Sunday, September 4, 2011
My Achilles Tendons have "yelled" at me all day. What those who do not have Fibromyalgia don't understand, is that because of Fibromyalgia, my pain is magnified. My abundance of Substance P seems to be working overtime. My next appointment with the Physical Therapist is Tuesday afternoon.
Dr. Emily put me on Tramodol 3x a day. I have not noticed a difference. I may need a higher dose.
We have had a quiet Sunday. I have done laundry, dishes and cooked meals. I did a lot of reorganization yesterday and cleaning. I feel good about what I accomplished.
We have nearly 160 sites in the park to clean tomorrow. Needless to say, not much will be accomplished at home. Dwain cooked a beef roast Saturday in the dutch oven. We have enough left over for hot beef sandwiches for dinner tomorrow.
You can .... smile in the face of pain.
You can .... forgive those who cannot understand Chronic Illness.
For we understand it is unseen.
Saturday, September 3, 2011
It's hard to believe we are in the month of September. There is approximately 3 months and a couple of weeks until Christmas!!!
Our schedule in the park has changed. We will be cleaning sites, five days a week through September 15. Our next destination is Wallowa for a week before heading to Fort Vancouver National Park.
I've had pain and a throbbing sensation with both of my Achilles Tendons for a couple of months. I spoke to my medical doctor and she arranged for me to receive Physical Therapy. I had my first appointment last week. He worked on relaxing my tendons and muscles. The Physical Therapist thinks my A. Tendons are painful because of a fall when I was 9 years old. A little hard to grasp the possibility. Here's a thought...could that fall from a barn hay loft, triggered my Fibromyalgia? I have another appointment on Tuesday.
I have good news from the medical doctor. My blood pressure was the best it has been in years and I had a clear pap. I need to call and schedule my Mammogram. Also an appointment for a test at OHSU. I have been having trouble with my hearing. This test will let us know if it is hearing or cognitive problem. I will have the test done while we are in Vancouver this fall.
I very much appreciate my readers taking the time to leave a comment about my post. However, if you are unable to empathize or leave a positive comment, please do not leave a post. I recently read a comment that was negative. Negativity is not what this blog is about. This blog is to help me and others converse about living with Fibromyalgia and other chronic diseases.
You can .... be positive when you don't feel positive.
You can .... make time to be with family and good friends.
You can .... share your day, warts and all, with those who have open ears.
Saturday, August 13, 2011
I have enjoyed my Saturday. Dwain and I are staying home this weekend. We are both in need of "down time."
Dwain played his Dulcimer almost all day. I did a couple loads of laundry, gave Lucy a haircut, around her face and washed the dishes. Boy do I miss my dishwasher! :-D
By 11:00 I was ready to lay down. I reclined in my chair and checked email and Facebook. By 1:00 I was in bed. I took an hour nap. Lucy woke me because she heard a dog barking outside. I laid back down and slept for another hour. We had a good fish dinner with a salad of carrots, apples and raisins. Also fresh peaches! I read after dinner. "You're Late Again Lord" by Karon Phillips Goodman is an interesting read about how we ask God for things then become impatient while we wait. We forget that we are on God's journey and how to use the waiting time. God always answers us, but it may not be as we anticipate. We must listen when God speaks to us.
Preseason Football has started. We have enjoyed a couple games today.
I didn't sleep well last night. Other than hard cramping in my legs this morning, my Fibromyalgia has enjoyed the slower pace of my day.
I will wait for a more productive day .... on God's timing.
You can ... use your time wisely while you wait for your prayers to be answered.
You can ... give yourself permission to enjoy a relaxful day.
You can ... be patient.
Sunday, July 31, 2011
When I over exert my body, multiple things happen....I sweat excessively, my Irritable Bowel Syndrome (IBS) kicks into full gear, my stomach gets sick, muscles cramp; become weak and my headache worsens. I suppose that is enough to list for now! To help ease symptoms, I must be in a reclined position, either in a recliner chair or bed. I take one-half of a Dramamine. Dramamine is an OTC medication for motion sickness and helps my upset tummy and Vertigo. If I take a whole tablet, I go to sleep. Sleep helps, but I can sleep without the additional medication.
I had a week off from my State Park duties. I played with my Granddaughter, Lyla, who is 2 1/2 years old. I spent Monday with Heather, traveling to Vancouver, Washington. It was a nice "Mommy and Me" day. We stayed with Adam, Carrie and Lyla for a couple of nights before picking Patrick up at the airport upon his return from visiting his Uncles, Seth and Steve in Chicago for two weeks. One more night all together, then we kidnapped Lyla for four days. While Lyla busied us all, we celebrated Grandson Josh's 13th birthday. By the time these activities were complete, I was a goner or maybe a groaner!! I've always said that it would be all worth the pain if I am able to participate. After this weekend, I may change my mind! For now, it's one hour at a time.
YOU CAN .... have humor when your body is betraying you.
YOU CAN .... accomplish a chore on the way to the bathroom.
Friday, June 24, 2011
We worked in the park this morning, gathered our things and headed for Josh's house. We hooked up to the little RV and headed for Pendleton. I'm pooped but excited to watch the ball games. The kids have worked hard for this honor. The coaches select a team from the top ball players in their area. The weather is supposed to be mid-70's with a breeze Saturday and Sunday. Monday it will be in the 80's. We have a canopy to have over our heads. I soooo thankful. Will let you know how I survive being outside all afternoon. No time to write further tonight.
Wednesday, June 22, 2011
"10 THINGS "NOT" TO SAY TO SOMEONE WHO HAS FIBROMYALGIA...
by Pam Scott-Ryan on Wednesday, June 22, 2011
10. We all get more aches and pains as we get older.
The pain of fibromyalgia is much more severe than the normal aches and pains associated with aging. Little things that shouldn't hurt at all can be excruciatingly painful. Plus, most people develop FM long before they should be experiencing age-related aches and pains.
9. I think I have that, too – I'm always tired.
This statement shows a basic misunderstanding of the severity of the fatigue associated with FM. The fatigue of fibromyalgia is so much more than just being tired. It is an all-encompassing exhaustion. You are like someone pulled your plug, cutting of your source of power. It's kind of like taking the batteries out of the Energizer bunny.
8. My friend has fibromyalgia and still manages to work. Maybe you just need a job (hobby, etc.) to take your mind off the pain.
Translation – you must be lazy. The fact is, the severity of FM symptoms varies. Some people have fairly mild symptoms and are able to continue working. Some continue working longer than they probably should because they have no other choice, but they suffer tremendously. Others are so disabled they are confined to a wheelchair much of the time. While getting involved in a project can help to distract your mind from the pain for short periods of time, if you have a more severe case, it doesn't work well enough to allow you to consistently work a 40-hour week. And it doesn't help dispel the extreme fatigue that usually accompanies FM.
7. My doctor says fibromyalgia isn't a real disease; it's just a wastebasket diagnosis.
First of all, this doctor obviously hasn't kept up with the latest research, which clearly demonstrates that FM is a very real, physical disease. Also, to date the FDA has approved three medications to treat fibromyalgia and they generally don't approve medications for imaginary illnesses. There are a few doctors who will tell patients they have fibromyalgia if they can't figure out what is causing their symptoms and just want to get the patients off their back, but I have to question the ethics of a doctor who would do that.
6. If you got more sleep, you'd feel better.
Well, duh! One of the major problems with fibromyalgia is that something prevents the body from going into the deepest stage of sleep, when the body naturally restores and replenishes itself. Even if you manage to stay asleep for several hours, you're most likely not going to awaken feeling refreshed. And most sleep medications do little to help you achieve that deep sleep. They may help you get more hours of sleep, but probably will still not give you the deep sleep you need.
5. I read about this new product that cures fibromyalgia.
This can be one of the toughest comments to deal with because it is usually said by well-meaning friends or relatives who genuinely want you to feel better. The products are frequently some kind of “natural” supplement being sold through a multi-level marketing plan and are very expensive. If those making the suggestions are casual acquaintances, I generally just tell them I appreciate their concern and will look into the product. However, if it's someone closer to me who is likely to keep asking if I've tried the product, I go on to explain that there are dozens of products out there claiming to cure or at least improve FM and I just can't afford to try them all. Read Let the Buyer Beware for tips on how to evaluate product claims.
4. At least it's not fatal.
My first thought in response to this comment is always, “Yeah, but sometimes I wish it was. At least then I'd know there was an end to the pain.” I rarely say that, though. Of course I'm glad it's not fatal. But that doesn't help reduce the level of my pain or the depth of my fatigue. Nor does it help to raise research funding or bring attention to the needs of FM patients. Understandably, people tend to be more interested in preventing death than in improving the quality of life. Maybe I should start actually saying what I'm thinking when someone makes this comment. At least it might get their attention.
3. You just need to exercise more.
Often this is another way of insinuating that you're lazy. This comment in particular has always bugged me. Perhaps it's because I used to be a dancer and aerobics instructor. If more exercise were the answer, I'd be all over it. Yes, exercise is an important component of any fibromyalgia treatment plan, but it's only one part and it has to be approached slowly and carefully to avoid triggering a flare. Read Fibromyalgia and Exercise for more information on how to incorporate exercise into your FM treatment plan.
2. But you don't look sick.
This comment puts the FM patient between the proverbial rock and hard place. If we let ourselves go and show how we actually feel, people are uncomfortable and don't want to be around us. On the other hand, if we manage to fix ourselves up and put on a brave face, no one realizes we're sick. If you think about it, most chronic illnesses are invisible. My dad had heart disease but looked great until the moment he died from a massive heart attack. My mom had pancreatic cancer but looked fine. She didn't even know anything was wrong until it was too far gone to treat. She didn't “look sick” until the last couple of weeks of her life when she was confined to bed. Just because someone doesn't have visible sores or a crippling deformity doesn't mean there's not a serious illness just under the surface.
Ta Daaa...... Here it is - the number one thing you should NOT say to a fibromyalgia patient:
1. It's all in your head.
This is the all-time worst and most insulting thing you can say to someone with fibromyalgia. I used to launch into an explanation of how FM is a very real physical illness, complete with symptoms, etc. Now I simply say, “You're right, it is in my head. Researchers have found that there is a problem with how my brain processes pain signals.” Enough said."
I hope this article allows you to think before you comment. Fibromyalgia and Chronic Fatigue Syndrome are real diseases. Although the person looks like there is nothing wrong, if you watch, you will notice how they gingerly stand from a sitting position or lower themselves into a chair. You will notice periodically that they substitute a word for another. Their cognitive process works as if the electricity can't get through the line without interruption. Their balance is not as good as it once was. They have trouble lifting a ten pound bag of potatoes. They are always physically and mentally tired. Be observant of your friends with Chronic Diseases, including Fibromyalgia and Chronic Fatigue Syndrome. Your friendship with be better for it.
You can .... be of help to those with Chronic Diseases, ask how
You can .... explain your Chronic symptoms to your friends. If you are like me, you will cry while explaining.
You can .... take a nap today .... do it!
Tuesday, June 21, 2011
Our grandson Josh spent two days with us. Josh and Dwain cooked a yummy meal with dutch ovens. We had pork roast and potatoes with peach cobbler for dessert. I'm sure his favorite activity was fishing! He caught several trout. The coming weekend will find us in Pendleton, Oregon at Josh's All Star Baseball games. Can't wait!!!
Before beginning my post today, I read comments left on my Fibromyalgia Blog. I am disappointed that individuals choose to post advertisement on my blog for prescription medication without permission. I am asking those individuals to cease their advertisement.
You can .... see the best in everyone
You can .... take time to enjoy the sunshine
You can .... sweeten your ice tea, if you must
Sunday, June 12, 2011
Saturday afternoon a high school classmate came by for a visit. While he was here, my Aunt stopped by. Both were good visits.
Today, was an easy-going day. Dwain fixed a yummy pot roast in the dutch oven for dinner. As I write, we are sitting next to a nice campfire. Dwain is off to get a hot dog! Myself, I'm waiting for the wood to burn down to fix a smore!!!
You can .... take time to visit with your spouse.
You can .... stretch your muscles multiple times a day.
You can .... smile often, it's better than frowning.
Wednesday, June 8, 2011
My combination washer and dryer quit a couple of days ago. Dwain thought it was the heating element and we ordered one. Come to find out, it was a wiring problem. I have been using the machine since it was fixed!
Our Lucy is in training not to bark when someone knocks on our door. She is showing improvement. She has an appointment with the Vet next week to update her shots...rabies, etc
You Can .... allow yourself to rest when your body needs the rest.
You Can .... remember to prepare part of your dinner meal in the morning.
You Can .... help one in need.
Tuesday, May 31, 2011
We find things that people leave behind, besides dirty campsites. Today I found a blow gun dart. I found out that there are blow guns that shoot small animals. I can't think of any small animal that should to be shot with a sharp dart. :-(
We were busy over the weekend visiting with friends from out of town. I did not catch up my home chores. Now it is all staring at me. I'm hoping tomorrow I can accomplishing something in my house. :-D
My pain level increased this week. I know I've overworked my body. I regret it because of the increased pain. I've tried so hard to have the park be perfect when campers come in and I have not accomplished my goal. Therefore, I find myself working more than my required four hours a day. In a way, I feel I've failed at this volunteer job and I've also failed keeping my house tidy. I'm afraid my Type A personality is to blame for this failure.
Tomorrow, Dwain will take Josh to his ball game. I'm going with Heather to an academic dinner and program. Patrick will receive an academic award, but we don't know for what class. Their Dad will miss both as his job will take him out of town. I hate missing Josh's game, but sometimes I must chose.
Wednesday, May 25, 2011
Heard of Fibromyalgia and Chronic Fatigue Syndrome?
Had to ask a loved one not to hug you?
Slept an hour and a half, then awake the rest of the night?
Had to get out of bed because you were so stiff and sore?
Been so physically exhausted that you couldn't be on your feet long enough to shower?
Had your head throbbing and aching all day long?
Had excessive migraines headaches?
Felt like your neck was in pain could no longer hold up your head?
Had your arms and legs tingle and loose feeling?
Had your body ache continuously?
Felt like you had a sunburn on your skin .... but you don't?
Had shooting pains??
Experienced Irritable Bowel Syndrome or constipation as an ongoing issue?
Had an Irritable Bladder?
Stumbled or fell because you couldn't pick your leg up from total exhaustion?
Fallen upon rising from a sitting position or passed out?
Experienced Restless Leg Syndrome?
Felt like you had bugs crawling on you ... commonly called "The Creepy Crawlies?"
Had such a dry mouth that you couldn't get your tongue off the roof of your mouth to form your words?
Had such dry lips that they hurt?
Tried to swallow food and have it stick in your throat?
Had muscles that feel like ropes in your body?
Had excess mucus in your throat?
Been out of control with your cognitive function?
Had depression or an anxiety attack?
I hope not!
Saturday, May 21, 2011
A second day in a row I have woke to sunshine. I believe it is SPRING! It sure raises my spirit to have the sun shinning on my world. When the summer weather is hot, I feel worse. I move slower and think at a slower pace. Most with Fibromyalgia have less pain and fatigue during the warmer season. I feel best between 65 and 72. Dwain said if he could put me in a weather controlled living space, the temp would be 70. :-D
I hope everyone has a nice weekend. We are off to Josh's double-header baseball games. An fun time. :-D
Sunday, May 15, 2011
We got our call to move up to Wallowa Lake State Park to begin our park hosting duties. We enjoy being in this park. It is beautiful. By coming the month of May, the park is coming out from under the snow. We spend our work days raking sites and picking up blown down tree limbs. Combine the physical work and the stress of Dwain and I not communicating well during the week, equals a Fibromyalgia High Alert!!! Oh and grandson Josh's 2 to 3 baseball games a week! Needless to say my favorite part of last week were Josh's ball games.
Gave Lucy a haircut yesterday and a bath this morning. She is a fun little dog and I'm so glad we have her. I found her a sweatshirt and coat last week at a local farm store. They were on sale, which made me happy. Now she doesn't look like she had outgrown her clothes (which she had).
One other thing I enjoy is blogging and keeping up with Fibromyalgia Friends on Facebook. The comments I receive from both are encouraging and helpful. We are a community of friends brought together as a family and we all truly understand what the other is describing.
My newest symptom are my Achilles Tendons on both feet. It has bothered me for about three months. I've tried exercises and that is not relieving the soreness. Although, the more I'm on my feet the less it hurts. However, when I do sit to rest my body then get up....it is much worse. Can't win!!!
I wish you all a wonderful Sunday. Spring is showing up at Wallowa Lake. The fishing boats can now be on the Lake, little flowers are carpeting the landscape. Children are playing in the park, but probably the biggest sign of spring is that we have a bear in camp. He tends to come into camp at night and tries to raid the dumpsters. I hope the sun is shining where you live. Being springtime, it rains one day and sunshines the next in NE Oregon. Today it has been raining. At least it is not snowing like on Mother's Day!
Friday, April 29, 2011
I lost my Godmother recently. She was also my Aunt. I was given the schedule for her multiple services. Dwain and I worked out how we could attend. This was a feat as our oldest Grandson's 15th birthday and our youngest Grandson's baseball tournament both fell on either side of her service. It would be a mega-full schedule, but could be done. By chance my brother called to see if I had received the service schedule. I told him I had and that we were leaving about 8 pm, after having Patrick's birthday dinner and cake with him. We would drive for several hours, stop for the night, then drive the rest of the way Friday morning, arriving in time for her graveside service. I had even made arrangements to pick our Granddaughter up on our way through Portland, keep her over night and return her on our way through Portland the next day. My brother was surprised we were leaving so early. This was a red flag and I questioned his comment. One of my cousins gave me the wrong schedule. The graveside service would not be until Sunday. Anxiety took over my being. I couldn't think. Emotion welled up and I couldn't figure out how to handle it. It was the most out of control feeling. It lasted for quite awhile. It slowed down when I made the decision not to attend the funeral. I was on the verge of tears all day. Sometimes they flowed. But there was always more. Today while I was reliving this situation, I had the realization that Fibro won. Ever feel the mixture of anger and sadness? What an over-whelming combination. My cognitive behavior has been worse, I'm very tired. I'm battling to keep depression at bay. I wish I could have over-powered my emotions and sat on them. I have had these emotions before, but this, by far, has been the worst. I've been able to handle them before. Not this time.
Yesterday, Fibro won.
Friday, April 22, 2011
I'm glad Easter weekend has arrived. I understand we are to have a nice weather. My Patrick and Joshua informed their Mom that they didn't want to have an egg hunt this Easter. Guess they have grown up. Dwain's Dad and his wife, Lenora are driving across the state on Saturday to spend Easter with us.
Heather shared information with me today that has drained my strength. Anyone with Fibromyalgia knows that emotional stress increases your pain. I hope that a good night sleep will help. I ask those that read my blog to say a prayer of strength for me.
Looking forward to Josh's opening day of baseball tomorrow. He has one game. I love watching his team play. They are learning and growing as players right before your eyes. I'm a proud Grandma!
Dwain, Lucy and I took a walk after dinner. It was nice to be outside although the sun was going down so the cool of the evening chilled us. I would prefer to take a daily walk earlier in the day, like late morning. By afternoon, my energy level is less. But I did it. :D
Thursday, April 21, 2011
It snowed most of the day. Didn't stick until this evening. Will be interesting to see what happens overnight. Grocery shopping with Heather tomorrow. Will enjoy her company. Also, will be nice to be out.
My Fibro has stayed in check today. Just a slight headache. Had an hour nap this afternoon.
Received a phone call from Seth this evening. It's been too long since we have talked. I miss him. I wish we lived closer. He is settled in his new home. Excited for him to have his first home.
Lucy will have a bath tomorrow. She is starting to smell like a dog!!
Wednesday, April 20, 2011
My Fibromyalgia did fine as long as I was able to stretch and walk every four hours. We had one day going to Rapid City and two days heading to NW Montana that we didn't stop as often. Boy did my body feel it and I felt my body! Only once took a pain medication. Otherwise I shifted alot. :D
We arrived in Wallowa, Oregon at 9:30 pm this Monday. It was a long drive from NW Montana. It feels good to be here. It's like returning home. We have spent many summers in this little NE corner of Oregon. We have almost two weeks until we return to Wallowa Lake State Park. We will be spending the summer at the Lake, park hosting.
My Chronic Fatigue continues to play havoc. I sat down about 11 am. I'd been on my feet for several hours and my body needed a rest. It wasn't two minutes and my eye lids were closing. I was able to battle the fatigue until 1:00. I then took a two hour nap. Exhaustion is not fun. You move in what feels like slow motion and you can't think straight.
Time to get to bed for the night. Hope you all have a good night sleep. Hugs
Sunday, April 3, 2011
Yep, I have hitch itch. It does not cause a rash, upset tummy, diarrhea or hunger. Hitch itch is a term my husband Dwain and I use when we are ready to hit the road. In case you don't remember or you are a new reader, Dwain and I are full-time RVers. We have a 37' Fifth Wheel Montana. After being in an area for awhile, we get hitch itch to get out of Dodge. Well, we are itchin'! We are waiting for our mail to arrive from eastern Oregon then we will hitch up the RV and go! While traveling, we stop every two hours to stretch. We keep snacks and plenty of water in the truck.
I enjoy traveling, seeing new places. It also provides me with time to read or knit. We rarely eat out. The RV is our home so the fridge/freezer is full. Although I don't cook a large meal as we are never as hungry after sitting all day. Also my Fibromyalgia is height on. My butt gets tired and my pain increases. I'm thankful that the drive is not a long day. The drive is always interesting. Not only new scenery, but we always see wildlife...deer, elk, mountain goats ad lots of birds, to name a few.
I'm a lucky girl to be living as I like. It is easier on my body and for that, I am thankful.
Monday, March 28, 2011
Saturday, March 5, 2011
Then one day we wake up and can't finish our shower because of the fatigue. Maybe the sensation of the water hitting our bodies feels like a million needles stabbing into our skin. Climbing upstairs is difficult to accomplish. We must climb half way, rest, then continue on. For some, different foods cause our pain to increase. We are unable to be on our feet long enough to make our kids' school lunches let alone make their breakfast. The dirty clothes are piling up. You rise from your chair and fall to the floor because of muscle weakness. You are afraid to drive for multiple reasons...you can't remember how to get to a location that you have driven to many, many times before. You are worried that your body will betray you before you can deliver your child to their football or play practice. Holidays are extremely difficult. It takes longer to accomplish tasks. Anxiety kicks in and confusion becomes evident. Cognitive issues are apparent to not only you, but to everyone you are in contact. You always remembered to acknowledge the birthday of others. It's on your calendar but you don't notice it until the day of, leaving your cards to be received late. You can't walk as far as you once did, leaving hikes with your family out of the question or a fun day of shopping. Volleyball games are to physical. To have a friend visit over a cup of tea is strenuous. Writing cripples your hand.
We must "always get back up on the horse" and put our best efforts forward. If we sit in pity, we can't ride.
Sunday, February 27, 2011
My Chronic Fatigue (CF) has been more active than usual. Falling asleep before 11 am is not how life should be. My night sleep has been great so not trying to catch up on my sleep.
I am having trouble with remembering situations of family and friends. I've always kept up with their birthdays, anniversaries, family situations and their health. I haven't been remembering anything. I'm not sure if that is connected with the CF flaring and my cognitive issues. It is common for Fibromyalgia and Chronic Fatigue sufferers to have problems with names and dates. I've had a few problems in that area, but this has gotten worse. I read an article that said that dealing with our pain is all we can do. Therefore, we place everything on the back burner that happens in our day or to our body, except trying to control our pain. Where once we were multitaskers, now we must deal with the pain being racked through our body.
I leave you with this thought:
Friday, February 11, 2011
I enjoy these little men more than I can express. Patrick is 14, will be 15 in April. Josh is 12, his birthday is in July. They have been raised well. I know their parents are challenged by them at times, as it should be, but we are bless grandparents. We spent several hours on the beach yesterday. It was a beautiful day on the Oregon coast. Today we will attend a music night where many musicians gather for the love of music (Heather P you would enjoy Friday night music) and they play for two hours. Both boys are very musical. Patrick wants to play with them and he brought his guitar. Josh doesn't like to be looked at yet, so he will sit with me. They will see their great grandparents there and their great Aunt and Uncle. I'm excited to share them. :D
Saturday we will leave early and drive to Woodland, Washington. We will help move our youngest son and his family. They are moving to Vancouver, Washington. They have our 2 year old grandaughter, Lyla. So they will all have the day together. The boys live 8 hours across the state of Oregon from Adam and family so it's always a treat to get them together.
Will post photos when I get them transferred to my computer. I hope everyone has a good of day as I'm having. :-D I may not be worth a hoot on Monday, but that's ok!!!
Wednesday, February 9, 2011
Dwain's Dad has a dominating personality. He has the need to constantly talk, all the while making no sense. He had some sourdough. I said I might make sourdough bread the next day. Well, I made sourdough biscuits the next day and they did not turn out. Now, it took an hour to prepare and cook the biscuits. After that I lost the desire for bread. My friend Marie came for an unexpected visit, so would not have had the time for bread preparation in time for dinner. The next day, while Dwain was talking to his Dad, he asked how the bread turned out. When Dwain told him that I did not make bread, he exploded and was angry. It upset Dwain. Because I have also experienced Dad's rath in the past, it upset me too. He cares about himself and does not consider others have opinions.
Our son-in-law, Matt's Mom is on life support. Matt and family will leave early Thursday morning to drive the eight hour trip to his parents. When they have said their goodbyes, she will be taken off life support. We will meet them and our grandsons will come home with us through the weekend. I feel guilty that I'm excited to see the boys when their Dad is loosing his Mom.
I know there are many more problems in the world, but right now these personal issues are increasing my stress level and in return my Fibro pain has increased. I'm hoping for a good night sleep. I haven't had problems sleeping since I've been on Trazodone to help me sleep....so thankful.
I have accomplished several projects in our home. Feels good to accomplish something. :-D
Saturday, February 5, 2011
Monday, January 31, 2011
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?
Friday, January 28, 2011
Monday, January 24, 2011
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
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
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 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. :-)