one tablet in the morning.
This will be a good lesson to ALWAYS read the directions on my prescriptions, even if I've been taking the medication for years.
We are due to warm up and rain tonight. Right now it is still freezing outside. the transition could be nasty.
Went to the pharmacy yesterday. The doctor had ok'd my refill of Venlafaxine. However, the pharmacy didn't have enough to fill my prescription. They gave me ten tablets and said I can pick of the remainder in two days. That's ok with me.
I did notice the instructions on the prescription bottle states to take one tablet in the morning and two tablets in the evening. I looked at the just emptied bottle and it had the same direction. I have been taking this medication for nearly ten years and my doctor's verbal instructions were for one a day, taken in the morning. I have been taking this prescription bottle out of my medicine cabinet everyone morning for nearly a year and I did not notice the additional two at night. I must call my doctor for clarification. We are not in an area where our telephones work so will call tomorrow when we go to town.
Two questions arise for me. One, if I had seen and accepted the additional two pills a day and took them would I have had a reaction? The second question is if I had taken the two additional pills, could I have felt much better starting a year ago? Guess I will wait until Wednesday to find out and will only take my usual one tablet in the morning.
This will be a good lesson to ALWAYS read the directions on my prescriptions, even if I've been taking the medication for years.
We are due to warm up and rain tonight. Right now it is still freezing outside. the transition could be nasty.
Sunday, January 2, 2011
Football and Fibromyalgia
I love watching football! I don't have a favorite team right now, but I enjoy if the guys are playing the top of their game. This time of year we are headed for playoff season, which starts next Sunday. They will eliminate teams down to the last two, who will play in the Superbowl.
Football is good for my Fibromyalgia. It holds me in my chair. My body relaxes and sometimes I sleep through a quarter. There are times that I get excited and my body tenses, my mouth starts blabbing, which causes my head to hurt, so I need to be careful.
This week I've spent a lot of time in my chair. I am out of my Venlaflaxine 75 mg. I take 325 mg total and am thankful it was not my 150 mg prescription. I didn't know my doctor's office was closing the week between Christmas and the new year. The pharmacy sent a request for a refill and it's sitting in the fax machine waiting for the office to open Monday morning. I've been out since Wednesday. I have tried to keep my activity at a low level, afraid I will flare. My busiest activity has been carrying items downstairs. I limit myself to three carries each day. Thankfully, I'm done with that activity. Tuesday, I will take down the Christmas tree and decorations. A trip to the pharmacy is at the top of my list on Monday. I must make priorities. If I go to the pharmacy and pick up a few groceries, that's the end of my day...back to my trusty chair. :-)
Football is good for my Fibromyalgia. It holds me in my chair. My body relaxes and sometimes I sleep through a quarter. There are times that I get excited and my body tenses, my mouth starts blabbing, which causes my head to hurt, so I need to be careful.
This week I've spent a lot of time in my chair. I am out of my Venlaflaxine 75 mg. I take 325 mg total and am thankful it was not my 150 mg prescription. I didn't know my doctor's office was closing the week between Christmas and the new year. The pharmacy sent a request for a refill and it's sitting in the fax machine waiting for the office to open Monday morning. I've been out since Wednesday. I have tried to keep my activity at a low level, afraid I will flare. My busiest activity has been carrying items downstairs. I limit myself to three carries each day. Thankfully, I'm done with that activity. Tuesday, I will take down the Christmas tree and decorations. A trip to the pharmacy is at the top of my list on Monday. I must make priorities. If I go to the pharmacy and pick up a few groceries, that's the end of my day...back to my trusty chair. :-)