Taking it up again!

You may remember that I had to give up knitting and crocheting as it hurt my hands too much. It was so disappointing!  

I was visiting my twin sister one day and I found her crocheting a beautiful baby shawl. Now her hands are sore with her lupus and arthritis, and when I asked her how she managed and  told her I could not longer knit or crochet, she encouraged me to take it up again. 

She assured me that her hands had improved since she took up her handcrafts again, and I resolved to give it a try. My hands improved and I had better flexibility in my hands and wrists. I was rapt! I needed to do something creative and those last few months

With fibromyalgia it is important to find something to take my mind off pain, and I find knitting or crocheting does that to some degree. I believe it is healthy and very satisfying to be creative and I have knitted, crocheted or sewn many gifts for family and friends over a lifetime.

I also enjoy blogging and so I thought to create a new one, highlighting a lot of those creations, mainly to remind myself of happy hours making and giving each one.

Currently I am working on making baby shawls and jackets for my grandchildren to use for their own children when the time is right... an heirloom gift or legacy if you will.

With being 71 years of age, I obviously don't know how long I will be able to continue doing this, so I am working on them now, either giving them directly to those old enough to keep them themselves, or to their mothers to keep until the time is right.

I hope you enjoy looking at my creations...

Keep clicking and stitching,

Glenys                    

 https://nanasclicksandstitches.blogspot.com/

Ordinary and good!

It's Wednesday morning here. I have just finished putting the groceries I got online away. It's so convenient for Chris and I seeing as we both are unwell

I have done a couple of loads of washing and am thinking about doing some lunch. Toasted cheese and tomato sangers sounds good and easy.  

My kitchen needs to be cleaned but I am out of spoons as I didn't sleep well last night. The weather is changing as it's autumn here and we can experience all seasons in one day. It plays havoc with my fibromyalgia. It's making me feel miserable.

I am thinking of taking a nana nap before I do the kitchen. But before that I will take some Panadol Osteo   to help relieve my fibro pain. Pacing and resting are not an option with fibromyalgia: it's a necessity. 

After I clean the kitchen I will cook chow mein and rice for dinner and if I have enough spoons I will fold the day's clean clothes and put them away.

It's an ordinary day here and I am glad. When you think of what's happening in the world, I can truly gratefully say that God has blessed me with a day that's ordinary and good! 

Dead tired

A woman who suffers from a chronic illness or disability often finds herself at the end of "normals'" ideas of being tired. We are often looked at with contempt for being so tired that we can't perform our daily duties properly. Or that we have to go to bed early, rise late, or cancel social engagements at the last minute. We are not lazy. 

Before Corona, we were regarded with suspicion when we couldn't make it to church regularly and people harshly judged our spiritual health, deeming us backslidden.  Emotional and spiritual hurt exacerbates our ill state. We feel worse and they lack compassion.

Often we have to cancel doctors' appointments because we are too sick to get there. We find we can't drive and even if we could, we haven't got the strength to even get washed and dressed. It is not unheard of that some of us have crumpled in the shower, unable to get out and totally winded...

Our "tired" goes far beyond a sleepiness or drowsy feeling. We are so fatigued that breathing is too much effort and not for the first time we are grateful it's automatic.

Furthermore, our "tired" is not helped by a nanna nap or even 9 hours of sleep.  We fight our illness and pain even in our dreams and wake up unrefreshed and have to face another day when we haven't recuperated from the day before. We simply have run out of spoons.

"Tired" is overused and doesn't come close to the bone sucking quagmire of desperate fatigue we chronically ill people find ourselves sinking into constantly.  To have "normals" flippantly say, "Me too!" when we tell them we are tired invalidates us and makes us long for their brand of tiredness that can be restored through a good sleep.

We cannot even enjoy a shower or bath to help us sleep as the effort it takes to do this not only drains us of whatever energy we can find, but does not always bring a restorative sleep. Just muscle pain.

Such is my own pain on going to bed that I find I cannot place my arms anywhere comfortable. My fibromyalgia and polymyalgia rheumatica make it impossible to raise my arms upwards and extending them hurts my muscles and tendons. So I go to sleep with my arms folded on my chest.

I indeed look like a cadaver which has been laid out and testifies somewhat to the feeling of being dead in my tracks.  Because that's the type of exhaustion we face every day: we truly feel dead tired.

© Glenys Robyn Hicks

Cast me not off in the time of old age; forsake me not when my strength faileth. Psalm 71:9

Failing fast

You may have noticed I haven't been posting much lately. Fibromyalgia, heart disease, high blood pressure and now boils have taken over my body all at once.

My body is failing me and the fatigue is not only sapping my strength but my mental faculties. It is hard to formulate a sentence these days.

I have been to the doctor. My blood pressure meds have been increased (200/86) and that in itself makes me tired.

These days it takes me all my time to look after Chris and my home. Forget socialising.

I am on the strongest oral antibiotics, taking 9 a day. They have brought the boil on my spine to a head. I am waiting for it to pop itself, rather than try to squeeze it. Though I think I would die from the pain if we tried to do that. The boil is quite large.

I pace myself to try to eke out my meagre spoons but I find I just have to have a nana nap in the day to have enough spoons to cook dinner.

I am praying that I feel better for Christmas as we are having family here for lunch Christmas Day. Most certainly I will have to be stronger than what I am now. My body is failing fast.

Invisible illnesses hurt as much as a broken arm.

So yesterday I got my tooth seen at the dentist. I was overjoyed that she managed to save it. It was a gruelling 45 minute sit in the chair.

Those of you who suffer from fibromyalgia know that sitting stretched back with one's head tilted to the side is not an easy pose to stay in. Add ankylosing spondylitis and polymyalgia rheumatica to the mix, and it's a half hour of torture.

I must say though that the lady dentist was very patient, kind and efficient. I told her about my many ailments as required for a new patient, and I was amazed that not only did she know what fibromyalgia was, but was very careful to not touch my neck roughly. 

She also gave me double the novacaine because she knew I would be very sensitive to pain.

It so happens that her friend suffers from fibromylgia and she has a really bad time of it. To have the dentist allow me to sit up and have a rest every ten minutes was a blessing. In fact, she was a godsend.

She lowered the chair as far as it would go as I got out, and being aware of my torn knee ligaments in both knees, she helped me get out and stand up. 

Today, my tooth is not aching at all, but my jaw, ear and neck are. I suspect from the injections and keeping my mouth open for so long. I have TMJ as well.

Today I have been doing meals, cleaning my kitchen and folding washing whilst medicating with paracetamol. I have had to take it every 6 hours, but it is what it is. I am still better off filling the tooth as opposed to pulling it.

My plan for tonight's meal is to make a sweet curry pork dish with rice. Chris loves that and it's easy to do in the slow cooker.

My online shop will be coming in an hour or so, and I will put that away. That's it for today.

I loved that the dentist took fibromyalgia seriously. It's not often that it is. When you find someone like that, the validation lifts one's spirits. Thanks goodness some people believe that invisible illnesses hurt as much as a broken arm.

 

Hanging on by a thread revisited

We chronically ill women always have times when we feel that we are barely holding it all together. We are literally becoming unravelled and we feel like we are hanging on by a thread.

Flares, unrelenting pain, immeasurable fatigue, depression and lack of restorative sleep can all add to the feeling that we can't go on. Even breathing seems like an effort.

It is in those times that we must reach out to God and ask Him to give us the strength to get through each day- or especially the night which seems the longest when we long to sleep but can't.

We need to try to listen to the Word or put on some Christian worship music, and give ourselves over to relaxing as much as is possible for someone in the grip of pain or depression. But we have to focus on something positive, or else we will be getting a one way to the Pit of Despair. We don't want to go there.

By focusing on something positive, we can actually release endorphins, those chemicals that reduce pain and increase a feeling of well-being. 

Reaching out to God during these times is critical to our staying in control emotionally. But we must do it, in faith.

If the woman with the issue of blood hadn't reached out to Jesus by touching the hem of His garment, she would not have been healed.

I am not necessarily saying that you will get healed, even though it is possible of course. But you will be lifted up to a higher level of coping with it all.

Worship and praising God whilst suffering is the most exquisitely beautiful act of trust and reverence. It will lift us up and set the enemy of our souls to flight.

So, next time you are feeling you are hanging by a thread, make sure it's the hem of Christ's garment.

© Glenys Robyn Hicks

And suddenly, a woman who had a flow of blood for twelve years came from behind and touched the hem of His garment. Matthew 9.20

Pain is a disability

Anyone who suffers from chronic pain knows that it precludes us from a lot of enjoyment of life. Pain makes the vicissitudes of life that much harder to bear. 

Everything is exaggerated both physically and mentally, and the only thing I can do is accept that this is not my usual self, for pain changes people.

Pain disables us in many ways. from physical activity. from family life. from sex. from sleep. from patience. from social life. from functioning normally. from life generally.

The effects of pain cause us to withdraw from people and become reclusive. It makes us feel isolated and unable to really feel understood or validated. We learn to be distrustful of others.

Because chronic pain, in my case fibromyalgia, causes us so much mental as well as physical angst, we decide to retreat to our home often preferring it even if we had enough spoons to leave.

Seeing as pain is such a disabling affliction, it makes no sense to me that we are often regarded by doctors with suspicion when we request heavy duty pain relief such as opiates.

Most of us cannot get enough medication to adequately help us with our pain. We often then succumb to depression and live as recluses  due to agoraphobia. 

We who suffer from chronic pain know that it is a disability. Invisible and destructive. We live in the knowledge that pain is disabling. 

We just wish doctors were as aware of the ongoing relentless disability called Pain.

We aren't just tired: we're dead tired

A woman who suffers from a chronic illness or disability often finds herself at the end of "normals'" ideas of being tired. We are often looked at with contempt for being so tired that we can't perform our daily duties properly. Or that we have to go to bed early, rise late, or cancel social engagements at the last minute. We are not lazy. 

Before Corona, we were regarded with suspicion when we couldn't make it to church regularly and people harshly judged our spiritual health, deeming us backslidden.  Emotional and spiritual hurt exacerbates our ill state. We feel worse and they lack compassion.

Often we have to cancel doctors' appointments because we are too sick to get there. We find we can't drive and even if we could, we haven't got the strength to even get washed and dressed. It is not unheard of that some of us have crumpled in the shower, unable to get out and totally winded...

Our "tired" goes far beyond a sleepiness or drowsy feeling. We are so fatigued that breathing is too much effort and not for the first time we are grateful it's automatic.

Furthermore, our "tired" is not helped by a nanna nap or even 9 hours of sleep.  We fight our illness and pain even in our dreams and wake up unrefreshed and have to face another day when we haven't recuperated from the day before. We simply have run out of spoons.

"Tired" is overused and doesn't come close to the bone sucking quagmire of desperate fatigue we chronically ill people find ourselves sinking into constantly.  To have "normals" flippantly say, "Me too!" when we tell them we are tired invalidates us and makes us long for their brand of tiredness that can be restored through a good sleep.

We cannot even enjoy a shower or bath to help us sleep as the effort it takes to do this not only drains us of whatever energy we can find, but does not always bring a restorative sleep. Just muscle pain.

Such is my own pain on going to bed that I find I cannot place my arms anywhere comfortable. My fibromyalgia and polymyalgia rheumatica make it impossible to raise my arms upwards and extending them hurts my muscles and tendons. So I go to sleep with my arms folded on my chest.

I indeed look like a cadaver which has been laid out and testifies somewhat to the feeling of being dead in my tracks.  Because that's the type of exhaustion we face every day: we truly feel dead tired.

© Glenys Robyn Hicks

Cast me not off in the time of old age; forsake me not when my strength faileth. Psalm 71:9

It's a pain in the neck

 

Lately I have been trying to keep off the computer. I have had a horrid fibromyalgia flare and I suspect along with neck and shoulder pain, I have also got TMJ and polymyalgia rheumatica back as well.

We  recently sold our GMC Sierra ute and with no more vehicles needing a driveway to park on, we have turned our attention to finding another rented home. It has proven to be a nightmare.

There are not many affordable homes to rent and we find we are vying with up to 20 different people at a viewing, all hoping to get the same property. It is terribly stressful.

I think the stress has exacerbated my fibromyalgia. I have been clenching my jaw and this has seen my TMJ return. Without a blood test to check ESR creatines and so on, I can't say that my PMR has returned, but judging from the pain and inability to raise my arms, I would not be surprised.

I have done 5 loads of washing and dryed it in the dryer as it's too painful to hang it outside. I have run the dishwasher and been to the chemist to pick up my Januvia for my diabetes. Just that small bit of work has exhausted me. My spoons have left the building.

Lately I have been thinking it isn't worth moving, but the possums in the roof wake me up with their thumpings and scratchings and the cold weather has meant that central heating is calling my name and beckoning me to a newer more modern abode.

Just typing to you has stirred up all my sore muscles, and it's traveled down my arm. So I will be taking some paracetamol Osteo soon and maybe I'll be having a nana nap.

Fibromyalgia, PMR or plain arthritis makes for a bad day by any name. Whatever ails me, it boils down to the fact that today, it's a pain in the neck. 

 

We have gone mad!

It may seem strange to some, but even in the worst pain, you will find me playing Candy Crush in an effort to distract my mind from the pain.

The rheumatologist suggested to my daughter who suffers from fibromyalgia and pain post chemo, to use it as a distraction from the pain. She was one of these mind over matters kind of doctors. We were not very optimistic to be honest.

As a sufferer of not only fibromyalgia but ankylosing spondylitis, spinal canal stenosis coupled with bad arthitis and angina, I thought it may help me. It helps a little. But Tramadol would be better!

My doctor won't let me have them. Even though he knows I only take them as required for high pain days like today.   He gave it to me when my second knee tore and it helped my fibro pain so much. Then he closed shop!  

I  know there have  been many who abused pain-killers but when  basic pain relief is available only with a chemist's approval such as Panadol with codeine, it makes life more difficult for the person like myself,  to get any relief at all. 

With fibro flaring and another episode of polymyalgia rheumatica, I have been tempted to take some of my Prednisolone, but I am worried about the side effects. I tell you truly, I am feeling desperate.

So even though you may see me playing Candy Crush or online a lot, I can honestly say that it's for  medicinal purposes. I will be a Candy Crush addict any day if it will relieve the pain.

Just don't tell the do-gooders. If they think we are liable to become addicts, they'll make FB take it off their site! You fellow pain sufferers know they will. We have gone mad in our correctness!

Ordinary but good

It's Friday morning here. I have just finished putting the groceries I got online away. It's so convenient for Chris and I seeing as we both are unwell

I have done a couple of loads of washing and am thinking about doing some lunch. Toasted cheese and tomato sangers sounds good and easy.  

My kitchen needs to be cleaned but I am out of spoons as I didn't sleep well last night. The weather is changing as it's autumn here and we can experience all seasons in one day. It plays havoc with my fibromyalgia. It's making me feel miserable.

I am thinking of taking a nana nap before I do the kitchen. But before that I will take some Panadol Osteo   to help relieve my fibro pain. Pacing and resting are not an option with fibromyalgia: it's a necessity. 

After I clean the kitchen I will cook chow mein and rice for dinner and if I have enough spoons I will fold the day's clean clothes and put them away.

It's an ordinary day here and I am glad. When you think of what's happening in the world, I can truly gratefully say that God has blessed me with a day that's ordinary and good! 

The only nice thing about it

So we went to the doctor yesterday to get our results from blood tests taken a few days ago. My blood pressure was 140/90 which was slightly better than last time, but still high.

He asked was anything bothering me and I had to tell him I am worried about Chris. Both of us have heart failure, high blood pressure, diabetes and cellulitis plus I have fibromyalgia. 

We both have pitting oedema on our feet and legs and the fatigue that comes from obesity and feeling sick. Dressing and showering is shared in that we help each other and because of exhaustion from showering, we shower every second day, taking opposite days. That way, we can help each other.

Our love language is touch in the form of massaging each other's feet and legs and our speech revolves around spoons and how much sugar is in everything that passes our lips.

We rarely leave home any more except for the doctor or chemist and our rubbish bins go out more than us. The highlight of our day is to discover we don't have any appointments or need a blood test. We are extremely relieved to know we can just stay home and have a PJ day.

It is unusual to call on us and not find at least one of us having a nana nap, particularly if we haven't slept well the night before.

When massaging Chris's feet or watching him sleep upright so that he doesn't feel like he's drowning in his fluid, I become anxious about how ill he looks and I fret that I will lose him.

I can't bear to think of that and when I do, I have to give it to the LORD in prayer and trust that He will grant us more time together.

All this angst does nothing to alleviate my fibromyalgia pain or help me get over a flare and I find myself taking mild pain relief every 6 hours. As the doctor advised.

Our home is able to be company ready in half an hour as it is basically tidy all the time. True, there may be slippers in the lounge or a cup on the table, but this can easily be fixed. I just close our bedroom doors to hide the permanently clean but unmade beds.

We love our home as we feel it nurtures us and even though we only may be gone a few hours when we have to go out, we find we are really looking forward to coming home again.

When we were engaged, we agreed that it would be nice to grow old together and we have. Twenty-five years later, it isn't so nice. But thank goodness we have each other and that's the only nice thing about it.

Keeping dainty with chronic illness

I have been ill with fibromyalgia for about twenty years now. In that time, lots of things have changed, and one of them is my personal hygiene routine.

One would think that taking a bath or a shower would be an easy thing to accomplish, but if you suffer from chronic fatigue, fibromyalgia, back problems or angina problems like I do, you would realise that it consumes a lot of your spoons. So I had to do a bit of rethinking of my daily routines. I've discovered that one of the places that takes a lot of my spoons is the bathroom.

Because bathing and drying and dressing exhaust me, I varied my time in taking a bath depending on how well I feel. If I have enough energy, I would bathe in the morning, if not I would take a shower before bed as Chris is home and he helps me get dried and into my nightie. (When you are chronically ill, you quickly get over being humbled by needing assistance- you are grateful for any help available.)

I have found that if I take a bath or shower in the morning I am left with no energy for the rest of the day. If I take my shower at night, I have just enough energy afterwards to get myself to bed, which works out much better.

Hot baths or showers leave me too exhausted and give me angina pain, so I take showers with only warm or tepid water. While I would prefer to shower every day, showering is best done every other day for me to avoid flare-ups of pain, fatigue and soreness. I have decided on some new course of action to make time in my bathroom more fibro-friendly.

One of the first things I changed was how I take a shower, or rather, the position in which I shower: sitting. Here I find those telephone type showers are useful. When I get out of the shower, I sit down to dry off.

I can no longer blow dry my hair so by necessity my hairstyle has been wash and air dry for years now. Time in front of the sink brushing my teeth or washing my face has been modified by resting one foot on a stool while standing. Because of spinal problems and being a short person, I have a glass in my bathroom which I fill with water and use for rinsing and cleaning my toothbrush without straining to reach the tap.

I no longer wear makeup, the standing in front of the mirror and the use of my hands in holding the various tools of the task, is now limited to special occasions only; it is too painful a task to do on a daily basis. Also, my face is so sensitive that it breaks out in red welts at the slightest pressure... which includes smearing on foundation. This is called dermagraphia.

The bottom line is taking a shower is a real workout now. In addition to modifying how I take a shower, I am going to follow these 3 rules: I will only take a shower at night, I will only take warm water showers and I will only take a shower every other day. With the employment of a good deodorant after each shower and a fresh change of underwear each night and morning, I have found that I don't offend anyone and remain feminine and dainty.

Life with chronic illness is complicated, but at least I manage to stay clean while living it!

© Glenys Robyn Hicks

So teach [us] to number our days, that we may apply [our] hearts unto wisdom. Psalm 90:12

You can say that again

So today we have shopped online but most of the food we ordered was unavailable. So we took a trip to Aldi  and managed to get  meat,  chicken and cat food.  Most products are being limited now.  There are distribution shortages of staff due to Covid. 

There's a four hour queue to get tested or one can do a Rapid Antigen Test at home, but there's a shortage of tests and it's very difficult to get one. People who can't get tested are isolating and missing out on work just in case they are positive.

Our Prime Minister suggested that as most Australians will test positive soon so he told us to make sure we have paracetamol aka Panadol on hand so that we can manage symptoms at home. (Lotsa luck with that one!) So people went out and stripped all pharmacies and supermarkets of all brands of paracetamol. 

To top it all off for me is that once again, my antidepressants haven't made it off the wharves. They don't know when they will be available again. So it's lucky that I have extra Panadol on hand for my fibromyalgia and an extra box of antidepressants. I am so grateful to the Proverbs 31 wife in scripture who was always prepared and laughs at the time to come. 

A past Prime Minister of ours once famously quoted that life wasn't meant to be easy. You can say that again. 

My new wheels

                                               

So if you have read on my other blog, I am now wheel-chair bound. I am relieved that I have an easier method of transportation and that it will be easier for Chris to push, but I am also sad that my life has come to this.

So, the MRI results are in. I have a meniscus tear, fabella, torn posterior crucius ligament, bursitis and osteo arthritis behind the patella. It needs surgery as it does not repair itself.

I am to see an orthopaedic surgeon and meanwhile I must rest the knee and use pain killers. 

We have bought a shower chair and a wheelchair. I have had Chris push me on the seat of my walker, but it is a big strain on his heart and I worry about him. 

It is difficult to focus enough to write at the moment and I spend a lot of time on the couch aka the beach, or in bed with my electric blanket.

I am just able to stand enough to wash some dishes, cook a meal and stack the washer and dryer. Chris helps sometimes and has been my legs.

I am making use of the slow cooker a lot, cooking the meals as I am able to stand.

As with all new health issues, I am trying to come to terms with this "new normal" and the constant struggles with fibromyalgia are now "normal" and this new challenge is calling for all my ability to accept my new lot in chronic illness.

I am disheartened that both my knees have now given way (I have a torn meniscus in my other knee), and am trying to feel grateful that I could afford a wheelchair. Thank goodness for afterpay.

I am trying to be thankful for my new wheels, and I am also trying to give this new situation over to the LORD. I guess it's all a part of grieving what I have lost and accepting it, and not giving way to self-pity. It's hard.

However romantic a picture I can find really doesn't cut it for me as I struggle to accept that I am now wheelchair bound, and instead of a new car, a wheelchair is my new wheels.

© Glenys Robyn Hicks

My flesh and my heart fail; But God is the strength of my heart and my portion forever. Psalm 76:26

Our little haven

 

So yesterday was a day of horrible fibromyalgia pain and fatigue. I felt a little down so I came to my couch and sat next to Chris for a cuddle and rest. 

We love feeding the birds that come into our back garden and all through the day, our garden is like an airport. Birds of all types come to dine and drink and it is so restful and fun to watch them.

They have their own little antics and natures and they can be quite amusing. And apart from watching their different natures and antics they have something else that we find very attractive: they have babies.

It's such fun to watch the mothers feeding their babies and to watch the babies venture further and further from her as they learn to feed themselves. They fly but are still juvenile and yesterday their mothers were distancing themselves from their chicks and refusing to feed them, much to their annoyance. 

The magpie juveniles are especially raucous and squawk even with food in their mouth. They are almost always feeding. The minor bird mummy also is weaning her chicks from her and as soon as she moves away, they follow like the duckling family juveniles do. So fun to watch.

But by far, my favourite birds are the Kingfishers which have also had babies. Whilst laying on the couch, I can see outside and I was delighted to see a mother Kingfisher with one of her three babies on our garden swing.

They were watching the porch which was covered in birdseed for the galahs and rosellas. I had thrown out some cut up luncheon meat, and they were waiting for the magpies to vacate the porch so that they could dine. Kingfishers are shy and besides, magpies are three times their size. So they wait.

It is the season for little white cabbage moths too. They are flying around the agapanthus plants and I guess they are mating because they seem to be in pairs. As are the pigeons that come for the seed.

There are three that regularly call in and partake of the parrot seed on the ground. There's a little female who just wants to eat, but there also is an amorous male who has romance on his mind. He pursues her constantly and hopes to make her his by dancing for her. 

He fans out his tail feathers and hops towards her, then takes a few steps back. He repeats this courting gesture until she tires of him and runs a few feet away. But he is insistent and pursues her over and over again. I hope that he wins her heart as it is such fun to  watch the young birds as they leave the nest under their mothers supervision.

We have a bird bath/feeder in the back garden which we used to fill with seed, but now with torn meniscuses in both knees, I cannot get down the steps to fill it, so they get fed from the back sliding glass door. I just toss the food onto the back porch. They don't care where it is. 

They are quite used to me now and I have them almost eating out of my hand. So much so that as soon as I open the door, they come flying in to the garden from all directions, calling each other.

We have water in the bird feeder and in a plastic container in front of the steps. They bathe and drink and sing and they enjoy our back garden as much as we do.

It's a lovely place to recoup one's spoons during a fibromyalgia flare. The daily scenes are so peaceful and we love our little haven and we know the birds think of it as their haven as well. Their constant visits and frequent broods of chicks speaks of a place of plentiful food, water and safety.

We are grateful God lead us to this little country town- it is a gift from Him: our little haven

Cleaning for older women

I read this and thought not only would it be helpful for us older sisters, but also for us Sacrificial HomeKeepers especially those of us who suffer with fibromyalgia.

There are many websites that have detailed instructions teaching young women how to clean and organize their homes. However, I haven't been able to find much on teaching older women how to adjust to not being able to stay on a routine cleaning schedule due to health problems, yet keep a clean home.

This article can also apply to younger, healthier women too because of the unexpected occurrences that do happen in all our lives.

One thing you need to know about me is that I've always had the problem of perfectionism, which I have learned to control in recent years. You may be wondering why I consider perfectionism as a problem. For most people with this characteristic, they are uptight and easily upset when things don't go as planned. The least little thing that goes wrong immediately puts them in a bad mood. Why? Because they have lost control of the situation.

I have had to ask the Lord on many occasions to help me adjust my attitude and He has been faithful in doing so. I am MUCH more relaxed than I use to be and give the Lord all the credit because I don't think it is something you can change on your own. Oh, I occasionally will fall into my old way of thinking at times, but quickly realize that old enemy and put it away.

As we age, we usually end up with a few health problems along the way and we also tend to move a bit slower, thus taking longer to do one chore. It can be very frustrating to those who have always tried to keep a clean and tidy home. Maybe bending or stooping is causing you pain at times or you just can't seem to do as much in one day.

* My number one recommendation is to RELAX!!!!! I don't mean to sit all day eating bon-bons and watching soap operas, but relax your attitude.

If you are like most women, you dread another woman coming into your home if it isn't absolutely and perfectly clean and tidy. We are always apologizing for the way the house looks when most of the time, it is just fine.

Your children are grown and maybe already left the nest, so it is just you and your husband. This alone will help you because there are now only two to make a mess. Yet, the house still needs tender, loving care.

* Clutter in your home can appear to others as uncleanliness, so make sure to put things back where they belong and keep your home as clutter-free as possible. A tidy home will appear clean even when there are a few dust bunnies around. Maybe it's time to get rid of some things you no longer really need. Maybe that collection doesn't have the same appeal or meaning to you as it once did. Ask your children if they are interested in having it. If not, why not donate it or have a garage sale? The less "things" you have, the less dusting. Take a picture of it and put in a memory scrapbook! Then be happy you have less dusting to do.

* Your laundry loads will be greatly diminished when it is just the two of you. I have found that on days my back is acting up, I can sometimes still accomplish doing the laundry by having a low stool by the dryer to sit on. That way I can reach into the dryer without bending over and sit there folding each item. My husband and daughter frown on me doing anything when my back is bothering me and they say, "Why didn't you call me to do that?!!!!" Well, I'm the type of person that if I can find a way to do something myself, I'll do it. Asking for help is my last resort.

* Depending on your ailment, sweeping, mopping, and vacuuming can be difficult along with cleaning the tub/shower. May I suggest to look at alternative cleaning equipment? A couple of years ago my daughter gave me a Swiffer floor vac and Swiffer wet jet. These two items have been a tremendous help to me. They are VERY lightweight and easy to use. Of course these are to be used on hard floor surfaces only. I read once where a woman used an old-fashioned mop to clean her tub and shower. Prevented her from having to bend over. If you are completely unable to do these tasks and your husband isn't able to do them either, why not consider asking one of your children if they have time once a week to do this for you? Or maybe someone from your church? I would recommend that you try to get someone you know very well.

* If you have clothes and shoes in your closet that you haven't worn in a long time, get rid of them. Same thing with bed linens. Get rid of excess. It's that much less to collect dust or mold. Haven't you ever noticed the "old person" odor when you walk into someone's home? Just because you are getting older doesn't mean you should quit caring for your home and yourself. Be sure to bathe/shower daily. Don't forget to wash your hair! Get in the habit of laundering small loads instead of letting clothes and damp towels set around until you have a big load to wash. At least once a year, ask a strong person you know to come in and move furniture for you so that you can clean behind those items. Don't forget to take care of those curtains! Wash and dry or have them dry cleaned.

What I am still trying to get through my thick skull is to pace myself on the good days. Give myself less tasks to complete and to take frequent breaks. It is difficult to change our habits, but it can be done. I am having to break a lifelong habit of "Get all your work done and then you can rest."

A typical day for me goes like this:

Before getting out of bed, I thank the Lord for the day and for my family and ask Him to guide each of us in all we say and do that day.

Then it's time to get up, get dressed, and have a cup of hot tea with honey (sometimes I treat myself to a cup of coffee, black only) and watch the news with Hubby while waking up. Then it's time to prepare something for breakfast.

No, I do not wear heels around the house. It's socks and slippers during cold weather and sandals during hot weather. I don't wear a head covering, but I do like wearing an apron.

After breakfast I clean up the kitchen and then sit down to check email and decide what I'm going to try and accomplish that day. Depending on what is to be done, I remind myself that if it is going to take longer than 15-30 minutes, I MUST take a break. This is usually when I'll do a blog post or visit a few blogs and check emails again.

Since my Hubby is retired on disability, we have our lunch together around noon each day. If I'm having a good day, I will try to accomplish another task after lunch. If not, then I keep my hands busy. I'll do...knit or crochet.

As a homemaker, we all would love our husband and children to really take notice of what we do. Sometimes we feel we are taken for granted and wonder, "Is my family really grateful for the things I do around here?" You all KNOW what I'm saying. We don't expect them to come home everyday and gush over how clean the house looks, but every once in a while it's nice for one of them to thank us for what we do. Well, this feeling DOES happen to the man of the house. Here's what happened:

I've not been able to vacuum lately and my daughter has been busy and gone a lot. Hubby and I both have been having back troubles, but last Friday I was feeling a bit better and told him I had to get out of the house for a while. I went shopping.

Later in the afternoon, he said, "Did you notice I vacuumed?"

I looked down and said with a grin, "When did you do that?"

"While you were gone to town. You know when I vacuum, it really needs it!"

Then he said that he was going to wait and see if I noticed that he had vacuumed, but couldn't stand to wait any longer and had to tell me what he did. LOL! So, I thanked him. :) Written by Sharon from Sharon's Roses blog which has been deleted now...

That they may teach the young women to be sober, to love their husbands, to love their children. To be discreet, chaste, keepers at home, good, obedient to their own husbands, that the word of God be not blasphemed.  Titus 2:4-5 

Nothing to be ashamed of!

Fibromyalgia has made many changes in my life and one of them is my dislike of wearing clothes. The mere touch of fabric on my skin, or the tags on my clothing can send me into an itching frenzy.

Before I wear something new, I will cut off all the tags and if it has lace, particularly around the neckline, I will not buy it or I will cut the lace off.

Mohair drives me insane with itch and brings me up in a rash wherever it touches my skin. I won't buy it. If I have a woollen top on, I have to wear a blouse with a collar under it to stop the itching.

In dressing, I have to put layers on because fibromyalgia sufferers' thermostats are broken. They can't be adjusted or fixed. It is not uncommon to feel cold when everyone is hot and vice versa. Anyway, it is important to me that I can reduce or add on clothing as required.

Not that I really enjoy wearing clothes anymore. In fact, if I could be naked without offending, I would. Not that I do go publically naked of course. And I do dress modestly as it's important to our witness. Not to mention I don't want to be arrested! lol

I do go around the house naked in the summer. In case of visitors, I have my sundress in easy reach. It is never a problem to quickly slip it on if there is a knock at the door. Chris will always wait for me to get into our bedroom to change before he answers the door.

We are mindful of others at all times and keep our drapes closed when I walk around. Of course,  it's not when we have guests or when grandchildren stay. If we are expecting company then of course I get dressed. If we are on holiday or guests, I wear a loose nightdress at night and clothes in the day.

I know I am in good company with Winston Churchill often holding interviews whilst in the bathtub or naked, even in his office. I am not that brazen...

But I know I am not alone in hating wearing clothes in the World of Fibromyalgia. I do not doubt that many fibro sufferers will join me in saying that they sleep in the nude as well. 

Clothes can make one feel that they are strangling you in bed.  Sheets, no matter how soft, end up causing the most awful itches and feelings of heat that most fibromites sleep with one leg out and a fan on. Even in winter.

There are so many changes in one's life with fibromyalgia and some you won't hear about. Such as a hatred of wearing clothes.  We keep it secret, like it's something to be ashamed of. 

Trying to keep oneself from scratching until one bleeds is a reason for compassion. If I only walk naked around my own home, with only my husband seeing me, I am not flaunting myself and being immodest. 

Coping with illness is nothing to be ashamed of: it's all part of accepting it and moving on. I know my God would understand. I am not ashamed at all. 

© Glenys Robyn Hicks

Sing, O heavens; and be joyful, O earth; and break forth into singing, O mountains: for the LORD hath comforted his people, and will have mercy upon his afflicted. Isaiah 49:13

You can still be a Proverbs 31 woman!

The Proverbs 31 woman is an example of a godly wife. It's not something we are going to be able to do all at once and for some of us, we may never accomplish all she did. But I believe emulating her example is a good thing. We have to have a goal. If you aim for nothing, you are always going to hit it. I used to get up real early, about 4.30 to get my husband off to work. I would have my quiet time then before my 4 children would wake up.

This worked for me when they were quite tiny too and I just carried it through. Until about 22 years ago when illness came in. I don't sleep well and wake up in lots of pain and I find if I try to get into the Word the fibro fog makes it impossible to focus. I don’t glean much from the Word and my prayers are disjointed. I put on some praise and worship music and just thank the LORD for giving some sleep and so on. After a hot shower and breakfast, I can study the Word and pray better. I think anyone with an illness or pregnant, or who has had a sleepless night with a sick child etc, has to be realistic and in tune with their body. She has to know what her own limitations are and modify what is an excellent goal to achieve it.

My modified morning routine now works better for me. And let's face it, any time is a good time to be in the Word! We all have to work out when it is best for us....then do it. My time of choice would be early mornings though. But I have had to learn to modify things in order to achieve them. And later is better than never! I believe that for all of us women trying to live a godly life, the Proverbs 31 woman is a guide of what to strive for. Even if we can't achieve all she has done (and you will notice that she achieved this over seasons of her life- not all at once!), still our hearts will be in the right place.

If women look at the whole picture with the view of doing it all NOW or not modifying it for themselves, they will most likely give up and not even try to emulate her example. Sometimes there are unresolved heart issues that the LORD has to work through with some women who won’t even try to emulate the Proverbs 31 woman. Not even with modifications. It may take some time until they are convinced that this holy calling in their lives is truly for their own good and contentment. Sometimes it takes a lot of washing with the Word before the soil of the world is cleared out of some women's eyes. They just need encouragement as God works in their lives.

© Glenys Robyn Hicks

‘She girds herself with strength, and strengthens her arms.’ Proverbs 31:17