My thermostat's broken!

 

Once I passed menopause, I thought I would be free of hot flushes and sweaty nights, waking up in a bed of sweat and feeling nauseous.

However, fate was not kind to me and as soon as I finished the menopause, I became ill with fibromyalgia.

To be honest, I am never at a normal temperature. On blood thinners for heart stents and antiphospholipid syndrome (or sticky blood), I feel the cold keenly and on any given day while everyone in my home wants to turn the heating off or down, I am there pleading my case for more heat.

Ten minutes after the heat is put up for my benefit, I have to turn it off again. I feel sick- I am sweaty and unwell.

About an hour before I go to bed, I turn my electric blanket on as I feel the cold so much. I sink into the warmth as it soothes my fibro muscle and spinal pain. A couple of hours later, I wake, sweaty, nauseous and out of sorts.

I strip the minkie blankets off but I feel cold so I put some back. Five minutes later, I am hot again and I stick one leg out of the blankets and fall sleep again.

This cycle of hot/cold repeats through the night. I am turning like a rotisserie chicken! Thanks to fibro, my thermostat's broken.

It's all too much

 

So recently I have had chest pain in angina and breathing problems coupled with what I thought was fatigue from an ongoing fibromyalgia flare.

My blood pressure sky rocketed, requiring a visit to a cardiologist who ordered an echocardiogram. My general practitioner told me if the results were bad, he would contact me. And he did.

I got the call last Friday telling me to make an appointment for a phone consult so I ended up speaking to the doctor on Monday. He told me I have heart failure due to Pulmonary Hypertension.

There is no cure for it but there are some treatments. I am already on blood thinners which I will stay on as PH can cause blood clots in the lungs. I already take 7 blood pressure tablets a day.

I often have felt dizzy and this is another symptom of PH and I feel like I can't get enough air in at times. The time will come when I will probably need oxygen at home.

Forget about exercise- I nearly collapse with exhaustion after walking up our long passage to answer the door.

I will know more tomorrow when I see the doctor in person. This is needful because he wants to check out the swelling in my feet, ankles and legs. I suspect I have fluid in my abdomen too. It hurts and is tight like a drum.

I had a blood test yesterday to check on my kidney function and this will be a regular thing.

Lately it's been one thing after another and I am a tad depressed. Prayers would be much appreciated. It's all too much! 

One leg out, one in!

So today we signed a new lease for another year at our little country cottage. We love it here and if one has to be in lockdown like we are, there is no better place for it. 

Because we have cold winters here, we have bought an electric portable heater with realistic flames like the one we have in our living room.  So as we still have cold days in October, I am hoping the heater comes soon. The cold is the only down side of living in this little cottage. 

With my fibromyalgia, I feel the cold especially and some days I feel like I can't warm up. Sometimes I go to bed with my electric blanket just to warm up.

Anyone who suffers from fibromyalgia know that our thermostat is broken. We act like someone who has a fever: we are hot, then cold, then hot again. It's a conundrum as well as a nuisance. Like so many symptoms of fibromyalgia, there's no real explanation as to why.

I used to think it was because I am on blood-thinners for my antiphospholipid syndrome and stents. That was until I joined a really helpful online group for fibromyalgia sufferers called Fibro Blogger Directory. 

There the other members shared about this and many other fibromyalgia symptoms and I quickly learned that I was not the only one with a broken thermostat who slept with one leg out and one in the covers.

 

It's like a fridge in here tonight.

                                                         

We are just into the seventh day of Spring and I am so glad to see the back of our winter. This house is old and has no insulation and I feel the cold real bad with watered down blood. Chris laughs at me, saying that Australian winters are mild and don't last long. 

I have no desire to live in England or anywhere that has long dark winters and snow. We average out no lower than 1C or 33.8F though we did see -1C a few mornings. As nice as snow looks, you can be sure I won't be joining in making snowmen!

Although changing weather effects my fibromyalgia, I still enjoy the different seasons in each day of Spring and autumn. And I just adore the smell of early spring mornings and the abundant blossoms on our neighbour's tree overhanging the fence. It's such a pretty pink and when it loses its leaves, it leaves a pink carpet all over the lush green of our grass.

With some Spring  mornings and evenings still being cold, I am looking to buy a heater for my study. I am sitting here with a wheat pack on my chest to warm me up!  It's like a fridge in here tonight.

Painted in to a corner

So we visited our doctor last week and he asked us if we wanted the Covid 19 vaccine. With both of us with weak hearts, diabetic and obese, plus being older he told us we should consider it.

Well, we have considered it. With ordinary flu vaccines, both of us had a really bad reaction to it, and we both swore we wouldn't have another one. So we declined.

We pointed this out to him, plus the added problem with my blood being sticky and my propensity to make clots, it seems too risky. Even with Clopidogrel and aspirin blood thinners which I am on for life.

The doctor said if I wanted it that he would consult with my specialist who deals with my antiphospholipid syndrome. When I told him I didn't have one, he said that he would have to refer me to one and take it from there.

I asked if he was planning to have the vaccine and he said he and all in his clinic had already had it. I asked him which one. He replied AstraZeneca. 

Now AstraZeneca has been ceased in some European countries because it seems to be linked to many cases of blood clots.

As an older person, I would be given AstraZeneca here in Australia to leave the other vaccines for those under 50 who may be at greater risk of blood clots. 

With severe muscle pain already from fibromyalgia, I can do without feeling even worse. Especially for a disease that has a 98% survival rate if you are unlucky enough to catch it in the first place.

So we declined and the doctor was OK with that. For the moment. Because I can foresee in the near future that there will be more pressure on people to be vaccinated, especially as more vaccines become available.

I will never agree to being vaccinated and it's OK now, but with a muted message on Twitter from our Prime Minister that "certain things will have to be done to ensure all are vaccinated" and revealing that even Australian citizens may not be able to return to Australia if unvaccinated, the die is cast for some coersion in complying.

We will be standing our ground on this experimental vaccine, but we feel that it's only a matter of time before we are ordered to comply and are painted in to a corner.

I am wearing my blanket!

We are in our winter here in Australia and where we live in a small country town, it gets very cold. Sometimes it even snows. 

With my thermostat being broken due to fibromyalgia and then being on blood thinners for my stents and antiphospholipid syndrome, my blood is like water and I really feel the cold.

You kinda know your blood is thin when you get a blood test with your husband and when it's standing in vials next to mine, his is dark red and mine is watery pink! So yes, I feel the cold keenly.

Our home is all electric and of course our only heating is electric too. So when the bill came, I gasped when I saw how much it cost! 

When I saw the Oodie on Face Book, I asked Chris if I could have one for my birthday! I ordered it in April but didn't get it until the beginning of June. Just in time for the coldest months in Australia. I figured that if it was as warm as they say, that it would recoup the cost in just one billing cycle!

Now Chris is from England, and he is quite used to the cold and doesn't feel it like I do. When he saw how warm I was without using the little fan heater in my study, he mentioned that he might like one for his birthday!  Since getting older and feeling ill with high sugars and vertigo, he declared that he was now feeling cold too.

So he tried it on and apart from mine being the pink you see in the picture, it was perfect! So I ordered a navy one for him. Size is not a factor as they are made oversize and one size fits all! 

The only problem is that he won't get it until July as they are pre-ordered and very popular here!

They are expensive and I got mine on Afterpay which helps a good deal. We love Afterpay!

Today is Monday and I am doing Sylvia's Lists today as I am feeling under the weather with fibromyalgia flaring. The last few weeks have been stressful, especially the day Chris was taken ill and I thought he had suffered a stroke.

We then had to sort out his new insulin regime which I did, and although he is now improving, I still am suffering rebound fibro flares from the stress.

I am planning to cook lamb strips in a marinade of mongolian beef with green veg and mashed potato for dinner. Depending on Chris's sugars, I will serve some artifically sweetened jelly and sugar free icecream for dessert.

By the way, I am not getting paid to advertise my Oodie. I just wanted to pass on my great comfortable friend for your consideration to anyone here who feels the cold. I really love mine: I can find anywhere is a great place to sit and be cosy as I am wearing my blanket!