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Clexane
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APS awareness
I received three shots of
Clexane
while waiting for the scan, this was then stopped post scan. Following a private scan and DVT diagnosis 6 months later I finally pushed for and got the tests I needed. This site, and now 'The Graham Hughes International Charity' is a great resource.
I received three shots of
Clexane
while waiting for the scan, this was then stopped post scan. Following a private scan and DVT diagnosis 6 months later I finally pushed for and got the tests I needed. This site, and now 'The Graham Hughes International Charity' is a great resource.
RazD
in
Hughes Syndrome APS Forum
7 years ago
Newly diagnosed with APS
I have flown transatlantic several times and have injected myself with
Clexane
. My haematologist is fantastic & continues to thrombophilia test me every 6-12 months.
I have flown transatlantic several times and have injected myself with
Clexane
. My haematologist is fantastic & continues to thrombophilia test me every 6-12 months.
juanacalpe
in
Hughes Syndrome APS Forum
7 years ago
Clexane
Just about to take
clexane
anybody got any good success stories with it ???? X
Just about to take
clexane
anybody got any good success stories with it ???? X
kc21
in
Fertility Road Mind, Body & Wellbeing
7 years ago
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CLEXANE GIVEN LATE
Is it ok if you have your
clexane
just over 4 hours late! I am panicking a bit (actually more than a bit) I have been taking it everyday for 5 months for a PE which was found in November. It's the first time I have forgotten.
Is it ok if you have your
clexane
just over 4 hours late! I am panicking a bit (actually more than a bit) I have been taking it everyday for 5 months for a PE which was found in November. It's the first time I have forgotten.
Pinkbubble28
in
Hughes Syndrome APS Forum
7 years ago
Its been a while hello all
its been a while since i have posted on here but just wanted to update you, I have had my stem cell transplant I won't go into gory details but if you would like to know more here is my blog http://beckyb8.wixsite.com/stemcelltransplant As far as blood clotting goes they are still unsure so I am on
clexane
its been a while since i have posted on here but just wanted to update you, I have had my stem cell transplant I won't go into gory details but if you would like to know more here is my blog http://beckyb8.wixsite.com/stemcelltransplant As far as blood clotting goes they are still unsure so I am on
clexane
beckyb
in
Hughes Syndrome APS Forum
7 years ago
Advice from daily injection users please
This will be my forth year of daily
Clexane
. My skin is becoming 'resistant' in places, needing either a second jab or forceably giving extra pressure. Has anyone any advice please regarding skin care or treatment to relieve the problem? Grateful for any comments
This will be my forth year of daily
Clexane
. My skin is becoming 'resistant' in places, needing either a second jab or forceably giving extra pressure. Has anyone any advice please regarding skin care or treatment to relieve the problem? Grateful for any comments
Julie_T
in
Hughes Syndrome APS Forum
7 years ago
Clexane.....no bruises
I know this is going to sound really weird but last time I was on
clexane
I was covered in bruises on my tummy. I've been taking it for 3 days so far and not one single bruise....just aggressive looking red puncture marks. Is it still working? Xx
I know this is going to sound really weird but last time I was on
clexane
I was covered in bruises on my tummy. I've been taking it for 3 days so far and not one single bruise....just aggressive looking red puncture marks. Is it still working? Xx
Marita15
in
Fertility Network UK
7 years ago
Bridging with clexane for surgery
I have a day procedure coming up next week and I'm meant to bridge with
clexane
. Stop warfarin 3 days before surgery and start
clexane
. The doctor didn't say what to do at the other side of the procedure. Do I take both
clexane
and warfarin until my INR is back in range?
I have a day procedure coming up next week and I'm meant to bridge with
clexane
. Stop warfarin 3 days before surgery and start
clexane
. The doctor didn't say what to do at the other side of the procedure. Do I take both
clexane
and warfarin until my INR is back in range?
tassie
in
Hughes Syndrome APS Forum
7 years ago
Feeling fed up and low!
Dreading it is a dvt because of the
clexane
injections, I dreaded everyone and the thought of having them for three months is making me feel sick! Its a real pain! x
Dreading it is a dvt because of the
clexane
injections, I dreaded everyone and the thought of having them for three months is making me feel sick! Its a real pain! x
triplets
in
My Ovacome
7 years ago
Egg Transfer all done, taking clexane this time. Hoping it's our time 😀
I have had lots of tests which came back ok which is great, but I just felt I should be doing something different to hopefully have our miracle(s), so I am on
clexane
(blood thinner) we will try anything to keep them safe inside me.
I have had lots of tests which came back ok which is great, but I just felt I should be doing something different to hopefully have our miracle(s), so I am on
clexane
(blood thinner) we will try anything to keep them safe inside me.
Kelly-03
in
Fertility Network UK
7 years ago
Prothrombin Factor 2 and MTHFR
For my fertility they will give me
Clexane
a blood thinner as part of my treatment. The MTHFR gene I'm more worried about as this stops my body absorbing B9/folic acid which is critical for my body to function normally but crucial in foetal development .
For my fertility they will give me
Clexane
a blood thinner as part of my treatment. The MTHFR gene I'm more worried about as this stops my body absorbing B9/folic acid which is critical for my body to function normally but crucial in foetal development .
Hannah143
in
Fertility Network UK
7 years ago
APS awareness and treatment
I was diagnosed in 2009, following extended illness with UC and several clotting incidents (DVTs and PEs), at the time thought to be caused by UC and periods of illness induced inactivity - even though some clots occurred in hospital while under
clexane
/heparin cover.
I was diagnosed in 2009, following extended illness with UC and several clotting incidents (DVTs and PEs), at the time thought to be caused by UC and periods of illness induced inactivity - even though some clots occurred in hospital while under
clexane
/heparin cover.
CormorantWatcher
in
Hughes Syndrome APS Forum
7 years ago
Heparin (CLexane) injections
Hi all, newbie on here but not to Lupus or Hughes syndrome! In addition I have another clotting disorder ( reduced activated protein C) Warfarin became unstable about 4 years ago and management changed to daily heparin injections. What I would like help with is information on the alternative medication
Hi all, newbie on here but not to Lupus or Hughes syndrome! In addition I have another clotting disorder ( reduced activated protein C) Warfarin became unstable about 4 years ago and management changed to daily heparin injections. What I would like help with is information on the alternative medication
Julie_T
in
Hughes Syndrome APS Forum
7 years ago
Stopping IVF drugs post scan
So after my scan early this week I was told how to finish off my drugs for IVF and took the last cyclogest, progynova, 5mg folic acid and
clexane
yesterday. I have to carry on with my aspirin until I'm 36 weeks. Did anyone else just feel scared in stopping the drugs?
So after my scan early this week I was told how to finish off my drugs for IVF and took the last cyclogest, progynova, 5mg folic acid and
clexane
yesterday. I have to carry on with my aspirin until I'm 36 weeks. Did anyone else just feel scared in stopping the drugs?
KittyK
in
Fertility Network UK
7 years ago
been put on sintrom tablet finished loading dose now on one a day do I need regular blood tests
Body test bloods ecg chest x rays loading dose 3
clexane
injection and4 sintfrom tabs over 3days
Body test bloods ecg chest x rays loading dose 3
clexane
injection and4 sintfrom tabs over 3days
tb74
in
Anticoagulation Support
7 years ago
Newby currently being investigated for APS
i am now on
clexane
for 6 months. At the time i was tested for APS and it showed borderline lupus anticoagulant. i have got to be retested in March I suppose to confirm if I have APS.
i am now on
clexane
for 6 months. At the time i was tested for APS and it showed borderline lupus anticoagulant. i have got to be retested in March I suppose to confirm if I have APS.
Pinkbubble28
in
Hughes Syndrome APS Forum
7 years ago
And so it began....
Boobs are just fine, and no aches or pains or spotting from the pessary
clexane
Injections giving me nice bruises though and that's it absolutely ZILCH...
Boobs are just fine, and no aches or pains or spotting from the pessary
clexane
Injections giving me nice bruises though and that's it absolutely ZILCH...
Hidden
in
Fertility Network UK
7 years ago
What are Micro Clots? Are they dangerous?
O was treated with
Clexane
inj I finally flew back to the UK and into a local hospital. Three days after the first MRI another showed no clot.
Clexane
was stopped. Hospital general consultants said that's not possible. The first MRI must be wrong.
O was treated with
Clexane
inj I finally flew back to the UK and into a local hospital. Three days after the first MRI another showed no clot.
Clexane
was stopped. Hospital general consultants said that's not possible. The first MRI must be wrong.
WendyWoo50
in
Hughes Syndrome APS Forum
7 years ago
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
Obviously my warfarin was increased and I was put onto
Clexane
injections daily. My warfarin dose has increased slowly over the last few months until now I am taking 20 mg daily.
Obviously my warfarin was increased and I was put onto
Clexane
injections daily. My warfarin dose has increased slowly over the last few months until now I am taking 20 mg daily.
WendyWoo50
in
Hughes Syndrome APS Forum
7 years ago
if you were switched from warfarin to clexane/lovenox, what differences, if any did you notice?
Besides being able to eat/drink whatever you want... did the memory fog return or any other symptoms change or occur? Want to get your facts, I know you aren't medically trained but am curious to everyone's experiences. Thanks 🤔💕. Cindy from NJ, US
Besides being able to eat/drink whatever you want... did the memory fog return or any other symptoms change or occur? Want to get your facts, I know you aren't medically trained but am curious to everyone's experiences. Thanks 🤔💕. Cindy from NJ, US
Wittycjt
in
Hughes Syndrome APS Forum
7 years ago
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