Help: hi my name is val and I was... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,411 members10,622 posts

Help

val4 profile image
val4
7 Replies

hi my name is val and I was diagnosed with sticky blood last September and told to take 150mm of aspirin a day but that was it can anyone please give me more information as I know very little about it or what to expect from it other than baby loss.

thanks

Written by
val4 profile image
val4
To view profiles and participate in discussions please or .
Read more about...
7 Replies
maximus31 profile image
maximus31

Hi Val4,

Have you had a clot event as well as diagnosed with APS?

val4 profile image
val4 in reply tomaximus31

hi Maximus31 I have not had a blood clot other than when I have my cycle and I only found out I had this after 5 miscarriages in a row

maximus31 profile image
maximus31 in reply toval4

Hi Val, thanks for the update. Sorry that you had 5 miscarriages. My understanding is that after multiple miscarriages, they test for APS and if positive , asprin or another blood thinning drug is given to reduce the chance of another miscarriage.... After baby is born, I am unsure if mother continues with blood thinner or stops. Maybe other members could comment.

Lure2 profile image
Lure2

You have not told us where you live and if you have got a Specialist of autoimmun illnesses (we need a Doctor who has had patients like us before). Also what symptoms from APS you have got and if the Asprin helps.

Usually it is enough with 75-100 mg of a baby-Aspirin as a bigger quantity may give you stomach problems.

I suggest you do as APsnotFab has said and then stay with us to learn a lot from our helpful and friendly members.

Best wishes!

val4 profile image
val4 in reply toLure2

I'm sorry lure2 I live in Blackpool in the UK hun, I'm not shore wat iv got exactly just my consultant told me iv got sticky blood and to take 150mm aspirin eveyday

MaryF profile image
MaryFAdministrator

HI, I hope you enjoy looking at our new charity and website. It will inform you immensely, and do also feel you can continue to ask questions, as we are all in a similar boat with regard to this disease, and some of us have several other things also. If you look over on the right hand side of our forum, we have pinned posts, and under that is our list of recommended specialists, we also have quite a few on the actual charity website MaryF

val4 profile image
val4 in reply toMaryF

thankyou maryf

Not what you're looking for?

You may also like...

Help?

Hi I'm 23 years old and live in Sussex I was diagnosed when I was 21....I have a 10 month old...
Jazz3914 profile image

Help

I have a meeting with my ward manager tomorrow to discuss going back to work. I've been off for 5...
bevers1 profile image

HELP PLEASE

Hi all I’m after some advice please. Here’s my story.. I am now 45 years old and basically I had 3...
LSTP2018 profile image

Help

I had some blood tests taken about a month ago ordered by a Rheumatologist and went to the GP for...
lorac1 profile image

Getting help!?!

Hi , what a great site.... I would love to hear people's ideas , I feel very alone and like nobody...
juzza profile image

Moderation team

See all
KellyInTexas profile image
KellyInTexasAdministrator
HollyHeski profile image
HollyHeskiAdministrator
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.