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Hrt obstetric aps
I didn’t have a second test as Professor Quenby prescribed
heparin
and on follow up with her she said suspected Aps due to my bloods and fibrin deposits in my placenta. I went on to have 2 more babies on the treatment of
heparin
.
I didn’t have a second test as Professor Quenby prescribed
heparin
and on follow up with her she said suspected Aps due to my bloods and fibrin deposits in my placenta. I went on to have 2 more babies on the treatment of
heparin
.
Burtie-bengal
in
Hughes Syndrome APS Forum
4 years ago
Presence of a lupus anticoagulant may explain prolonged activated partial-thromboplastin time in COVID-19
“Additionally, fixed dosing of low-molecular-weight
heparin
would be favoured in these circumstances over intravenous unfractionated
heparin
because of difficulties in monitoring the latter when the baseline aPTT is prolonged, and in this setting anti-Xa levels may provide a better guide to
heparin
dosing
“Additionally, fixed dosing of low-molecular-weight
heparin
would be favoured in these circumstances over intravenous unfractionated
heparin
because of difficulties in monitoring the latter when the baseline aPTT is prolonged, and in this setting anti-Xa levels may provide a better guide to
heparin
dosing
lupus-support1
Administrator
in
Hughes Syndrome APS Forum
4 years ago
Covid-19: rough morning
He is on
heparin
because he is still hypercoagulable so we are in this catch22- his blood is so thin that the bleed won’t stop, but we cant stop the
heparin
or else he will clot again. He is getting more units of blood transfused, and they’re giving him platelets bc his platelet count dropped.
He is on
heparin
because he is still hypercoagulable so we are in this catch22- his blood is so thin that the bleed won’t stop, but we cant stop the
heparin
or else he will clot again. He is getting more units of blood transfused, and they’re giving him platelets bc his platelet count dropped.
Angelssavepoppy
in
ICUsteps
4 years ago
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Progesterone injections
I’m black and blue from
heparin
I already take, I feel sick all the time and now more injections. I’m cramping but nauseous and still have to eat as I was told to put on weight today.
I’m black and blue from
heparin
I already take, I feel sick all the time and now more injections. I’m cramping but nauseous and still have to eat as I was told to put on weight today.
Corchi
in
Fertility Network UK
4 years ago
Covid19 is starting to remind me of CAPS
Plasma, monoclonal antibodies, HCQ and now most recent success stories include anticoagulant therapy specifically with
heparin
drip. Just an observation. https://www.medrxiv.org/content/10.1101/2020.03.28.20046144v2 https://www.ncbi.nlm.nih.gov/pubmed/32220112
Plasma, monoclonal antibodies, HCQ and now most recent success stories include anticoagulant therapy specifically with
heparin
drip. Just an observation. https://www.medrxiv.org/content/10.1101/2020.03.28.20046144v2 https://www.ncbi.nlm.nih.gov/pubmed/32220112
Roarah
in
LUPUS UK
4 years ago
Ozone is curing COVID-19 IN 1-2 DAYS
Several hospitals are using Major AutoHemo Therapy (MAHT), a protocol that extracts the patient's blood, bubbles oxygen ozone through the blood in a saline or
heparin
bag, and is infused back into the patient.
Several hospitals are using Major AutoHemo Therapy (MAHT), a protocol that extracts the patient's blood, bubbles oxygen ozone through the blood in a saline or
heparin
bag, and is infused back into the patient.
bepo
in
Cure Parkinson's
4 years ago
Does Eliquis affect APS test results?
I'm only 28 and I'm worried that I'll have a reduced life expectancy and can never get pregnant ( I'm allergic to
Heparin
too :( What have your experiences been with APS? Is it possible to lead a normal life?
I'm only 28 and I'm worried that I'll have a reduced life expectancy and can never get pregnant ( I'm allergic to
Heparin
too :( What have your experiences been with APS? Is it possible to lead a normal life?
annabanana23
in
Hughes Syndrome APS Forum
4 years ago
Noise sensitivity
Hello, hope you are all keeping well. 🙂 Quick background as I'm new here - My struggles with tinnitus started in October 2019 when I felt as though my left each was blocked. This lasted for a few weeks, then became a bit more intermittent but I then also kept hearing a continuous whoosh. I was referred
Hello, hope you are all keeping well. 🙂 Quick background as I'm new here - My struggles with tinnitus started in October 2019 when I felt as though my left each was blocked. This lasted for a few weeks, then became a bit more intermittent but I then also kept hearing a continuous whoosh. I was referred
B113
in
British Tinnitus Association
4 years ago
Any hope for reactive tinnitus and distortion or hypercusis to improve or go away after 7 months with it?
I've had my reactive tinnitus for 7 months now. It still reacts to music well lots of music. Classical music is where I noticed the least distortion but pop music I noticed whistling and beeps over it. Been going on like this 7 months now. My dad's voice sounds robotic and so does the tv and my own
I've had my reactive tinnitus for 7 months now. It still reacts to music well lots of music. Classical music is where I noticed the least distortion but pop music I noticed whistling and beeps over it. Been going on like this 7 months now. My dad's voice sounds robotic and so does the tv and my own
Alugo6340
in
British Tinnitus Association
4 years ago
A 25 year old guy that loves the gym from the Netherlands.
Hey guys! I usually don't post on anything, but this time, I feel like I need to get and give support to those that are experiencing something similar, since I learned that professionals and friends & family have quite a hard time understanding the severity of this condition. When I say severity, don't
Hey guys! I usually don't post on anything, but this time, I feel like I need to get and give support to those that are experiencing something similar, since I learned that professionals and friends & family have quite a hard time understanding the severity of this condition. When I say severity, don't
strawberrymilk
in
British Tinnitus Association
4 years ago
Alternative to Pentamidine
I am currently on Ibrutinib for my SLL. I am allergic to Septrin so I am having Pentamidine by nebuliser every 4 weeks. I am just wondering if there may be another alternative ?
I am currently on Ibrutinib for my SLL. I am allergic to Septrin so I am having Pentamidine by nebuliser every 4 weeks. I am just wondering if there may be another alternative ?
Grannajan
in
CLL Support
4 years ago
What am I gonna do? Anyone with reactive tinnitus still listen to music?
I was looking at the questions on quora and a whole bunch of answered the question "is life worth living without music?" and MOST people have said things like "without music, life is dull it's like a sky without trees and stars " or "music is good for the soul" or "I'd die without music ". Most people
I was looking at the questions on quora and a whole bunch of answered the question "is life worth living without music?" and MOST people have said things like "without music, life is dull it's like a sky without trees and stars " or "music is good for the soul" or "I'd die without music ". Most people
Alugo6340
in
British Tinnitus Association
4 years ago
Nocturnal Dialysis Problems
One technician asked if I was on a blood thinner, and I said "No", and he mentioned that he thought it was strange that there was no
Heparin
(blood thinner) in the dialysis fluid. 8) I'm not able to sleep during nocturnal dialysis because the machine keeps beeping (due to the issues I mentioned above
One technician asked if I was on a blood thinner, and I said "No", and he mentioned that he thought it was strange that there was no
Heparin
(blood thinner) in the dialysis fluid. 8) I'm not able to sleep during nocturnal dialysis because the machine keeps beeping (due to the issues I mentioned above
steve680
in
Kidney Disease
4 years ago
Practical guidance for the prevention of thrombosis and management of coagulopathy and disseminated intravascular coagulation of patients in
Pharmacological thromboprophylaxis should be given to all immobilised and severely ill patients with COVID-19 patients unless otherwise contraindicated
For CrCl > 30: Give LMWH or fondaparinux s.c. according to license
For CrCl < 30 or AKI: Unfractionated
5000
Pharmacological thromboprophylaxis should be given to all immobilised and severely ill patients with COVID-19 patients unless otherwise contraindicated
For CrCl > 30: Give LMWH or fondaparinux s.c. according to license
For CrCl < 30 or AKI: Unfractionated
5000
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
4 years ago
Sea Cucumber blocks selectin mediated metastasis
while researching untoward effects of needle seeding after biopsy I stumbled onto this article https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3402858/ seems A fucosylated chondroitin sulfate (FucCS) from sea cucumber is 4–8 fold more potent than
heparin
in the inhibition of LS180 carcinoma cell attachment
while researching untoward effects of needle seeding after biopsy I stumbled onto this article https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3402858/ seems A fucosylated chondroitin sulfate (FucCS) from sea cucumber is 4–8 fold more potent than
heparin
in the inhibition of LS180 carcinoma cell attachment
sammamish
in
Advanced Prostate Cancer
5 years ago
Does this sound like Eustachian tube dysfunction?
my tinnitus reacts to every word spoken like this undertone to people's voices on tv, I hear it with music too almost doesnt matter what type of music or volume. I was born with severe hearing loss but this didnt happen til 6 months ago after a cold. I had clicking noises everytime I swallowed and sinus
my tinnitus reacts to every word spoken like this undertone to people's voices on tv, I hear it with music too almost doesnt matter what type of music or volume. I was born with severe hearing loss but this didnt happen til 6 months ago after a cold. I had clicking noises everytime I swallowed and sinus
Alugo6340
in
British Tinnitus Association
4 years ago
Hi everyone I’m new to this community. I’m wondering if anyone is having slight breathing problems when having a cold after having PE twice.
I had unprovoked pulmonary embolism in September 2016 ,treated with 3 months of
heparin
injections. In July 2017 I had another one. Now I’m on lifelong Warfarin. My life /lungs never been the same again. When it was diagnosed I had shortness of breath on any physical activity.
I had unprovoked pulmonary embolism in September 2016 ,treated with 3 months of
heparin
injections. In July 2017 I had another one. Now I’m on lifelong Warfarin. My life /lungs never been the same again. When it was diagnosed I had shortness of breath on any physical activity.
Bakery40
in
Lung Conditions Community Forum
5 years ago
APS & Severe Diverticulosis? or anything similar
Eventually after several days the bleeding was arrested and warfarin was reintroduced together with
heparin
shots as my INR was down to 1.1 - now after several days it's up to 1.7.
Eventually after several days the bleeding was arrested and warfarin was reintroduced together with
heparin
shots as my INR was down to 1.1 - now after several days it's up to 1.7.
JPMcGee75
in
Hughes Syndrome APS Forum
5 years ago
Losing ground on movement or my mind...my rant, sorry it's long.
I got high score on the blood pressure machine everytime and lots of
heparin
shots. I was placed on seizure protocol due to the risk of injury. They were trying to get me squared away. So I'm not allowed to move around and they pumped me full of lots of drugs to try to make it stop.
I got high score on the blood pressure machine everytime and lots of
heparin
shots. I was placed on seizure protocol due to the risk of injury. They were trying to get me squared away. So I'm not allowed to move around and they pumped me full of lots of drugs to try to make it stop.
Daesin
in
Functional Neurological Disorder - FND Hope
5 years ago
Hearing test
Has anybody else suffered from hearing loss? Just had Audiologist home visit and assured me that RA was responsible even though my Consultant said it wasn't! Who's right?
Has anybody else suffered from hearing loss? Just had Audiologist home visit and assured me that RA was responsible even though my Consultant said it wasn't! Who's right?
Ladyfairfax
in
NRAS
5 years ago
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