Should I get a second opinion? - Hughes Syndrome A...

Hughes Syndrome APS Forum

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Should I get a second opinion?

SEJ19 profile image
11 Replies

I had been having pins and needles in my chest, arms and back on and off for about 4 days. Therefore I went to my local GP, he checked my pulse which was 115 ((after I got home it had gone down to about 80)) my oxygen and pressure was fine. I can lift both of my arms up totally fine, I can breathe fine. He told me that it was just my muscles playing up, I don't know If I should go back or have a second opinion or not. Can't help but worry.

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SEJ19 profile image
SEJ19
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11 Replies
daisyd profile image
daisyd

Hi, I would be concerned if my pulse was 115, i am surprised that he didn't do more tests. I would go back

MaryF profile image
MaryFAdministrator

Hi, Do you have a diagnosis of Hughes Syndrome/APS? If so who is looking after your care? MaryF

SEJ19 profile image
SEJ19 in reply to MaryF

No I don't.

MaryF profile image
MaryFAdministrator in reply to SEJ19

Ok, sorry you feel unwell but this is a forum specifically for Hughes Syndrome/APS. You certainly need to go back to the GP or hospital to help get to the bottom of your troubles, however I don't think we can help you any further, best of luck to you. MaryF

Manofmendip profile image
Manofmendip

Hi. As my colleague Mary has asked you, do you have Hughes Syndrome/APS and, if so, who is managing your condition/care?

Dave

SEJ19 profile image
SEJ19 in reply to Manofmendip

How is it diagnosed?

Manofmendip profile image
Manofmendip in reply to SEJ19

With various blood tests. You need to go back to your GP. If you do not know what Hughes Syndrome/APS is may I ask how you found this group and why you posted on it?

Dave

SEJ19 profile image
SEJ19 in reply to Manofmendip

I think it might have came up when I was googling my Symptoms.

I didn't know it was called Hughes Syndrome as well as Antiphospholipid syndrome.

Manofmendip profile image
Manofmendip in reply to SEJ19

Ok. that makes sense.

Have you looked at the Hughes Syndrome Foundation website, which you can access by clicking on the HSF logo at the top right of this page. On there you will find a guide to the symptoms and also details of the blood tests that your GP should do, if you feel that your symptoms match those of Hughes/APS.

Dave

SEJ19 profile image
SEJ19 in reply to Manofmendip

I have taken a look, thank you so much for the help. I think going back to my GP is best.

Manofmendip profile image
Manofmendip in reply to SEJ19

Please let us know if you are diagnosed with APS and we will be pleased to help you. Where are you from?

Dave

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