Is any body has headches b/c of hughe... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,404 members10,613 posts

Is any body has headches b/c of hughes disease or lupus, have a stroke in Feb 2007. My inr regular is 3.1 -3.4. Thks.

msperling profile image
9 Replies

Have headaches every day my GP and blood spec and nero spec, have no idea of cause.

Written by
msperling profile image
msperling
To view profiles and participate in discussions please or .
9 Replies
MaryF profile image
MaryFAdministrator

Hi there and welcome, have you been given a diagnosis of Hughes or Lupus? Both can give you unremitting headaches. In Hughes Patients INR often set higher. The first thing, is where are you located, as our charity has a list of UK specialists that your GP can refer you to, or privately if you wish to self refer. If not in the UK we do know a few names in other countries, which is aided by other members. Also not a bad idea to email the charity website to your doctor's secretary: hughes-syndrome.org/

Also within the charity website a list of tests that can be conducted, although some people are sero negative and don't pass a test but nevertheless still have Hughes Syndrome.

Let us know how we can help further. Mary F x

msperling profile image
msperling in reply toMaryF

Thanks for your response, i have diagnosis with Huges and somewhat with lupus, they think the lupus cause my stroke and 2 yrs ago had Gran mall seizere, i am not med for that i am on kepra. Also i am living alberta canada.

MaryF profile image
MaryFAdministrator in reply tomsperling

Well it is great that you have a diagnosis... it really is, some people have a real struggle to get a diagnosis. Some patients as well as their anticoagulation for their Hughes Syndrome, also do well on a medication called Plaquenil added along side which is useful with Lupus and allso Sjogrens which often rears its head with Hughes and Lupus. However it takes many weeks and months to work, many do well on it. Here is a list.. showing some help in Canada: (Bottom left), you or your doctor could contact them to find out further advice. Hughes patients do at times have a higher INR setting. So alongside forwarding the charity website to your medical doctor, here also is the list with a name in Canada.. they may know more for you:

apsaction.org/

Mary F x

msperling profile image
msperling in reply toMaryF

Thanks alot i am also on plaquenil (200mg once a day) so you says people with my disease causes h/d all the time, also i exercise alot and run alot, i ran half marathon twice after my stroke and my disease, i am very thankful for this. Not one my g.p and my spec says anything h/d they says it could be my scar tissue after my stroke, i am on warfarin since 2007.

KathrynKathyKate profile image
KathrynKathyKate

I have APS and have daily headaches. Diagnosed with Chronic Migraine. I tried propranolol for awhile with no real difference. I was put on topamax a year ago and have had nothing but problems with it. First round seemed to control migraines but gave me nasty squeezing headaches. My eyes were sensitive to it and pressure rose in both eyes but higher in right eye. I stopped then started again. I stayed on a low dose for awhile but finally gave up on it a few weeks ago. It's not worth damaging my eyesight over. I just had Botox for migraines and that isn't working either. Seems like I just have to suffer forever.

sarahlou1801 profile image
sarahlou1801

Hi I have APS and also suffer with daily migraine waiting to see a neurologist at the mo x

Manofmendip profile image
Manofmendip in reply tosarahlou1801

Hi Sarahlou

What medication are you on for APS? I was on Warfarin for 10 years and that stopped my migraines for 7 years and then they came back. I was then put on Amitriptyline and have not had a migraine since. I am now off Warfarin and on Fragmin instead but I have not been brave enough to stop the Amitriptyline to see if the migraines come back.

Best wishes.

Dave x

beautymonster85 profile image
beautymonster85

Most definitely! That is part of your new disease, APS.

*********** ADMIN REMOVED LINK******************

Please see the HSF Posting Guidelines

healthunlocked.com/hughes-s...

MaryF profile image
MaryFAdministrator in reply tobeautymonster85

Hi I have never heard of the organization mentioned above, but we do tend to recommend this one, having widely heard of it: americanaps.org/ Mary F

Not what you're looking for?

You may also like...

I have a stroke in Feb 2007, the spec realized have Huges or APS disease. My kids our 15, 20, 23. When should they get tested?

Also what test should they have see, to see they have disease that have? Another question i had...
msperling profile image

2 questions in 1 A) Is the erratic nature of my INR due to APS or azathioprine? B) Is anyone else taking huge doses of warfarin eg. 20mg/day

Is the erratic INR due to APS or azathioprine? Despite eating, drinking and on the same meds every...
WendyWoo50 profile image

Originally diagnosed with Lupus which has now been changed to Hughes. My IGM is 114 but I have not been put on any medication-

I am wondering if I need to be on any medication. Is it only if you have had a clot that you are...
JOEW profile image

Memory loss and a feeling of "can't cope" with work

For the past 2 years every time I've been to see the specialist or my GP, I've mentioned that I...
Nat1969 profile image

I

I have all the symptoms of APS including 2 positve ACL's 22 and 19 and the specialist will not...
whynotme profile image

Moderation team

See all
lupus-support1 profile image
lupus-support1Administrator
KellyInTexas profile image
KellyInTexasAdministrator
HollyHeski profile image
HollyHeskiAdministrator

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.