Petition Update May 2018
Hi Everyone, many of our supporters have been following the posts on our Facebook page and our website, regarding our petition to get T3 reinstated as a prescription drug.
Many of you will have seen the post by Ursula Power from the ITT group. Ursula very kindly posted the link to the question John Woodcock MP was allowed to put to the house on the 30th April. John’s question was answered by Steve Brine, Parliamentary under-secretary for Health and Social Care. If you have read the post you will see that Steve Brine quoted the present guidelines to answer the question.
Put simply the guidelines are that;
- No new patients will get T3 prescribed
- Patients presently being prescribed T3 will be phased off T3 gradually and eventually just have T4 prescribed
- Patients who have had T3 in the past, and have had it withdrawn, can ask their GP for a referral to an Endocrinologist. If the patient can show they have a clinical need for T3. The Endocrinologist can then write to your GP. Your GP has to put in a request to the CCG to fund the T3 for you. If your CCG is supportive of the use of T3 and they can afford the cost, you may be able to get T3 via the NHS.
As you can see the situation depends on a lot of IF’S, AND’S and BUT’S and a lot of luck as well. I recently had a discussion with John Woodcock’s office about the unfairness of the situation.
Following on from this discussion John will be interested to know if;
- Your GP has refused to discuss T3 because they do not support the use of T3 or has told you the CCG will not support T3.
- Your Endocrinologist will not support T3 saying that there is not enough evidence to support the use of T3
- Your Endocrinologist supports T3 but your CCG does not
- You have had T3 withdrawn, and are not confident to order T3 yourself, so you just use T4 but do not feel well using T4 alone
If any of the above situations have happened to you, can you please let me know. John has said he will look into this if we can show evidence to prove patients are still struggling to get T3. We would particularly like to hear from patients in the Morecambe Bay area
Many thanks to everyone who are supporting our petition and our efforts to get T3 reinstated.
Many thanks Moyra x
Petition Update April 2018
Hello everyone, For the last 3 month’s I have been waiting for an update from John Woodcock our MP, regarding the questions I submitted to be used in one of the Prime Minister’s question sessions. On Friday I received word from John’s office that one of the questions has been sent to Parliament. I don’t have any more news about this at the moment but will post a further update as soon as I do.
Meanwhile we will continue with our fight to have T3 reinstated as a prescription drug, available to patients on the NHS. The total number of supporters for our petition now stands at 2,600. This, is a fantastic result for a small group like C.A.T.S. however we do need to increase this total. Please can everyone who have supported us so far, share this petition far and wide. Also, if you are reading this and have not signed yet, can you please consider doing so. The link for our petition is https://www.change.org/p/the-secretary-of-state-for-health-jeremy-hunt-reinstate-t3-liothyronine-as-a-prescription-drug-available-on-the-nhs?utm_source=embedded_petition_view
There is also a national petition group (ITT Campaign group). This group are actively fighting to have T3 reinstated, the same as C.A.T.S are. However, this group are also fighting for better care for Thyroid patients. I am sure you will all agree that there needs to be better Thyroid care. So please support this group by signing and sharing their petition. The link for this is https://www.change.org/p/itt-campaign-group-improve-thyroid-treatment-for-millions-of-people-stop-the-withdrawal-of-t3
Many thanks to all the wonderful people who are supporting C.A.T.S. with this mission. Without this support we could not have got this far. Since my last update some patients have told me they have seen the Endocrinologist and have had their T3 reinstated, however it is still a postcode lottery if you can get T3 or not. Take care everyone
Many thanks Moyra x
Hi Everyone, I have received word from our MP John Woodcocks office that his London team, are looking into the T3 issue. I have submitted 3 questions (all T3 related) and hope that John will be able to use these questions in one of the parliamentary question debates I have no further information about this at the moment. So please keep checking our website and our Face book page for updates.
Our petition has reached the fantastic total of 2,550 but unfortunately we still need more lovely people to support us. The link for the petition is https://www.change.org/p/the-secretary-of-state-for-health-jeremy-hunt-reinstate-t3-liothyronine-as-a-prescription-drug-available-on-the-nhs?utm_source=embedded_petition_view
There is also a national petition run by the ITT (Improve Thyroid Treatment) Campaign group. This petition has only been running just over 6 months and has already reached almost 30,000 supporters. Apart from the T3 issue, this group is, also fighting for better treatment for Thyroid patients. Please help this group to get their petition to parliament. The link for this petition is https://www.change.org/p/itt-campaign-group-improve-thyroid-treatment-for-millions-of-people-stop-the-withdrawal-of-t3
Many thanks, to everyone who have already supported these petitions. If you have not signed yet can you please consider doing so. Can you also share this update with your friends or any groups you belong to. Many thanks Moyra x