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Decapeptyl has stopped working?
Hi all. I have been having monthly decapeptyl injections since the summer and my Consultant has said he would like me to stay on them for as long as possible. I am also taking Indivina HRT. I am due my next injection on Wednesday. For the past few days I have had that familiar gnawing burning pain on
Hi all. I have been having monthly decapeptyl injections since the summer and my Consultant has said he would like me to stay on them for as long as possible. I am also taking Indivina HRT. I am due my next injection on Wednesday. For the past few days I have had that familiar gnawing burning pain on
ANK1173
in
Endometriosis UK
9 years ago
Can low INR cause depression/mood swings/anxiety?
Hi, with the help of my clinic nurse we are nearly on track with getting the correct warfarin dose to get my INR within its target range (2.5-3.5), however my husband and I have noticed when it drops below the range I am depressed, anxious and moody. It's really causing problems. Before I started warfarin
Hi, with the help of my clinic nurse we are nearly on track with getting the correct warfarin dose to get my INR within its target range (2.5-3.5), however my husband and I have noticed when it drops below the range I am depressed, anxious and moody. It's really causing problems. Before I started warfarin
Tess43
in
Hughes Syndrome APS Forum
9 years ago
Pulmonary embolism
Hi this week I have been diagnosed with 2 pulmonary embolisms one on each lung. I am 29 years old & this was caused from the contraceptive pill. I am still in shock that I have these & don't know how long recovery will be or anything else apart from the medication I'm on. I was only in hospital 24 hours
Hi this week I have been diagnosed with 2 pulmonary embolisms one on each lung. I am 29 years old & this was caused from the contraceptive pill. I am still in shock that I have these & don't know how long recovery will be or anything else apart from the medication I'm on. I was only in hospital 24 hours
Kate020885
in
Lung Conditions Community Forum
9 years ago
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Rivaraxoban
So.....I have Hughes with very high levels of antibodies. I was on Fragmin injections which I got on with very well. However, after a consultation in October it was agreed that I would try Rivaraxoban and see how I got in with that. I was initially apprehensive when I saw the long list of possible side
So.....I have Hughes with very high levels of antibodies. I was on Fragmin injections which I got on with very well. However, after a consultation in October it was agreed that I would try Rivaraxoban and see how I got in with that. I was initially apprehensive when I saw the long list of possible side
CalebJacob
in
Hughes Syndrome APS Forum
9 years ago
PCOS after switching from depo-provera injection to coil.
Hello. Am new here. I am in my late 30s. I was on depo injections for about 12 years with no PCOS. No hirsutism. No dodgy ovaries ( I've had several scans over the years for nonPCOS reasons, the last clear ovary scan being 3 years ago). Last year I switched to the hormone coil and rapidly developed hirsutism
Hello. Am new here. I am in my late 30s. I was on depo injections for about 12 years with no PCOS. No hirsutism. No dodgy ovaries ( I've had several scans over the years for nonPCOS reasons, the last clear ovary scan being 3 years ago). Last year I switched to the hormone coil and rapidly developed hirsutism
strawberryflower
in
PCOS UK (Verity)
9 years ago
Anti phospholipid antibody with Hemorrhagic disorder
I have a rare blood disorder and I inject Arixtra(Fondaparinux) at this time. Heparin and Agatraban both had the opposite effect on me. Due to the expense, my doctor has recommended possibly switching to Rivaroxaban. I am a little nervous to change what I know is working. Camie
I have a rare blood disorder and I inject Arixtra(Fondaparinux) at this time. Heparin and Agatraban both had the opposite effect on me. Due to the expense, my doctor has recommended possibly switching to Rivaroxaban. I am a little nervous to change what I know is working. Camie
Coblondie13
in
Hughes Syndrome APS Forum
9 years ago
Rivaraxoban
So.....I have Hughes with very high levels of antibodies. I was on Fragmin injections which I got on with very well. However, after a consultation in October it was agreed that I would try Rivaraxoban and see how I got in with that. I was initially apprehensive when I saw the long list of possible side
So.....I have Hughes with very high levels of antibodies. I was on Fragmin injections which I got on with very well. However, after a consultation in October it was agreed that I would try Rivaraxoban and see how I got in with that. I was initially apprehensive when I saw the long list of possible side
CalebJacob
in
LUPUS UK
9 years ago
Ablation Day +1
Well I'm one day on now. Wasn't half as bad as expected more uncomfortable than painful and if it became too bad I just told them and morphine and medazalam were given. Today just have slight discomfort in my chest and upper back which is to be expected. One medic said 'just because you don't have a
Well I'm one day on now. Wasn't half as bad as expected more uncomfortable than painful and if it became too bad I just told them and morphine and medazalam were given. Today just have slight discomfort in my chest and upper back which is to be expected. One medic said 'just because you don't have a
SuzieA
in
Atrial Fibrillation Support
9 years ago
Rotator cuff tear & hypothyroid?
About 3 years ago I had to have a stroid injection into my right shoulder because I had impingement syndrome due to a rotator cuff tear in my shoulder. I can`t figure out how it happened, but the problem has returned, & I`m wondering if being hypothyroid could have predisposed my to this type of injury
About 3 years ago I had to have a stroid injection into my right shoulder because I had impingement syndrome due to a rotator cuff tear in my shoulder. I can`t figure out how it happened, but the problem has returned, & I`m wondering if being hypothyroid could have predisposed my to this type of injury
hairyfairy
in
Thyroid UK
9 years ago
Haircut?
I know this may seem like a silly request, but I can't stand my itchy dry scalp and ready to cut all my hair off. I have used a lavender shampoo to calm it down. I used a psoriasis shampoo, helped. But ,I think I need a more manageable haircut because my scalp is always pink. What does everyone else
I know this may seem like a silly request, but I can't stand my itchy dry scalp and ready to cut all my hair off. I have used a lavender shampoo to calm it down. I used a psoriasis shampoo, helped. But ,I think I need a more manageable haircut because my scalp is always pink. What does everyone else
Natura
in
LUPUS UK
9 years ago
Dry scalp problems
I have had dry skin and also dandruff and dry scalp since before becoming hypothyroid. I had been using head and shoulders until recently to try and ease symptoms, however, this did not work. I was given the 'black tar' shampoo on prescription and this didn't work either. The last few weeks, my scalp
I have had dry skin and also dandruff and dry scalp since before becoming hypothyroid. I had been using head and shoulders until recently to try and ease symptoms, however, this did not work. I was given the 'black tar' shampoo on prescription and this didn't work either. The last few weeks, my scalp
Hidden
in
Thyroid UK
9 years ago
Buying Our Cottage Brought Surprises
We didn't much care for this cottage when we first saw it...the 'garden' at the front was so terribly over-grown that the windows were hidden behind long grass and unruly shrubs...the roof was covered in clumps of bright green moss and baby trees were growing out of the guttering. But the estate agent
We didn't much care for this cottage when we first saw it...the 'garden' at the front was so terribly over-grown that the windows were hidden behind long grass and unruly shrubs...the roof was covered in clumps of bright green moss and baby trees were growing out of the guttering. But the estate agent
Hidden
in
Lung Conditions Community Forum
9 years ago
Diabetic problem
I m 50 year old and suffering from diabetic from 4 year and taking GLUCONORM G-2 and GLUCONORM G-1, bur its not intake regularlly from last 15 days i m feeling my left arm and hands bone are doing pain kindly suggest the proper medicine
I m 50 year old and suffering from diabetic from 4 year and taking GLUCONORM G-2 and GLUCONORM G-1, bur its not intake regularlly from last 15 days i m feeling my left arm and hands bone are doing pain kindly suggest the proper medicine
anilverma19091964
in
Diabetes India
9 years ago
Rotator cuff injury
I had a rotator cuff injury to my right shoulder about 3 years ago, & I had a steroid injection at my local hospital which cleared it up. The problem seems to have recurred, with the usual pain & discomfort. I`m wondering if having an underactive thyroid would make someone more prone to this kind of
I had a rotator cuff injury to my right shoulder about 3 years ago, & I had a steroid injection at my local hospital which cleared it up. The problem seems to have recurred, with the usual pain & discomfort. I`m wondering if having an underactive thyroid would make someone more prone to this kind of
hairyfairy
in
Thyroid UK
10 years ago
MRI Scan - T2 Hyperintense white matter lesions reported
My recent MRI Scan reported T2 Hyperintense white matter lesions in the frontal region. Anyone else have any experience of this finding, and willing to share information please? Also, recent A & E admission with chest pain and breathlessness. D-Dimer test elevated, so was given a VQ scan, no PE found
My recent MRI Scan reported T2 Hyperintense white matter lesions in the frontal region. Anyone else have any experience of this finding, and willing to share information please? Also, recent A & E admission with chest pain and breathlessness. D-Dimer test elevated, so was given a VQ scan, no PE found
LupusKaren
in
LUPUS UK
10 years ago
Rivaroxaban
Hi, I have been injecting Fragmin since August this year and I get on well with them, however I am about to be swapped over to Rivaroxaban. I have just picked them up and read the side effects! Wow! Does anybody else have any experience of this drug and if so how do you find it? Any horrible side effects
Hi, I have been injecting Fragmin since August this year and I get on well with them, however I am about to be swapped over to Rivaroxaban. I have just picked them up and read the side effects! Wow! Does anybody else have any experience of this drug and if so how do you find it? Any horrible side effects
CalebJacob
in
LUPUS UK
10 years ago
Diagnosed with autoimmune hepatitis
Hi this is my first post on this site so please forgive if I sound naive, have been having trouble with my liver functions showing very high readings, I thought it was down to the fact that I had my gall bladder out, however not been able to get over the op or I thought I wasn't, having hot sweats,joint
Hi this is my first post on this site so please forgive if I sound naive, have been having trouble with my liver functions showing very high readings, I thought it was down to the fact that I had my gall bladder out, however not been able to get over the op or I thought I wasn't, having hot sweats,joint
Time4care
in
British Liver Trust
10 years ago
Interesting feature on Inside Health
This is always an interesting programme to listen to, but this week's episode is particularly pertinent as the latest types of anticoagulants are discussed. http://www.bbc.co.uk/programmes/b04mctw7 There's a transcript of the programme on this site as well (if you're unable to listen on iPlayer). Has
This is always an interesting programme to listen to, but this week's episode is particularly pertinent as the latest types of anticoagulants are discussed. http://www.bbc.co.uk/programmes/b04mctw7 There's a transcript of the programme on this site as well (if you're unable to listen on iPlayer). Has
Jo60
in
Hughes Syndrome APS Forum
10 years ago
Pulmonary Hypertension
I have just found this community and don't know whether I belong to this one or not. I have Limited Systemic Sclerosis which has now progressed to Pulmonary Hypertension. There aren't that many in this country that suffers with it, only around 6 to 8,000 in the UK. It affects the pulmonary artery
I have just found this community and don't know whether I belong to this one or not. I have Limited Systemic Sclerosis which has now progressed to Pulmonary Hypertension. There aren't that many in this country that suffers with it, only around 6 to 8,000 in the UK. It affects the pulmonary artery
PaleIndian2
in
Lung Conditions Community Forum
10 years ago
Spontaneous Referral!
Just had to share this as slightly excited - my Rhuematologist has spontaneously asked if I would like her to arrange for me to be seen by Dr David D'Cruz!! It may have something to do with the fact that I had just emailed her to say that I want to inject Heparin if my INR goes below 2.5 rather than
Just had to share this as slightly excited - my Rhuematologist has spontaneously asked if I would like her to arrange for me to be seen by Dr David D'Cruz!! It may have something to do with the fact that I had just emailed her to say that I want to inject Heparin if my INR goes below 2.5 rather than
Elaine77c
in
Hughes Syndrome APS Forum
10 years ago
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