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Gaucher disease type 1 (GD1)
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What is a cardioversion?
If you have AF you may have been offered a cardioversion, but may be unsure of what to expect? A
cardioversion
is a procedure to convert your heart from AF back into normal (sinus) rhythm. This is achieved by administering a rhythm control medication (antiarrhythmic drug) by mouth or through
If you have AF you may have been offered a cardioversion, but may be unsure of what to expect? A
cardioversion
is a procedure to convert your heart from AF back into normal (sinus) rhythm. This is achieved by administering a rhythm control medication (antiarrhythmic drug) by mouth or through
TracyAdmin
Partner
in
Atrial Fibrillation Support
3 months ago
Request for advice looking for possible new diagnosis
Hi, this is my first time back on the forum after a few years break just bimbling along whilst struggling as we all do. But I've really hit a wall. I've also posted this on the Fibromyalgia and Lupus communities.I don't want to write too long a post so will try and keep the background brief. Basically
Hi, this is my first time back on the forum after a few years break just bimbling along whilst struggling as we all do. But I've really hit a wall. I've also posted this on the Fibromyalgia and Lupus communities.I don't want to write too long a post so will try and keep the background brief. Basically
Wispymisty
in
NRAS
4 months ago
Request for advice looking for possible new diagnosis
Hi, this is my first time back on the forum after a few years break just bimbling along whilst struggling as we all do. But I've really hit a wall. I've also posted this on the Fibromyalgia/Rheumatoid Arthritis communities.I don't want to write too long a post so will try and keep the background brief
Hi, this is my first time back on the forum after a few years break just bimbling along whilst struggling as we all do. But I've really hit a wall. I've also posted this on the Fibromyalgia/Rheumatoid Arthritis communities.I don't want to write too long a post so will try and keep the background brief
Wispymisty
in
LUPUS UK
4 months ago
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Lopressor dose titration
Permanent afib 100mgm of Lopressor am & 50 pm plus eliquis. Decided to cut back to 50 in am because of blurred vision and now have had upset stomach times 1 week plus HR back up to low 100's. Thought I felt better on lower dose but maybe not??
Permanent afib 100mgm of Lopressor am & 50 pm plus eliquis. Decided to cut back to 50 in am because of blurred vision and now have had upset stomach times 1 week plus HR back up to low 100's. Thought I felt better on lower dose but maybe not??
farewelltoarms
in
Atrial Fibrillation Support
3 months ago
Too Much Omega 3 triggering AFib?
I care for a family member with an AFib history. It has recently reared its head again after several years without an issue. I have been trying to find a possible trigger. One of the possible things I suspect is that it may be the overhaul in her diet the last couple of months. I noticed one day
I care for a family member with an AFib history. It has recently reared its head again after several years without an issue. I have been trying to find a possible trigger. One of the possible things I suspect is that it may be the overhaul in her diet the last couple of months. I noticed one day
Mulan1
in
Atrial Fibrillation Support
3 months ago
Happy but not really
Hello.i was so excited when I found this post but not really after seeing that no one has really gotten over it. Apparently it's permanent for the most part.i just got my 6k bill from hospital because I couldn't take it I thought it was a serious lung or heart problem but I'm cleared.i have the same
Hello.i was so excited when I found this post but not really after seeing that no one has really gotten over it. Apparently it's permanent for the most part.i just got my 6k bill from hospital because I couldn't take it I thought it was a serious lung or heart problem but I'm cleared.i have the same
EliezerCan2
in
Pain Concern
3 months ago
Updated diagnosis of autoimmune thyroid disorder
Just an update. Unsurprisingly with elevated thyroid antibodies I have been diagnosed with an autoimmune thyroid disorder. As I currently have some hyper symptoms as well as hypo ones, the private GO who’s diagnosed me very sensibly, imo, wants to test again to ensure she gets the diagnosis and treatment
Just an update. Unsurprisingly with elevated thyroid antibodies I have been diagnosed with an autoimmune thyroid disorder. As I currently have some hyper symptoms as well as hypo ones, the private GO who’s diagnosed me very sensibly, imo, wants to test again to ensure she gets the diagnosis and treatment
Fizzwhizz
in
Thyroid UK
4 months ago
Gut analysis
I recently provided a sample for analysis and received the results last week. I had a follow up appointment with Gemma my Funtional Health Practitioner (in training) yesterday. I wanted to share some of the info I have learned here. I have Helicobacter Pylori, unsurprising as around 50% of the population
I recently provided a sample for analysis and received the results last week. I had a follow up appointment with Gemma my Funtional Health Practitioner (in training) yesterday. I wanted to share some of the info I have learned here. I have Helicobacter Pylori, unsurprising as around 50% of the population
IdasMum
in
PMRGCAuk
4 months ago
Fitbit versus Apple watch
Thank you to everyone who replied to my post re Apple watch and Kardia. I decided on the Kardia 6 as part of the kit mainly because cardiologists seem to think they are accurate. I am still not decided on the watch yet. I havnt been diag with AF yet as some may remember , Ectopics yes , and they are
Thank you to everyone who replied to my post re Apple watch and Kardia. I decided on the Kardia 6 as part of the kit mainly because cardiologists seem to think they are accurate. I am still not decided on the watch yet. I havnt been diag with AF yet as some may remember , Ectopics yes , and they are
ainslie
in
Atrial Fibrillation Support
3 months ago
If I Didn't Have Faith and Family Like You!
Now, I just shared my story about my weekend in NY seeing Chris Botti; now I'm sitting in the Family Waiting Room of Jefferson Hospital for hubby to get out of surgery. He kept complaining of bad back and stomach pain. Well, large Kidney Stone causing a blockage! He needed a different procedure; not
Now, I just shared my story about my weekend in NY seeing Chris Botti; now I'm sitting in the Family Waiting Room of Jefferson Hospital for hubby to get out of surgery. He kept complaining of bad back and stomach pain. Well, large Kidney Stone causing a blockage! He needed a different procedure; not
GratefulNeeC
in
My MSAA Community
7 months ago
⁹Newbie: can anybody help with local support to me? Surrey/Sussex/South London
Hello! I was diagnosed with UCTD 3 years ago after contracting awful covid. However during routine check-up bloods last month, for the first time, my Rheu picked up positive Lupus screen, ANA, rheumatoid factor alongside others i cant remember. (I have always had a negative autoimmune panel, but high
Hello! I was diagnosed with UCTD 3 years ago after contracting awful covid. However during routine check-up bloods last month, for the first time, my Rheu picked up positive Lupus screen, ANA, rheumatoid factor alongside others i cant remember. (I have always had a negative autoimmune panel, but high
Gm131987
in
LUPUS UK
4 months ago
Thyroid blood test results
I have been on thyroxine since 2017 to treat my underactive thyroid (confirmed Hashimotos).My bloods from this week are in the attached screenshot. I haven't felt like me for many years. I wondered what peples thoughts were on my results?
I have been on thyroxine since 2017 to treat my underactive thyroid (confirmed Hashimotos).My bloods from this week are in the attached screenshot. I haven't felt like me for many years. I wondered what peples thoughts were on my results?
SusieR68
in
Thyroid UK
4 months ago
Is atrial enlargement serious.
hi guys and girls. Just had a phone appointment over the phone with cardiologist. I think it went well.? But it seemed to be a rushed appointment and I didn’t have time to ask him all the questions i wanted to unfortunately.! but the main thing im worried about is that he mentioned my ECHO in December
hi guys and girls. Just had a phone appointment over the phone with cardiologist. I think it went well.? But it seemed to be a rushed appointment and I didn’t have time to ask him all the questions i wanted to unfortunately.! but the main thing im worried about is that he mentioned my ECHO in December
Jetcat
in
Atrial Fibrillation Support
3 months ago
Rythm changed
hi I was diagnosed with AF three months ago was put on apixoban and bisoperol however bisoperol has been changed to verapamil after a four day stay in hospital where due to them using a nebuliser my heart rate went to 210 nebuliser was used for an asthma attack told never let anyone use a nebuliser
hi I was diagnosed with AF three months ago was put on apixoban and bisoperol however bisoperol has been changed to verapamil after a four day stay in hospital where due to them using a nebuliser my heart rate went to 210 nebuliser was used for an asthma attack told never let anyone use a nebuliser
KelliEAnniE
in
Atrial Fibrillation Support
3 months ago
New NICE guidelines
On the Pernicious Anaemia Society forum, there is a new thread re the newly released NICE guidelines for Pernicious Anaemia/B12 Deficiency Diagnosis and Treatment in Over 16s [i]
New NICE guidelines
[/i] https://healthunlocked.com/pasoc/posts/150619728/new-nice-guidelines Within that thread,
On the Pernicious Anaemia Society forum, there is a new thread re the newly released NICE guidelines for Pernicious Anaemia/B12 Deficiency Diagnosis and Treatment in Over 16s [i]
New NICE guidelines
[/i] https://healthunlocked.com/pasoc/posts/150619728/new-nice-guidelines Within that thread,
helvella
Thyroid UK
in
Thyroid UK
4 months ago
NICE guideline on B12 Deficiency diagnosis and monitoring in over 16s
The Vitamin B12 Deficiency Guideline in Over 16's has been published.
What does this mean for those with Pernicious Anaemia whether formally diagnosed or not?
What does it mean with those struggling to get sufficiently frequent treatment for their B12 deficiency?
What does
The Vitamin B12 Deficiency Guideline in Over 16's has been published.
What does this mean for those with Pernicious Anaemia whether formally diagnosed or not?
What does it mean with those struggling to get sufficiently frequent treatment for their B12 deficiency?
What does
PAScomms
in
Pernicious Anaemia Society
4 months ago
Dr Guptas video
Has anyone seen the video re cardiac anxiety? I'm trying to figure out what comes first the anxiety or the list of symptoms ie palpitations chest pain etc. Has anyone dived into this research?
Has anyone seen the video re cardiac anxiety? I'm trying to figure out what comes first the anxiety or the list of symptoms ie palpitations chest pain etc. Has anyone dived into this research?
TillyBoss
in
Atrial Fibrillation Support
3 months ago
Oxygen therapy
I am helping to look after my 88 year old sister at present. She has been prescribed ambulatory oxygen therapy following a diagnosis of pulmonary hypertension, I think related to her Protein S Deficiency. She is frail and even the small oxygen cylinders are heavy and difficult for her to use but oxygen
I am helping to look after my 88 year old sister at present. She has been prescribed ambulatory oxygen therapy following a diagnosis of pulmonary hypertension, I think related to her Protein S Deficiency. She is frail and even the small oxygen cylinders are heavy and difficult for her to use but oxygen
mozart27
in
Lung Conditions Community Forum
3 months ago
Muscle wasting?
Is this a PD sign? It happens anyway with age so how do you know what the root problem is? A few days ago I finished a treadmill workout in our shed and as I was walking away my legs gave out. Suddenly I was on the ground. Ultimately I was able to get up and shuffle into the house. I posted
Is this a PD sign? It happens anyway with age so how do you know what the root problem is? A few days ago I finished a treadmill workout in our shed and as I was walking away my legs gave out. Suddenly I was on the ground. Ultimately I was able to get up and shuffle into the house. I posted
kaypeeoh
in
Cure Parkinson's
7 months ago
atypical trigeminal neuralgia
Recently diagnosed with atypical trigeminal neuralgia, pain on left side of face/eye/head. I also have rheumatoid arthritis which I take methotrexate 20mg once per week for. Does anyone else know anything about this, or what helps, in a lot of pain.
Recently diagnosed with atypical trigeminal neuralgia, pain on left side of face/eye/head. I also have rheumatoid arthritis which I take methotrexate 20mg once per week for. Does anyone else know anything about this, or what helps, in a lot of pain.
PurpleDuckie
in
PMRGCAuk
4 months ago
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