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Well - the grand total has now gone up to £41.50 - included

in that is a donation of £10, and two donations of £5 plus two members buying

two quizzes - 15 members in all - out of over 1414.   Rather sad.

Luv - Sheila

TPA is not a government agency. TPA does not

get government funds to fight for your health. Sheila and I have exhausted

every avenue of government related to your regaining your health. We have spent

thousands upon thousands of hours each researching medicine and law in our vain

attempt to persuade those who are supposed to be properly caring for you to do

so properly. However, they will not listen.

It appears that the only way, aside from the Lord producing a miracle, that

this whole matter will go to court. That is going to take far, far more than

the 22 quid that has been collected so far for a little light hearted game that

will end with a prise. It makes me wonder....

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Yes come on everyone get your paypal accounts out of moth balls, I know for a fact at least 5 of the 15 are non-members - how sad is that!!

RE: Support TPA

Well - the grand total has now gone up to £41.50 - included in that is a donation of £10, and two donations of £5 plus two members buying two quizzes - 15 members in all - out of over 1414.

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Dear ,

Reference your call for funds to take the relevant authorities before the

courts. I agree that after many years of campaigning we are getting nowhere and

the reasons, I suspect, are many and varied including pride, arrogance, and

financial!

I believe that the law can work, as it did for a local group campaigning against

a wind farm on an adjacent airfield. They set up a fighting fund and used it to

take the local council to the high court and won. No wind farm! However, a

fund for such legal purpose would need to be set up as an entirely separate

entity to the normal TPA account and potential subscribers would need to be

properly informed as to the full strategy of such legal action, prior to

offering their support and contributions. Legal fees are horrendous these days

so a very large amount of money will be needed and that sort of cash MUST be

seen to be looked after safely, used conscientiously and with complete

transparency.

I agree that it is, probably the only type of action that may produce the

desired effect and providing that the infrastructure is in place, I for one,

will be very willing to make a donation and also to be a witness in any

proceedings taken.

I should also like to encourage patients to be more pro-active at local level

and challenge their GP's attitudes and those of the Endocrinologists etc..,

where appropriate, in writing, so that there is a record. I have been doing

this, in recent months and will continue to do so until a common sense approach

to my treatment, is adopted.

I offer you my full support in this matter and I look forward to hearing about

your policy in due course.

Best Regards,

Sheena

>

> TPA is not a government agency. TPA does not get government funds to fight

for your health. Sheila and I have exhausted every avenue of government related

to your regaining your health. We have spent thousands upon thousands of hours

each researching medicine and law in our vain attempt to persuade those who are

supposed to be properly caring for you to do so properly. However, they will

not listen.

>

> It appears that the only way, aside from the Lord producing a miracle, that

this whole matter will go to court. That is going to take far, far more than

the 22 quid that has been collected so far for a little light hearted game that

will end with a prise. It makes me wonder....

>

>

>

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Hi

Sheena - many thanks for writing this - we need all such experiences on board.

We are, at the moment, registering TPA-UK as a Charity because funding will be

much easier to get - if, indeed, there are people willing to help fund our

campaigns for justice for the tens of thousands of sufferers in the UK alone

who are being left without a proper diagnosis for their symptoms of

hypothyroidism and therefore given no treatment - but for those who are being

treated, they are not given a choice of treatment and a large minority do not

regain their normal health on levothyroxine sodium-only.

Have

you any ideas of details this group used to set up a fighting fund?

We

certainly do appreciate we have a fight on our hands, but if I didn't believe

we could win, I wouldn't be wasting my time here. We have all the medical science

and rights on our side - the endocrinology specialty and the British Thyroid

Association, including the Royal College of Physicians do not.

Luv

- Sheila

Dear ,

Reference your call for funds to take the relevant authorities before the

courts. I agree that after many years of campaigning we are getting nowhere and

the reasons, I suspect, are many and varied including pride, arrogance, and

financial!

I believe that the law can work, as it did for a local group campaigning

against a wind farm on an adjacent airfield. They set up a fighting fund and

used it to take the local council to the high court and won. No wind farm!

However, a fund for such legal purpose would need to be set up as an entirely

separate entity to the normal TPA account and potential subscribers would need

to be properly informed as to the full strategy of such legal action, prior to

offering their support and contributions. Legal fees are horrendous these days

so a very large amount of money will be needed and that sort of cash MUST be

seen to be looked after safely, used conscientiously and with complete

transparency.

I agree that it is, probably the only type of action that may produce the

desired effect and providing that the infrastructure is in place, I for one,

will be very willing to make a donation and also to be a witness in any

proceedings taken.

I should also like to encourage patients to be more pro-active at local level

and challenge their GP's attitudes and those of the Endocrinologists etc..,

where appropriate, in writing, so that there is a record. I have been doing

this, in recent months and will continue to do so until a common sense approach

to my treatment, is adopted.

I offer you my full support in this matter and I look forward to hearing about

your policy in due course.

Best Regards,

Sheena

>

> TPA is not a government agency. TPA does not get government funds to fight

for your health. Sheila and I have exhausted every avenue of government related

to your regaining your health. We have spent thousands upon thousands of hours

each researching medicine and law in our vain attempt to persuade those who are

supposed to be properly caring for you to do so properly. However, they will

not listen.

>

> It appears that the only way, aside from the Lord producing a miracle,

that this whole matter will go to court. That is going to take far, far more

than the 22 quid that has been collected so far for a little light hearted game

that will end with a prise. It makes me wonder....

>

>

>

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found in this incoming message.

Checked by AVG - www.avg.com

Version: 8.5.432 / Virus Database: 270.14.137/2617 - Release Date: 01/13/10

19:35:00

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Hi there,

There are solicitors out there that are willing to

take on a case for free – No win no fee – I have previously

approached them but was unable to go forward myself due to health issues that

do not meet the criteria i.e I had an ongoing illness that went alongside the

thyroid condition – so not a pure case.

Regards

Mandy

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