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Fighting a legal battle with very few resources

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Pie chart explained at  the end.


It feels like most of this year has been taken up trying to deal with 2 very big problems that have occurred as a consequence of my Bankruptcy. Which is dealing with legal and financial “debt” actions for bills and charges relating to one of the flats I used to rent out. In Motherwell.

Both the council for the area and the factors that manage the property want me to pay for things that have arisen or been charged after I went bankrupt in Sep 2014. This is why I referred to “debt” in inverted commas – as it is debts I haven’t run up myself. And no reasonable person would expect to be liable for these – as the properties had all been handed over to a Trustee In Bankruptcy in 2014.

My Trustee In Bankruptcy (say) they have repeatedly explained my situation to these 2 organisations (particularly the factors) over the last few years – ie, I am bankrupt, went bankrupt because of health, gave all assets away on becoming Bankrupt, have no income or savings now. And can hardly manage to deal with anything because of my health. Which is WHY I opted for Bankruptcy. Sorry, I know this is the 1000th time I‘ve mentioned this . . . . !

I have also made (been forced to make) some efforts at explaining all this myself to these organisations – usually in long emails. At great cost to my health every time, as even small exertions usually make me more ill. And can cause me to crash/relapse even further for days, weeks, etc.

Trying to think and type out an email will usually take me hours and is a very big exertion with my level of health and ability (or disability).

Again, this is why I went Bankrupt.

But these 2 particular organisations don’t care a jot about this. They seem determined to push on for their pound of flesh.

Some of this stuff I’ve probably written about in earlier posts – sorry about this. And for maybe repeating stuff.

But I desperately need to try and pour some of this out – as it is all keeping me very ill indeed. It feels like it has consumed most of this year. And it is consuming me. My physical health and my mental and emotional health too. Nightmares all the time, increasing this year – with all this worry.

Oh, and the Bankruptcy itself is still ongoing.

Still being administered.

Still dragging on.

Some other flats still to be sold.

So for me, being “discharged” from Bankruptcy in Sep 2015 has meant absolutely nothing. I have no idea what benefits there are from saying a person is discharged. Not that I expected any benefits as such – I just mean what is that actual point of the statement saying you are “discharged” when you were a landlord with various properties ? Because they don’t get disposed of overnight. And it is also pretty unlikely they will be disposed of within 12 months either. (By “disposed of”, I mean sold or repossessed.)

Given that one mortgage lender has taken almost 3 years to repossess an empty flat. A flat that was not tenanted, was unoccupied, ie. vacant – in Sep 2014. And well before that too I believe.

Yes, you read that correctly – 3 years . . . .

This of course, is the flat that has produced the bills I am now having to “fight” these legal and financial battles for.

I put “fight” in commas too, because I have so little ability to fight this.

As well as all the pages of physical symptoms I have with Severe ME, the awful cognitive dysfunction (AKA brain fog) prevents me being able to express myself or remember things when I most need to. Well, it causes problems for me all the time of course. Its very frustrating not to be able to remember stuff I have just read in a book, or having to re-read an email 5 times, or cannot digest something just heard on TV perhaps. It is miserable actually – but not essential in the way it will be in a court case.

The legal battle the firm of property factors are waging against me – is now in the 2nd part.

This firm (I will call them Apollo Property – not their real name) are suing me in 3 stages for factors bills, charges and “estimated” bills for communal maintenance/repairs. The total I think, adds up to somewhere between £9000 and £10000.

I think the reason they are doing it in 3 parts is so it comes under what is called the Simple Procedure in Scotland. It used to be called something like Small Claims. Either way, it is dealt with by the Sherriff Court. And I think the legal charges for the person bringing the action are cheaper than a normal court case. And the top limit for these types of cases I’m told are £5000.

So I am assuming that is why Apollo are doing it in this way.

It makes no difference to me really – as I have no funds with which to pay any of this. And would never have expected to be liable to pay these things. No reasonable person would surely ?

As I mentioned in this post, IF the flat had still been tenanted – the tenant’s rents would have been taken over by the Trustee. But I would still be liable to pay bills like these factors bills – from fresh air .

No reasonable person would expect this to be the position.

And I still don’t know for sure if this actually IS the legal position.

The previous solicitor I had requested to send or email me the specific legislation relating to this, ie. The Act and section, paragraph etc, where this is stated and detailed. So I could read it myself – as it seems so unbelievable.

He hasn’t replied.

But then he has been paid. (You have to pay the legal fees in advance and ongoing for this type of legal assistance. You do not get a bill at the end.)

 

For this 2 nd Stage – Apollo are claiming approx £5000.

For “estimated” bills for communal repairs and maintenance.

I don’t understand how it can be estimated – you would think they must know what they have paid out exactly ?

And is legal detail not meant to be accurate and specific ? I thought that the whole essence of legal stuff was the preciseness of the detail ?

So I am baffled by this.

 

Ironically, the whole communal area where this flat in Motherwell is located had, as I understood, been allowed to go downhill. And this was probably a result of the previous factors failing to carry out any maintenance or repairs over a period of a few years. (They eventually went into Administration and the current factors Apollo took over.) And of course, this would be why the letting agent I used said they just couldn’t get any decent tenants for the flat. And it had sat empty for quite some time before 2014.

No landlord would just choose to have a property sitting empty. Just saying . . .

At this particular scheme where my flat was – there are 3 small blocks of flats. Each with 11 flats in them.

They would all have needed similar work to mine I am pretty sure. So anything I am being charge for can be multiplied by 11 for definite. And then by 3,  as 3 blocks.

Very recently it also came to light these factors Apollo are also charging the mortgage lender a sum of £16280 which they want paid to them from the sale of the flat.

(The lender finally repossessed it in March this year, and it was sold in July. )

The only detail Apollo seem to have given the bank’s solicitors is vague descriptions like “essential maintenance” and “charges”.

So that means the total of these repairs for my flat = £5000 + £16280

= £21280

And for the full block (as communal works)

X 11 flats = £234,080

And for the scheme of 3 blocks :

An absolutely whopping £702,240 . . . . !!

These figures seem astronomical.

I didn’t mean to type so much detail and make this into such a long post. But my head is spinning with all of this . . . .

And how to fight it with so little energy.

 

The pie chart in the picture at the top is a screen shot I took from an app called ME/CFS App. I try to record my daily energy use on it – in the hope of it helping me in the future. Or maybe as a visual aid perhaps to show a GP of how my life is.

I’ve been doing this off and on for a few years.

The dark blue is the amount of time I am either sleeping – or completely disabled.

Possibly resting or recovering from doing stuff, but certainly unable to “do” anything at all. Not even listen to soft music, certainly not read.

Just totally non-functional.

And this is at least 80% of my life.

Probably more actually – as you fill in the areas of “activity” in 30 min boxes. Nearly everything is a high or medium energy activity for me. A low energy activity may be listening to meditation music lying down. Or maybe eating food.

A simple text message might take me 20 mins to type out – but I would probably fill a 30 mins box for this on the App. So I tend to overstate my time being active.

I imagine my actual level of functioning is around 10 % .

Which is a pretty shit life – lets be honest.

10% is the figure the App keeps telling me is my baseline. I don’t even know what “baseline” means, as haven’t had enough spare energy to read all the instructions in 2 or 3 years.

So anyway – I’m trying to fight this legal battle with Apollo Factors while being functional only 10% of the time.

Not to mention the firm of Debt Collectors now employed by the Council for Motherwell as well.

I don’t feel very hopeful.

But its good to vent . . . .

And if the sheer effort of typing all this gets some of this horror out of my head, and reduces the number of nights a week I have exhausting nightmares – then it has been worthwhile for me.

Sorry its such a long read.

 

 

 

 

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Bankruptcy in Scotland:  The law is an ass ? 

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I enjoy writing as it can be theraputic. But this is only the 3rd post I have done this year. And it will soon be the end of June. Half the year gone.

This is because I am still horribly limited by my ME and can manage to do very little. Everything takes me ages to recover from. Maybe 90% of the time I’m sleeping, resting or recovering. Some days a bit better.  And some even worse – when in bed 24 hours out of 24.

Resting or recovering isn’t much different from sleep for me. Well, apart from not having nightmares when awake. But I’m usually unable to do anything. Just pretty much non-functional. It feels like attempting anything, no matter how small, triggers off an increase in symptons. Which is miserable.

The Bankruptcy stuff is STILL ongoing. Since 2014. Shock after shock after shock. A constant battering to my health. And my husband’s health. It has been endless.

And is actually getting worse.

In my 2nd last post I had appealed for a solicitor to help. Because I was being sued by a property factor for their factors bills dating back to 2014. These bills were for their regular management charges, plus general repairs and maintenance.  And of course I was very shocked at this.

The property was one of my 14 buy-to-let flats which were handed over to the Trustee In Bankruptcy in 2014. When my health totally crashed.  All correspondence, bills, statements etc have been getting posted onto the Trustee every week since 2014. (By my husband as I have rarely been well enough to get out.)  And the point of this was that the Trustee would deal with everything. Handle everything.

That is what I was told by the bankruptcy Adviser. That was why I was advised that bankruptcy was the best option for me, as I understood it. And why I accepted this. To “give away” the properties and all responsibility for them. I was too unwell to even think about trying to sell them myself. I wouldn’t have wanted to do this anyway at that time. I would have waited until the property values had improved. As to sell then would just have resulted in many shortfalls against the mortgages.

I know I have laboured this point before. In this post – The Bankruptcy Stuff Keeps Getting worse.

And this one – A Long Slow Road. (This is quite a long post about various things. The comments about Bankruptcy are in the 2nd section.)

And this one – Unwanted Visitors.

And this one – My Life So Far – Not What I Expected.

But it is all the more shocking to me the more that happens and the more I find out.

IF I understand correctly what has happened recently :  It seems the original owner of the property (ie. me) is still liable for payment of bills like Factors bills from ONE DAY after their bankruptcy date. Up until the date the flat is either sold by the Trustee or legally taken back (ie. repossessed) by the mortgage lender.  Even if this takes years and years.

In this particular case it has taken years. From 2014 until March 2017 in the case of this flat. Almost 3 years. 3 years for the mortgage lender to repossess a property which was empty. Not tenanted. And no mortgage payments getting paid on it.  And its not just this flat. As I understand it – there are still 2 other flats left.  Therefore it would seem I still legally own these also.

Jesus wept . . . .

Just to talk about this a bit further.

As I understand it – all rents that were paid by tenants are taken by the Trustee. Even if any had been paid to me by the letting agents – the Trustee still gets them. As bank accounts get frozen.

But I am still meant to (legally) pay all these bills. I mean, seriously . . . . ?   And how am I meant to do this ? Or any other ex-landlord in the same situation.

To give a more extreme (but simple) example :

If a bankrupt landlord owned 100 flats. And they were all tenanted. All these rents would be taken by the Trustee In Bankruptcy. And if the Trustee doesn’t sell the flats themselves and the mortgage lender takes 3 years to actually repossess them – the bankrupt ex-landlord is still liable for all these bills. So the Trustee would get 3600 rents (monthly rents for 3 years).  But the landlord would still be legally liable to pay 3600 factors bills (if the factors bill monthly).  Does he/she magic the money to pay these out of thin air ?

IF this is the law – then the law really is an ass.  (I’m in Scotland. I don’t know if it is the same in England.)  I can still hardly believe it. It seems so unreasonable.

I have requested my solicitor to email me the details of where this is wtitten in the bankruptcy legislation. ie. The name of the Act and location (section, paragraph, whatever) of where this be found.  Not that I really know what I’ll do with this once I have it. But I need to be able to actually see it for myself. And it should be made widely known I think.  So that nobody else can be given the advice we were, without being told of these consequences.

Another point is : If any flats have been empty (not tenanted) a while – it gets even worse. As council tax bills build up too after exemption periods have been exhausted. Exemptions usually only last 6 months.

This then implies that utility bills for any empty flats, or empty periods, are my responsibility too. Where the supplier applies a standing charge.

This particular flat had been empty for quite a while before it was given to the Trustee in 2014.  Possibly a year, but maybe longer.  This was because the letting agent could not get any tenants for it. As I think the communal areas had deteriorated and fallen into a poor condition. This was because the previous firm of property Factors (who eventually went bankrupt themselves) failed to deal with any repairs or maintenance.

The irony of this is not lost on me . . .

Now I do realise (or assume) that when most people go Bankrupt they do not have a choice.  Because finances and debts have got to such a position where there is just no way to rescue things.  But my situation was different. As mentioned in previous posts – our assets well exceeded the debts.  But voluntary Bankruptcy was taken purely because the Bankruptcy Adviser clearly said that the Trustee would deal with everything. Take everything off my hands. All mail, demands, forthcoming  threats (once things stopped getting paid),  phone calls, etc,  just had to be passed onto the Trustee.  (And we knew we had to pay a big price for this financially and emotionally. The loss of our home of 15 years and all the equity in it. It was no easy option or get-out.)

At the time of getting the bankruptcy advice nothing was in arrears. Everything was getting paid and there had been no missed payments.  I was even still getting 0% credit card offers thru. My credit score (with Experian) had been 999 (the highest in the Excellent range) for a long time. Although it had dropped down a level by early 2014 – to the Very Good range I think. I suspect because the amount of capital debt was rising, even though nothing was in arrears.  It was getting harder though – but that was more because of my health.  This previous post from Feb 2013 gives an example.

I know they say ignorance of the law is no excuse. And it seems to be no defence either. But seriously – would anyone reasonably expect this to be the case?  Even my administrator at the Trustee said she would dispute the claim because it wasn’t my fault all those factors bills had built up. Plus the fact that I have no income or savings with which to pay, or even make a payment arrangement. (This wasn’t legal advice of course. She told me the Trustee do not have any in-house solicitors that could advise me.)

To add insult to injury – I have no way of knowing if any of the work billed for by these Factors has actually been done. Plus – I don’t even have the bills I am being forced to pay. They were all sent onto the Trustee over the last 3 years. (Everything has been sent onto them. It is what we were told to do.)  Then everything regarding the Factors claim was sent to the solicitor.

Words cannot describe how unjust this whole situation feels.

Now this same firm of Factors have started more court proceedings for “planned maintenance” bills.  The next one is for £4900.00 and has been allocated a claim number for court.  And they have stated they will be further suing for yet another amount for “planned and ongoing maintenance” – this time for a sum below £2000.00 .

In addition, the council for the Motherwell area where this flat is (North Lanarkshire Council) have now sent me a demand for almost £2600.00 for council tax. It was delivered by sherriff officers acting for the council. I  sent it the Trustee right away. As they are still administering my Bankruptcy. They have now sent it back to me and suggested I ask the solicitor about it.

We cannot afford to pay for any more legal help. Husband has been working 7 days a week for a while now to be able to pay for the recent legal fees.  And towards repaying the friend who very kindly gave us a cheque to settle the factors demand. 

Neither of us would be able to obain any loans now as our credit records will be utterly trashed as a consequence of the bankruptcy.  And hubby working 7 days a week is hard – given that I can hardly do anything around the house. And he does almost everything.  Just a week or two ago he had the lovely task of emptying plastic jugs I was having to use in the bedroom – as I was too ill to manage to the bathroom. Too much info I know, but this is how bad it can be. And scrunching up A4 envelopes so I could use them to breathe into (like a paper bag) when I felt panic attacks coming on.

How much more can he be expected to do?

And how much more battering can my health take ? Or husband’s.

Trying to communicate with the solicitor over the last few months has taken a massive amount out of me.  If I was well enough to do this sort of thing I wouldn’t have needed to consider voluntary bankruptcy in the first place.

It was made harder for me as I don’t think they could understand how bad ME actually is, especially when symptoms are severe.  For example : how do you sucessfully communicate how bad your brain fog (aka cognitive dysfunction) is – when this is one of my worst symptoms?

Sometines I wondered if they actually thought I was exagerrating about how limited I am. And how long it takes me to “recover” from the exertion involved in a simple thing like an email or a phone conversation. A simple thing to them but a very exhausting thing for me. Always triggering a big worsening of ME symptoms and being more ill for days on end.  And I found myself trying to explain over and over how badly limited I am. Then giving examples. Not because I was looking for sympathy or anything. But because all this legal and court stuff have time limits set. And I was terrified of what would happen if I couldn’t do things in time. This was so exhausting and I had been hoping for some reassurance that some accommodations could be made if needed.

I don’t know what to do now.

I’m really not well enough to use the internet to look for ideas. Or make longish phone calls. I don’t mean these things are impossible 100% of the time. But I can only manage a very short time doing things without it making me more ill. Then I’m knocked out for days.  And I get nothing done.

I can’t think straight about any of this. The only thing I do know for sure – is that bankruptcy has been a terrible option in my situation.  3 years of Hell for mothing.

Any suggestions would be welcome. (About the forthcoming claims.) Any info that might be helpful would be great, eg. phone numbers, websites, email addresses.

Thanks for reading.

PS.  I haven’t put the links in yet – where I’ve mentioned previous posts.  Will add soon.

Unwanted Visitors

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Last Friday was a very bad day.

An incident happened in the morning which sent all my ME symptoms into freefall. And me into a big meltdown.
It was stressful and unnecessary.

The day started well and I was up and dressed at 9 am. 
I’d had a bath or shower the night before, and had gone to bed very exhausted after it. But had slept soundly. So I was quite refreshed for a change.
The plan was have some breakfast then get outside for a short walk. Even if just very short. It looked lovely outside – bright and sunny. I was desperate to get out.

I was sitting enjoying my breakfast when the doorbell rang at 9.30 am.
I was expecting a delivery from Amazon of Co Enzyme Q10 capsules (taken to try to reduce my chest symptoms). So I opened the door without hesitation.
Two men were standing there and one of them introduced himself and showed me some ID.
I didn’t take in much of what they said or where they were from – but I managed to hear the bit about repossessing a property. I knew they didn’t mean the one we now live in which is our home now. But my head was immediately spinning.
I think I said something like “Oh for God’s sake, how many times . . . ” And then “you better come in” .  And I brought them into the living room.

I wouldn’t let them talk as my whole system had gone straight into a red alert state. From a stress/panic level of zero (totally relaxed) right up to a 10 (off the rails) in a spilt second.
No thinking about this and no choice in it at all.
I mentioned this in a previous post – the effect just a text or voicemail about the Bankruptcy stuff has on me now. To the extent I feel I cannot switch my mobile phone on now, as my body’s automatic stress response is so damaging for me (and my ME symptoms).
And that is just a simple phone message.  This event probably caused a much worse reaction.
I managed to digest the fact they represented solicitors who were acting for the mortgage lender Mortgage Express. Who now wanted to repossess 2 properties. Or they may have been from Sheriff Officers (like bailiffs) who the solicitors had employed.
Anyway, I got the gist of it.

I wouldn’t let them talk – instead I went straight into a sort of rant that must have lasted 25 minutes.  Hardly stopping for breath. A few times I did almost stop as tears were threatening to take over. But I just  kept on and on – like a steam train.
I was saying (maybe yelling) stuff like :

I am Bankrupt and have been for a year now
You (ie Mortgage Express) have been told this over and over and over
How many times do you have to be told ?
Why does NOBODY update your records ?
The whole reason for the bankruptcy was my health – to give away ALL CONTROL OF ALL THE PROPERTIES to the Trustee In Bankruptcy. So they would deal with EVERYTHING.
That is what I was told would happen
But it hasn’t happened
This is going to kill me
If I was well enough to sit here and have meetings – I wouldn’t have had to go Bankrupt in the first place
If it was just about finances – then I wouldn’t have volunteered for Bankruptcy. We could have sold our house yourself.
I used to have a perfect credit rating of 999 with Experian  (nothing to do with anything now – just misplaced pride I guess !)
I shouldn’t be getting treated like this
The Bankruptcy advisor told me the flats would all be handed back to the mortgage lenders. Then told us that the Trustee would be selling them instead.
Which was totally fine. Either way was fine
This was the WHOLE point of the Bankruptcy.
I’ve been trying to give you (Mortgage Express) these properties back for well over a year now
What is the point of repossessing properties that I am trying to give you back ?
How hard can you make it ?
It’s all such a shambles and its killing me
If you’re going to speak I’ll have to record it, as I won’t be able to remember anything you’ve said . . . !  (they couldn’t get a word in edgeways)

And on – and on – and on I rambled and ranted, until I finally ran out of energy.

The 2 men seemed fairly sympathetic, but that was maybe just because they couldn’t get a word in.
They did manage to mumble about procedures and stuff.  To be honest I wouldn’t have taken in anything they said – even if I had allowed them to speak a bit more.  They gave me some legal letters and tried to explain what they were.  But I just grabbed them and was saying stuff like
“I can’t even read this – it will just get posted onto the Trustee In Bankruptcy for them to deal”
“EVERYTHING gets sent onto them . . . ”
“They are supposed to deal with EVERYTHING . . .”

I think they were glad to get away.

After they left all my energy just evaporated.
I sat looking at my cold cup of tea for ages.
Then the tears started. From exhaustion, frustration, anger, etc etc.
Then I decided to phone my husband at work.
I shouldn’t have done this. But I had got myself into such a state I had to tell him. But all I did was rant on the phone to him. I kept saying things like – this shouldn’t be happening, they (the Trustee) must be able to stop this stuff, they were meant to deal with everything, etc etc etc

He then phoned the Trustee. But he said he ended up going into a rant himself on the phone, as he felt helpless and frustrated at not being able to do much to help.
When he called me back later, the only update was they had said they were very sympathetic to my health situation, but this stuff is just procedure.

And they suggested that I just do not answer the door to anyone . . !

How long for, I wonder . . . ?
These visitors were talking about 2 properties. There are another 12 to go . . .

I spent the the rest of the day curled up in a tight ball on the sofa. And just cried and wept for a few hours.
My temperature must have plummeted as I was very cold although it was sunny outside. So I needed the heating on for the whole day.
And all the usual symptoms were there – headaches, out of breath, heavy weight/feeling of compression on chest, legs and arms like jelly with no strength at all, head spinning and feeling dizzy, chest pounding – I dread to think how high my heart rate must have been
etc etc etc

So, to sum up the current situation :

Can’t bear to switch mobile phone on – because of unwanted missed calls and voicemails.

And cannot risk answering the door for the foreseeable future.

Given that I heavily rely on things being delivered (eg health items from Amazon) this isn’t ideal.

This situation is not conducive to improving my health in any way at all.
It is damaging it further.
It’s like constantly being made to walk on broken legs – destroys all chance of healing and recovery.

I just wanted to run away.
But I didn’t have the strength left to walk to the kitchen.

On Sunday night/Monday morning I was sick during the night, and had a lot of bouts of diarrhoea.
Horrible.

My whole system felt wrecked.

I just hope things improve soon.

A Long Slow Road

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image

Everything is very very slow.

HEALTH/ME :

Trying hard to get a bit better health-wise.
But it’s like walking such a fine line with ME.
Do just that bit too much and the payback is punishing. You crash, so many symptoms go thru the roof, and it feels like back to square one again. Then you rest to recover, try to build up a bit, feel a bit better, physically stronger, some more energy. And you try to do something big – like just go out!
Then wham and crash – all over again.
This condition is such a nasty piece of work. And I have to manage it on my own.
No medical help at all.
Last weekend I managed to get out twice – late on the Friday and also the Sunday afternoon. This was marvellous and I enjoyed both so much. But then “crash” – and I had to spend most of the last 6 days in bed again. I’m not even going to bother detailing all the different symptoms as I’m so sick of them.
But its not easy.
And painfully slow.

BANKRUPCY STUFF :

This is painfully slow too.
I don’t mean the waiting to be discharged from bankruptcy. This can happen after 1 year – or it may take up to 3 years. And of course is on your record for ever. Well, 6 years I think is technically correct. But as good as forever I feel.

That’s not the problem.

The problem for me is the amount of mail, phone calls etc that I still get from people like mortgage lenders, etc. And the adverse effect it has on me every time.
Last week alone my husband posted off 3 big A4 size envelopes stuffed full of letters, demands, threats, etc to our Trustee In Bankruptcy. We try to send any mail on every week. Last week was admittedly worse than usual – but even then.
It’s not ideal.
And this is maybe 18 months after we first took advice from the bankruptcy adviser.
And later decided to proceed. My health had totally crashed to my lowest ever level of functioning in Feb 2014 so I really felt this was the best, if not the only option.
All this time – and still it all goes on and on.
Nobody seems to even acknowledge that we are Bankrupt. The Trustee say Yes they tell everyone. But still I am being pestered.
Getting to the stage (again) that I don’t even want to switch on my mobile phone. Because of missed calls, voicemail messages, etc. This isn’t good because I still want to be able to use text messages at times, or maybe listen to calming music on the U Tube app in the phone. Even if I can do very little else some days.

I think I have said this before – this process has been torture for me. And has had the effect of worsening my ME overall. I have more symptoms now than when it started.
Plus recurring nightmares over the last 18 months.
My automatic stress response to this stuff is very heightened now. Very over sensitive. The smallest of things sends my nervous system into orbit some days. And this triggers off so many debilitating symptoms (eg, the severe headaches). It’s automatic and just happens without any thought about it. Or choice. And it takes ages (sometimes days or more) for me to “come down” again. And for the symptoms to lessen.

Basically, my whole nervous system feels like it is in shreds.

And the point of the Bankruptcy (the WHOLE point) was to give away all control of everything to a Trustee In Bankruptcy. So they would deal with everything and everybody. Most especially all the properties and all the mortgage lenders.
That was what we were told would happen.
If I was able to continue to do stuff like this – then I wouldn’t have chosen voluntary Bankruptcy in the first place.

If I had a pound for every time I’ve said this over the last 12 months . . . .

I do realise that people may read this and think – yeah, but you must have been in a big mess financially ?

And yes, of course debts had accumulated. I had been hemorrhaging money over a few years leading up to Feb 2014 because my health had been getting even worse. I mentioned this in a previous post somewhere.
BUT – if I had been able to keep going then these would have been cleared in a few years by selling maybe 2 or 3 properties. But I couldn’t keep going – as there was no way of getting a reasonable break from everything.
ALSO – if it was just about financial reasons then we could have sold our home ourselves. Rather than handing it over the the Trustee. They sold it at a cheap price (as expected). And within just a week.
And the profit made (or equity released) was approx £150,000.00. No small sum.
Plus our 3 mortgage Endowments were taken from us and cashed in. (This was a total shock.) Producing over £40,000.00. Again, no small sum.
So we “gave away” almost £200,000.00 in “available assets” to the Trustee.
My business debts (property debts) when my health crashed early 2014 were nowhere near this sum. And at this point everything was being paid ok, nothing was in arrears, no missed payments or anything like that.
I was even still getting 0% balance transfer offers from a few of the credit cards that I was using for business cashflow and expenses.

So the issue wasn’t the amount of debt being carried – but more the fact that I could do no more. Physically (and mentally) I had nothing left.

So everything given up in return for Bankruptcy = a Trustee taking over and dealing with everything = total rest and peace of mind for me = the chance of my health improving.

It has been nothing like this.

I have no idea what’s going on. And it’s very hard to get anything in writing.
From day 1 – I begged for everything in writing. From the bankruptcy adviser and then from the Trustee In Bankruptcy.
(Because of my health and most especially the brain fog.)
But it just doesn’t happen.

But I know the only way thru this – is to go thru it.
And short of medicating myself into a stupor with perhaps very strong anti-depressants – I just have to take it.

GP PROBLEM :

After 10 months of trying – I’m not much further on with getting an ME friendly GP or any help or support.
The health centre I was trying to join – I had to admit defeat. And give up. A GP there had been mentioned as being good. But the staff (a nurse and 3 different medical receptionists) had no knowledge or time for people with ME. They just kept telling me to do things I wasn’t able to do. And were abrupt and totally lacking in any understanding or patient care. Every interaction I had (one appointment and 3 phone conversations) resulted in just making me more ill with the upset and stress of it.
These people are being paid salaries to treat people like this.
So it was 9 months of time and energy wasted for me.
As I’ve said before – you need to be much more well to be able to cope with this sort of stuff.

However, I think I am now successfully registered with a new small GP surgery.
I say I think – because I haven’t had any card from the health board or anything in writing to confirm this yet. The receptionist said I should get a card to confirm after a few weeks. Hasn’t arrived yet. But hubby phoned and the receptionist said it was OK.
This surgery is small with just one GP. But there was no in-person appointment with a nurse or GP required to apply to join. Just a form which was fairly simple. OK, it still took me ages to complete with the brain fog, headaches, etc. But fairly simple by most people’s standards.

The only thing is – I have no idea what the GP’s view and attitude towards people with ME is yet.
I will just have to hope for the best . . .
Anyone reading this who has no experience of ME may think I am over-worrying about this.
Here are just 2 examples from folk on twitter very recently of how it can be :

example 1
A sufferer’s GP told her father that he “didn’t believe in ME” and that it was “a charter for malingerers” .
This resulted in a long standing family break up. As it presumably resulted in the person’s father disbelieving his daughter and giving no support.
Which to be honest is absolutely unforgivable. But the GP did terrible damage here.

example 2
A male sufferer changed to a larger health centre to try to get better treatment, more respect.
There were 8 GPs in this health centre.
Over time (probably a long time) he found out that 7 out of the 8 GPs did not believe in ME. And only 1 did.
At least there was one.
But that’s a rate of 88℅ who would treat you poorly at that centre. And just 12% who would be likely to give you any support at all.

I do hope this isn’t reflective of the nationwide average . . . .

– – – – – – – – – – – –

Ok, thats all for now.
Incredibly exhausting to write all this. Much longer than I planned.
But it is therapeutic.

My Life so far – NOT what I expected

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image

I save a lot of pics like this if I see them on twitter or somewhere – just because I like them.  Mainly funny, upbeat,  philosophical, inspiring,  motivating etc.
Something a friend said to me in a text message recently reminded me of this picture.
It certainly describes my life.

But I’m not OK with it – yet. That will take a while.

I’m 55 – and now have nothing.

The post from 7 Feb 2015 titled Battered, Bruised and Bankrupt explains.

When I say nothing – I mean nothing financially. And no security.

No money
No income
No savings
No ability to earn any income because of all the ME symptoms severely affecting my life. (Certainly not just now.)
No Benefits – I am not well enough to deal with the process. Nowhere near well enough.
No GP ( or as good as no GP).
I do own 50% of this flat I now live in with my husband – but at the moment this is 50% of nothing (financially). As it has a large mortgage on it and there is no equity in it.
And we now have nothing to pay off the interest-only mortgage with in 8 years time. We did have various mortgage Endowments – but they were taken from us by the Trustee In Bankruptcy and cashed in.

Worked hard since 17

With Commercial Union Assurance (now part of Aviva) for 19 years.
Then Prudential for almost a year.
Then NTL ( now Virgin Media) in telecoms for 4 years

Studied for professional qualifications in Insurance (Life and Pensions) and Financial Services (for Compliance work).
Obtained A.C.I.I ( ie. Associateship Of The Chartered Insurance Institute) in the Life & Pensions branch early 1980s .
Obtained MLIA {Dip) and FPC (Financial Planning Certificate} in early 1990s.
During the early 1980s I also worked in pub jobs for 3 (sometimes 4) nights a week – on top of my full time job. I did this over a period of a few years and think I worked in 5 different pubs.
The reason – to save up for my 1st flat. For the deposit, costs and fees, furniture, etc.
I was keen to do this but not have any debt when I moved in.

All these jobs/careers I had to give up and resign from due to my health. And all the symptoms of what I now know to be ME (or CFS as it was called at my diagnosis).
NB. I left all these jobs with nothing – even after 19 years in Commercial Union.
There was no help or support from my GP at all. And I just wasn’t well enough to be able to push for more help.

Finally got diagnosed with what was called CFS in 2003.
After more than 12 years of going back and forwards to GP – but feeling I was being treated like a time-waster each time. As if I was just being lazy.
Appalling treatment really.

By 2004 I had to accept I just couldn’t risk working for an employer again. Assuming anyone would have me . . .
Although I was feeling a bit better again after some rest time, I still had a lot of symptoms to cope with. I knew I could only work when I was able to. And would often need big rest and recovery periods.
No employer could be expected to cope with this.

So the only option left was to work for myself.

In 2004 I started up the Property stuff seriously.
Buying the 2nd flat to rent out (ironically the one we now live in and are very glad to have !).
By using savings and remortgaging our home I got started.
Then managed to build up to owning 15 flats by 2014.
Mainly by remortgaging them or using additional borrowing to raise funds for the deposit, fees and costs to buy the next flat. When the value of the property had increased enough to allow this.

The point of this was to get to a point where I would have been able to sell off a property every year. Or maybe every 2nd year.
And the profit would give me an annual income.
(It is very hard to make any real monthly income from the rent – there are so many expenses and things to deduct from it.)

Ironically, if I had done nothing at all we would now be much better off financially.

Hindsight again . . . . A totally useless thing.

Remortgaging our home was a calculated risk. But it was the obvious and only option to use. Neither of us have ever had any inheritances or lottery wins !
It had loads of equity in it at 2014.
Partly because of the increase in the property market. But also because we had bought it in 1998 with a very small mortgage. We put down a large deposit of 65% of the purchase price.
This was done partly by saving up very hard for a few years and going without most things. Really scrimping on everything.
And the reason for this – our future security . . . .

Now at July 2015 – Bankrupt.

Husband dragged down with me – as some properties were bought in joint names.
But he has been totally supportive and never blaming me. And I’m so grateful for this.
So, the loss of everything – apart from the flat we are living in.
Oh, and we were allowed to keep our beloved BMW. Because it is so ancient now ! (Think I mentioned this in a previous post.)

As I explained in previous post, the Bankruptcy was voluntary because of my health.
I couldn’t go on.
And this was the only way, as I understood it, to give away all control and responsibility for all the properties. And hand over all dealings with everyone to a Trustee In Bankruptcy. ie. All dealings with banks, letting agents, tenants, insurance companies, etc etc.

It hasn’t worked out quite like that . . . .

But that’s life isn’t it ?
You get told something but the reality turns out to be quite different.

But at some point all this horrible Bankruptcy stuff will come to an end. And I will be able to “relax” and have some peace of mind.
No idea when this will be – impossible to get any clear info in writing.
And I will have the energy (well, more than just now) to hopefully find a decent “ME friendly” GP.
Not really for treatment – not expecting miracles. But just for some symptom control and support.

At the moment I have none of this. Just nothing at all.

But I’m still here.
And there are many people out there with ME or CFS who are much much worse than me.

So I’m grateful that I’m not even worse than I am. And that I do have “mini bursts” of energy. And can do some things. Even if the recovery time after it takes days . . . !

PS.
Apologies for any typing errors. I tried my best to check it before hitting the publish button.
But I really struggle to use my laptop or tablet etc. And am all out of energy now.

Battered, Bruised and Bankrupt

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Voluntary Bankruptcy

This was the biggest and most life changing event which dominated most of last year.
And is still going on now.
I became voluntarily bankrupt w.e.f September 2014.
Or “in Sequestration” to use the correct scottish term,

I had to make this hard decision because my health was so poor. It had been steadily getting worse over the last few years and I was living a “non-life” really. In bed most of the time (maybe 80% or 90% of the time) struggling with all the horrible ME symptoms (an ever lengthening list). And at the same time trying to keep the property stuff afloat – mainly from bed. With my mobile phone for texts, emails, internet banking. And of course – actual phone calls. But phone calls had to be kept to an absolute minimum as I was too ill most of the time to carry out a business type phone call, or remember accurately what had been said . I relied mostly on emails as I could take breaks in a way you can’t in the middle of a phone call. Plus I needed a written record of almost everything – as my brain fog was severe.

But this was in no way ideal. You can’t deal with everyone purely by email or text. Plus a simple email that should take maybe 20 mins would often take me 4 hours to type. And that could often take me a day or two to recover from the exertion of doing even that.

My “PEM” or “PENE” (post exertional malaise / post exertional neuro exhaustion) has been severe and punishing.

Sometimes I would manage out of bed and get to my desk in my dressing gown and slippers. Looking like an unwashed wreck. Often I had to choose between washing/showering and getting any work done.
Almost every small bit of energy I could muster up had to go on work/property stuff. But over the last few years, I had built up a massive backlog of stuff that I would never have gotten on top of.

In the end I had to choose between my health and my ME getting even worse – or giving everything up.
When I write it like this, I can see there really was no choice.
But I went thru a lot of mental agony and anguish before deciding. Even started to have panic attacks at one point.

Doing this stuff had been my life for the last 11 years.
And I had struggled on for a very long time – because you can’t just get rid of 15 flats overnight. And I knew the consequences of “giving up” would be awful.
It wasn’t like resigning from my career in insurance in 1997 because of my health, after almost 20 years with the same employer. And walking away with nothing. And that door just closes behind you.
That was simple compared to this.

This has been terrible, and caused my health to go even further downhill. Which was one of my fears about doing it.
But it had to be done – and it was done to give myself a decent chance to improve again in the future.

When everything is more settled, and I get to a stage where I have some peace of mind.
I feel sure I can start to improve then.

I’ll probably write more about this in later posts.
As it has been traumatic, and I do need to get stuff out.

 

Moved house

For 2 reasons :

1) I wasn’t managing in our home very well any longer.
It was a semi-detached house with stairs (obviously). The stairs were hard. I could manage them some days – but with bad exhaustion after. Other days I couldn’t manage at all. My bedroom had been moved into a downstairs room some time ago – but the bathroom was still upstairs. (Had a downstairs loo, thank goodness.) My office was also upstairs (and I was hardly managing into it). The kitchen was too far away from the bedroom and living room for me. And when I did get into it, I often couldn’t stay in it for more than a few minutes at a time – as there was nowhere to sit down. And various windows throughout the house (incl my bedroom) I was unable to open – which would drive me mad.
It had a garden of course, but I rarely managed to get out in it over the last year or two. Any “good” days were spent trying to work and keep everything afloat. Not every one of course, but most of them.

2) The other reason was that we knew we would later voluntarily hand over our house to the Trustee In Bankruptcy. It would have been “taken” off us anyway. We had lived in it since 1998 and there was plenty of equity in it. So we knew it would be sold off to take the equity.
It has just gone onto Rightmove for sale this week. And it looks so sad and empty.

A house move is a stressful event anytime.
We moved well in advance of the bankruptcy taking effect. I actually moved into the flat before my husband at the end of May 2014. As I was desperate to get away from the house, its stairs, and all the other problems.

But as anyone with ME will know – a house move takes a huge toll on your health. Even when it’s a happy house move.
But in these circumstances . . .
I’m just glad its over – and I pray that we don’t have to do it again.

 

Had to change Banks – twice

How would I describe doing this (with ME) ?
Complete bloody torture . . .
The 1st change was recommended by the financial advisor and done ages before the bankruptcy. Bank manager clearly informed of probable future bankruptcy therefore ensuring everything done properly.
It took me months to get all the direct debits set up again – as I can hardly manage to tolerate using the laptop, or phone, etc with my ME being so bad.

Everything was just getting settled and running fine – then the bank decided that they were freezing and closing down all accounts (nationwide) for any bankrupt people. No notice was given at all. It just happened instantly.
This threw us into chaos.
Husband’s salary had just been paid in a week before this happened and we couldn’t get it back out. Well, we did eventually. But with a lot of hassle.
And trying to get a new current account once you have actually become bankrupt is very difficult. (No surprise really.) Most banks don’t want to know, and I actually thought we weren’t going to be able to open one at all at one point.
It was chaos, and mega stressful with ME.
Because you can’t pay many things without a bank account. And, as already mentioned, I am very limited in even being able to make phone calls. Or use the internet. And physically going out to places to try and pay things in cash was totally beyond me. (Still is most of the time.)
We now have a new account up and running (thank god).
But almost everything (DDs etc) have still to be set up all over again.

Not easy . . .

 

Homeopathic Hospital (or Centre Of Integrative Care)

Had a 5 day in-patient stay in January 2014.
This was a huge disappointment and actually resulted in my condition getting even worse afterwards. Especially when I read the doctor’s report a few weeks later.
There were many good things about the stay – I must add this.
Eg, the company of the other patients, getting good food at a regular time, the garden view from my bed (and got out into it twice), some of the meditation classes, a marvellous massage (called a Bowen Therapy massage), a great adjustable bed, a chair in the shower area to sit down on.
But there also a lot of odd, weird things that I tried to ignore and block out while I was there. This was hard work to do mentally, as a lot of things didn‘t “feel“ right.
But I didn’t speak up while there.
Partly because too exhausted – the whole effort of getting organised and getting there had taken its toll. And my husband was ill too and I was worried about him.
And the brain fog doesn’t make it easy to think clearly or express yourself when needed.
The other thing was – I didn’t want to be labelled as being “over-anxious” or having a “depressive/negative mood”. So I just kept quiet about things I was concerned or confused about.
But when I read the doctor’s (fairly short) report later – I was horrified. Angry, upset and despairing at what a waste of time and energy (mine) it had turned out to be.
Most of my symptoms had been ignored. And I reckoned about 80% of what I had said (or tried to say) had been dismissed or ignored. Or I hadn’t been allowed to talk about some symptoms.
Looking back – the total time the ward doctor spent with me was maybe 45 mins on the 1st day. Out of a 5 day stay. For 25 years of illness . . .
And a list of symptoms that was getting longer and longer. And more severe.
I had been so “grateful” and “positive” and “upbeat” while I was there. And on the last day, And even when I was just home.

But it all knocked the stuffing out of me.

I tried to reason with myself that I maybe had been expecting too much. But I just expected a doctor/doctors who had some knowledge and understanding of ME/CFS. Then I used up even more energy trying to go back over how it had gone so wrong, why had I not been able to make myself understood, did I not speak clearly enough, had I been speaking too fast (trying to get 25 years of history out remember), etc etc etc.

But it was damaging.

 

Have no GP now

Well, that’s not totally correct. But as good as.
The combination of having moved house to a different post code (although I’m actually closer to the surgery now), and the fact I haven’t been able to get into to surgery since 2011, means that I was told in October 2014 that I had to find a new GP.

I’m still reeling from the phone call that day.

A GP that I had never met or even spoken to before phoned me after my husband went into the surgery before going to work that morning. To ask for better (any) painkillers for me. My headaches have been very bad the last few years (mentioned while in the Homeopathic Hospital, but not taken seriously). And I had been awake most of the night actually crying with the pain. One of the worst nights ever, pain-wise.
The GP who phoned was abrupt and aggressive, wouldn’t let me speak, and I’m not sure she even understood what I was trying to say part of the time. She had a foreign accent.

She used phrases like :

“What’s wrong with you – are you housebound or something ?“
(Re why I haven‘t got to the surgery since 2011)

“We only do home visits for elderly people or people who cannot walk”.
(I didn’t want a home visit – just some effective medication.)

“If we come out to visit you and find out you CAN walk – we will be very angry with you.”
(I didn’t want a home visit but I was speechless at this.)

“I am noting your records now that you are not to be given any more prescriptions.”
(She talked to me like I had done something wrong. And was therefore punishing me.)

“There’s no rush – just within the next few days.”
(Telling me I had to change to another GP surgery – despite me trying to explain I hardly managed out, or even to make phone calls most of the time.)

And it went on and on.

I was in tears (of frustration) after it. And my heart rate felt like it was thru the roof for days later.
I have been with that surgery since 1987 and l don’t think I’ve had a home visit (or even asked for one ) in all those years.

 

Asked 2 ME Charities for help in finding a new “ME/CFS friendly GP”

1) Most recently (a few months ago) :
Paid £20 to join one and used a lot of time and energy emailing their advocacy worker. To explain in detail how limited I am and why I was asking for their help with the GP issue.
She was very nice, but explained she had a big backlog of people with ME needing help. And couldn’t really spend any time with me at this point in time.
She did mention one GP but I don’t think the practice is going to be suitable for other reasons. Even if he still works there, which she wasn’t sure of. And I would still have be a lot more well than I am just now to be able to make enquiries, or go there.

2) A few years ago :
The other charity (or maybe its more of a support group) – I used to be a member of years ago. But only managed to go to 2 or 3 meetings.
Anyway, I asked if I could pay the annual membership and rejoin. And explained my main need was for help finding a decent GP.
(This has been a big problem for me for years.)
I had hoped that somebody/anybody could just give me a recommendation for a decent one. I got an email reply just suggesting I come along to their next meeting – although I had tried to explain how limited I was, and rely mainly on email. I emailed back a few times asking could I pay their membership and rejoin anyway – but they just stopped replying.
So I gave up.

 

Car broken down at end of road – 5 weeks ago

I went into bankruptcy for health reasons.
To relinquish all the properties, and all the work and responsibility that went with them. And all the dealings with Letting Agents, Tenants, Banks, Mortgage Lenders, Tradesmen, Factors, Insurance Companies, etc etc etc.

It wasn’t so much for financial reasons – although debts had certainly built up over the last few years with me not being able to deal with things well, or quickly enough. I was making losses and haemorrhaging money.
But before the process started, everything was getting paid ok and nothing was in arrears. But it was a struggle trying to juggle it all.
Our assets well exceeded any debts – on paper anyway.
After the process we are left with almost nothing.
The Trustee is allowing us to keep this one flat to live in – mainly because it has a big mortgage on it and no equity in it.
But any life assurance and mortgage endowments were taken off us and cashed in.

But – the one bonus for us was they allowed us to keep our beloved BMW.
Only because it is so old – it is a Y registration. Which is roughly 15 years old I think. And it is probably worth less than £1000.
I have always loved this car.
It is the most reliable car we have ever had – and it looks good. And is so comfortable and secure to drive (when I’m able to.)
I was forever boring people with how reliable is has been.

5 weeks ago it broke down at the end of the street . . . .

A major suspension issue – involving a lot of labour time to fix (as well as an expensive part). To have it fixed by a BMW dealer or even a smaller garage would be unaffordable. The repair would cost more than the value of the car itself.
However, we are lucky that a friend of husband’s is working on it. Which will be much cheaper. But its a very slow process as he can only do bits at the weekends. In daylight. And the weather hasn’t helped.
But it will get fixed – eventually

 

– – – – – – – – – –

 

This blog post has taken me ages to write. I changed it so much. And didn‘t want it to be so long – but felt the need to get all this out.

And it will be the first that most people in my real life will learn about the Bankruptcy.
I have only managed to tell a very small number of people. Mainly because my health has been so bad and I have hardly managed to see anyone.
(And it’s not really suitable for a text message . . . )

I’ll probably write more about much of this stuff in future posts.
I’m desperate to be writing again.
It is a struggle as I’m still feeling quite unwell much of the time. And just trying to think and concentrate is exhausting. And using my laptop feels like torture some days.

Doing this post will no doubt wipe me out for days. I feel totally wrecked after doing it.
But in this case, it will be worth it.
The more I can pour all this stuff out (onto this Blog) – the more it is out of my head. And creates “headroom” for better stuff.

That‘s the plan anyway . . .

Am I getting worse ?

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Its now Jan 2013 and not much has changed. In terms of my day to day life and CFS.
I actually wonder if my health has got a bit worse over the last 2 years. But its hard for me to be objective and measure this clearly.
My head is filled up thinking about work (property) issues and problems. And household problems. And money matters – household and business. And practical problems of so many things I need to do, but haven’t been able to :
eg :
get my hair cut (over 12 months now), visit to dentist (maybe over 2 years), go for breast screening, was due 3 years ago. (have had 3 appointments but wasn’t well enough for any of them).
With all this going on, plus my CFS neurological smptoms of “brain fog” and the “racing brain” (to name just two), this is probably why I haven’t got the ability to tell.
But I am getting more severe and longer-lasting symptoms some weeks. And it seems to  take me longer to recover from my “crashes” each time.
People with CFS and ME will know what I mean by crashes. But for the benefit of others – it is more commonly called post exertional fatigue or post exertional exhaustion. And its nothing like the natural tiredness, or exhaustion, people can feel after a long hard day. Or even after doing something out of the ordinary which been exhausting. Like a marathon run. This tiredness/fatigue/exhaustion is entirely natural and a normal healthy person usually just needs adequate rest to recover from it.
But with CFS and ME it is so much worse.
The level of exhaustion, and severity of  other symptoms, can be very bad indeed. And often totally out of all proportion to the amount of time and energy the person had used. On whatever they were doing. And to make it even harder to control – it can fluctuate from day to day, week to week, etc. (Making planning things often a real challenge, if not impossible at times.)
An example from my day to day life :
I find that I’m often exhausted now after having a shower and may need hours to recover. Not every time but too often.
By “exhausted” I mean – I am too weak and out of breath to be able to do much other than rest. My arms are sore and weak with the effort taken holding them up long enough to shampoo my hair. And my chest is pounding and heart racing. I took my pulse after a shower a while ago – it was 141. This is maybe 2 to 2.5  x  the average rate of a fitter person ?
Yet it was a simple, short and non-stressful activity, done slowly under no pressure.
This makes me wonder how high my heart rate goes when I feel under any major stress.
eg. In November 2012 when relations turned sour with a firm of tradesmen I had used for lots of work in my properties. And spent much money with them. One of the 2 partners turned into a total scumbag and actually threatened voilence against the properties. Saying he would “rip the fittings out of all of them”. Or words similar. And this in writing to me by text message. . . Then a 2nd text message to me confirming it was “a promise, not a threat” . Unbelievable.
Just to add here : I had an ongoing account with this firm and faithfully paid them every month as had been agreed. So I wasn’t in default to them in any way. But I had been raising my dissatisfaction with some of their work, and various broken promises with time-scales etc.
And they just turned nasty.
That week I was in bed almost the entire time – and my worst symptom was feeling like an elephant was sitting on my chest. That heavy, weighty feeling.
Just awful.
But I still had to deal with the situation as best I could – from my bed. And not very well admittedly.
Its all over now and these people are out of my life.
But I hate to think that this could have worsened my condition. As I was experiencing so many bad emotions that week – fear, anger, disbelief, frustration, despair. But anger more than anything.
However they say what doesn’t kill you makes you stronger.
I certainly hope so  . . .  !

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