Manfred

Nov. 1st, 2024 05:11 pm
watervole: (Default)

 I just had a horrible shock. The Physiotherapy centre in Broadstone just phoned to say that Manfred no longer works there and would I like to book someone else for my appointment next week?

No, I blooming well don't!

They won't/aren't allowed to say why, but it has to be one of two things - either his mother (who is frail and elderly) in the Netherlands can no longer cope.(though I thought they might have told me if that was the case), or he's fallen out with the new owners of the practice.  It changed hands a couple of months ago.

I'm currently searching the Internet to try and find where he will be working, if he's still in the UK.  He has an inactive Facebook page (but I'm trying to message him just in case he ever checks there ) and I've found a place in Wimborne (local) which has his name on their books - so I've left a message on their answerphone.

Fingers crossed, the man is a miracle worker. Won't give you social chit chat, or run loads of tests - just listens to you saying where it hurts, then proceeds to massage in a totally different place.  And magically, the pain goes away.  Referred pain.  Tension in one area causes pain in another.  I think he just has an incredible knowledge of anatomy, combined with fingers that can detect tight muscles.

Trained at a university in the Netherlands - they must do damn good courses there...

Back again

Oct. 27th, 2024 09:01 pm
watervole: (Default)

I haven't been here for a while, becuase  I had horrible sciatica.

I'm pretty much a sciatica specialist this days...

I've had identical pain in the leg (If you've ever had sciatica, then you'll know just how painful this is.  If you haven't - I hope you never do) caused by multiple causes.  Pressure on the sciatic nerve from a herniated disc in the spine, an inflamed bursa pressing on the nerve, and a tight piriformis nerve pressing on the nerve.  Only an expert can tell which cause it actually is, and even they may need an MRI scan to confirm it.

Thank heaven, I know a really good physiotherapist...  Manfred had the right diagnosis when I had bursitis, and I trusted him enough even than to see a second doctor when the first one insisted it wasn't bursitis.  The second doctor (I find young doctors are useful when you want them to accept a physio's diagnosis) agreed.  I arranged for a jab in the bursa (can be done in a doctor's surgery) which removed the pain in around 60 seconds...

Manfred was away when I first went down with pain this time (he goes to the Netherlands a lot, as he has an elderly mother who needs help), so I saw three other physios who all agreed that the problem was a herniated disc in my spine pressing on the sciatic nerve and giving me horrendous pain in my leg.

I wasn't surprised, as I've had that before, and was successfully treated for it with an epidural injection in the damaged disc - which was a magical treatment that made half a year of pain vanish in about 60 seconds.  I joined the waiting list for an MRI scan (long) and went to see Manfred when he returned in the hope that he could help a little.

I hobbled in with my walking stick, couldn't walk without it at that point. I expected him to say 'Herniated disc' He didn't. Well, I trust him.  His diagnosis was a lot of very tight muscles in my back (caused by sleeping on very uneven ground while fighting the Civil War - faulty airbed - carrying heavy boxes, and a very long train journey.)

That session reduced the pain enough for me to ditch the walking stick, and weekly visits since then have improved thing much more.  I'm back dancing again. Still a little bit of progress to go, as there's some tightness to exercise/massage out, but I can now sit down long enough to play a board game and write to you all.

Basically, if other experts disagree with Manfred, I'll back him every time!

I've said a massive thank you to him.  My first grandson will be born sometime in the next three weeks. I now know that I will be able to sit and cuddle him, walk round carrying him, and smile at him without pain.

There is no greater gift.

 

Back again

Feb. 27th, 2024 02:23 pm
watervole: (Default)

 Apologies for the long hiatus.

As some of you may recollect, I broke two bones in my foot, seven and a half weeks ago.  Which made getting to my desktop computer difficult...  It's in a corner of our office and is hard to reach on crutches, or when you have to shuffle sideways past  a chair to reach it.
I have a tablet, but I normally touch type, which isn't possible on the tablet, so no posting.

Plus, I went down with flu just as the foot started improving.

However, I think I've come out pretty well overall. I can now go on a walk for about 15 mins. I'm tired when I get back, but the foot isn't aching too much.
I can do a little bit of morris dancing - tried for the first time last week. (The physio amazed my by saying I was okay to try step-hops)  I can't cover any distance yet with a step hop, but I did manage to get -badly- through the entirety of two dances.
Went sword dancing last night (which is slightly less demanding on the leg muscles, but requires really good balance for some moves) and had a blast. I chose to walk sedately through a spin move, and sat out of a dance that needed fancy stepping, but still got in a decent number of dances.

Not bad for a 65 year old with mild osteoporosis!

I'm making a note here of things that I think helped me to recover reasonably quickly, in case I break it again.

0.  If you think you have a really bad sprain or a break (I thought it was a sprain originally), then remember RICE

Rest - two of my fellow dances helped me to a chair and I didn't even attempt to put foot to floor.
Ice - A team member managed to locate a frozen drink in the freezer, so we used that to keep the injury as cold as possible.
Compress - Ankle bandage, as soon as possible. Crepe bandages are best, but you can use all kinds of things in a tight corner.
Elevate - We got another chair, put it in front of mine, and rested the foot on that.

Common sense - after checking her insurance was good, another team member drove me home at the end of the evening.

See the doctor!  The doctor diagnosed the fracture and had me off to the fracture clinic the same day.

Post diagnosis...

1.  Be reasonably fit to start with - I morris dance, sword dance, and try to for a daily walk if it isn't raining (that last was difficult this last winter...).

2.  A really useful exercise to do on a daily basis is to stand on one foot for 30 seconds every day. This really improves your sense of balance and also strengthens muscles around the ankle.  I've been doing this for years, and it was on the hospital's list of exercises to do daily once it was safe to put weight on the foot again.  I found it very easy to start up again, and it helps reduce the time between the fracture being healed, and being able to do normal activities again.

3.  Read the information provided by the hospital.  Re-read it at least once a week.  Do what it says!

4.  There are useful things you can do that aren't on the official list - I checked with the hospital fracture clinic (who give their contact email address and phone number so you can ask questions without needing an appointment at the hospital) - things like lying on your back and doing cycling feet, or going swimming, are fine.  Basically, any exercise that is not weight-bearing is likely to be safe in the early phase after an ankle break. The benefit of this kind of thing is that it reduces the risk of muscles atrophying and also helps keep your blood moving while giving your heart and lungs some exercise.
  (I was really surprised to find that I could swim gently for half an hour with hardly any difficulty at all. I was harder to get to the pool on crutches, than it was to swim. I had to use different swimming styles, but basically, it's not about elegance, just about keeping moving.

5.  I found the official walking boot didn't suit me very well.  I used it when outside the house, but indoors, after the first few days, I generally went barefoot and used the crutches.

6.  Never put more weight on the foot then is comfortable.  A mild ache is okay, anything else is not.
I have a tendency to try and overdo things.  This is not good when it comes to broken bones.

7.  Keep moving.  Don't sit down all the time.  It's not good for you.  Even if it's only to lie down and wave your legs in the air, or hobble to the kitchen and back on crutches, try and move a little every half hour or hour.

8.  Keep in touch with your friends - social contact is important. I kept going to dance practice - courtesy of lifts from friends - I just shifted to playing the concertina rather than dancing.

9.  Be married to the most wonderful and helpful man in the world!  (I'm very lucky, and I know it)


 

watervole: (Default)

 I'm making good progress on the ankle. Nearly four weeks since I broke it, and I can now walk round the house (albeit slowly and carefully.) without crutches.

Swimming is definitely helping - my leg muscles are still reasonably strong, and the foot is far more flexible.

It also looks as though my long-term habit of trying to balance for 20seconds a day on each foot has also had a long-term pay off. (Thank Michael Moseley's 'Just one Thing' podcast for that tip)  It reduces your risk of falls, by improving your balance and strengthening your ankle muscles.

One of the official  post broken ankle exercises is to do this for 30 seconds per day, and I can already do it without holding onto a chair. The next aim will be to try and do with with my eyes shut - which is much harder. 

My morris target is to remain firmly with the band this week.  Next week, and probably the week after, I may try walking through one or two dances.  Trying to actually dance again is on hold until I've definitely got full muscle strength, balance, etc. back again.

Sword dancing will probably be viable a couple of weeks before morris dancing is, though I'll have to be careful as to which dances I attempt. Some are much easier/safer than others, so they will be the ones I try initially.  And certainly none for the next two weeks.

So what am I actually doing?

I'm repairing tatter jackets. I'm 'ragman' for Anonymous Morris, so while I'm unable to get out much, I'm taking costumes one by one and tidying them up and doing any necessary repairs. Some of the older ones are being tarted up a bit ; some will have new tails added as dancers have grown taller.  

This is what the tatter jackets look like.

May be an image of 6 people, people dancing and crowd

 

watervole: (Default)

 The most irritating thing about moving around on crutches is that you can't carry anything.  

Want to read a book?  The reading part is fine, but I still need a crutch in each hand - fortunately, I am married to a marvellous man who is willing to go and pick things up for me!

I'm making reasonable progress on the foot.  The swelling is going down - probably won't be gone entirely for a couple of months, but it looks a lot better than it did two weeks ago.  I've still got some very interesting coloured bruising, but nothing like the initial balloon.  I've got a large beetroot coloured splotch on the instep which is fairly tender - I suspect there was some muscle damage there, as it's actually more painful than the two fracture points!

The beetroot blotch makes it too painful to wear the support boot, so I've been going around barefoot at home (luckily the hospital physio confirmed this was okay).

Added  few days later..

 

It's now three weeks since the accident.

My metatarsal is healing slightly slower than predicted, but I think the ankle is healing slightly quicker.  I'm still using the crutches if I'm moving around the room or between rooms, but I can do one or two very basic Tai Chi routines without the crutches. The big advantage of Tai Chi is that all changes in balance are very slow and controlled. Thus, I can control exactly how much weight shifts onto the injured foot.

The most unexpected thing is that I'm sleeping far better than normal.  I have to sleep in a different position than normal in order to have the injured foot on top, but because I'm finally free of the various problems that were causing pain on a pinched nerve in my leg (sciatica type pains have at least three different causes - and I've had all three in turn over the last few years).

Hopefully in a few more weeks, I'll be able to walk through dance moves, but step-hops will probably have to wait a bit longer, as they put far more stress on the joints.

I'm going to attempt what I suspect will be a very short swimming session tomorrow - I did a test run yesterday, so I know I can get up the entrance steps on crutches, use a lift to the lower floor, get my shoes off in the changing room and use crutches to get to the pool.  So, back tomorrow, for the quietest swimming spot of the day (8:30) and we'll see what my body thinks of non-weight bearing exercise that moves the joints in different directions.

I ran both swimming and the Tai Chi past the physio at the hospital - just in case you're worried :)

 

 


 

watervole: (Default)
 Fifth metatarsal shaft fractures

Fractures to the shaft of the 5th metatarsal are often referred to as "dancer’s fractures.

No prizes for guessing which morris dancer currently has her foot in a air boot... (Looks rather like something you'd wear to walk on the moon...)

Apparently, the fast spins in dances put a lot of strain on the long thin bone between the little toe and the ankle. That's the 5th metatarsal.

I went over trying to correct a turn where I realised I was going the wrong way. Fell (not sure if it was before or after I broke the bone) and hit the floor (albeit with a slight reflexive roll.  I assumed I'd sprained my ankle, and as I had a very bad sprained ankle five or six years ago, I did everything right this time.  I'm glad to say that I didn't try to walk on it.  With the help of my wonderful fellow dancers, I got to a chair (Rest), found a bottle of some kind of drink in the freeze compartment of the fridge in the hall) (Ice), raided the first aid kit for a bandage (Compression) and propped my foot up on a chair (Elevate) RICE

Got to the doctor the following morning, who suspected an ankle fracture.  Down the hospital at 2pm, through X-ray and various other departments at truly amazing speed - it was a quiet time of day, and we didn't need anything major, but had a diagnosed break from the X-ray. But 4pm, we were heading for home with air boot, crutches, instructions and the assurance of a follow up appointment next week!

And lovely friendly staff throughout.  When the NHS works well, it can be like magic. (I hope our next government will help the NHS work like this more often)

 

So, I've been spending a lot of time with my foot raised up on a pile of cushions on top of a stool, and icing it. I'm allowed to take the boot off when icing and also in bed.  I'm allowed to do a little bit of walking, but no more than a few minutes at a time.

 

It should heal up without surgery as long as I follow orders, but I'm probably looking at 2-3 months before normality.  I'll be able to walk on it quite a while before it will be safe to dance on.  I see physiotherapy in my future, but I've had lots of practice at doing what physios tell me :)

 

 

 

 

 

watervole: (Default)

 I'm actually gaining on all the health problems now. And I promised I'd tell you all what I found helpful.

Realising that the far worse than normal asthma of the last few months was probably due to stress was the key in this case.

Over the course of a couple of weeks, I focused on tai chi, meditation, gentle walks, etc. (and also just telling myself that I was caught in a vicious circle where being unable to breathe was triggering panic attacks which were making the asthma worse, etc.)

The asthma is now back to its normal level for this time of year.

I've still got some remaining stomach pain, but it's not nearly as bad as it was, and googling suggested that IBS was a strong possibility. I've had irritable bowel syndrome before.  It's essentially caused by stress - so no surprise that it's responding to the same treatment I've been giving the asthma.  It always vanishes when I'm dancing... (ie. when I'm happy and distracted)

Things that helped:

1.  Tai Chi, Leia Cohen in particular.  

She has several 5 minute tai chi videos on YouTube - this first one is now upto 13 million views...

 

I subscribed to her app a year or two ago, and have found many useful videos there.  I use one most days. There are some that are especially helpful with hip problems, great for people who spend too much time sitting down. (helpful for piriformis syndrome too)

2.  Meditation

I use Insight Timer - This site is free and has thousands of guided meditations on many subjects and also relaxation music.  I have the paid version purely becuase it was so massively helpful when I had depression five or six years ago that I would gladly have paid them far more than the annual fee in gratitude. (You get some handy bonuses with the paid version, but the free version is still fantastic)

3.  Dealing with pain

When my sciatica was really bad, I got some help from Curable (I had the operation on my spine not long after, so didn't get to test it on to the full, but I did find it helpful enough that I've kept the app, though I may drop it soon as I've memorised the best bits)

It's essentially a brain-training technique. I read about the technique in New Scientist and went searching for a site that used the technique. In very simple terms, the brain can become conditioned to respond to pain in certain ways.  This means that it sometimes continues to send strong pain signals in situations where they are not helpful.  (phantom limb syndrome is probably the one most people will recognise.)

But the brain can also turn off/reduce pain signals in some situations.  If you're running from a tiger, the pain in your hip is unlikely to stop you...

What the app does is to help you tell the brain which pain signals are too strong. eg.  Sciatica...

I find the 'helpful assistant' on the Curable app to be incredibly annoying, but there are some very good exercises in there and I found them helpful.

watervole: (Default)

 I'm pretty much free of the pain from sciatica/bursitis/piriformis now.

The next stage, which is proving harder than anticipated, is to regain all the muscle strength that atrophied away when I was having to lie down nearly all day.

I've made progress, but I tire horribly easily, and I always have muscle aches the next day after any serious exercise.

But, on the positive side, my balance is fully recovered.  I can stand on one leg for a full minute of a Tai Chi exercise and both legs are good for that.

I can swim for 25 mins (even if I am wiped then next day) and my speed is picking up. I can believe that I will be back at my normal swimming speed (which used to be faster than 80% of the other people in the pool) before very long.

I can do 15-20 mins Tai Chi, but 40mins is way beyond me. (I did that class on two separate days - I use Leia Cohen's "Tai Chi 5 minutes per day" which I recommend highly.)

I can go for a 20 min walk, but start flaking out after that. (But as Richard says, it's a vast improvement over struggling to walk across the lounge!)

I'm doing some very light weight lifting with hand weights. (Lighter than the smallest handweights at the gym, which were too tiring)  I have horrible bingo wings.

I'm also working on my mental health, which took quite a bash when things were at their lowest.  Feeling completely useless is not good for one's self-confidence....

I'm starting to settle into a pattern (forcing myself to remember to do it even on days when I don't really want to) of meditating for 10 mins a day.  There's a very good app called 'Insight Timer', though I sometimes meditate without the app when I'm in the flow.

I shall go and do it now while I'm thinking about it...

And I shall try and write more often here to share other things that I've found to help both mental and physical health.  Some are quite trivial, but they nearly all seem to be helping and hopefully may be of use to others.

 

 

 

watervole: (Default)

 I'm gradually gaining on the bursitis

(I don't think that cut tag worked correctly, can someone remind me how to use them....)

 

Mostly boring health stuff )

The injection a couple of months  ago in the bursa in my left hip definitely helped.  It meant I could sit down for about half an hour, which was a vast improvement on nothing!

And gradually making further gains.  The big catch was that every time I overdid it (I was able to walk for five or ten mins, which was good, but if I walked too far or tried swimming front crawl as I would normally do with  straight legs, then that could trigger intense pain behind my knee), I lost about three weeks of progress.

I was still having to lie down on the floor cushion for a fair chunk of the day, and to sleep on my right side at night - which means it's no surprise that I eventually developed bursitis in the right hip...

I got a steroid jab in the right hip bursa about a week ago, and that does seem to be helping further.  It's taken about a week for the right hip pain to mostly die down.  He didn't want to do two hips at the same time as that uses a lot more steroids (I already have osteoporosis and steroids are not good for it...)

The effect has only kicked in gradually, but it's definitely there. I suspect the right hip pain was affecting the way I was walking as I've noticed an improvement in the left leg pain even though that didn't get injected this time around. 
Bursitis can cause sciatica. The inflamed bursa presses on the sciatic nerve, causing extreme pain down the leg.

My walking range has now improved to about half an hour.
I'm able to swim more too.  Did 20 minutes earlier in the week. Went for half an hour today, but that turned out to be too much.  It's evening now, and my left hip is still very painful.

it's just a case of finding the balance. More exercise is good overall, but I need to scale it up very gradually.  The long term aim is to be able to drive again, but I don't think I'm ready to try that yet. Car seats are soft and tend to trigger pain quite rapidly.

 

 

watervole: (Default)
 Interestingly enough, I'm now thinking twice about the iron tablets.

Following up on a couple of comments people made, I decided to do a bit more reading.

Liquid iron supplements can stain the teeth, but not tablets, so that wasn't an issue.

However, the interesting question is the causes of iron deficiency.

I eat a diet with a reasonable amount of beans, green veg (veg box and allotment), brown rice and a small amount of red meat, so should have enough.  Therefore, it was either the pain from the pulled chest muscles that was causing the tiredness, or, if I am actually anemic, there is probably an underlying cause.

In people over 60 (and I'm on the good side of that by fewer years than I'd like...) one of the potential causes of anemia (once you rule out several that are unlikely to be me) is bowel cancer.

My mother-in-law died of bowel cancer that was diagnosed too late.  She was diagnosed as anemic and put on iron tablets for a couple of years, but it's clear from the NHS website that she should have been tested for bowel cancer at that time.

I would be extremely angry about this, except for the fact that she had gone blind.  Her quality of life had dropped dramatically and she was bored to tears.   She had an active mind and was no longer able to read the book she loved, do her cryptic crossword or even garden reliably.  I nearly cried when I realised she'd planted half her cyclamen upsidedown.  Her garden was her life.  The cancer gave her an escape from a life she no longer wanted.

(brief pause while I cry.  It's eleven months since Molly died and I still miss her.  I have many of her plants growing in my garden and I tend them with loving care)

Back again.  To cut a long story short.   I should stop taking the tablets and if I find I'm getting tired again, I should visit the doctor and get a blood test to see if I'm actually anemic, and if I'm actually anemic, whether there is an underlying cause.

So, let's do this scientifically.  

I'm going to stop the tablets today and see if I continue to improve.


watervole: (Default)
 Fingers crossed,  I seem to be getting better.

I've had a lot of problems since my last bad asthma attack  (you have to be me for a bad asthma  attack to be an automatic forerunner to pulled muscles)

Firstly, the weather is getting warmer and that means fewer people burning wood in their stoves, so that pulls the air pollution down a bit.

Second, the pulled muscles are healing up - stretches help, and I'm now well enough to start exercising to build up my strength again.

Thirdly, I've been trying iron tablets to see if they help with the feeling of total exhaustion - I know I have low iron levels as I frequently got turned down as a blood donor (though I was told that I wasn't anemic at the time).  They may be helping, or it may just be the reduction in pain that's making me feel more energetic.

I managed three dances last morris practice (at intervals, not one after the other), before feeling wiped, and that's better than I've managed in quite a while.

I'm also making progress in the garden.  Several beloved plants are being rescued from a sea of ransoms or celandines.

Leg pain

Feb. 17th, 2013 05:51 pm
watervole: (Default)
 I'm hoping someone on my flist will have a suggestion that may help as this pain has been ongoing for weeks now.

I had very bad chest around the Xmas/New Year period and had to pretty much give up any kind of exercise as even walking made me feel as though I was being shot in the chest.

That's gone now, I finally found a way of dealing with it (vicious massage of what was clearly a pulled muscle of some kind)

The hard part has been getting fit again from an almost zero baseline.  I've now got pretty much back to normal again, I can swim fast, do my normal gym workout (though it still leave me wiped), morris dance and walk for a couple of hours.

The real problem is that I can manage the exercise without pain, but about 5 mins after I stop, I get severe pain in my left thigh.  The pain can last a whole day and nothing seems to stop it.  Stretching helps a little, but only a little.  If I go through my warm up routine, the pain will reduce for a few minutes, but then it comes back again.

After a day with no exercise the pain will have reduced, but I don't want to become immobile again!

Can anyone suggest (the doctor had no ideas) why it doesn't hurt until I stop exercising?

Cold makes it even worse, but heat doesn' t make a lot of difference (tried hot water bottles)

Working on the computer is really difficult, because the leg gets really painful after a few minutes stilling down.

I'd really like this pain to be gone by Redemption, or I won't be able to sit down for any programme items!

Help !  All advice welcome.

Omeprazole

May. 4th, 2012 04:06 pm
watervole: (Eeek!)
 Omeprazole is a medication for heartburn.  One of the common side effects is stomach pain.

And when I say stomach pain, I mean really crippling stomach pain that takes days to go away after you stop taking the tablets..
watervole: (Default)
I may not be posting much for a while.  The elbow pain is bad again.  I pretty much know what's triggering it.  Driving, concertina playing and stress.  Driving while stressed is probably the worse.  I don't have to do it often now Henry's learning to drive, but I need to occasionally.

The unemployment thing is the biggest stressor by far.  We're into the third month now and from past experience, I know it can get a lot worse than this.  I can feel my stomach muscles starting to tense up - I hope the IBS isn't going to make a return.  I remember that from the last long stretch of unemployment.

Anyway, typing isn't as easy as I'd like.  I'll be doing all the  stretches and exercises - they stop the pain from progressing past a certain point and they stop all the other muscles going as well, but they don't totally cure it. 

The good news is that Richard's being very active on the job-hunting front.  He's following multiple lines of attack on the job-hunting front, and doing a astrophysics Phd in between the job research to keep his morale up.

Here's Richard's Linked In profile.  
"A highly experienced and creative system, network and software engineering specialist. Key ability lies in problem solving in the most demanding technological environments within critical time and budget constraints. Profound analytical and trouble-shooting capabilities are combined with knowledge of a wide range of techniques to solve apparently intractable technical problems. Solutions are communicated imaginatively with clarity and precision. Seeking a senior technical role in a high technology environment where the application of smart and innovative technical solutions can make a substantial difference to the bottom line. "

watervole: (Toothache)
I think I'm starting to defeat the tennis elbow, so I'm going to record here what's working, so that I'll be able to look back to it in the future if I get a recurrence.  We're not totally there yet, but there's a significant reduction in pain levels since two weeks ago.  I'm now starting to try and rebuild the muscles that have vanished in the two months I've been unable to use my arm.  The trick is to do that without setting off a fresh bout of tennis elbow...

1.  Do stretches.  In particular the one given me by the physio which basically involves crossing wrists, bending my hands forward, interlacing fingers  and then twisting the hand  of the sore arm round in an outside direction as far as it will go.  Hold for 30 seconds.  Do three sets three times a day.

2.  Do no lifting or twisting motions with bad arm.  Also avoid actions that need you to hold onto something with a strong grip.  Especially avoid opening jam jars, turning door knobs, knitting, washing dishes, concertina playing, weeding and sewing. Minimise computer use.

3.  Find the sore tendons joining the elbow.  Massage them several times a day.  Find the muscles attached to them and massage those too.  They will be sore before you massage them and easy to find with probing fingers.  Follow the sore muscles all the way to wrist/shoulder and massage every bit that is sore.

4.  Do all arm exercises that do not trigger elbow pain (so as not to let the rest of the muscles atrophy)

5.  Once elbow pain subsides, start (with no/minimal weight) doing the arm exercises that trigger the elbow pain.  Especially the one using the wrists to raise and lower weights with the palms down and the elbows at right angles.  Very gradually increase weight over time. Do three sets three times a day. If muscles ache continue.  If elbow pain recurs, immediately reduce weight to a level that does not hurt.  Carry on doing this for three weeks after elbow pain is gone.  Go swimming, but stop if elbow pain (as opposed to muscle ache) starts.
watervole: (Toothache)
Sometimes, I hate recovering almost as much as I hate being ill.

I had flu and the after-effects of that for nearly three weeks, then a chest infection before I had a chance to get back to normal.

The net result is that I'm tired all the time and my muscles ache.  (and I've still got catarrh in my lungs and a nasty cough caused by that)

Still, at least I'm mobile again.

Now I've got to start the long hard slog to getting fit again.  I have a very strong incentive.  If I don't get fit in the next few weeks, my asthma will get worse, my knees will start to hurt and my shoulder trouble will get worse (it's playing up already).

So, gentle swim Tuesday.  Very gentle gym class Wednesday (body balance, which is basically slow stretches and balances).  Walk to Post Office Thursday.  Gentle half-hour walk on the heath today - that's left me feeling totally exhausted. 

Maybe I'll try a short walk tomorrow or another slow swim.  I need to work the shoulder muscles and I'm not yet ready to tackle my normal routine on the stepper and the rowing machine.

I'll get there, but it's going to be a slow process.
watervole: (Toothache)
Down with the lurgi again, though at least it's only a cold rather than flu.

Nose streaming, eyes watering.

One contrast I'm noticing with the flu is that I really didn't want to eat much when I had flu, whereas with the cold I still feel grotty, but I want to eat.  I wonder if there's any truth in the old adage about 'Feed a cold and starve a fever' and if there is, what the biological reason for it is.
watervole: (Toothache)
One of the hardest things I find about taking a steroid course for asthma is coming off them afterwards.

The side effect I generally notice is muscle weakness (though this may also be due to the fact that I've been ill).

The catch is, that it's hard to tell shortness of breath caused from asthma apart from shortness of breath caused by the lungs being weak after illness and steroids.  Thus, this tends to be a time when I'm never far from my peak flow meter.

I went swimming this morning (imperative after being ill as I need to build up the lungs again asap).  I'm now pretty breathless, but my peak flow meter tells me that my lung function is actually only 30 points below max (ie.  Well within what I'd expect on a normal healthy day).  The feeling of being out of breath is actually a result of my body not having had a decent work out in over a week.  The lungs are tired after exercise, rather than actually asthmatic.

Without the peak flow meter, I would have assumed it was asthma and taken more medication.  (yesterday, the same sensation WAS asthma and I did use the inhalers).

I'm planning on cutting the steroids by 10mg a day (took it down by that much this morning), seeing how much salmeterol I need to maintain lung function, and using that as a guide to see if I can keep stepping the steroids down.

And I'll need to get some form of active exercise every day for at least the next week.
watervole: (Bloody Torchwood)
I can hear the fireworks starting and I'm a little bit nervous.

I'm indoors, which will help, but I'm already on pretty much the  max medication I can take, because of the flu.

The two worst asthma attacks I can remember were both on New Year's Eve and triggered by firework displays.

Fingers crossed.   We don't usually get many fireworks in the village.

It's quite possible that the steroids I'm already on will prevent any problem.  Here's hoping.  (and it'll be useful data for the future if they do)

My mind's mostly with Anonymous Morris.  They've danced out a few times before, but this was our first really big event.  I'm so hoping it all goes well.  (But  I would in no way be helping them if I was there and collapsing on the spot - which I would be.  One has to be realistic.  I'd be a distraction, not an asset right now)

They're all good people.  They'll do fine without me.  (Though I do hope the band are okay.  Our new band members have only been with us for two weeks and that's not long to get confident with all the tunes.)
watervole: (Toothache)
I'm definitely past the worst.  My body temperature is stabilising now.  No hot or cold sweats today.  Still very tired, but more able to move about the house.

The asthma is holding steady (but only because I'm taking max salmeterol and the steroid tablets).  I'm not needing to top up with ventolin today, which is good.  I took so much yesterday that I was getting tremors from it.  I'm almost shaking from the salmeterol alone, but not quite.

I'll keep taking the steroids until I the asthma is stable on half the salmeterol dose I'm taking at present.  (Or the tablets run out.  I've only enough for a four day course, but that should be enough)

Modern medicine may have some problems with side effects, but by Golly, that's massively better than being collapsed on the floor unable to breathe.
watervole: (Toothache)
There are times when you have a bad cold and you think you have flu.

Then there are the times when you actually have flu, and you remember what the difference is.

This is one of the latter occasions.

I started shivering Tuesday evening (even when wrapped up in a cloak and a blanket on top of three layers of clothing).  Since then, I've been through the hot spells, the cold spells and, increasingly, the wheezy spells.

This is why I got a prescription for steroid tablets from the doctor a month ago.  I didn't need them then, but I knew that if I did this winter, I would be feeling far too crap to go to the doctor.

I can't use inhaled steroids - which are the standard preventative treatment for asthma.  This means that when an infection goes to my lungs, I'm in real trouble.  The only recourse I have is massive doses of bronchiodilators (I'm at max now) and short courses of steroid tables.  I don't like the tablets, the side effects include really nasty insomnia, but I don't have much choice.  My peak flow is way down and the slightest amount of effort leaves me coughing and wheezing.  So, I'm now on the tablets.  (It's only about one year in four that I get an attack this bad)

Annoyingly, this means I'll have to miss morris practice tonight.  I hope the new musicians can manage without me...  I'll probably have to miss the dance-out tomorrow which is a real bind. I'd been looking forward to this one. It's the big firework night on Poole Quay and Poole Tourism asked us to dance for it.

I was already planning on taking extra asthma medication to cover myself against the fireworks (I've had some very bad reactions in the past).  But if I'm on maximum dose now because of what the flu has done to my lungs, then I've no higher dose that I can go to.  

I want to be there very badly, but I also don't want to end up in hospital.  (Been there, done that)
watervole: (Toothache)
Another couple of days with a high fungal spore count.  This is really starting to get to me. My chest feels tight a lot of the time.  I've tripled my normal dose of asthma medication and the side-effects are starting to kick in now.  I'm finding it harder to sleep.  It's a choice of feeling tired from the asthma, or tired from the insomnia caused by the salmeterol.  And as the tiredness kicks in, it gets harder to exercise, which increases the chance of setting up a vicious circle in which the asthma gets worse overall.

I hope to goodness it eases up soon. Apparantly this has been a really good Autumn for fungi.
watervole: (Toothache)
Something has been badly triggering my asthma this last week or so. Particularly in the last couple of days.  I'm taking way more medication than usual and still feeling wheezy.

I suspect the cause is fungal spores of some kind.  Grass pollen and weed pollen don't give me much of a problem, but I notice that one of the sites (Zirtek) that lists fungal spores is giving a high count across most of the country at present.

My asthma is always worse in winter.  I need to start going to the gym more often.  My maximum peak flow isn't bad at all, around 490 today after ventolin, but that will fall over the winter if I don't keep up the exercise.

Over the years, I've found the best thing for my asthma is to maximise my lung capacity so that I can better cope with losing some of it to the asthma.

It's probably time for another dust blitz as well. Dust and dust mites are a known allergen for me, and they're always worse in winter as well.  A really good house cleaning can make a surprising difference.

Knees.

Jun. 23rd, 2010 07:34 pm
watervole: (Toothache)
My knees are killing me.  I'm not exactly sure why, but they got bad on Saturday (when I was dancing, but not excessively so) and I can barely walk at present.  I can cycle to some extent (uses different muscles and isn't weight bearing) but standing is very painful.

And it's the Quayside Cloggies 25th anniversary tour/party this weekend.  Unless things improve, I'm going to have to miss it.
watervole: (brocolli)
I've had a suspicion for a long time that sugar and highly-refined foods are probably the biggest factor behind obesity (more so than fat).  This research seems to confirm that.

I stay at a comfortable weight by the simple tactic of choosing wholefood options (brown bread/rice/pasta instead of white), beans, plenty of veg, etc.  I eat far less meat than most people, but still include it in several meals a week.

I try and avoid anything that contains sugar.  That means eating on of the very small number of breakfast cereals that don't contain sugar (watch out for crystallised fruit that several brands now slip in in order to try and make you think there's no sugar when there is).  Dorset Cereals muesli, and Grape Nuts are the usual ones at present.  (they started adding sugar to my previous brand).

I don't buy or make cakes (but the occasional slice when out for an afternoon is okay - this is a lifestyle, not a prison).  I eat small amounts of chocolate (a couple of squares of Green and Black each day), and that's pretty much it on the sugar front.

I've stopped eating things like baked beans and other similar tinned foods.  The sugar content has risen so much that I now find them unpalatable.

Cheese is wonderful, and we eat all kinds of varieties.

If I had to offer just one tip for a healthy diet, I'd say to eat nothing with sugar in it.  (and no artificial sweeteners either)
watervole: (allotment)
The vertigo has eased off a lot recently (fingers crossed) and I'm able to do a lot more.  My wrist (that I hurt five or six weeks ago) is almost recovered and I'm finally starting to get back to that dimly recalled thing called 'reality'.

Massive backlog of jobs on the allotment, but I've managed to go down for a while every day for the last four days.  My work capacity (measured in 'buckets of weeds' seems to be improving a little each day).

I've now weeded all round the beetroot and am starting round the leeks. Those leeks are seriously big, especially considering the skinny little things we dropped into the holes when we transplanted them.  Definitely a testament to all the compost we dug in before transplanting them.

I've also started work on the summer fruiting raspberries.

If you have summer fruiting raspberries (defined as ones that have finished fruiting by now, in the south at any rate), then sometime during the next few months, you need to do the following:

1.  Cut out all the canes that have borne fruit. Cut them right down to ground level (you can leave an inch or so if it makes the job easier, it won't do any harm)

2.  Look at the canes that are left (the new ones that have grown up this year).  Any that are weak and spindly, cut down to the ground.  Leave the strongest canes only. The weak ones don't bear enough fruit to be worth it and they'll only take light/nutrients from the stronger canes that will bear the decent crop.

3.  If any of your canes are more than four foot tall, then you're going to need to support them - otherwise, the poor things will only flop over when they start having the weight of fruit to support.  The simplest way is to knock in a six/seven  foot post at the end of each row, stretch some gardening wire between them at three and four feet (the height of the wires isn't a precise art.  Look at your canes and pick a couple of heights that make sense for your plants.)  Then use string to tie the canes to the wires.   It will project them from blowing over in strong winds and also stop them going floppy and trying to grow sideways...

4.  If you have a compost heap, spread the cut out canes across it in a loose lattice pattern and pile your weeds on top. The canes help maintain air pockets in the pile and also add carbon to balance the nitrogen in the weeds/grass clippings.  If you have a compost 'dalek', then chop up the canes a bit to get them to fit in.  Because canes are so weak, they rot a lot faster than most woody stuff, so I find them really handy in compost making. 


Autumn fruiting raspberries are fruiting nicely now (yum!) and should keep going for some time.  I'll cover what to do with those later on in the year.
watervole: (Toothache)
Just to balance downright incorrect propaganda on other parts of the web...

I had both my children in NHS hospitals.  I had easy births both times and friendly, helpful nurses.

I had an emergency appendix operation the same day that my doctor referred me to hospital after I had a pain in my side.

I had radiotherapy for my Dupuytren's Contracture (I had to argue for it, but it was a treatment unknown in the UK at that time and the system eventually took on board the German research and gave me what I requested)

I've had nothing but friendly, effective help for recent 'female' problems.

I get medication for my asthma at a price I could afford even when my husband was out of work.

I've just had an MRI to investigate the causes of my ongoing vertigo and I'm seeing the specialist again next week.

My husband's dislocated his patella three times (which is incredibly painful) and had plaster, physiotherapy, etc. on the NHS (not forgetting the ambulances).

We'd better not forget treatment for concussion, visits to casualty with severe asthma, health checkups, an upcoming eye operation and other things that I'm sure will happen to the family in years to come.

For part of our lives, we had medical insurance as a job perk. All of the things I've listed above were treated on the NHS.

Do I love the NHS?

You bet I do.

MRI Scan

Jul. 28th, 2009 09:55 pm
watervole: (Toothache)
I had an MRI scan last week (won't know if it's produced any useful information for a week or two).  I suspect it's only looking for long-shot options on the cause of the vertigo.

Having a scan is staggeringly boring.  You wait for ages in the waiting room (but at least there's decent magazines), then you lie down with your head in a ring just like on your average hospital TV show.  You effectively have your head in a box, but they thoughtfully provide an angled mirror so you can see the guy at the controls. I suspect this makes people a lot less likely to panic.

They offer you a choice of music on big, padded, headphones.  There's a reason for this...

Being in a scanner is noisy - that's the bit the TV shows gloss over.

They give you the headphones for a reason.

Being in a scanner is not just noisy, it is very noisy.

When you have the headphones on, playing banal music of  limited choice, you can just about hear the music over the sound of a pile driver.

It really, truly, sounds just like someone is operating  a pile driver right next to you - and that's WITH the headphones and music.

I shudder to think what it sounds like without the headphones!  The medical staff all sensibly retire to another room with a closed door before they switch it on.

Being a fairly phlegmatic person, I lay back, closed my eyes for most of the 1-15 mins the scan took and day-dreamed about Doctor Who.  I suspect some people might find it a little scary, but personally, it was reassuringly dull.



watervole: (Morris dancing)
The three of us (Richard, Henry and myself) are back again. We're absolutely exhausted. Too tired even to be hungry.

We collected during Friday's procession, danced in Friday's ceilidh, collected all day Saturday (10-6), went to Saturday's ceilidh, collected all day Sunday, then went home and collapsed.

Serious offer: if anyone running an event that needs a lot of collectors wants a workshop on how to collect effectively, then I could probably help. There are definite tricks to doing it well.

I'm gradually homing in on the things that trigger my vertigo.  I can twirl round in a ceilidh without any problems, but I had an attack when I put my specs on to read the titles of the CDs at the music stall. As soon as I started moving my head sideways to scan the titles, the room started wobbling.  Saved me a lot of money on CDs...

The next time it kicked in was Saturday evening.  We always go to the local Italian restaurant after the street dancing finishes on Saturday.  This time, reading the menu outside the restaurant cause me to feel dizzy. It also kicked in inside the restaurant while eating.  I found myself clutching the side of table to try and feel stable.  I had to leave the restaurant at intervals and walk up and down the street to recover some balance.

Conclusion: although ear trouble is at the base of this (I often get a sense of pressure in the ears, occasional tinnitus and my hearing seems to be a bit off), the triggers may be mainly visual.  (Working at the computer is a minor trigger.)
watervole: (Toothache)
Good things.  Body balance class at the gym.  I think the Cawthorne-Cooksey exercises may also be helping.

The vertigo (certainly when I'm indoors) is better when I'm wearing contact lenses than when I'm wearing glasses.  (the peripheral vision confusion of focus with glasses makes it worse)

Bad things - working at the computer can definitely trigger it sometimes.  The most likely occasions seem to be when I'm scrolling down the screen (I'm trying to use page down when that is an option).  Also looking at the computer to a piece of paper and back again several times can sometimes be a trigger.  I've got the screen on the highest refresh rate.

Bonus symptoms - I'm getting a little bit of tinitus in my left ear.  I only notice it when I'm trying to go to sleep as other sounds mask it during the day. (and it often goes away all together).  It's not very loud, just a small pulse of white noise at intervals of around a second, but it's surprisingly annoying.

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