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Heparin
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Anticoagulation and Surgery
They then would have discharged me without any
Heparin
but instructions to start taking warfarin again after 2 days and in small doses at first which would have left me out of therapeutic range for a further week at least.
They then would have discharged me without any
Heparin
but instructions to start taking warfarin again after 2 days and in small doses at first which would have left me out of therapeutic range for a further week at least.
Hidden
in
Anticoagulation Support
12 years ago
1 Year and Counting
We noticed that when I was in the hospital with the PEs while being treated with
heparin
and warfarin, the episodes stopped. My INR is set to be between 2.5 and 3.5, but I continue to have episodes. Does anyone else have seizure-like episodes?
We noticed that when I was in the hospital with the PEs while being treated with
heparin
and warfarin, the episodes stopped. My INR is set to be between 2.5 and 3.5, but I continue to have episodes. Does anyone else have seizure-like episodes?
Willa
in
Hughes Syndrome APS Forum
12 years ago
Thanks for comments.
I will also ask him if maybe I should be on a combination of
Heparin
and Warfarin, but I don't want to have to give myself shots. I already feel like a slave to this condition.
I will also ask him if maybe I should be on a combination of
Heparin
and Warfarin, but I don't want to have to give myself shots. I already feel like a slave to this condition.
Willa
in
Hughes Syndrome APS Forum
12 years ago
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Haematologist vist
Given
heparin
injections for when INR below 3.0. Nice to have a positive contact with a doctor/consultant.
Given
heparin
injections for when INR below 3.0. Nice to have a positive contact with a doctor/consultant.
sharonap
in
Hughes Syndrome APS Forum
12 years ago
Has anyone had a pregnancy with ET?
I am 13 weeks pregnant and on Pegasys, consultant just added
heparin
injection daily as well but happy with me so far. Would love to hear about other people's experience thank you
I am 13 weeks pregnant and on Pegasys, consultant just added
heparin
injection daily as well but happy with me so far. Would love to hear about other people's experience thank you
Dingwall1979
in
MPN Voice
12 years ago
Is it possible to take Lovenox injections (heparin) to treat APS? Instead of Warfarin. I don't think my insurance will pay for it.
I am on Warfarin for my diagnosis of APS. I had a clot in 2008. I also have Lupus, and fibromyalgia. I have had horrible stomach problems since being on warfarin since 2008. I am sick and nauseous all the time. I do not tolerate the warfarin very well at all. I wish there were another alternative to
I am on Warfarin for my diagnosis of APS. I had a clot in 2008. I also have Lupus, and fibromyalgia. I have had horrible stomach problems since being on warfarin since 2008. I am sick and nauseous all the time. I do not tolerate the warfarin very well at all. I wish there were another alternative to
smjohn
in
Hughes Syndrome APS Forum
12 years ago
Pardon!!!
Hi all just been on another post and it mentioned hearing problems so i wondered how many of you have problems hearing. I can't tollerate high pitched noises as they are painful i find it difficult to hear in noisy areas and tend to tune out in crowds which can come across rude but i can't help it thankfully
Hi all just been on another post and it mentioned hearing problems so i wondered how many of you have problems hearing. I can't tollerate high pitched noises as they are painful i find it difficult to hear in noisy areas and tend to tune out in crowds which can come across rude but i can't help it thankfully
Hidden
in
Fibromyalgia Action UK
12 years ago
Professor Graham Hughes' September blog
What about
heparin
? Its usefulness is, of course, limited by the fact that it needs to be injected. Nevertheless, we have found a new use for
heparin
.
What about
heparin
? Its usefulness is, of course, limited by the fact that it needs to be injected. Nevertheless, we have found a new use for
heparin
.
Hidden
in
Hughes Syndrome APS Forum
12 years ago
Our experience of strep b
When I delivered my son he apparently 'came out' boiling hot. The hospital staff acted quickly and we were told he just had an infection and whisked him away to set up IV access for antibiotics. My husband and new baby boy then were brought back to me after this and we went to the post natal ward. The
When I delivered my son he apparently 'came out' boiling hot. The hospital staff acted quickly and we were told he just had an infection and whisked him away to set up IV access for antibiotics. My husband and new baby boy then were brought back to me after this and we went to the post natal ward. The
Bellalondon2012
in
Group B Strep Support
12 years ago
on warfarin but INR changes daily - my ideal INR for me is3.5
Having been on Warfarin and
Heparin
(the later should my INR fall below 3) I find of late that my INRs change daily, have the warfarin same time each night. When my IN either falls below 3.5 or higher I go woozy etc etc.
Having been on Warfarin and
Heparin
(the later should my INR fall below 3) I find of late that my INRs change daily, have the warfarin same time each night. When my IN either falls below 3.5 or higher I go woozy etc etc.
daisy11
in
Hughes Syndrome APS Forum
12 years ago
Update on pregnancy
Been up hosp cos baby wasn't moving put on weekly monitoring as I have + protein + keytones + blood and I'm sick everyday, but my blood pressure is stable I was wondering if I'm getting pre eclampsia again even though I'm on
heparin
and aspirin daily I want to bring my baby home this time round so I'm
Been up hosp cos baby wasn't moving put on weekly monitoring as I have + protein + keytones + blood and I'm sick everyday, but my blood pressure is stable I was wondering if I'm getting pre eclampsia again even though I'm on
heparin
and aspirin daily I want to bring my baby home this time round so I'm
hartnell5
in
Hughes Syndrome APS Forum
12 years ago
Someone pass me a fresh wet fish!
I am totally over the shock of losing my ESA Tribunal. I have been more focused on a point of anger this last few days. At the end on the Drs questions the judge had two things to ask me, or discuss with me. 1. Q.You claim to have hearing problems, yet you have heard us throughout! A. Because
I am totally over the shock of losing my ESA Tribunal. I have been more focused on a point of anger this last few days. At the end on the Drs questions the judge had two things to ask me, or discuss with me. 1. Q.You claim to have hearing problems, yet you have heard us throughout! A. Because
Ozzygirl64
in
Fibromyalgia Action UK
12 years ago
Prof Hughes' August blog
In the meantime, as with other patients with this clinical picture, we are left with a clinical trial, either firstly aspirin or, at some stage, with three weeks of low molecular weight
heparin
. Such an important issue. I will keep you posted.
In the meantime, as with other patients with this clinical picture, we are left with a clinical trial, either firstly aspirin or, at some stage, with three weeks of low molecular weight
heparin
. Such an important issue. I will keep you posted.
Hidden
in
Hughes Syndrome APS Forum
12 years ago
What are the alterntives to Warfarin if one faces a life time on it (age 46) for PVT and MPD. Heparin intolerant so that is not an option.
Daws
in
MPN Voice
12 years ago
Is it APS or MS or both?
I became pregnant in 2004 and was treated with aspirin and
heparin
which I took throughout pregnancy and for 8 weeks after the birth of my daughter.
I became pregnant in 2004 and was treated with aspirin and
heparin
which I took throughout pregnancy and for 8 weeks after the birth of my daughter.
mitzygaynor
in
Hughes Syndrome APS Forum
12 years ago
We do NOT have APS. We have AUTOIMMUNITY!
But what he/she has failed to do is understand that Warfarin and/or
Heparin
(my strong drug of choice), only addresses the clotting; it does not address your overall inflammatory state. As such, you continue to endure the stress of constant chronic inflammation.
But what he/she has failed to do is understand that Warfarin and/or
Heparin
(my strong drug of choice), only addresses the clotting; it does not address your overall inflammatory state. As such, you continue to endure the stress of constant chronic inflammation.
TheKid
in
Hughes Syndrome APS Forum
12 years ago
Re heparin
Also if you wanted to stay on the
heparin
do they allow this or do they make you take warfarin. Thanks h.
Also if you wanted to stay on the
heparin
do they allow this or do they make you take warfarin. Thanks h.
Moonbug
in
Hughes Syndrome APS Forum
12 years ago
Please help!!
Until now it's has only affected me during pregnancy but after being diagnosed and placed on aspirin and
heparin
I now have a little girl.
Until now it's has only affected me during pregnancy but after being diagnosed and placed on aspirin and
heparin
I now have a little girl.
Gemgem
in
Hughes Syndrome APS Forum
12 years ago
Best way to give birth?
Im now nearly 26 weeks pregnant taking aspirin and 10,000 units of
Heparin
a day. Im looking for some advice on the best way to give birth to our child, is a C Section or Vaginal birth best? and what kinds of pain relief would be suitable? Thank you
Im now nearly 26 weeks pregnant taking aspirin and 10,000 units of
Heparin
a day. Im looking for some advice on the best way to give birth to our child, is a C Section or Vaginal birth best? and what kinds of pain relief would be suitable? Thank you
katrinahug03
in
Hughes Syndrome APS Forum
12 years ago
Pregnancy and medication related question
I have always been on
heparin
and aspirin as soon as I get a positive pregnancy test results but he has had poor results for me as I have had 7 miscarriages out of 8 pregnancies and the 1 pregnacy that did make it wasn't ideal with my daughter being low birth weight due to placenta problems at full term
I have always been on
heparin
and aspirin as soon as I get a positive pregnancy test results but he has had poor results for me as I have had 7 miscarriages out of 8 pregnancies and the 1 pregnacy that did make it wasn't ideal with my daughter being low birth weight due to placenta problems at full term
kateb81
in
Hughes Syndrome APS Forum
12 years ago
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