Fibromyalgia and your Heart

Living Daily with Fibromyalgia

Fibromyalgia sucks lolly-pops. (That is a much nicer way to say something crass.) And it really does! Like, really, really, really bad. When you are dealing with the pain that befalls you on any given day, it is overwhelming! The pain of Fibromyalgia is indescribable!

Here I sit after my second rest of the day. My morning began with the usual stiffness and sore, achey feeling. I moved around like my battery needed to be charged desperately! I felt very mechanical. But, for those who read and follow this blog, you know that this is nothing new! However, today is my son’s birthday. I wanted to make the day enjoyable for him and I set out to do just that!

We had a nice leisurely breakfast and a lovely lunch while playing board games-we just enjoyed the day! However, here I sit at 3:30 in the afternoon waiting for those pains to subside before I begin again.

The birthday boy has taken his siblings outside for a ping-pong tournament in the shed and so I decided to rest a bit.

What my son doesn’t realize as he lovingly tries to give me these opportunities to rest, is that my older daughter and I have been planning a surprise birthday party for him tomorrow evening. 23 young people will be hosted on our property in honor of his 17th. Because it is a surprise, preparations cannot be done out in the open! Therefore, things such as the baking of a cake, the gatherings for the bonfire, and the purchasing of the items for the hot dog roast must be done secretively. Many of this has been done gradually over the last few days and (hopefully) has gone unnoticed. I have been buzzing around for days overextending myself out of love!

~Sidebar~                                               The weather in the midwest is extremely bizarre this time of year. Less than 5 days ago the temperatures were in the upper 20s for the lows with highs in the 40s. Now, here I am with lows in the upper 60s and highs in the mid-70s today. A major thunderstorm is due tonight and 3 days from now the temps are supposed to drop yet again. The constant up and down and back and forth in the weather wreaks havoc on a Fibro body!                                           ~End of Sidebar~

Okay, so I have six out of ten children under the age of 22 still living at home. Some days it is very difficult to continue on doing as I have always done. I want each of them to have happy and pleasant memories of their childhood with an active mom; a mom who can be the mom like I used to be!

Sometimes, the reality of my present situation is something I do not wish to face.

Yesterday was a relatively decent day for me. 2 days ago, whatever I did must have caused my extreme issues today. It gets very tiring trying to remember what I did two days ago to cause me the pain and I’m in 2 days later. My brain does not allow me to remember a lot of the mundane, everyday things I do. Things like cleaning and moving this or that, vacuuming air vents, cleaning ceiling fans. All that hurts as I do it and hurts worse later.  But, hey, it needs to be done and I love to do those things! My body, however, does not.

I try to make a mental note saying I shouldn’t do this or that because it will cause me problems tomorrow or the next day. But my brain has let me down. I’ve tried to keep notes and write things in a journal. It does help, but that, too, is hard to remember to do.

Throw weather into the mix and you have the makings for some intense pain days!

Oh, I just want to be normal again!

To think and remember like I used to.

To be active and play like I used to.

To enjoy the little things like I used to.

But, alas, I must accept the new normal. There are days, weeks even, when I feel I have whole-heartedly accepted this.

And then….there are moments like this…

Why do I write this to you? To let you know that I am only human. I have real feelings, real concerns, real frustrations and real anxieties.

I also have a real faith, a real love for my family and a real love of life. Pain and all.

It’s just some days are more painful than others. Some days are harder than others to get through. But each day is a day that the Lord has given to us.

My pain is constant, but so is my faith in God.

Please know that I take Fibromyalgia seriously. I know what it has done to me, to my family and to my life.

Do you find that pacing helps? How do you handle the normal struggles in your  day? Do you suffer from the lack of support from loved ones?

Pray about these issues and lift them up to a heavenly God! He hears your cry!

My day is not yet over…and neither is my pain. The smiles on my kiddos faces is enough to see me through. I’ve been blessed with a great family and I do not take that lightly!

So, Happy birthday, son! I’d do it all again for you because I love you!

Blessings and gentle hugs!

The ~FibroMomofTen~

 

Fibromyalgia and your Heart, Living Daily with Chronic Invisible Illness

Heart Arrhythmia and Autoimmune Disorders

Heart Arrhythmia and Autoimmune Disorders-Do they go hand-in-hand?

For the past two weeks I have been resting after being admitted to the hospital for heart palpitations. Needless to say, it was a little bit scary to have your ticker out of joint. For me, it began at noon on a Wednesday and was still occurring at 6:00pm the same day when I decided I probably needed to have a doctor take a looksie.

After the ER doctor ran an EKG it was found that I had some irregularities on the test. My blood tests had come back as nothing life threatening or immediate, but the doctor felt I needed to be on a watch and therefore, I was transferred to a larger hospital and kept overnight.

The ER heart monitor was replaced with a hospital version of the same thing once I got to my room. More sticky stuff on my body…more sticky stuff removed…I awaited for the morning where an Eco-cardiogram was to be done-with continued heart palpitations regularly throughout the night.  It turned out that the outcome of the Eco would determine the next test. The Cardiologist came in, introduced himself and explained everything that was ordered and what I should expect.

Once the Eco results were finally in, it was decided that a Stress test was needed. More heart pics, IV dyes and a treadmill set at “uphill” from the onset. (Okay guys, remember that I DO have Fibromyalgia and extensive exercise is gonna kill my joints and make me suffer the next day.) Nonetheless, I was a trooper! (or so they said) and did everything as I was told, like a good girl! They got their test and pictures and I got out of breath and joint pain! I was then wheeled back to my room. More waiting. More palpitations.

Enter the Cardiologist once more! The good news was I did not have to have a procedure called a heart-cath. My heart was strong, he said, and what I needed to be on was a medicine called a Beta-blocker to help regulate my heart beats. Two hours after receiving the first dose, my heart palpitations ceased and my heart felt much better. The doctor said what I have is called a PVC Heart Arrhythmia.

Sounds bad, but basically, it is not life threatening, just needs to be monitored and I need to be medicated…and stay one more night to be sure the dose he prescribed is adequate and the palpitations stay away.

Well, true to my normal Fibro history-self, I awoke the next morning with the beginnings of a Migraine and severe joint pain. Yep, from the treadmill test. And I was told that I was only authorized to be given Tylenol. Not good for me since Ibuprofen is the only med able to kick this monster out of the park. I took the 650mg of Tylenol, thinking it was all I was going to get and then I lovingly expressed my thoughts to the nurse, who passed them along to the doctor, who authorized Motrin, which had to be sent to the Pharmacy, which had to be filled and then brought to my room. Meaning two hours and one ****of a Migraine later I was able to take the Ibuprofen. Five hours later, my head pain was waning. It seriously was an awful thing to live through. Now, had I had that Motrin from the get go….

The Beta-blocker was working after tweaking the dose and the doctor decided I could go home. Yippee! Also, A heart monitor was being ordered for me to wear for one month to make sure my heart was not doing something behind the scenes that I was not feeling due to the meds.

Now, I am not going to lie and say that I was doing okay mentally. Any problems with one’s heart will cause anxiety, which leads to a more rapid heart beat and staying calm is vital.  So I asked the doctor if he thought there was any correlation to the Fibromyalgia, Lupus or other autoimmune issues I have and my heart arrhythmia. He said that certain heart issues from Fibromyalgia and Lupus can happen, but at this time he did not feel there to be a connection, but for me to see my Rheumatologist and to update him, let him run other tests, if needed, and go from there.

So, is there a connection between this heart arrhythmia and my auto-immune issues? Maybe. My next appointment with the Rheumatologist will (hopefully) shed a broader light on this subject.

In the meantime, I am taking this new med and my heart is staying more regular then it used to be. I feel very “chilled-out” and the meds keep my heart from allowing my adrenaline to make it beat faster, which is a very weird feeling. It’s like stress can’t rile me up because my heart won’t speed up.

I am now wired for sound with this heart monitor attached to me for about a month. It is not too cumbersome…really…

So, as I try to take it easy I guess the thought is it (the meds) will help me to not over-do the body. We’ll see.