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Old 07-04-2006, 05:01 AM   #1
SJLGI
Junior Member
(female)
 
Join Date: May 2006
Location: Hampshire UK
Posts: 32
Hope this helps someone

Hi
Just wanted to tell my story in the hope that it might help someone else and to encourage people to never give up. I’m in the UK so this could be useful to anyone here hitting the same brick walls as I did.

In November 2004 I had my third child, I suffered from uncontrollable shaking straight after the birth which the midwife told me was probably shock. I continued to have spells of shaking for several weeks after the birth but otherwise felt quite good. Then in January I contracted impetigo and from then on picked up just about everything that was going. I started to get mood swings, became very tired, developed carpal tunnel and other joint and muscle pains. By October I had admitted to myself that something was wrong and as we have a strong family history of thyroid was fairly certain that my thyroid was the problem.

In Dec 05 I went to see my GP told him my symptoms and that I felt, given the family history, my thyroid was the problem. He said no, I was suffering from post natal depression, prescribed anti-depressants and said he’d run a thyroid test just to be sure. The test came back 2.74, I was told that was “normal”. I was shocked and thought I’d got it wrong and started taking the anti-d’s. Over Christmas I had severe welling of the glands in my face and my ear canal, it was agony. The anti-depressants had numbed my emotions. I went back to the GP he upped the dose of anti-depressants, told me to wear splints of carpal tunnel and see a chiropractor if I had other pain. The gland and ear swelling got worse.

In Feb 06 I went to see another GP because my neck was now slightly swollen – she stopped the anti-depressants – arranged for an US scan, antibody test (1042) and an appointment with an Endocrinologist.

In April I saw the Endocrinologist he said antibodies don’t mean anything, asked me how many children I had and what there ages were and said “ah now that must be stressfull”. The US scan showed a nodule but I was told it was nothing to worry about.

I arranged to have blood tests done privately as in the UK they will only test TSH and if that is not in normal range T4 (I found the info to get this done through thyroiduk.org). I had TSH (3.4) FT4 (12.7 – 12-22) and FT3. I took these results to a private doctor who said he felt I needed treatment but light of recent cases of doctors being hauled up before the GMC he could not risk his license.

In June I went back to my GP showed her the blood test results, gave her a list of symptoms and she also agreed that the cause of my problems were my thyroid. She said it was too controversial to treat me especially as she would be going over the specialists head in doing so. She said she knew a private doctor who would treat me – this was very expensive and I said I’d use that as a last resort. She said she could refer me to another specialist. I asked her to contact the Endo who treated my sister when she was diagnosed with Graves – she said she would sound him out rather that perhaps waste my time with another appointment.

On Friday I had a call from the surgery, would I go in and see the GP. I did on Monday and the Endo had contacted them as said start treatment immediately.

It took 7 months and a lot of effort and energy on my part to get here (energy I didn’t have). Thank goodness for the internet and sites like this.

End of first chapter.
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Old 07-04-2006, 12:15 PM   #2
daisy01
Senior Veteran
(female)
 
Join Date: Jul 2005
Location: Kent South East England
Posts: 713
Re: Hope this helps someone

welcome to the board, i am also from the UK and so very very greatful to my net buddies from across the pond. they have saved my sanity on so many occaisions. these guys have told me all i need to know and have helped me back to health both emotionally and physically.

if it wasnt for this board then i would of still been merely existing on levothyroxine and not living well with Armour.
i am one of the lucky ones who managed to get an elightened endo in the NHS who actually listened to me and treated my views with respect and prescribed me Armour.
My Gp knew i had hypoT 3 yrs before anyone chose to let me into the secret by the time I found out, my TSH was unmeasurably high and my T4 was unmeasurably low. The way we with thyroid disorders get treated in the UK is nothing short of criminal.
anyways, glad to have you around
take care
daisy xxxx
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Old 07-04-2006, 01:42 PM   #3
jdn5764
Senior Member
(female)
 
Join Date: Oct 2004
Posts: 245
Re: Hope this helps someone

Well done on getting some help. I've been going back and forth to my gp for nearly 4 years now. As my first tsh came back as 2.68, everything to them is normal. Had two other blood tests since then but the GP won't let me see the results.
Why dr's don't listen to us instead of looking at results is beyond me.
I am sure that when any Dr at my practise, looks at the pc screen it says hypocondriac, and all I get issued with is anti depressants. Which I don't both getting, why should I pay nearly £7.00 for something that I know won't help with the problem I have.
I wish you well with your medication and hope you feel better soon.
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Old 07-05-2006, 07:38 AM   #4
rozzihippychick
Senior Member
(female)
 
Join Date: May 2006
Location: London, England
Posts: 102
Re: Hope this helps someone

I agree with everything you two are saying I have had 8 yrs of struggles. here in the uk we are so dismissed especially us women its such a problem and now I have had the surgery I feel really stranded I don,t know how I shall ever get my life back together and get back to work. You have to fight the medical profession when you feel least able to stand up for yourself. I wish there was some m.p out there with a thyroid condition we could lobby for recognition and support. Good luck to you both.Rozzi

Last edited by rozzihippychick; 07-05-2006 at 07:39 AM.
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Old 07-05-2006, 11:54 AM   #5
lookin4aclue
Veteran
(female)
 
Join Date: Apr 2006
Location: Idaho
Posts: 333
Re: Hope this helps someone

Hello and welcome to the board. I know the treatment there in the UK must really be a fight to get, and I couldn't imagine how bad it really must be, here in the states it's bad enough. We all have to fight to get tests done, and are told so often that the problems that we are having are not thyroid related(when we know they are). It makes you want to SCREAM! I hope that they soon figure out for everyone(UK and US) some real standards on testing, why can't they just perform the stupid TSH, Free T4, and Free T3, and antibodies when they think it is thyroid related instead of the standard TSH? It doesn't make since to me, because if any of these are out of wack, then you have a thyroid problem. I know some one here in the states that posted she had here GP do TSH, Free T4, and Free T3, and the Free T3 turned out to be the cheapest test they ran!! I can't believe the lies they tell us so we won't push to have the Free T3 tests done. I wonder if us thyroid sufferers should push for these as a standard. Anyway sorry about the ranting about the testing! I hope that people find your story helpful, and gives someone the push they might need to get the medical help they need.
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