Search
Search
About
Log in
Join
Experiences with
Heparin
Posts
Communities
1,021 public posts
Filter results
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
Want to take advantage of all our features? Just log in!
Log in
or
Join
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
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
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
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
Hughes syndrome.... very anxious
Also will
heparin
make any difference to me if I'm to start it as soon as I have a positive??, I feel that may be too late. Sorry to babble on, I'm so confused and have little understanding on the whole diagnosis. Thank you for reading Rachel
Also will
heparin
make any difference to me if I'm to start it as soon as I have a positive??, I feel that may be too late. Sorry to babble on, I'm so confused and have little understanding on the whole diagnosis. Thank you for reading Rachel
Rachel-c
in
Hughes Syndrome APS Forum
7 years ago
Heparin hit
I think regulars on here are aware of my recent health issues and hospital stay. This morning I had what is known as a Anti X Tena Assay blood test. The results have shown I have reduced platelets so the hospital have arranged another test on Tuesday. They seem quite
I think regulars on here are aware of my recent health issues and hospital stay. This morning I had what is known as a Anti X Tena Assay blood test. The results have shown I have reduced platelets so the hospital have arranged another test on Tuesday. They seem quite
Jillymo
in
Hughes Syndrome APS Forum
7 years ago
Baby is here!
Heparin
and aspirin truly are amazing. Blessed to have our 2 miracles. Never hesitate to contact me for any support on the journey to becoming a mum. It's been a challenge but so worth the perseverance!
Heparin
and aspirin truly are amazing. Blessed to have our 2 miracles. Never hesitate to contact me for any support on the journey to becoming a mum. It's been a challenge but so worth the perseverance!
Hopingforababy
in
Hughes Syndrome APS Forum
7 years ago
Vertigo bppv ectopics beats anxiety Severe depression please help!
, Get ready for an essay as im desperate. Im 35 so about roughly in my early 20s developed dizzys in my sleep. It would wake me. Closed eyes would make it worse. Yrs passed i decided to see a neurologist. Head scans were fine was told it was bppv. Few urs later i developed graves disease.. the torment
, Get ready for an essay as im desperate. Im 35 so about roughly in my early 20s developed dizzys in my sleep. It would wake me. Closed eyes would make it worse. Yrs passed i decided to see a neurologist. Head scans were fine was told it was bppv. Few urs later i developed graves disease.. the torment
Contra21
in
Thyroid UK
7 years ago
Apixaban
Hi diagnosed with DVT 2 weeks ago had two shots of
heparin
and been on APIXABAN since, been advised about bleeding so far so good, no adverse symptoms as of yet only mild symptoms is lightheadedness every so often, My only anxiety is it feels like a ticking time bomb, Consultant and his pharmacist
Hi diagnosed with DVT 2 weeks ago had two shots of
heparin
and been on APIXABAN since, been advised about bleeding so far so good, no adverse symptoms as of yet only mild symptoms is lightheadedness every so often, My only anxiety is it feels like a ticking time bomb, Consultant and his pharmacist
Bazaafc
in
Anticoagulation Support
7 years ago
Im newish on here & 15 yrs of vertigo/bppv on and off & ectoptics. Ive had enough its taken over my life. :(
Hi all, Get ready for an essay as im desperate. Im 35 so about roughly in my early 20s developed dizzys in my sleep. It would wake me. Closed eyes would make it worse. Yrs passed i decided to see a neurologist. Head scans were fine was told it was bppv. Few urs later i developed graves disease.
Hi all, Get ready for an essay as im desperate. Im 35 so about roughly in my early 20s developed dizzys in my sleep. It would wake me. Closed eyes would make it worse. Yrs passed i decided to see a neurologist. Head scans were fine was told it was bppv. Few urs later i developed graves disease.
Contra21
in
Tinnitus UK
7 years ago
Tinnitus GONE! A chance for everyone?
I am new to this forum. Amazingly I am no longer plagued with the nightmare of tinnitus. After suffering for more than ten years it is under absolute control. Here is my story. I had read in a local newspaper of the work of Dr Cunningham of Newcastle University who had been recognised for his successful
I am new to this forum. Amazingly I am no longer plagued with the nightmare of tinnitus. After suffering for more than ten years it is under absolute control. Here is my story. I had read in a local newspaper of the work of Dr Cunningham of Newcastle University who had been recognised for his successful
NoTinitus
in
British Tinnitus Association
7 years ago
Prof Graham Hughes Monthly Blog - September 2017
She was admitted to hospital and treated initially with
heparin
. “To my amazement, I could read, my eyes were totally clear”. She recovered from the heart attack, but went on to suffer episodes of pain between the shoulder blades, sometimes in a ‘tight band’.
She was admitted to hospital and treated initially with
heparin
. “To my amazement, I could read, my eyes were totally clear”. She recovered from the heart attack, but went on to suffer episodes of pain between the shoulder blades, sometimes in a ‘tight band’.
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
7 years ago
1
...
27
28
29
...
52
Next page
10
20
30
40
50
Filter results
Clear filters
Posted in
All communities
Hughes Syndrome APS Forum
322 results
British Tinnitus Association
119 results
Tinnitus UK
63 results
View top 10 communities
Sort by
Most Relevant
Newest