more new symptoms: Does anyone else get... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,354 members10,542 posts

more new symptoms

donnabrain profile image
6 Replies

Does anyone else get a "stinging" across their chests?

I have had this for a week so I saw a gp today who gave me some capiscal cream to rub on it

I have had a reaction to the cream (bright red where I rubbed it on)

I am also getting numbness in my chin,lips and toungue so I am now waiting for a call from the gp to see if that is a reaction to the cream or if I need to trot off to A&E

Written by
donnabrain profile image
donnabrain
To view profiles and participate in discussions please or .
6 Replies
GinaD profile image
GinaD

A rash that's a reaction to a cream for a rash? Sounds like something I'd do. But seriously --that is possible. I'm allergic to aloe Vera - but how allergic varies. Sometimes I react to a cream I didn't realize had it immediately, and sometimes it takes a few days for the reaction rash to get going.

Lure2 profile image
Lure2

Hallo donnabrain,

Are you still only on Aspirin for your APS?

Have you had that numbness in your chin, lips and tongue before? If so what has your APS-Specialist said about that?

I had that when I was on Aspirin just before I had my TIA or ministroke. After Warfarin I have never had it again.

Best wishes to you and take care

Kerstin in Stockholm

donnabrain profile image
donnabrain in reply to Lure2

never had it before kirsten

I went to Dr who sent me to A&E,who admitted me

Just got home, been in four days, had MRI,was clear,still got symptoms :/

Lure2 profile image
Lure2 in reply to donnabrain

I know that you did see prof Kamashtha (sorry do not know exact Spelling) and after that he left the country! How terrible for you.

Anyway you must ask for a Heparin trial or some other drug stronger than Aspirin that is obviosly not enough for you now.

You need to be properly anticoagulated as you may have microclots. They do not always show up on our MRIs as they are so very tiny. But they do damage! I know.

Mary had some very good solutions for you earlier. It is difficult for me in Stockholm to suggest how you go on now.

Good luck from Kerstin

donnabrain profile image
donnabrain

thank you

Dr Sangle was adamant that I dont need anything stronger than aspirin and that my APS only affects my pregnancies

I am not due to be seen again for another year

Not got the oomph to insist on anything else at the moment

donnabrain profile image
donnabrain

Rang GP and begged her to speak to Dr. Sangles secretary as stinging in chest much much worse and pins needles numbness in while face as well as alldown left side

Everyyone is adamant that the MRI clear MRI means everything is ok but I just feel that it is not

Quoted Kirsten, but gp said mri best for showing "everything"

I know that a lot of it is stress related as daughter was assaulted by a neighbour four weeks ago and there is acourt case,i am trying to tidy up as a lady is coming to view my house at 11am tomorrow and I am the queen of clutter and teen is off on NCS challenge on Monday and due to my being four days in hospital and him managing to wear about 7 pairs of chinos whilst I was away and not think to put a wash on,,so he has nothing for me to pack, and I have houseguests arriving from the north tomorow 3pm

Breathe!!!

You may also like...

New symptoms arrising

Ive had Aps and lupus for over ten years now and its been reasonably managed with daily steroids,...

Hi, new to this community and looking for advice/help with my symptoms.

* I get recurring headaches and migraines. * I get pain in the backs of my eyes. * I have had high

More information. More confusion.

very grateful for the information he gave me and the information I get from this site, I cannot say...

New to Hughes, want to find out more about Apixaban

here and on Apixaban for Hughes. Don't know anyone else on this mess! Is there any one out there?

Is breathlessness a symptom of APS?

improved a little bit. Just wondering if anyone else had this?