When I was diagnosed it was when I was covering three other people's jobs and had a leader that was absolutely inadequate. It was holiday season, frustrating family dynamics... developed a headache, blah, blah, blah. Developed stroke was tested for APS, was + and so on. Now I am wondering if this was just lying dormant in my body until I just couldn't take anymore and the coagulants were awakened? Anyone else feel this way? I am always wondering what brought this to the surface. I should explain I had had a TIA 28 years ago with the pregnancy of my son. That passed after delivery... he was born approx a month early and was healthy. For 28 years nothing ( no symptoms) then h-E-l-l-O, bam...as above.
Here I go thinking again.... anyone e... - Hughes Syndrome -...
I'm sure it is a contributing factor. I was diagnosed whilst doing IVF. Left on aspirin 75mg for 7 years with no events. Had very similar experience of work stress and long haul flight over a 4 week period and bam TIA in work and called ambulance on myself.
Luckily no major ramifications except change to warfarin and adding a cholesterol tablet for good measure.
Now going through a similar work situation in another shop. Blood pressure went sky high last week due to the pressure. So scared it will happen again so now treating the stress blood pressure with tablets to try to protect myself.
Yes I too had TIA 4 month after birth of my son! Had hi blood pressure in last 2 months and had him 3 weeks early! Had my first blood clot at age 24 in my lung and several blood clots soon after that, in my legs! Lots of medical illnesses throughout my life! Doc think had all my life! Just at all these times APS EASNT EVEN A KNOWN DISEASE! Very sickly as a child! Always in and out of hospitals, but came out without a diagnosis!!!
My mother passed away this time last year after a stroke. She had been on warfarin following a stroke 18 months earlier. Her funeral was just before Christmas. The period between her last stroke and then death was 12 days, and those days were the most difficult as her palliative care in a nursing home wasn't the best. I fully believe the stress associated with this caused the trigger to have the jugular DVT 6 weeks later and eventual APS diagnosis. I had been on very low dose HRT for over 10 years with no issue.
Caught my attention when read this.I have APS too and other auto immune diseases but last year n this have had involuntary movements and can't walk due to trippy jerking walking on right side.saw neurologist yesterday and he reckons it's stress.my biggest stress was bereavement of my mother 6 years ago but his answer doesn't seem plausible due to my now disability . I feel I am insulting my two sisters if this is the case and NOW it's stressing me.
I know 3 months ago you said that you were waiting for a Top Neurologist at Sheffield hospital (this after 7 weeks in hospital and they did not find anything) and after that, if that did not work, be referred to prof Hughes at St Thomas.
Instead he wants to refer you to a psycohtherapist!!!
What are you going to do about it?
Why do not give him a call and ask to be referred to St Thomas where there are Specialists even if prof Hughes does not take patients any more.
I have understood that you have been promised this from a Doctor at the hospital or .......... Do not let them loose you another time.
Good Luck and let us hear how it goes for you please.
Apologies... I forgot to explain that after the birth of my son I wasn't on any precautions, meds or otherwise. Although when I was pregnant with him my sister was causing me a lot of stress... maybe that was why the TIA, warning. At that time I don't think they knew about Hughes disease or it was just evolving🤔