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When writing the press release please remember that if it turns into one long

accusation no paper will print it. It needs to be abjective, accurate but

naming NO names and not taking anyone to task.

I know it is very tempting to ram home the message but in reality this will not

happen as it just won't get printed.

YES you can say that the charges were innaccurate but NOT trumped up.

Yes you can say how unfair it is that doctors have no protection against such

charges but the GMC must not be criticised.

I say this knowing how hard it is to get anything printed in a newspaper - even

in the 'letters to the editor' column.

Please don't waste this opportunity by trying to take revenge.

Glynis

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To get justice you need a platform, I understand how you must feel, I only hope

that you will understand how I feel and the reason I started this thread. I do

not want to see this opportunity wasted either.

>

> I am aware of all of these things Glynis and aware of the importance of

> getting this right. I have no intention of wasting this opportunity. This is

> NOT about taking revenge - this is about getting JUSTICE - not just for tens

> of thousands of patients in the UK alone who have been left suffering, but

> for tens of thousands of doctors too.

>

> Sheila

>

>

>

>

>

> When writing the press release please remember that if it turns into one

> long accusation no paper will print it. It needs to be abjective, accurate

> but naming NO names and not taking anyone to task.

>

> I know it is very tempting to ram home the message but in reality this will

> not happen as it just won't get printed.

>

> YES you can say that the charges were innaccurate but NOT trumped up.

>

> Yes you can say how unfair it is that doctors have no protection against

> such charges but the GMC must not be criticised.

>

> I say this knowing how hard it is to get anything printed in a newspaper -

> even in the 'letters to the editor' column.

>

> Please don't waste this opportunity by trying to take revenge.

> Glynis

>

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I disagree, I dont see how 'shouting from the rooftops'about such a huge

achievement could be construed as revenge. If it becomes public knowledge how

this particular doctor was treated by the GMC I dont think they would dare try

to bring new 'trumped up' charges either. Bad publicity is often a good

deterrent to any body !

I say publish and be damned, as it were !

>

> To get justice you need a platform, I understand how you must feel, I only

hope that you will understand how I feel and the reason I started this thread.

I do not want to see this opportunity wasted either.

>

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But you have to remember who you're working with here. The BTA / drug companies

can and will quash any detrimental publicity - whether that is letter or

article.

To get something published (even a letter) the paper publishing has to ensure it

cannot be sued - name names or criticise and they won't print it.

>

>

>

>

>

>

> I disagree, I dont see how 'shouting from the rooftops'about such a huge

achievement could be construed as revenge.

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This is true - this country is getting more like communist China every day.

Newspapers have to watch who they upset. This has to be done oh so subtley ...

and probably gently gently bit by bit. I think the general public are noticing

that something is going on with thyroid matters. So are doctors and endo

specialists - most of them are already on the defensive and they don`t like us

getting knowledge from the internet. As my doctor said " I suppose you got that

from the internet " as if you only get false information from the internet.

Jane

> >

> >

> >

> >

> >

> >

> > I disagree, I dont see how 'shouting from the rooftops'about such a huge

achievement could be construed as revenge.

>

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…and the BTA et al also have to remember who they are

working with, i.e. patients with symptoms of hypothyroidism who need to be

properly diagnosed and given a choice of treatment. As I am the one who will be

writing the PR, then I will decide whether what I write might be considered

detrimental or not. I have been running TPA for quite a few years and to date,

I am not aware of every having written anything that would be considered

detrimental or run the risk of ever being sued. I'm quite a cautious old bird

you know because I do try to think first!

If I paid attention to all those people telling me to " be careful "

and not upset " them up there because they won't like it " , I would

have blown TPA into the ether long, long ago.

Certain people and organisations need to be upset, but there are

ways of doing this, and then there are other ways……

Sheila

But you have to remember who you're working with

here. The BTA / drug companies can and will quash any detrimental publicity -

whether that is letter or article.

To get something published (even a letter) the paper publishing has to ensure

it cannot be sued - name names or criticise and they won't print it.

>

> I disagree, I dont see how 'shouting from the rooftops'about such a huge

achievement could be construed as revenge.

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My response to such doctors Jane is to say " Are you telling

me that you do not check out the research that is published in all the top

medical journals THAT are published on the Internet - I am VERY surprised at

this Doctor! This is the ONLY place I can be sure of getting the most up

to date information about the latest research and studies " . I would then

suggest that if they are not sure where to find such information, I would be

happy to give them some links. That should shut them up. This is so ignorant

and arrogant, it's beyond belief.

Luv - Sheila

.. So are doctors and endo specialists - most of

them are already on the defensive and they don`t like us getting knowledge from

the internet. As my doctor said " I suppose you got that from the

internet " as if you only get false information from the internet.

Jane

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"Certain people and organisations need to be upset, but there are ways of

doing this, and then there are other ways..

Sheila "SheilaGo for it ! I cannot think of suitable title but I'm sure you will get this to the attention of the general public, and those who are still publishing misleading or at worst incorrect information will have to rethink their publicity.Sue x

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Oh Sheila - I do wish I was as `on the ball` as you. You sound such a confident

gutsy person. Of course, your response is absolutely right and I have seen my

doc google stuff himself before. But he just made me feel as if I`d been a

naughty girl for looking on the internet. Its the illness - it tends to make us

all weak and wobbly and a pushover. But I`m learning, thanks to you and this

forum - thanks.

Jane

>

> My response to such doctors Jane is to say " Are you telling me that you do

> not check out the research that is published in all the top medical journals

> THAT are published on the Internet ...

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Thanks for the encouragement Sue - without such encouragement,

it can sometimes be very difficult to carry on. Afshan has posted the GPC

Panel's Determination to me and I should be in receipt of this on Monday, so

cannot do anything until I have got that, and then, I have to type it all out -

and it was LONG, but I will only be posting the part referring to their

decision regarding Dr Skinner's fitness to practice.

Luv - Sheila

" Certain people and organisations need to be upset, but there

are ways of

doing this, and then there are other ways..

Sheila "

Sheila

Go for it ! I cannot think of suitable title but I'm sure

you will get this to the attention of the general public, and those who are

still publishing misleading or at worst incorrect information will have to

rethink their publicity.

Sue x

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It is certainly difficult being the one holding their head above the parapet

-and we must give whoever is doing that not only the bullets to fire but the

support to do so.

And a thought - why not present the evidence - there is a growing register of

counterexamples - why not a similar one which simply asks - were you

successfully treated by the NHS or are you still struggling - and when you took

your health into your own hands and saw someone who listened and treated did you

recover more or less full health?

Something along those lines - a thousand or so short paragraphs of before and

afters - to prove that it is OK to medicate despite lab results and it does not

have bad side effects.

My only worry is that if I completely self medicate and do not at some stage

have the blessing of a GP then what will happen in say 25 yrs time when I am in

my 70s and maybe not able to order meds from overseas for whatever reason and I

become dependent on the NHS. I visit a lot of elderly folks in my job and in

carrying out assessments - I do come across - mainly women who have a diagnosis

of hypothyroidism on 25 mcg of T4 , overwieght,levels of confusion, etc etc. Or

worse, no diagnosis of thyroid issue but on thyroxin - one lady was so tired she

slept most of the day, was so overweight it was getting harder for her to

mobilise and she was puffy faced etc - I alerted her GP that she may need bloods

and looking at he said she was fine and they had been done the previous week!!!

SO - however, proactive and able most of us might be now in sticking two fingers

up at the system and doing our own thing - we need to make it work properly for

now and the future and some times we need to jump up and down and make a noise -

as long as we can provide the evidence why and keep banging on about how things

should be.

Well, rant over.

Stacey

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Hi Jane, actually, I am still often quite weak and wobbly and

have to remember to be as assertive as I can muster to get the message over. I

just hate it when doctors treat us like prime idiots, when most of the time, it

is them that are the idiots and not us, and they hide behind their title of

'doctor'. They want you to feel naughty so you will go away with your tail

between your legs, but don't allow that and stick up for yourself and others,

and that way, perhaps they will eventually learn. And Jane, remember that in

the past, before I started natural desiccated thyroid extract, I was ~VERY weak

and wobbly with brain fog, and a complete push-over. What I write now is only

what I have learned through the members of this forum and the information

available for all on the Internet.

Luv - Sheila

Oh Sheila - I do wish I was as `on the ball` as

you. You sound such a confident gutsy person. Of course, your response is

absolutely right and I have seen my doc google stuff himself before. But he

just made me feel as if I`d been a naughty girl for looking on the internet.

Its the illness - it tends to make us all weak and wobbly and a pushover. But

I`m learning, thanks to you and this forum - thanks.

Jane

_,_._,___

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Hi Stacey

You are so right.

We need to show the evidence as to why people on forums such as ours with

medical advisers such as Dr Peatfield and Dr Skinner are getting back their

normal health, which they are not doing following mainstream statements about

how to diagnose and treat those with symptoms of hypothyroidism. I am hoping

today to get the Panel's Determination in the Post and will get on with writing

a press release or press report.

Stacey, if you had

no other choice but to take your thyroid health into your own hands and

self-treat, then in 25 years time, you would not need a doctor - in fact, from

starting to self-treat, your health would be in better hands than with the NHS

at the present time as we know there are as many as 250,000 UK citizens who are

being left without the correct thyroid hormone replacement that will make them

well. You can turn your question around and ask what would happen when you are

your 70's and still having your thyroid sysmptoms being treated (or not

treated) within the NHS - will you even still be here. I stuck too

fingers up to the NHS and started natural thyroid extract 8 years ago and now

in my 70's and still going amazingly strong, everybody telling me at all turns

how well and healthy I look - and I AM. Natural thyroid extract is now a lot,

lot cheaper than when I first started out self medicating, but I persuaded my

endocrinologist that as I was having to take this for life, would he recommend

it on the NHS, which he did, and now has several of his other patients on NDT.

We at TPA at least,

will carry on banging the drum and jumping up and down until our message gets

out to everybody, and we need to thank doctors such as our medical advisers for

sticking with their beliefs and proving the NHS wrong - and now, even the GMC

has accepted it - so little by little, we are getting there. It is up to each

one of us though to fight our corner - get the facts (we have them all on our

web site and in our files if only members would read them) and pass them on to

our doctors. Without these, my endocrinologist would never have changed his

mind and continued to believe that L-thyroxine was the only medication needed,

and that natural thyroid extract had potency problems in the past and the T4

and T3 levels couldn't be standardised in all batches. He now knows how wrong

he was and is delighted to be making his patients well again.

Luv - Sheila

My only worry is that if I completely self medicate and do not at some stage

have the blessing of a GP then what will happen in say 25 yrs time when I am in

my 70s and maybe not able to order meds from overseas for whatever reason and I

become dependent on the NHS. I visit a lot of elderly folks in my job and in carrying

out assessments - I do come across - mainly women who have a diagnosis of

hypothyroidism on 25 mcg of T4 , overwieght,levels of confusion, etc etc. Or

worse, no diagnosis of thyroid issue but on thyroxin - one lady was so tired

she slept most of the day, was so overweight it was getting harder for her to

mobilise and she was puffy faced etc - I alerted her GP that she may need

bloods and looking at he said she was fine and they had been done the previous

week!!!

SO - however, proactive and able most of us might be now in sticking two

fingers up at the system and doing our own thing - we need to make it work

properly for now and the future and some times we need to jump up and down and

make a noise - as long as we can provide the evidence why and keep banging on

about how things should be.

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Snap - in the mental health sector, I saw many ladies and probably a couple of

gents that obviously had thyroid (some hyper, some hypo)symptoms. Many, many

mental health issues can stem from a dysfunctioning endocrine system - yet its

never considered by the professionals - easier to bung them on anti-psychotics,

anti-depressants etc which have awful side affects. It really annoyed me when

colleagues labelled clients as lazy and hassled them into action they just

didn`t have the energy for. Grrrrr.

Jane

>

>

>

>

> I do come across - mainly women who have a diagnosis of hypothyroidism on 25

mcg of T4 , overwieght,levels of confusion, etc etc. Or worse, no diagnosis of

thyroid issue but on thyroxin - one lady was so tired she slept most of the day,

was so overweight it was getting harder for her to mobilise and she was puffy

faced etc - I alerted her GP that she may need bloods and looking at he said she

was fine and they had been done the previous week!!!

> > Well, rant over.

> Stacey

>

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