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As if MS wasn't enough, I have osteoporosis
HelloAs if MS wasn't enough, I now have osteoporosis. Which could be why I fell and broke my shoulder in December. My primary doctor has put me on boniva. So again I am afraid to take it. Side effects just don't sound l ike fun . I am only 53. I am taking vitamin D and eating 2 tums daily for
HelloAs if MS wasn't enough, I now have osteoporosis. Which could be why I fell and broke my shoulder in December. My primary doctor has put me on boniva. So again I am afraid to take it. Side effects just don't sound l ike fun . I am only 53. I am taking vitamin D and eating 2 tums daily for
jkdavid99
in
My MSAA Community
3 days ago
Itch Relief?
While vacationing last winter, I developed an unbearable itch on my feet. They felt like they were on fire and I was itching so hard I was afraid I’d tear the skin off. I grabbed some aloe vera (for sunburn) and rubbed it on my feet. Instant relief. Certainly easier than jumping in the shower! Hope
While vacationing last winter, I developed an unbearable itch on my feet. They felt like they were on fire and I was itching so hard I was afraid I’d tear the skin off. I grabbed some aloe vera (for sunburn) and rubbed it on my feet. Instant relief. Certainly easier than jumping in the shower! Hope
ILik3Pizza
in
PBC Foundation
4 days ago
Swollen red cheek andslight jaw pain on one side.
My friend was diagnosed 6 weeks ago with PMR and GCA. Great improvement on steroids. Yesterday she had slight jaw pain and this morning her face is red and swollen. Could this be a flare. She is on 20mg per day of prednisolone.
My friend was diagnosed 6 weeks ago with PMR and GCA. Great improvement on steroids. Yesterday she had slight jaw pain and this morning her face is red and swollen. Could this be a flare. She is on 20mg per day of prednisolone.
BleatingsheepMAA
in
PMRGCAuk
4 days ago
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Work on healing balance
My balance is no longer a major issue. I am working on improving it. I do work on my core. I consider my balance issues to be a neurological issue. I balance on both feet or one foot and focus on one point. Then I move my eyes back and forth in focus and same up and down. I also move my head to change
My balance is no longer a major issue. I am working on improving it. I do work on my core. I consider my balance issues to be a neurological issue. I balance on both feet or one foot and focus on one point. Then I move my eyes back and forth in focus and same up and down. I also move my head to change
WIZARD6787
in
Pernicious Anaemia Society
4 days ago
Recovery from pneumonia
70 YO F with bronchiectasis - I developed double pneumonia 3 months ago and completed 2 weeks of IV antibiotic treatment in hospital and at home 2 months ago. Is it normal for recovery from pneumonia to wax and wane, to be "nonlinear"? I was getting better 2 weeks ago, the fatigue was starting to lift
70 YO F with bronchiectasis - I developed double pneumonia 3 months ago and completed 2 weeks of IV antibiotic treatment in hospital and at home 2 months ago. Is it normal for recovery from pneumonia to wax and wane, to be "nonlinear"? I was getting better 2 weeks ago, the fatigue was starting to lift
eoram25
in
Lung Conditions Community Forum
6 days ago
Airport travel with Injections
Can some experienced travellers who use Pegasys give me some advice please. I am travelling this week from the UK to Mexico, and have bought a Disoncare insulin cooler to keep my Pegasys syringes in whilst travelling. I will keep this in my Hand Luggage, but I’m not sure what to do with the needle
Can some experienced travellers who use Pegasys give me some advice please. I am travelling this week from the UK to Mexico, and have bought a Disoncare insulin cooler to keep my Pegasys syringes in whilst travelling. I will keep this in my Hand Luggage, but I’m not sure what to do with the needle
swimswam
in
MPN Voice
7 days ago
combined therapy help
Hi a little advise if possible: normally levo 125mg and thybon 5mg. A new endo has taken me off thybon to try and work out if I have diabetes inspidius (water balance issues). I think I was slightly too hyper but 3 weeks later and I feel terrible - weight gain, constipation, no apetite. I don’t think
Hi a little advise if possible: normally levo 125mg and thybon 5mg. A new endo has taken me off thybon to try and work out if I have diabetes inspidius (water balance issues). I think I was slightly too hyper but 3 weeks later and I feel terrible - weight gain, constipation, no apetite. I don’t think
DancerLisboa
in
Thyroid UK
8 days ago
nose bleed
was rushed to hospital 2weeks ago for pneumonia. Was discharged after a week. Wasn’t home 24 hrs. And out of the blue my nose started bleeding. It hasn’t stopped. Has this happened to anyone else and what did the doctors do to stop it?
was rushed to hospital 2weeks ago for pneumonia. Was discharged after a week. Wasn’t home 24 hrs. And out of the blue my nose started bleeding. It hasn’t stopped. Has this happened to anyone else and what did the doctors do to stop it?
Daytym
in
British Liver Trust
10 days ago
wanting to share the news
Hi , I have had my CT scan and blood work again I just to say there is no evidence of disease!!!!!! It was last year had my removal of all my bits and then chemo and a stay in ICU with septic shock but I’m still here , I know it’s early stages yet and anything can happen in the future but I GOT THERE
Hi , I have had my CT scan and blood work again I just to say there is no evidence of disease!!!!!! It was last year had my removal of all my bits and then chemo and a stay in ICU with septic shock but I’m still here , I know it’s early stages yet and anything can happen in the future but I GOT THERE
Cazy1010
in
My Ovacome
10 days ago
Septic shock
My partner has been in ICU for six days with septic shock affecting all organs and iGAS. He's still fully sedated but now able to come off some meds. He was already struggling with severe bronchiectasis, depression and PTSD before this. I arrived home from work and had to phone the ambulance. Blaming
My partner has been in ICU for six days with septic shock affecting all organs and iGAS. He's still fully sedated but now able to come off some meds. He was already struggling with severe bronchiectasis, depression and PTSD before this. I arrived home from work and had to phone the ambulance. Blaming
Bee808
in
ICUsteps
12 days ago
Chronic Fatigue and PAF
I have been diagnosed with Paroxysmal Atrial Fibrillation and suffer from chronic fatigue. I know that fatigue is a symptom of PAF but I don't know if the fatigue is only meant to be present during bouts of Afib. I suffer from chronic and debilitating fatigue all the time. If I over exert myself, then
I have been diagnosed with Paroxysmal Atrial Fibrillation and suffer from chronic fatigue. I know that fatigue is a symptom of PAF but I don't know if the fatigue is only meant to be present during bouts of Afib. I suffer from chronic and debilitating fatigue all the time. If I over exert myself, then
Cablecar
in
Atrial Fibrillation Support
13 days ago
Frequent styes
I know that this is not a serious symptom, but I was just wondering if anyone else keeps getting styes. I seem to get rid of one and then a week later get another. My eyes are very sore.I do all the recommended things with eye hygiene, changing makeup regularly and heat pad on my lids. Could this be
I know that this is not a serious symptom, but I was just wondering if anyone else keeps getting styes. I seem to get rid of one and then a week later get another. My eyes are very sore.I do all the recommended things with eye hygiene, changing makeup regularly and heat pad on my lids. Could this be
Pippapot
in
MPN Voice
13 days ago
had mouth thrush a few times but never like this
went to Doctor with mouth thrush 4 weeks ago can’t get rid of it Doc sent for another Doc to look at it both hadn’t seen any so bad did take a swab to send away not back yet have given me 4 fifferent meds none working can hardly eat lips so sore now Fluconazole 5th day for 2 weeks not any better yet
went to Doctor with mouth thrush 4 weeks ago can’t get rid of it Doc sent for another Doc to look at it both hadn’t seen any so bad did take a swab to send away not back yet have given me 4 fifferent meds none working can hardly eat lips so sore now Fluconazole 5th day for 2 weeks not any better yet
primrose71
in
Lung Conditions Community Forum
13 days ago
Haemoptysis
Hi I have posted a few times over the years & Littlepom always gave me such reassurance as she also suffered from Haemoptysis ( coughing up blood ) I have finished a 14 day course of antibiotic but bleeding so slow to heal & I know infection is cleared . Has anybody any hints on what helps them
Hi I have posted a few times over the years & Littlepom always gave me such reassurance as she also suffered from Haemoptysis ( coughing up blood ) I have finished a 14 day course of antibiotic but bleeding so slow to heal & I know infection is cleared . Has anybody any hints on what helps them
Jk1957
in
Lung Conditions Community Forum
14 days ago
Polyneuropathy.
I treat my polyneuropathy with B6 and B12. GracePV shared their experience with B6, B12 nd B1. This inspired me to revisit my self treatment of my polyneuropathy. I came across information about Benfotiamine which is similar to Thiamine Hydrochloride and Thiamine Nitrate. There are indications
I treat my polyneuropathy with B6 and B12. GracePV shared their experience with B6, B12 nd B1. This inspired me to revisit my self treatment of my polyneuropathy. I came across information about Benfotiamine which is similar to Thiamine Hydrochloride and Thiamine Nitrate. There are indications
WIZARD6787
in
Pernicious Anaemia Society
16 days ago
night time pains
I have posted a number of times about night time pain …which I am still getting! However by taking an enema each morning when waking I get rid of the wind and normally have a bowel movement and can have a good day. However at night when going to bed I get wind and two hours later I am awake. I get
I have posted a number of times about night time pain …which I am still getting! However by taking an enema each morning when waking I get rid of the wind and normally have a bowel movement and can have a good day. However at night when going to bed I get wind and two hours later I am awake. I get
Reindeer1
in
IBS Network
18 days ago
SPARX3 study of treadmill exercise for Parkinson’s recruiting at 24 sites
Participants in the study, who must have a disease duration shorter than three years, will be randomly assigned to 18 months of treadmill exercise, for 30 minutes four times per week. This aerobic workout will be done either at high intensity — to keep patients’ heart rates at 80% to 85% of maximum
Participants in the study, who must have a disease duration shorter than three years, will be randomly assigned to 18 months of treadmill exercise, for 30 minutes four times per week. This aerobic workout will be done either at high intensity — to keep patients’ heart rates at 80% to 85% of maximum
Farooqji
in
Cure Parkinson's
18 days ago
shingles
I havnt posted for ages mainly because I’m generally very fit and well and do vast amounts of excercise but hoping for some possible explanations. Diagnosed 01/18 aged 71 now I had shingles 12 yrs ago but wasn’t very ill with it I arranged my first shingles jab for end Sept 23 No side effects but
I havnt posted for ages mainly because I’m generally very fit and well and do vast amounts of excercise but hoping for some possible explanations. Diagnosed 01/18 aged 71 now I had shingles 12 yrs ago but wasn’t very ill with it I arranged my first shingles jab for end Sept 23 No side effects but
Coffeejenny
in
CLL Support
20 days ago
What is an ICM?
An Insertable Cardiac Monitor (ICM) is a small thin device that is inserted under the skin on your breastbone to record the activity of your heart. It can remain in place for up to 3 years. The device will capture and record 'episodes'. The recorded data will be collated and assessed and help to diagnose
An Insertable Cardiac Monitor (ICM) is a small thin device that is inserted under the skin on your breastbone to record the activity of your heart. It can remain in place for up to 3 years. The device will capture and record 'episodes'. The recorded data will be collated and assessed and help to diagnose
TracyAdmin
ArrhythmiaAlliance
in
Heart Rhythm Disorders Support
20 days ago
Sezary Syndrome.
After many months of fighting a complete body rash, I was visually diagnose with Sezary Syndome and had to discontinue my CLL treatment with Venetoclax, only did 8 months out of 24 months due to the rash condition. Is there anyone with knowledge of this or was there any previous postings? I greatly
After many months of fighting a complete body rash, I was visually diagnose with Sezary Syndome and had to discontinue my CLL treatment with Venetoclax, only did 8 months out of 24 months due to the rash condition. Is there anyone with knowledge of this or was there any previous postings? I greatly
Champlain
in
CLL Support
20 days ago
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