Showing posts with label Pulmonary Embolism. Show all posts
Showing posts with label Pulmonary Embolism. Show all posts

Sunday, 7 February 2016

Otari-Wilton's Bush Walk

Jumping forward now to October 25th last year. I decided I wanted to push myself a bit and see how I went on a longer walk. Longer than 10-15 minutes I mean!

Growing up we spent a lot of time in Wilton's Bush as we knew it then. We lived in Wadestown and it was around a 15-20 minute walk from home. Pa often took us there on a Sunday afternoon. Or we'd go ourselves when we were 10 or so. No parents - just us! The fun we had - walking over the pipes across the stream - they're all boxed in now - going across the stream and I do recall on one occasion I met up with a stinging nettle bush! Suffice to say it was not fun.  :(

As my own children grew up we often walked here too and they almost always walked back along the stream bed. There should be a billboard:-

Source template meme



The board at the entrance to the walk. The green area is all within the boundary of Otari-Wilton's Bush.


Sunlight breaking through the trees, dappling the rocks and stream bed.


Tiny rapid, mossy green rocks, fallen down branches, nature will have her way!


Fungi growing on a stump


A hollowed out trunk . . . 


. . . Room for a Locket though!  :)


The walk into the picnic area is basically flat. Many of the trails are not! I was still feeling pretty good and so we decided to go on a bit. There was a short trail and I remembered it being not too steep. So . . . yeah . . .steps! I had to pause a couple of times to catch my breath wait for people to pass, but I made it to the top of the short hill.  =D>  I was glad to turn off the main trail though as I remember it goes on for quite a distance!


Pretty hard to see but we had to go down to the stream bed then up the other side. The trail is well marked but hard to see through the trees.


Near to the end you walk over the intertwined roots of these two trees, again the sun is peeking through the gaps.


On the way back Boar decided to walk along the pipe - and of course Locket had to as well! And I wonder where they get it from. This probably is one of the pipes I walked over too  :D  I was a lot younger than I am now though!


If you look closely you can see a grey patch near the middle of the photo - Locket! I'm standing on the trail. Boar is somewhere on the pipe too, just ahead I think.

Brachyglottis repanda

Rangiora - or colloquially "Bushman's loo paper"!


I love the way the sunlight is shining through from the back and you can see all the "veins" on the back of the rangiora leaves from the front.


The small yellow trail is the one we walked around from the picnic area. I edited my photo to show the arrows.


A larger photo which shows how small the trail we took really is in comparison with some of the others. For me on that day it was plenty. Since it was my first big walk since my PE I was really pleased with myself. I was tired but I achieved a few things:- a longer
walk, all up around an hour; steps!; pacing myself through the walk.

All in all a lovely way to spend an afternoon.  :)

Friday, 29 January 2016

A Frosty morning . . . and lungs!


A frosty morning - 14th July! Usually the wind is blowing . . . or it's raining, so we don't get too many of these really.

Source photo here
 If you've read a few of my other posts you'll know I had a a bit of a health scare in August last year. I found this photo online and I've added the red line, the long black arrow and the blue words blocked from here. I was trying to get my head around the scan report which said "Right main pulmonary embolus extending into all distal branches". I then confirmed with the Prof (my consultant) and, yes, my entire right lung was blocked off! I'm not sure exactly where the red line should be, possibly even closer to where the main Pulmonary Artery branches to the right and left - I'm just guessing. So looking at the photo everything to the left of the red line was blocked.

 During my second admission, a couple of days after I was discharged, I asked if I could see an image of the clot and the registrar kindly printed off an image for me. I've drawn the red line and added the words and arrow in green. The senior doctor told me the grey area (within my drawn red line) was the clot. This is a "slice" I think it is called from my CT scan. A friend who is a radiographer took one look and said, "Yes . . . all this should be white!" pointing to the grey area. Other people's scans would look different depending on where their emboli were.

On the surface a frosty morning and lungs do not seem to have anything to do with each other. To me they did though. In the weeks after the embolism I found that cold air hurt as I was breathing. That's what it felt like to me anyway. A scarf around my nose and mouth when I went outside and a heater in the room overnight both helped make life a bit more comfortable until the weather warmed up.


Friday, 1 January 2016

Recovery from Pulmonary Embolism - Part 2

A couple of weeks went by with the usual things happening. On Monday 5 October I had to get organised for the CT Colonography scan the following day. This involved a preparation sheet and some bowel prep.  :-? 

 

A long list of instructions, starting with a low residue diet the day before. No brown bread, red meat, cereals, vegetables, cheese or anything with seeds in it! Doesn't leave a lot. I got some Black Doris Plum Yoghurt as it has no seeds! It was thick, creamy and delicious  :)
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Apart from that I had white bread and honey and cooked myself some chicken for my evening meal. The next day it was clear fluids only. I'd bought some Barker's Lemon & Barley fruit syrup so I had more to drink than just water. I also made up some chicken stock - homemade in time honoured tradition - so I'd have some sort of sustenance!

 At 3:00pm I had to start the fun part of the bowel prep.  =))  First up at 3:00pm was 250ml of Picoprep - I decided if I had to drink this stuff I was going to do it in style! It didn't taste as bad as I'd feared. The advice was to "Stay close to a toilet as the laxative may begin to work soon afterwards" Straight after the Picoprep you have to drink another glass of water!

Picoprep

Now, there are 5 of us in the household and 1 toilet in the bathroom - which is not usually an issue. BUT Pa needs it sometimes in a bit of a hurry! What's a girl to do? Solution - I set up the Campa Potti just in case!  :D  Ours is similar to the one below - but quite a lot older. 


I had some of the chicken stock, at least it had some flavour! Made me feel like I was having something other than water.

Chicken Stock - homemade :)


This looks like milk. But it is definitely not milk! It is called E-Z-CAT dry. Didn't taste too bad either. Had to have this one at 7:30pm. Then more water at 8:00pm. Then at 9:00pm more of the Picoprep, 250mls. Then another glass of water!

Gastrografin -definitely not water!
10:00pm it was time for the Gastrografin above. 500mls of this to get through! It had an aniseed flavour so it's lucky I like aniseed! Then . . . you got it . . .another glass of water! By which time I felt as though I was ready to float! Finally about midnight, when all these laxatives stopped working, I was able to settle down to sleep! Oh! And the Camping Potti was not needed  :D

Next day was clear fluids . . . I stuck to water as after that prep no way did I want to have to repeat it! The scan itself was interesting. IV line for the contrast dye, then the fun part . . . gas pumped into your gut! Via your rectum/butthole of course! The comment, "Try not to release any, as it will just need to go back in . . " had me squeezing my gluteus maximus muscles as best I could. It was pretty uncomfortable as the gas pushes up against your diaphragm . . . but it didn't last too long.  #:-S  Though when I was told to roll over onto my tummy - well let's just say there was a bit of a gas leak  :-$

 

Once it was all over I took myself to the Wishbone cafe in the hospital foyer and had a coffe and some Macaroni Cheese! Needed something before I headed home.

 

Once I got home I had one of my fav Jarrah coffees and some mini squiggles. I felt like a wee treat after the scan I'd just had. 


Well!  That was all some time ago! Life sort of rushed along and I followed behind as best I could. Hence the gap of time between the last post and this one. I had this one mostly done . . . then got busy doing all the rest of the things that needed doing and by night time I was usually far too tired to do anything but read a few lines of a book before falling asleep! 

I also found an awesome blog Blood Clot Recovery Network (BCRN) which I've read many of the posts of. It has so much information and was a source of comfort as I sorted out my head space after the PE. I found that I was lucky as many folk had trouble with their breathing for months afterwards! Mine has mainly been tiredness, my stamina is not as good as it used to be . . . and the other thing I've noticed is my memory is not as good. It may be the medication, but I have to make notes on my phone or I'll forget things! It's been noticed by a few folk . . . but not many, only those closest to me. And I just now discovered I had completely the wrong month for the date of the embolism in an older post so I have now corrected it! I had July and it was August . . . normally I would pick that sort of thing up, but there you go! I didn't! Nuff said.

Over the last couple of months there have been more tests, a change in medication as the Rivaroxaban and periods were NOT a good combination for me! So I was changed to Wafarin which meant for 6 days I had to inject myself with Clexane which took a bit of getting used to! The actual jab didn't hurt . . . the fluid stung a bit. It was more psych-ing myself up to stab myself in the tummy! Thankfully my INR (International Normalised Ratio) got to 1.8 quickly and so I could stop the Clexane. Then it was blood tests every few days till my Warfarin stabilised into the 2.0 - 2.5 range the Prof wanted it to be in.

The CT Colonography showed that the clot had come from my femoral and iliac veins. They still don't know why though. I've had an ultrasound recenlty which shows the clot has gone . . . praise God that it has! It did show some "beading" on some veins so I've been referred to the Venous team. 

Throw in the studio dance concert, plus the one Locket does Tap at, and it was a busy few months.

I'm doing ok  :D  I still have to watch my energy levels as if I get too tired it takes me days to recover. I've just had a classic example with some dresses I was making for a wedding which left me sleeping 5 hours over 2 nights . . . after handing over the dresses I was exhausted and almost physically sick from the stress. A few good nights sleep have sorted that . . . though I can feel in myself I need a few more days to get back to my new normal, which is different to my old normal.

That's just life. Things change when your body throws a hissy fit! When I told my GP (doctor) who I've been going to for nearly 30 years that I went to bed and to sleep the night of the embolism he looked at me and said, "Many people don't wake up." Which I know . . . but it is still very sobering to hear it put like that.

So that is a very quick wrap up of the end of the year 2015. 

It is now 2016! It seems to have come around very quickly indeed. There will be new things happening and some of the old as well. This post is long enough though so I am going to wrap it up now.

Wherever you are I wish you all the best for a great year in 2016! 



 I hope it goes well for you. See you soon  :-h

Monday, 26 October 2015

Recovery from Pulmonary Embolism - Part 1

So, it is now 10 weeks and 3 days since my Pulmonary Embolism (PE). I'm in recovery mode and doing o.k I think.

I did have to go back to hospital in the early hours of the Tuesday morning, 18th August. I'd started coughing a bit before midnight, and it wouldn't stop, no matter what I tried. I was getting increasingly short of breath and had a feeling of pressure. I tried water which had usually helped, but not this time. I also had pain under my shoulder blade. My pulse was o.k. but my respiration rate was a bit fast at 25, and the same about 20 minutes later. In the end at about 1:00am I woke Boar and said I was going to talk to someone. I rang 111 (Emergency services number here in New Zealand) and before I was off the phone a rapid response vehicle was at the bottom of the drive! They were at the base in Johnsonville only a few minutes away. An ambulance was there soon after and I was taken into ED. Boar followed in the car.

What I didn't know till the next day was that Locket had heard the commotion and was sitting at the top of the stairs listening . . . poor girl. She said she knew I was o.k because she could hear me talking. She came down after Boar left to check the front door was locked and turn off the lights.

I was admitted to the Short Stay Unit around 5am and they kept me in for most of the day. It turns out that when the clot is breaking apart sometimes a piece gets stuck in the smaller vessels, causing irritation hence the coughing, and also a pleural rub - which is when the two layers of the lung rub together. There is a better description here. It was what was causing the pain.

I left the hospital around 5pm when Boar got off work and was able to pick me up. Brains and Locket came as well. They got me a wheelchair as walking was still a bit of an issue. Since there was a pretty cold wind I got Locket to run into the house when we got home and get my scarf  which I wrapped over my nose and mouth, as I'd found cold air didn't help and would start me coughing. Then it was up to the house. The only way to do this was slowly as there is a path up to the house and some steps. So I walked 5 steps and rested. And again . . . and again . . . until I was in the house. Mission accomplished!  :D

I took it pretty quietly for a few days and anyone who came to visit was greeted by me in my PJs and dressing gown. We were brought meals and my Life Group from NBC brought a whole heap of food to us, which made a lot of meals. So thanks a lot to everyone who helped out  :)

My first big day out was on Saturday. By then I was able to walk around the house pretty well, though still not quickly, and had even ventured upstairs! Up three stairs, rest . . . and repeat till I got to the top. Mainly to see if I could.

I got Boar to drive me out to Porirua to a couple of the shops. I managed o.k, but was tired by the time I got home. I saw some coasters I liked and so bought four . . . just because I wanted to.





They make me smile  :)

Friends were great at getting Brains and Lucy to and from dance which was a great help. I took it fairly quietly the following week however I did sew as I needed to get some dresses finished for Mrs C who was going to Fiji on the Saturday. They got done and delivered the day before she left!

The day before that was the first time I'd driven the car since my PE. I took Locket to dance and came straight home. I found I had to concentrate really hard, much more than usual. The short 10 minutes there and the same back was more than enough for a first outing! I did it as a test drive as Brains had an appointment I needed to take him to the next day. So I needed to drive for that.

The following week I took Pa to an appointment and also had my first follow-up appointment after the PE at the VTE clinic (Venous thromboembolism). It was a long and very thorough appointment! I had to have some blood tests done and also arrange to have a mammogram, plus there was another scan the consultant ordered - CT Colonography. Basically a scan of your gut and pelvis.

I was working through that week and weekend on a sewing job for a client and delivered it the following Monday. That night I got a call from Chuckles and Butcher. One of Butcher's best mate's wee son had passed away at only 18 months old. It was devastating news. I agreed to look after Half-pint and Lil Battler so they could go to the funeral. In the end Brains and Locket looked after the two boys as P had said it would be fine for me to go to the funeral. It was a beautiful, but very sad, service. They always are for wee ones  :(

I went for a short walk on the Tuesday - It was a flat easy stroll. 5 minutes one way and 5 - 6 minutes back. My first walk since the PE. I really enjoyed it but even though I took it really slowly I still found I was coughing by the time I got back to the car. It happens when I walk too far, or talk too long!


It was a lovely day and so I snapped a few photos of the calm sea at Oriental Parade.


I saw the small yacht and the ferry were going to pass and so decided to take a coupe of shots as the ferry dwarfs the yacht! It didn't take long for them to pass.


I managed to catch them just as they passed. By the time I clicked again they'd gone past each other.

Another thing that happened was Ma & Pa's 60th Wedding Anniversary celebration. It was held at Johnsonvale Rest Home where ma lives as Ma is not able to go anywhere these days. I had organised it - but in the end I couldn't go. I had a flu bug a couple of weeks before, and then came down with another virus bug that had me coughing a lot. Coughs and sneezes are not welcome at the rest home and so I stayed away. A good afternoon was had by everyone who was able to get there. I think Ma basically slept through most of the event. Her sister was able to come down from Palmerston North for it which was lovely, and there was a good number of family and friends there as well.

I had the mammogram done and thankfully it was all clear. Not having had one before it was an experience!  :-O   I think the poem below sums up the experience well!

Ode To The Mammogram

For several years they've told me,
"Be careful of your breasts.
Don't ever bruise or hurt them,
And give them monthly tests."

So I heeded all their warnings
And protected, both, they are!
I've guarded them most carefully,
And always worn a bra.

After thirty years of tender care,
The doctor found a lump.
He ordered me a mammogram,
To look inside that bump.

"Stand up very close," she said,
As she got my breast in line,
"And tell me if it hurts," she said,
"Ah yes, there… that's fine!"

She stepped upon a pedal…
I could not believe my eyes!
A plastic plate was pushing down,
My boob was in a vice!

My skin was stretched and stretched,
From way up by my chin.
And my poor breast was being squashed
To Swedish pancake thin!

Excruciating pain I felt,
Within this vice-like fit.
A prisoner in this vicious thing…
My poor, defenceless tit!

"Breathe deeply, now," I heard her say.
Who does she think she's kidding?
My chest's been smashed in her machine -
Can't breathe, can't do her bidding!

"There, that was good," I heard her say,
As the room was slowly swaying.
"Now, let's have the other one."
Lord, have mercy, I was praying!

It squeezed me from the up and down,
It squeezed from each side.
I'll bet she's never had this done
Upon her tender little hide!

If I had no problem when I came here,
I'm sure I'll have one now.
For if there'd been a cyst in there,
It would have popped - ker-pow!

This machine was made by men,
Of this I have no doubt.
I'd like to get their nuts in there -
For months they'd go without!

Author Unknown



Monday, 5 October 2015

Life changes . . . in a few seconds!

Thursday 13 August, 2015. It is an evening that will be forever etched in my mind. Not so much the date as the event.

I walked down the drive from my client's home, and as I walked I thought what a beautiful evening it was. Still, calm, not many clouds, quite a few stars out, almost balmy! One of the rare Wellington evenings at this time of year. I thought it would be a lovely evening for a walk. It was around 8:30pm. I got into the car and called Boar, to let him know I was on the way home, and to check if there were any other things needed from the supermarket.

I drove back to Johnsonville and decided to go to the larger Countdown on the main road. I parked and wandered in. I had an idea about the client's costume so sent her a text, partly to fix it in my mind and so I would have a record of it. It was a few minutes after 9:00pm. I got the few items we needed, went through the self checkout and headed back to the car. I went at my usual pace, which isn't fast. I suspect my iron (haemagblobin) is low again and I need to get it checked. It has been up and down since 2009 when it was found to be really low. Iron pills usually help.

When I got back to the car I felt a bit breathless and thought, "That's odd! Maybe I walked more quickly than I thought." However it resolved quickly, by the time I got to the lights, 30seconds, it was fine again.

I got home a couple of minutes later, got my bags out of the car and started up the path. By the time I was halfway up I was again feeling breathless. Got to the top, paused for a moment, then went across to and up the steps. By now I was feeling even more breathless. Made it inside the door, glanced in at  Boar who said, "Hello, dear," and didn't seem to think anything was out of the ordinary. I decided I needed to sit down so went to the sofa and plumped down there. NO! Still couldn't catch my breath and so thought I'd go and sit on a more upright seat, one of the dining table chairs . . . chucked off my jacket, and sat down.

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I felt as though someone had suddenly slammed me in the chest, or I'd been dropped on my back and winded . . . really badly. I was gasping, at the time I didn't think I was making much noise but I'm assured I was! I couldn't call out, my mind was going a mile a minute, "If this is an asthma attack they're not much fun!" I've never had asthma. "Maybe I've got that virus Mr Magoo (2yrs old) had that put him in hospital over the weekend,"    "What will happen if I collapse off the chair, will anyone hear and find me?"   "I can't breathe I cant breathe I CAN'T BREATHE!!" 

Then I started to talk myself down as I could feel I was beginning to panic, the nurse in me kicked in . . . it's still there. "O.k, calm down, you ARE breathing, slow your breathing down, that's it, slow deep breaths, you're doing o.k, you'll be fine, see your breathing is easier now . . . "  During this time Pa had appeared out and glanced at me as he went to the loo. A few minutes later Locket came down from upstairs and asked if I was o.k. At this point it would have been sensible to say, "Get Dad!" meaning Boar. Did I? Nope! Boar hadn't heard all my noise, he was in the bedroom, TV on, and is a bit hard of hearing these days after years of working with noisy tools.

"Yes," I said. "You sure, you don't sound o.k." Locket said, looking a bit worried.  "I was a bit breathless but I'm doing o.k now. I'll be alright."

I decided to go to bed, so I pottered around, got a hottie, went to the loo. I did find whenever I walked even a short distance I was breathless. I took my pulse at one stage and it was 135. I thought that was a bit fast! Did I do anything about it, like call Healthline? Nope! I went to bed!

Boar realised I wasn't feeling so great when Brains brought me his inhaler and suggested I have a couple of puffs, in case it was asthma.

I slept reasonably well, woke up once to go to the loo. Walked to the bathroom . . . 15 steps from bed to the loo, ordinary walking steps. Breathless by the time I got to the loo, and more breathless by the time I got back to bed. Fell asleep again. Woke again at 5:30am . . . a repeat of before. I ended up staying awake, sitting up in bed. I couldn't be bothered trying to get comfortable again. By this time I'd decided that I would go to the doctor. I was tossing up between my GP or after hours at Kenepuru. I thought that even if it was a virus and I needed Ventolin I shouldn't take it without a prescription. I mean, usually a walk to the loo and back doesn't leave me breathless!

I let Boar know I was going to see a doctor and got him to wake Brains as I decided on Kenepuru and I could drop Brains off at Whitireia before I went. I didn't feel like climbing the stairs though to wake Brains myself. Throughout this time I kept feeling basically fine . . . until I walked anywhere, even the shortest distance in the house would leave me breathless. No pain at anytime.

Into the car we climbed, driving was fine, dropped Brains at Whitireia and then drove myself to Kenepuru. Parked in the closest carpark and walked slowly in. By the time I got to the reception desk I was breathing pretty hard, coughing a little. The receptionist asked if I'd been there before . . . yes. Then my name. I was able to answer, but only by pausing and taking a breath for nearly every word! While I was confirming details the nurse, at the counter close by, got up to take a file to the back of the office. She stopped and eyeballed me, put the file away and sat down again, by which time the receptionist had said for me to have a seat and the nurse would be with me in a minute. The nurse said something to the receptionist who then told me to go right over to the nurse. Nurse took my pulse, temperature, oxygen levels and asked briefly what had brought me there. I replied, slowly, lots of pauses. Nurse asked me to sit down, then almost immediately a nurse came through from triage.

It was around 9:25am. This time I was put on the BP machine and I looked at the numbers as usual. 177/78 . . . "Gosh! That's a bit high!" I said. They agreed and asked if it had . . . "No, I've never known it to be that high before!" I said. The senior nurse popped out, the student continued the obs and next thing I knew they were taking me back to a cubicle. The senior nurse had spoken with a doctor and an ECG was wanted. As far as I knew it was fine. Then the doctor asked if I could walk to her room. I did . . . and she saw how breathless I was. Again obs were taken, then questions asked which I replied to slowly, and with many pauses. At one point I remember the doctor saying, "So, at no time did you not think it was strange that you were so breathless so suddenly?"  "Ah . . . no . . " and I told her what to me was my logical reasoning from the night before!

After taking my history the doctor rang through to speak with the ED doctor, questions, answers, and the comment that when I'd walked from the cubicle to her room I had been very breathless. There was also my history of high D Dimer and CT Scans for possible clots in 2009 and 2014. The upshot was that the ED doctor said I should be sent on there.

I queried whether I should drive myself there, absolutely not, I was told! I tried A-M Prof's home number but no reply. I was on the point of going online to find the church's office number when the doctor said not to worry, she was going to arrange an ambulance. Say what?! Dimly in the back of my mind I realised they were thinking "clot" again, but still I had no pain anywhere. Both the other times I did! So no pain, no clot, was my next piece of logical reasoning.

While I waited back in the cubicle the nurse took some bloods to go to ED with me, and put in an IV leur plug. I tried to get hold of Boar, or his work . . . no luck. I was taken in a wheelchair to the ambulance, took the two steps up into the ambulance . . . and sat down puffing! I was observed on the way in, as usual and then triaged by a nurse when I got to ED. Then I nearly cracked up laughing . . . because ED was really busy, no spare rooms and so they put me out in the main waiting area! Oh, well, I thought, at least there are people around if I fall out of the chair!

It wasn't that long before I was taken through to a cubicle. Another ECG, more bloods done, an X-ray and the questions. More thorough ones this time. They were looking for causes.

Have you had a long plane ride in the last few weeks?    No.
Have you had a long car ride in the last few weeks?    No.
Have you had a swollen calf or leg.   No?
Do you have pain when you breathe.    No?
Are you on an oral contraceptive.    No?
Are you on hormone replacement therapy (HRT)?    No.

So I didn't fit the criteria for what they were looking for! The blood tests discovered that my haemaglobin was low, very low. 75g/l when it should be between 115 - 160g/l. I also had an ultrasound of the heart to see if one of the chambers was enlarged. So the medical consultant decided I needed a blood transfusion. They were going to send me round to MAPU (Medical Assessment and Planning Unit) and do it there. They were still deciding about doing a CT Scan. My D Dimer was raised, which can indicate a clot, but can also indicate other things.

So I was taken around to MAPU. There I was admitted, then the consultant came to see me with a medical student. I had the consultant a bit puzzled! The medical student took a more detailed history. Then went to write it up. In a while the consultant and student came back.

It was about 8:00pm by this time. Boar had been driven out to Kenepuru by Smurfette to pick up the car from where I'd had to leave it. When he had dropped it home they, along with Brains and Locket, came in to see me. They brought me the things I'd asked for as I realised I'd be in for the night.

There was a plan. Instead of a blood transfusion they were going to give me an iron infusion. It is safer and gives as much iron in an hour as your body takes two to three months to absorb. Also the consultant had decided that they would do a CT Scan, just to be on the safe side. I do remember him saying, "I don't really expect to find anything though. I'm still a bit perplexed about your past history."

I was given a jab in the stomach of a drug called Clexane in case there was a clot. It would start to thin my blood. A new IV line was put in as the CT Scan contrast dye needed a larger one than I had in. Soon after that the orderly arrived with a trolley to take me to have the CT Scan. So my beautiful family had to go home.

Scan done it was back to the ward and the iron infusion went ahead. You are observed for the first 15 minutes, i.e. the nurse stays with you. This is in case you react to the infusion. I was all good and so I was checked on a couple of times over the next hour as it went through. Towards the end my neck was feeling warm, and I felt a weird pressure in my neck and my chest. I was thinking if it kept up I'd ring the bell, when the infusion finished and the feelings stopped. Since the machine was beeping the student nurse and a senior nurse arrived to disconnect it, took a look at me . . . and asked if I'd had that rash on my neck and under my chin before? No. Explained why my neck was feeling warm! They decided it had better be checked by a doctor.

By the time the doctor arrived I'd flung back the sheets and was rubbing my knees . . . the rash had come up there, on my arms, a bit on my chest, and it was darn itchy! The doctor prescribed an antihistamine. By this time it was around 10:00pm. I don't sleep well when I'm away from home so was sure I was in for a pretty sleepless night. Anyone who has been in hospital knows they are not the quietest of places!

I slept! Woke to go to the loo a few times, but went back to sleep straight away. Perhaps the antihistamine helped.

In the morning, Saturday, the consultant arrived, asked how my night had been and how I was feeling. Then he asked if they'd given me the results of the scan last night. No. (Cos nurses and technicians are not allowed to say till the doctor has  . . . I didn't even bother to ask!)

 "Oh!" he said, "There is a clot, a very large clot in the right pulmonary artery! Radiology rang me last night to tell me."

Now, I used to be a nurse, so I know that radiologists don't ring consultants after 9:00pm on a Friday night unless they really need to. I'm guessing the consultant was glad he'd decided to order the CT Scan!  #:-S

I know that Pulmonary Embolism can be fatal. I did not know that when they are in the vessel leading to the lung they do not always cause pain. 1 in 3 people die of a pulmonary embolism, sometimes within 30 minutes of it happening. I remember thinking that it could have killed me . . . silent, no signs, a clot sitting there somewhere had moved.  And I had gone to bed!

The consultant went on to say that he would prescribe an anticoagulant tablet, Rivaroxaban (Xarelto), for me to take, that I would be under the VTE (Venous thromboembolism) clinic after I was discharged, and that he wanted me to stay in another day at least so they could keep an eye on me. Also I wasn't to just stay on the bed. To try and walk around a bit, go further than I thought I could.

By the time I'd stood and talked to one of the nurses, then had a shower, slowly, I decided I'd rest for a bit. I fell asleep! Slept for around an hour or so. Most unlike me, and shows what my body had been through, to me anyway.

In the afternoon I had a few visitors, and Locket took my photo and put it on Facebook . . . no details though. After a few concerned queries from cousins, friends and family she edited it so folk would know what had happened. Turns out a number of the people who commented have had clots of various types.

The rest of the day went past . . . I was pretty tired and even though I had a book and knitting I wasn't able to concentrate on anything for too long. Mostly my thoughts just roamed. The one front and centre was that I was very glad to be alive! It's quite a surreal feeling to reflect that it could have gone the other way. Not that I'd know of course!

Later that night I was moved to another ward, the usual musical beds in the hospital.

When my obs were taken around 11:30pm, I think, my temp was up. Some blankets were taken off and it was checked again about 30mins later. Still a bit feverish. So I had to do a urine sample, and I think they took bloods. I had a urine infection of all things, again no symptoms of it. So I was given antibiotics for that. It took me ages to get back to sleep . . . around 4:00am or even 5:00am.

So then it was Sunday. I went for a wander, very sedately, but I made it most of the way round the ward, and my pulse wasn't too fast when I got back. Late morning or early afternoon the consultant arrived. He wasn't too worried about the fever, said that as the clot begins to break down it can cause a slight fever. It would take 3-4 weeks for the clot to break down. I queried whether it could happen again . . . not likely as I was on the anticoagulant.

"But if something like it happens again . . .?"      "If it does, don't go home, don't go to your GP . . . go straight to Emergency!"   O.k, message received and understood.

I called Boar to let him know I could go home. We had to pick up the medication from a pharmacy in Newtown as only certain ones stock it. I did find out I should be able to get it from my local pharmacy so long as I give them enough time.

I did get dressed to go home, but got into my PJs and dressing gown pretty quickly once I was home. Walking was still a major effort and if I walked too far - even in the house - I'd start to cough.


So good to be home, with family and enjoy a roast dinner. I wasn't able to eat much, but what I did was lovely  :D