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Heparin
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New member - looking for advice
Hello everybody, my first post and wondering of anyone has had the same experience as me. I have had tinnitus for a few years of the low rumbling kind but I didn’t realise I had it as I thought it was the hum of a motorway about 2 miles away! I spent over 20 years working in data centres and 40 years
Hello everybody, my first post and wondering of anyone has had the same experience as me. I have had tinnitus for a few years of the low rumbling kind but I didn’t realise I had it as I thought it was the hum of a motorway about 2 miles away! I spent over 20 years working in data centres and 40 years
JoeDea
in
British Tinnitus Association
7 years ago
IVC Filter/Clot Catcher Removal after 12 years, surgeon said its the worst case he'd ever seen! Sticky blood & filters are a bad combo.
He also said that he would keep me on
heparin
injections post op, until I am seen by the thrombosis team.
He also said that he would keep me on
heparin
injections post op, until I am seen by the thrombosis team.
leakeadea
in
Hughes Syndrome APS Forum
7 years ago
Where (not) to place a port
I was hospitalized for a day, treated with
heparin
and released. No further issues through the end of my first full treatment (18 weeks). Today, I went to have the port and the filter removed...
I was hospitalized for a day, treated with
heparin
and released. No further issues through the end of my first full treatment (18 weeks). Today, I went to have the port and the filter removed...
Hidden
in
My Ovacome
7 years ago
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Part II to Previos Post On Wide spread clotting/ Immuno Suppression Being Advised And Warfarin Abandoned. (?!?!)
INR is so high we can’t give
Heparin
. I have no idea how to stabilize you. We can only suppress you- I agree to move forward with suppressing with IV cytoxan.) Not to worry . My husband is flying home today. I’m walking around right now with a clot in my leg and no plan...
INR is so high we can’t give
Heparin
. I have no idea how to stabilize you. We can only suppress you- I agree to move forward with suppressing with IV cytoxan.) Not to worry . My husband is flying home today. I’m walking around right now with a clot in my leg and no plan...
KellyInTexas
Administrator
in
Hughes Syndrome APS Forum
7 years ago
New symptoms after self injecting?!
I began self injecting in October after loading injections did not improve the tingling and numbness. These were the only neurological symptoms I had and improved with the self injections. After a month the tingling returned and with some suggestions from this forum I believed it was due to too much
I began self injecting in October after loading injections did not improve the tingling and numbness. These were the only neurological symptoms I had and improved with the self injections. After a month the tingling returned and with some suggestions from this forum I believed it was due to too much
Padders12
in
Pernicious Anaemia Society
7 years ago
Lifetime Therapy of Warfarin at 10 milligrams a day since 2011. I have a Genetic Disorder Protein S and C deficiency
I am also allergic to
Heparin
. My surgeries include 10 inches of my colon removed from bleeding ulcerated colitis and diverticulitis in 2015. I had stomach and esophagus surgery called Nissin in 2016. I had my gallbladder removed March 2017.
I am also allergic to
Heparin
. My surgeries include 10 inches of my colon removed from bleeding ulcerated colitis and diverticulitis in 2015. I had stomach and esophagus surgery called Nissin in 2016. I had my gallbladder removed March 2017.
robinbird
in
Anticoagulation Support
7 years ago
The process of being diagnosed with an aneurysm.
Hello everyone This is my story of being diagnosed with a 15 mm brain aneurysm.i feel a little nervous about doing this as it will make it more real. {Oct 2017) My GP sent me to my local beacon to investigate my Tinnitus,he gave me a hearing test and within 10 min after telling him I have had no brain
Hello everyone This is my story of being diagnosed with a 15 mm brain aneurysm.i feel a little nervous about doing this as it will make it more real. {Oct 2017) My GP sent me to my local beacon to investigate my Tinnitus,he gave me a hearing test and within 10 min after telling him I have had no brain
54Apple54
in
Brain Aneurysm Support
7 years ago
Second Bacterial Meningitis Septicaemia - Advice needed
Dear all, I am hoping you can help advise me on the best way to help my mum. MENINGITUS ROUND 1 - MAY 2014 – GROUP A STREP In May 2014 she contracted Meningococcal Septicaemia (group A). She was treated quickly with antibiotics and steroids, was in ITU for a week and then on a ward for a following
Dear all, I am hoping you can help advise me on the best way to help my mum. MENINGITUS ROUND 1 - MAY 2014 – GROUP A STREP In May 2014 she contracted Meningococcal Septicaemia (group A). She was treated quickly with antibiotics and steroids, was in ITU for a week and then on a ward for a following
SHS7
in
Meningitis Now
7 years ago
Pregnancy/heparin Induced Osteoporosis - Forsteo or Zolendronic acid? Advice needed please...
I was recently diagnosed with Pregnancy induced Osteoporosis with the added complication of being on Fragmin/
heparin
blood thinners for 6 months across the pregnancy and after the birth.
I was recently diagnosed with Pregnancy induced Osteoporosis with the added complication of being on Fragmin/
heparin
blood thinners for 6 months across the pregnancy and after the birth.
CLaurence
in
Bone Health and Osteoporosis UK
7 years ago
Nightmare ENT appointment & self-contradicting doctor
The doctor confirmed that I had hearing loss and then told me I didn’t have hearing loss, he did not offer therapy, told me I have to accept the fact that tinnitus might be permanent (nah! State the obvious! What do you think I’ve been trying to do for 8 months?!), undermine everything I was saying,
The doctor confirmed that I had hearing loss and then told me I didn’t have hearing loss, he did not offer therapy, told me I have to accept the fact that tinnitus might be permanent (nah! State the obvious! What do you think I’ve been trying to do for 8 months?!), undermine everything I was saying,
jasmineam
in
British Tinnitus Association
7 years ago
Can Ear Wax Really Cause Tinnitus Or Make It Sound Worse?
I went for an hearing test a few weeks ago and when my ears were examined I was told I have impacted wax. I was offered micro suction but having experience it in the past there was no way I was going to have that performed again. I was wondering if anyone had impacted wax and having had it removed lessened
I went for an hearing test a few weeks ago and when my ears were examined I was told I have impacted wax. I was offered micro suction but having experience it in the past there was no way I was going to have that performed again. I was wondering if anyone had impacted wax and having had it removed lessened
Alan-
in
British Tinnitus Association
7 years ago
PMR since Sept 2017
After my original post, I think it was PMRpro that asked for a more indepth description of my journey. I have an appointment in December 2017 with my Rheumy and am wondering what questions I should ask. So here is my journey: February 22, 2017 – Saw Dr Gio for pain behind my clavicle bone he ordered
After my original post, I think it was PMRpro that asked for a more indepth description of my journey. I have an appointment in December 2017 with my Rheumy and am wondering what questions I should ask. So here is my journey: February 22, 2017 – Saw Dr Gio for pain behind my clavicle bone he ordered
Sunnyd7
in
PMRGCAuk
7 years ago
Really bad Tinnitus
About 6 weeks ago all of a sudden I got a loud ringing in my head. I got very worried about it and went up my GP who arranged for a hearing test which showed as expected as I’ve had high pitch heating loss for many years. I have been extremely stressed and began to have balance and a loss of sensations
About 6 weeks ago all of a sudden I got a loud ringing in my head. I got very worried about it and went up my GP who arranged for a hearing test which showed as expected as I’ve had high pitch heating loss for many years. I have been extremely stressed and began to have balance and a loss of sensations
Bandaid1
in
British Tinnitus Association
7 years ago
Itchy feet burning sensation while on heparin
Hi just wondering if anyone else gets itchy feet on
heparin
, as sometimes at night I feel a slight warm burning sensation then my foot feel really itchy this only seems to happen mainly at nighttime although have experience it in daytime on a few occasions very irritating
Hi just wondering if anyone else gets itchy feet on
heparin
, as sometimes at night I feel a slight warm burning sensation then my foot feel really itchy this only seems to happen mainly at nighttime although have experience it in daytime on a few occasions very irritating
Lopat
in
Anticoagulation Support
7 years ago
I'm new
Hi there, I have had tinnitus for 34 years,I can't remember life without it.Members of my family also have T and I often wonder is it genetic? I also went to a lot of loud rock concerts in my teens,I adore music, I find that now I can't listen to music very loudly as it makes my T worse.I get very embarrassed
Hi there, I have had tinnitus for 34 years,I can't remember life without it.Members of my family also have T and I often wonder is it genetic? I also went to a lot of loud rock concerts in my teens,I adore music, I find that now I can't listen to music very loudly as it makes my T worse.I get very embarrassed
day-break53
in
British Tinnitus Association
7 years ago
Bisoprol and Losarten
Hi, I'm new here. Has anyone suffered from constant buzzing in the ear, after being on these. Both are known side effects of these drugs. I'm on 2.5 mg Bisoprol and 25mg Losarten daily. Saw 2 NHS Cardiologists and both are in denial. They said it could be something to do with my ears, not the drugs.
Hi, I'm new here. Has anyone suffered from constant buzzing in the ear, after being on these. Both are known side effects of these drugs. I'm on 2.5 mg Bisoprol and 25mg Losarten daily. Saw 2 NHS Cardiologists and both are in denial. They said it could be something to do with my ears, not the drugs.
kunyuraman
in
AF Association
7 years ago
Low INR again
Think I might need
Heparin
as well 😐
Think I might need
Heparin
as well 😐
amy1808
in
Hughes Syndrome APS Forum
7 years ago
Awaiting CTscan results
Hi, I have had pulsatile tinnitus and fullness in ear in my left ear for over 6 months now. The ENT specialist conducted a hearing test and pressure test and although my hearing was not showing that different to my right ear the pressure was greatly reduced. I do get some pain like stabbing now and then
Hi, I have had pulsatile tinnitus and fullness in ear in my left ear for over 6 months now. The ENT specialist conducted a hearing test and pressure test and although my hearing was not showing that different to my right ear the pressure was greatly reduced. I do get some pain like stabbing now and then
SarahSing2021
in
Acoustic Neuroma Support
7 years ago
Seronegative APS?
Our doctor has offered lovenox (low molecular weight
heparin
) in the next pregnancy, but I feel we'd like some more reassurance as to what's going on. We live in San Francisco, CA. Does anyone know of any doctors who are knowledgeable about APS in the Bay Area or in California more generally?
Our doctor has offered lovenox (low molecular weight
heparin
) in the next pregnancy, but I feel we'd like some more reassurance as to what's going on. We live in San Francisco, CA. Does anyone know of any doctors who are knowledgeable about APS in the Bay Area or in California more generally?
tathougies
in
Hughes Syndrome APS Forum
7 years ago
APS & Extreme Fatigue
Hello, I've had APS for awhile and usually just take a baby aspirin except during pregnancy when I've taken
heparin
too. I'm in the Dallas, TX area. Recently, I've had very bad extreme exhaustion, migraines, Raynaud's phenomenon and bad circulation.
Hello, I've had APS for awhile and usually just take a baby aspirin except during pregnancy when I've taken
heparin
too. I'm in the Dallas, TX area. Recently, I've had very bad extreme exhaustion, migraines, Raynaud's phenomenon and bad circulation.
TxMama79
in
Hughes Syndrome APS Forum
7 years ago
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