Showing posts with label meals. Show all posts
Showing posts with label meals. Show all posts

Monday 29 November 2021

My four tasks of homemaking



With severe Fibromyalgia and fibro fog, I find making lists helps me focus on what needs to be done each day in my home. I love following Legacy of Home blog by Mrs Sharon White and I have adapted her daily lists to my needs. On bad days I follow Sylvia's Lists. Here is my list. I hope it helps you too. 


WAKE UP: BLOODS, JAB AND MEDS FEED XENA


1.  There is the breakfast hour, which includes tea-time. First we prepare the meal and set a table.  I often set up a tray- table and sit in the parlour before anyone else is awake.  I am an early riser so I have my tea while the sun is just beginning to rise.  I enjoy this quiet time of resting from the brief bit of morning work.


Later, when the family has their eggs and toast, or fresh baked muffins with fruit, it is time to do the dishes.   We wash the table and the counters and do the sweeping.   All the work of tidying and making things neat are part of the breakfast duties.


2.  Often, during the morning hours, we do the laundry or the dusting and vacuuming. Each day has its special work. It may be Wednesday is for washing floors. Perhaps Thursday is for cleaning the bathroom.  The mid-morning hours are a good time for many of us to do these special duties of making a home look pretty. LIST WORK FOR THE DAY


3.  The Lunch hour is such a wonderful time to stop and rest We put out a fresh, clean tablecloth.  I love my white-and-teal checkered cloth.  It looks so homey and old fashioned.  We can set up our plates and napkins. We can do this even if we are just serving grilled cheese sandwiches, pickles, and chips!  It makes the lunch - work like a reward when we sit at that pretty table and rest and eat while we enjoy the family.  Next we do the sweeping and the dishes, much like we did in the morning.


4.  The dinner hour is such a precious time in the day.  I often start working on the evening meal at 3 in the afternoon. I work slowly and take lots of breaks. Sometimes I peel potatoes and start getting a little casserole ready to bake.  Other times I might do much of the work for a pan of lasagna. I like to put these pans of prepared food in the refrigerator and then just take them out to bake when it is just about dinner time.  That way I get a great deal of rest between all the work. CLOSE BLINDS LIGHT LAMPS  BLOODS AND JAB. MEDS AND MILK


Sitting with the family and hearing the blessing (or the prayer before the meal) is such a peaceful experience.  It is lovely to just sit and enjoy dinner at the end of a long day.  Then the work of tidying, doing the dishes, and sweeping the floor happens.  We make everything look neat and pretty. But I do not like to rush.  I do not want to just "get the work over-with." I take my time and go at a steady pace.  The work of cleaning and accomplishing the beautiful work of making a neat home makes me happy.  It also brings peace.  Bathe or shower


These four tasks of homemaking do not take a great deal of effort.  They may seem simple and ordinary.  They may seem mundane.  But if we dress up in something pretty, wearing an apron, and keeping our hair up in a pretty style, we may find ourselves enjoying the work.  I have an old blue-and-white gingham apron that I love to wear. It is getting old and ragged. I will have to make a new one this coming fall.  I need a fresh supply of lovely aprons to wear as I do the housekeeping.


When we look extra nice as we do our work, we can find joy in the labor.  Doing the little tasks of keeping house, each day, with a feeling of contentment, will bring a true feeling of comfort and happiness to the family.  It will help them feel welcome and loved in a happy and simple home. adapted from Mrs Sharon White of the Legacy of Home


Wednesday 24 November 2021

Fibromyalgia is a wicked ruler.


So yesterday we went to see our daughter after lockdowns were lifted. The weather was beautiful and we bought some fish and chips for lunch and we ate them in the car overlooking some water. It was lovely!

We haven't been out socially for about 4 months, and it was a real novelty to keep on driving with no restrictions. We had a lovely cup of tea with our daughter and caught up. 

Driving home, we took the long scenic route. It made us feel glad to be alive. Last night, I slept like a baby but unfortunately woke up in top of the range pain. It's going to rain.

Fibromyalgia is such a wicked ruler. It can come and bite you on the heel, just  after you've had a lovely and special time. Maybe it was sitting so long yesterday, maybe because of the changing weather. I don't know. All  I know is I have another fibro flare.

Sitting here typing and in pain, I have come to realise that in spite of knowing that fibromyalgia will rear its' ugly head the next day, it's important to keep living.

The only alternative for me is to stay home permanently and wrap myself in cotton wool but be miserable doing it. I don't want that to happen.

So I will put up with rebound flares after using all my spoons if it means that I have a life other than that of an invalid. I am more than that.  I want to have episodes of pleasure in my life no matter how brief.

I need to make memories and keep in contact with my family. I will overcome it, even if fibromyalgia is a wicked ruler.

Things on my to do list are just basics today. Dishes, cooking and resting.



Friday 19 November 2021

Choppy waters ahead



Well our day is still in full swing. I have dishes to do and clean washing to fold up and put away. We went to the chemist and picked up prescriptions yesterday. Apparently there's a world wide shortage of one of my anti-depressants, Dothep 25 and I am on my last script. I have been waiting for 2 months for some.  The Dothep anti-depressants help me with my fibromyalgia pain. I hate to be without them.

The practice of keeping extra meds in case of emergency has paid off for me. But I will be out soon. That's a worry as the sea gets very choppy when I mess with my anti-depressants. I think they are in a container somewhere on their trip to Australia.. Apart from those few tasks, and cooking,  that will be all I can manage today. 

I am praying that I get those anti-depressants before I run out or there will be very choppy waters ahead.

Thursday 18 November 2021

Coming to terms with it


Fibromyalgia is flaring and my spoons are scarce today, so it's just basic home duties for me.  Dishes, washing and meals.

If I can get down the steps today, I want to sit in the garden swing. I need the fresh air and relaxation that watching the birds brings. They are getting quite cheeky and tame now. I only have to open the door and they converge on the back porch/decking chirping at me to get them something to eat. 

They stand there practically with their hands on their hips, feet tapping: why are we waiting? Quite funny. I know they case the house out- I see their shadows on the roof and carport. I will miss this place. Chris wants to move back into "civilisation" when we sell the fiver. With Covid, we haven't had any chance to get people here to see it. 

As with coming to terms with the knowledge that my fibromyalgia and other issues will not get better, so I am trying to come to terms with missing out on country life.




Monday 15 November 2021

Keeping my wheels turning!


 

Good morning. It's a new week! We have to go out today, just some grocery shopping and a trip to the post office. That will be before I tackle last night's dishes

I was so tired last night that I left them, hoping to wake up with some spoons (energy). That didn't happen so the grocery shop takes priority today. 

Some lamb chops are defrosting for dinner tonight. I will do mashed potato, vegetables and gravy with them. A sandwich will suffice for lunch. 

I use the frozen mashed potato, steam packs of vegetables and instant Gravox gravy. I am fortunate in that Chris loves meat of some sort with two veg and if one of them's mashed potato, he's a happy man.

Being able to go without peeling potatoes and shelling peas is a godsend for me. The arthritis in my hands, the torn knee caps and spinal problems make standing to cook to prepare a nightmare. I am too short to sit on a chair as I can't see over the benchtops properly. 

When in a fibromyalgia flare like today, it is just the icing on the cake. It literally tips me over. The pain is incredible and never lets up. I do have a high pain threshold but when the pain is 24/7, it wears you down.

I think I will make myself a cup of tea and take some painkillers. That's the only way I will be able to function today. They can join my other ten tablets taken this morning. I swear I rattle when I walk.  It is what it is!  But hey, whatever keep my wheels turning!



Thursday 4 November 2021

My day is all stitched up


Today is a bad fibromyalgia day. I am aching so badly I want to cry. But I don't think I even have the energy to do that! 

I meant to take up some cricket pants yesterday for my daughter in law. She needs them for next week's first match of the year. So that is on my priority list today. I finally found my sewing machine again. I haven't used it since we moved in here which is 2 years at Christmas. 

I have dishes to do as well as cooking. I had run out of bread and had to ring DIL who lives locally. She picked up a loaf for me at the local store as Chris was feeling too giddy with vertigo to drive today.  I can't because of my torn meniscuses. Woolworths ran out of bread at their online shopping food distribution centre, and although they refunded me, I needed the bread. 

Everybody is buying their food online and Covid seems to be the reason. Their shelves are getting low and every week there's something I am unable to order. I know I can bake a loaf  but I don't have the energy right now.

Would you believe me if I tell you I have psyche myself up to take those cricket pants up?- and that may use all my spoons for today! I guess you could say my day is all stitched up! 

  


Saturday 16 October 2021

Comfort from my kitchen


The weather has been shocking today and is forecast to be the same for four days. It's been so windy today and last night that I thought our tin roof was going to come off. It seemed to be lifting off. The rain just keeps pouring down with occasional hailstones. I think we are getting some of the tornado that came to Sydney.

I have been suffering from severe fibromyalgia pain, coupled with arthritis in my spine, fingers and knees. I have tried not to go to bed as I don't like sleeping my life away, but I will  have an early night.

Today seemed like the perfect day to warm up with some comfort food, so I made a slow cooker full of Jewish Penicillin.   Not only is it nourishing, but tastes great. I find it so comforting on days like today.

I had planned to do my overdue dishes today, but my spoons were vanishing as fast as my soup. Chris stacked the dishes for me and they are going to be waiting there till tomorrow now. I am planning on taking some Tramadol and go to bed about ten. 

I know I write a lot about fibromyalgia flares, but I think it's just the same long drawn out flare. Maybe this will be my new normal forever! I hate to think like that, so it's off to grab another bowl of comfort from my kitchen! 




Tuesday 12 October 2021

Tyrannical spoons



I woke up with high hopes of doing some baking this afternoon. It's been a few months now since I bought a food processor and I wanted to make Chris some sultana muffins with it.

But life had other plans and I had to handle some juggling of bills and made the necessary phone calls and then I took a shower. That's where the day spiralled out of control.

It took me forever to get showered and by that time, all my energy had been sucked off my spoons. I have barely enough to cook dinner.

My fibromyalgia seems to be always there, no longer flaring but constantly making me aware of every movement. Even my eyes seem to ache. Apart from physical torment, it now teases me with fleeting glimpses of spoons that disappear as soon as I flex a muscle. Most disappointing.

So apart from a few dishes washed and sorting out what to have for tea, nothing much as been accomplished.

She's a tyrant, Fibromyalgia. She dictates my days and even my nights and tantalises me with false promises. Ah well, it is what it is.

"The best laid plans of mice and men go awry!" comes to mind as does the scripture that says "a man's heart plans his way, but the Lord directs his steps!" 

So today is not a day for baking. Thanks to my tyrannical spoons.




Saturday 2 October 2021

Sometimes you have to be your own doctor!




It's Saturday evening here. Not much accomplished today except I washed some dishes and will cook dinner soon. 

Chris's face is improving already with his Bell's Palsy and he can open his eye almost fully and his mouth is not as drooped. He is regaining his speech again and is not slurring his words as much. 

His sugars are way up because of the Prednisolone he's been taking. Consequently, he has been sleeping on the couch most of the day. The doctor wants him to discontinue the steroids so this morning was his last day. 

I was awakened by asthma early hours of this morning. The inhaler didn't help much but I still went back to bed because I was needing to sleep. Especially with my night medications. If I don't sleep for 9 hours, I can't focus properly. Plus I am having the Mother of all Flares with my fibromyalgia and can't stay awake.

We have watched all 14 seasons of Heartland and are now waiting for Season 15 next month. We miss it. There's not much on TV or Netflix that we really want to watch. But I like watching something with Chris.

We put our clocks forward an hour tonight as daylight savings ends. I hope to get a better sleep tonight and I have decided to take some of Chris's Prednisolone if the asthma comes back.-it is an average of a week to get into a doctor up here.  

Ya gotta do what ya gotta do! Sometimes you have to be your own doctor! 



Friday 1 October 2021

Today was a washout.

 

We had an interesting day. On our way to the doctor and chemist, we found a roadblock because of the heavy flooding we've experienced these last few days. So we tried 3 other ways, only to find a police block on the third. The road has been washed away.

Our small township is cut off from travel at the moment, so we had to cancel. The receptionist got the doctor to ring us but it didn't do me much good as I was needing my blood pressure taken. More rain is forecast for the next 10 days. 

My orthopaedic surgeon for my damaged knee was cancelled as well. We are quite happy to stay home with 1400 new Covid cases today in Victoria including 22 from our area. I may not reschedule as I am determined not to have surgery as hospitals are best to be avoided at the moment. 

I have been shopping for extras in case of emergency, so it paid off today when we couldn't get out. I have plenty of medications in the house too. I am so glad I did some planning.

My only grumble was that we had to shower, dress and leave the house for nothing. My fibromyalgia pain is at a disabling level. I think the weather has caused a major flare. 

After dinner I will be getting back in my PJ's and taking a Tramadol and curling up with my electric blanket. At least the night won't be a washout. Today certainly was.

This is what met us trying to get out of our township.



Sunday 26 September 2021

Of fresh air and cats


I am a fresh air person. I can't wait for the opportunity to open all the windows and doors. The air, the smell of the new mown grass and listening to the birds and cows lowing make me glad to be alive! And like most of God's blessings to us: it's free! 

So today is freezing at the moment. (It's Sunday morning just before nine) Chris didn't sleep well, so I am keeping the house quiet. I am putting the oven on high and leaving the oven door down to warm the kitchen.

Soon I will take a cup of tea in to him and when he gets up I will cook an English breakfast for him. Bacon, eggs, tomatoes and baked beans with some toast. 

I managed to plow through those dishes yesterday but I didn't get around to putting away the washing. It sits on the empty side of my bed calling my name. I hope to get it today as we aren't going out. The chemist can wait until tomorrow. I have enough meds for today and the morning. 

Xena our cat hasn't made an appearance yet. She's sleeping in my side of the bed that's got the electric blanket on warm. Funny how cats always know how to look after themselves. But to be honest, she's helped me learn how to relax over the years. I love cats! 


Monday 13 September 2021

Finding beauty in a horrid day


I had trouble waking up this morning. My fibromyalgia has made me feel like I have been run over by a truck. However the day has not been a total loss.

I did a load of washing and now have to put it all away. I am not sure if I have enough spoons left for that because I also washed a whole stack of dishes and I am not sure if I have enough energy left to cook. 

I am still in my PJ's. I just might need to take a nana nap or rest at "the beach" so I can recharge. We will see...

The weather has been nice today and I left the back door open and listened to the birds and the stream running. The sun was shining on the water and the birds were calling and coming down to eat the seed and watermelon I left on the back porch for them.

It's important to try to find something lovely in every day, no matter how bad our fibromyalgia is to bring a balance of goodness and beauty in an otherwise horrid day.




Wednesday 1 September 2021

Life is good in spite of setbacks


I am trying to keep up with my home making duties. I have to do some dishes and clean my kitchen.. My knees are paining me so much today, that I won't be able to do much more. 

Fibromyalgia is back again and spoons are scarce. I am also psyching myself up to take a shower. Lucky we have a shower chair now. Funny how you don't think twice about it until chronic illness comes a'callin! 

With the brain fog, I get side tracked often too. Now I ask Siri to remind me to change the loads of washing over from washer to dryer. I need to find an app to tell me I have left stuff out that should go in the fridge or that I have nuked a night time snack and find it in the microwave in the morning hahaha

I am planning  on using  my slow cookers  a lot today.  I will be slow cooking the pork chops in a sweet curry sauce with  the rice.  I will be making some Jewish Penicillin in another slow cooker  and I will make  a chow mein in the other slow cooker for tomorrow.

After that, I plan to feed the birds and watch them eat...  sitting out on the porch under the apple blossoms on the neighbour's tree... it's the first day of Spring here in  Australia. Life is good in spite of setbacks..



Tuesday 24 August 2021

If I get those few things done


I didn't get some things done yesterday.  My spoons disappeared and I ended up taking a nana nap to ward off another fibromyalgia flare.

Waking up after a disturbed night's sleep, I realised that fibro has found me again. I have severe pain in my arms and neck as well as a newly diagnosed urinary tract infection. Hence the disturbed night's sleep.

In  spite  of  that,  I have a  few things I would like to do today.  I need to fold washing  which is easy as I can sit and do it. 

As I promised,  I will make some sultana muffins for Chris as I can reach it if I sit at our breakfast bar on the high stools. Same thing for dinner prep. Just a mixed grill for tonight.

Chris is  going to  change  my  bed and I  will wash  the  sheets  and anything  else in the hamper. With  my pain relief making me tired, that will be enough for today and if I get those few things done, I will be very happy.





Monday 23 August 2021

Living on a wing and a prayer


Before I injured my knee, I bought a food processor and I promised to make Chris some sultana muffins. It arrived Friday and I just unpacked it this morning.

I can't stand on my leg for long, but I think I can manage to reach the processor if I sit on my high barstool which graces our breakfast bar.

Whilst hoping to make muffins for afternoon tea today, I am hoping to make a sweet beef curry in the slow cooker for dinner. It feels good to actually have enough spoons to cook. My fibromyalgia flare seems to have gone.

Later on after dinner, I am going to take a shower as my new shower chair has arrived as well. I should be able to manage if I can sit down. I will time it so that Chris can be nearby in case I run into difficulties.

It was bad enough with a meniscus tear in the left leg without another one in the right now, however life goes on and it is possible to run the house seated. You learn to adapt.

My cleaning lady came today and the house looks nice. I had it tidy before she came so that all she has to do is clean and not tidy everything just so she can start.

I am hoping my knee doesn't require the Tramadol today as it makes me so tired that I won't achieve my goals in the kitchen.

I am mindful of every step I need to take so if I am careful, I should get away with just Panadol or Tylenol.  One thing I can't get away with is a quick prayer as I am literally living on a wing and a prayer.


Tuesday 17 August 2021

Wheelchair bound



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.

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.


Thursday 5 August 2021

Tomorrow may be better

 

So Friday night I developed a raging toothache. By Sunday I was so desperate for relief that I was seriously considering going to the ER at our local hospital.

I only had Panadol or Tylenol here and it wasn't helping at all. Waking up Monday morning, I rang the emergency department in our local dental hospital and they made an appointment for me that afternoon.

My tooth was cracked, exposing the nerve, so it had to be extracted. It was a difficult extraction and my jaw had to be planed down as it had jagged edges after the tooth was removed.

The dentist would not prescribe opiates for pain relief and told me to see my doctor. Fortunately for me, he did a phone consult and left a script for Tramadol for us to pick up. Chris got it dispensed for me and it was a life saver.

With my knees both paining me and a fibromyalgia flare brought on by the extraction, I felt like I was drowning in pain. So yesterday I spent most of the day in bed.

Today, I have a lot of dishes to wash and owing to how I feel, it will be the only job I make myself do.

I will make some Jewish Penicillin for dinner tonight and we will have a salad sandwich for lunch.

Hopefully tomorrow will be better.

Monday 19 July 2021

More than enough to do


We are on a snap lockdown.  I need to get some prescriptions filled.  Also I have some mail to pick up at the post office.

Apart from essential services such as post and chemist, everything else is closed or people are working from home. 

This is our fourth lockdown  this  year and  is mainly because  people  are not following protocols when they have been interstate. Oh well, as the young ones say, it is what it is. 

I  have dishes to do,  a  load of washing  to fold  from the dryer  and cook dinner.  After the chemist and post office. 

The way I feel today with my fibromylgia flaring and back pain,  it will be more than enough to do...

Thursday 6 May 2021

Just keeping my head above water

 


I have copped a double whammy with both a flare of my fibromyalgia and polymyalgia rheumatica.  The pain and fatigue are overwhelming.

No doubt this was caused by Chris's diagnosis of heart failure, my daughter's impending leukaemia specialist test results, my grandson going to prison and the pain this has caused to us as a family.

I am feeling extremely unwell and was hesitant to take the Prednisolone my doctor ordered, but after a phone consult with him today, we discussed the risks v advantages and decided the risk was worth it.

Although I am feeling exhausted, the Prednisolone has given me a high that precludes going to bed for a nana nap. I have just sat up in the loungeroom watching and feeding the birds.

I have a sink full of dishes to do but no energy to do them. The only reason I am blogging now is that I am sitting and it takes very little of my limited spoons.

Recently, adapting to our new normal, our dryer was placed on top of our front loader washer and this has helped me so much with not having to stoop too much with my sore back and hips.

If I was well, I would have hung the washing out to dry as the last few days have been lovely warm autumn days here in Australia. But I have to use the dryer as I can no longer peg the clothes out or stretch my arms above my head.

When I finish talking with you, I am going back to my couch aka "the beach".  I will be doing steak, chips, eggs tomatoes and baked beans for dinner. 

Spiritually I am doing fine, it's just the physical that pulls me down- and I am exhausted just keeping my head above water!



Monday 26 April 2021

It is what it is!


Many of you will know that my husband, Chris is facing serious health issues. He has recently been diagnosed with heart failure.

With fluid on his lungs, he feels like he is suffocating when he lies down, and so he sleeps sitting up in the recliner.

The fluid tablets don't seem to be moving much fluid off his badly swollen legs and feet either. His feet are so swollen that no shoes will fit him.

I was able to buy him some orthopaedic slippers that come apart and are fastened around the feet, ensuring a comfortable fit. They are quite warm as well which is a bonus in our autumn chilly mornings here.

We have many cardiologist and doctor appointments and tests in the coming weeks and  it really effects my fibromyalgia badly. But we keep on keeping on because we don't have any choice.

After a day out for medical appointments, I am usually running on no spoons and that is when Chris looks after me.

He makes me a cup of tea and turns my electric blanket on. He encourages me to rest and chooses an easy slow cooker meal for dinner. I usually cook that on the day whilst we are out.

I allow Chris full reign of what he wants to eat as his appetite is not as good as before he got sick. So you will find us discussing menus the day before.

I do all organising for his appointments, ensure his medications are made up, sort them out for the week and drive him to said appointments if he doesn't feel up to it.

He in return guards my health and makes sure I get uninterrupted sleep as I don't sleep soundly due to fibromyalgia pain.

In line with this, we now share separate bedrooms. Our marriage is as strong and loving as ever, but due to illness we both have found we sleep better apart.

It wasn't what we really wanted, but it is just part of our own new normal. We still sit together watching TV and we hold hands all the time. But with health issues causing insomnia, it is the only way we both can help each other. It is what it is.


When thou liest down, thou shalt not be afraid: yea, thou shalt lie down, and thy sleep shall be sweet. Proverbs 3:24a