Advice APS: Hi guys please can you tell... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,443 members10,641 posts

Advice APS

Sevenstar profile image
4 Replies

Hi guys please can you tell me as no -one seems to know , i am 68 years old with mild Bronchiectasis and Microvascular Angina and APS but am only on Clopidogrel, am I classed as vulnerable? I think I'm in category 5 at the moment , not wanting to rush just to know ! The APS website isn't clear about it !

Written by
Sevenstar profile image
Sevenstar
To view profiles and participate in discussions please or .
Read more about...
4 Replies
veganworld profile image
veganworld

Hi

I had this very same conversation with my GP last week and he told me I would have had a letter from the government to be classed as vulnerable. He read out the criteria from the government guidelines and it doesn't seem to cover us in any way shape or form. It was mainly cancer patients and extremely severe illness such as organ transplant etc. He did admit that due to the clotting if he had his way more people would have been put forward sooner and I would have been higher on the list but they had strict guidelines to adhere to. He didn't think it would be long to wait for the vaccine. I think it is still worth having the conversation and remind your GP that you are wanting the vaccine as soon as poss. When it is your turn you might get to the top of the list. Some GP's might go rogue you never know. Mine won't unfortunately.

Take care

Kaz

Sevenstar profile image
Sevenstar in reply toveganworld

Arh thanks for replying Kaz , yes it's the clotting issue should you become very ill that worries me , I understand it can become a problem! I'm having a telephone convo next week so I will run it past him, I don't want to queue jump in any shape or form but neither do I want a massive clotting issue !

Anyway looking at the headlines this morning the over 65s should be having letters from next week , so hopefully not long now !

Stay well !

MaryF profile image
MaryFAdministrator

Hi the GHIC charity website, did a question and answer session, which may interest you,

facebook.com/TheGrahamHughe...

I think there is a bit of confusion around which band people are in, it would be worth drawing your GP's attention to see if they can help in any way. I am sure you will be contacted soon, but no harm in sending an email to your GP to clearly express your concern, regarding your condition(s). MaryF

Sevenstar profile image
Sevenstar in reply toMaryF

Arh thanks 🙏 Mary excellent advice as always !

Not what you're looking for?

You may also like...

Aps newbie

Hi everybody I'm New here I was diagnosed with aps in 2010/2011, I have had 17 misscarriges and...
Totts1983 profile image

APS advice

Hi everyone, I've tested positive for aps. The doctor said it was at 1.4. I have no idea what this...
Heidi2791 profile image

APS Advice

Hi. I tested positive for Hughes Syndrome 26 yrs ago. Due to inflammation & bleeding from aspirin &...
coralinn46 profile image

Elevated Red cells and APS

I have APS and am on 6 mg Warfarin daily. My INR stays between 2.5 and 3.0 I was recently...
DannyBoy1 profile image

APS..Post Continued...

Hello...As now I have been studying about APS, one thing I came to know that it occurs much more in...
Abc91 profile image

Moderation team

See all
KellyInTexas profile image
KellyInTexasAdministrator
MaryF profile image
MaryFAdministrator
lupus-support1 profile image
lupus-support1Administrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.