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Magnesium
Sorry I'm asking lots of questions at the moment - I'm pretty new to the Hashis thing and the intricacies of it overwhelm me at times! My GP recently referred me to a neurologist re. numbness and tingling in my hands and feet. It's mostly noticeable at night, when I'm horizontal, and it keeps me awake
Sorry I'm asking lots of questions at the moment - I'm pretty new to the Hashis thing and the intricacies of it overwhelm me at times! My GP recently referred me to a neurologist re. numbness and tingling in my hands and feet. It's mostly noticeable at night, when I'm horizontal, and it keeps me awake
Hidden
in
Thyroid UK
5 years ago
Cardiomyopathy
Hi everyone, I am new here, been following people’s journeys since Feb and not yet commented. I suffer from severe anxiety and heart palpitations. around 2 years ago we found out that my dad has heart failure, his mum had cardiomyopathy which runs through the family and also 2/3of his uncles have died
Hi everyone, I am new here, been following people’s journeys since Feb and not yet commented. I suffer from severe anxiety and heart palpitations. around 2 years ago we found out that my dad has heart failure, his mum had cardiomyopathy which runs through the family and also 2/3of his uncles have died
Fiona1989
in
British Heart Foundation
5 years ago
Nerves??
Taking Pramipexole, started with 1/2 mg every night 1 hour before bedtime, 4 months ago after augmenting on roprinole. Had to go to 1 mg about 2 weeks ago. And now woke up this morning to my arm going nuts. My dad had rls bad in his later years, after 60. They said nerves were to fault, rls in the
Taking Pramipexole, started with 1/2 mg every night 1 hour before bedtime, 4 months ago after augmenting on roprinole. Had to go to 1 mg about 2 weeks ago. And now woke up this morning to my arm going nuts. My dad had rls bad in his later years, after 60. They said nerves were to fault, rls in the
Woody4
in
Restless Legs Syndrome
5 years ago
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Balance issues
Hi alll, wrote on this site a While back...I have a family history of PA and MS, after years of low ferritin, b12 and given ferrous sulphate and cobalamin tablets for a month or so, and never followed up by the GP. I was eventually diagnosed with MS in 2014... Iv been self injecting b12 since.. Did the
Hi alll, wrote on this site a While back...I have a family history of PA and MS, after years of low ferritin, b12 and given ferrous sulphate and cobalamin tablets for a month or so, and never followed up by the GP. I was eventually diagnosed with MS in 2014... Iv been self injecting b12 since.. Did the
Margomck32
in
Pernicious Anaemia Society
5 years ago
I did the 20 mins
I did it ran for 20 mins. Fantastic. Now a nice Epsom salts bath!
I did it ran for 20 mins. Fantastic. Now a nice Epsom salts bath!
Rogie55
Graduate
in
Couch to 5K
5 years ago
Weird FMS symptom
Hi all I have been diagnosed with post traumatic FMS this week following on from very bad birth of my daughter in 2017. I have had 2 years of hell. I have had every test in the book, seen every type of consultant going (including a rheumatologist in Jan 2018 who misdiagnosed me as being vit d deficient
Hi all I have been diagnosed with post traumatic FMS this week following on from very bad birth of my daughter in 2017. I have had 2 years of hell. I have had every test in the book, seen every type of consultant going (including a rheumatologist in Jan 2018 who misdiagnosed me as being vit d deficient
Tortoise84
in
Fibromyalgia Action UK
5 years ago
Dora phase 3 study when zytiga is working
Is Dora phase 3 the best treatment for him? Here is the history and questions: 83 years old , Gleason 8 , extensive Mets to bones and lymph nodes Diagnosed in October 2018 with PSA of 947 Initial treatment of firmagon first month then lupron and xygeva every 3 months. PSA from 947 to 20 from October
Is Dora phase 3 the best treatment for him? Here is the history and questions: 83 years old , Gleason 8 , extensive Mets to bones and lymph nodes Diagnosed in October 2018 with PSA of 947 Initial treatment of firmagon first month then lupron and xygeva every 3 months. PSA from 947 to 20 from October
Hidden
in
Advanced Prostate Cancer
5 years ago
Medichecks Results - what now?
Would love some input on my results please I started on Levo 5 weeks ago (50mg a day) after a slightly elevated TSH of 3.1 was detected by our IVF clinic, following a miscarriage. These are my latest results from Medichecks, I also had the standard TSH and FT4 done at my GP, which came back almost
Would love some input on my results please I started on Levo 5 weeks ago (50mg a day) after a slightly elevated TSH of 3.1 was detected by our IVF clinic, following a miscarriage. These are my latest results from Medichecks, I also had the standard TSH and FT4 done at my GP, which came back almost
Bramble83
in
Thyroid UK
5 years ago
Pills and food stuck in esophagus
Hi Everyone, I’m wondering if any of you have had a similar experience to what I’m dealing with. I had a laparoscopic hiatal hernia repair with toupet fundoplication back in September of 2018. Since December, I’ve experienced episodes of a full feeling behind my sternum that comes along with heart palpitations
Hi Everyone, I’m wondering if any of you have had a similar experience to what I’m dealing with. I had a laparoscopic hiatal hernia repair with toupet fundoplication back in September of 2018. Since December, I’ve experienced episodes of a full feeling behind my sternum that comes along with heart palpitations
Jdt1420
in
Oesophageal & Gastric Cancer
5 years ago
Concerning advice re A&E
I have silent Brittle asthma that has been fairly stable for around 9 years but been extremely unstable since Dec last year. I have posted before and had some fab support, but this has been a weird and disconcerting shift ..... I finally got to see respiratory Consultant at my local hospital, but gutted
I have silent Brittle asthma that has been fairly stable for around 9 years but been extremely unstable since Dec last year. I have posted before and had some fab support, but this has been a weird and disconcerting shift ..... I finally got to see respiratory Consultant at my local hospital, but gutted
Echoblue
in
Asthma Community Forum
5 years ago
Can’t sleep
I’ve had tinnitus for three years. Can’t sleep at the moment and the sounds I have have no longer been maskable or attenuated for ten days. I have 2 kids and a job, I’m at my wits end with nowhere to turn to. I’ve come off another forum as the negativity made me worse but other than forums what do we
I’ve had tinnitus for three years. Can’t sleep at the moment and the sounds I have have no longer been maskable or attenuated for ten days. I have 2 kids and a job, I’m at my wits end with nowhere to turn to. I’ve come off another forum as the negativity made me worse but other than forums what do we
Tmummy
in
British Tinnitus Association
5 years ago
Starting olaparib
Starting olaparib today. I have Mets to my bones and lymph nodes. One oncologist had recommended Ra223. The oncologist at UCSF who is recommending the parp inhibitor. Is not recommending Radium 223. Anyone have any input/ comments would be appreciated.
Starting olaparib today. I have Mets to my bones and lymph nodes. One oncologist had recommended Ra223. The oncologist at UCSF who is recommending the parp inhibitor. Is not recommending Radium 223. Anyone have any input/ comments would be appreciated.
Goldberg
in
Advanced Prostate Cancer
5 years ago
Today’s the day - the saga continues on..
Hello all! Went back to my primary doctor to talk about the results from the eye doctor. Also had my BP Meds increased, more blood work and urine checked. I know pred masks other things - but they found blood - so they sent it to the lab and I should know by Monday. I’m hoping it’s just a UTI - but
Hello all! Went back to my primary doctor to talk about the results from the eye doctor. Also had my BP Meds increased, more blood work and urine checked. I know pred masks other things - but they found blood - so they sent it to the lab and I should know by Monday. I’m hoping it’s just a UTI - but
Kern1410
in
PMRGCAuk
5 years ago
My RLS is slowly getting worse
My rls has been controlled the last few months but lately its getting so much worse. I take the lowest dose of pramipexole but also take 1800mg gabapentin and co codamol for chronic back pain. My rls is affecting me alot during the day even tho i have stopped having sugar which normally helps. I am wondering
My rls has been controlled the last few months but lately its getting so much worse. I take the lowest dose of pramipexole but also take 1800mg gabapentin and co codamol for chronic back pain. My rls is affecting me alot during the day even tho i have stopped having sugar which normally helps. I am wondering
Oscarsaurus
in
Restless Legs Syndrome
5 years ago
Diagnosis of achalasia
Achalasia affects only about 6,000 people in Britain who are at various stages of managing the condition, so it is rare. For some, it can be a long time before the condition is diagnosed, and can become confused with eating disorders, for instance. Achalasia prevents people from swallowing properly
Achalasia affects only about 6,000 people in Britain who are at various stages of managing the condition, so it is rare. For some, it can be a long time before the condition is diagnosed, and can become confused with eating disorders, for instance. Achalasia prevents people from swallowing properly
Alan_M
Partner
in
Achalasia Action
5 years ago
It is cold
It is cold but sunny, okay maybe not cold but cool, my toes are cold. I should walk downstairs and put some slippers on my feet. Nah, probably not, just to lazy to walk downstairs. Such is the life of a twenty year retired veteran of Relapsing Remitting ms (RRms) Life is good, is it not? Let’s
It is cold but sunny, okay maybe not cold but cool, my toes are cold. I should walk downstairs and put some slippers on my feet. Nah, probably not, just to lazy to walk downstairs. Such is the life of a twenty year retired veteran of Relapsing Remitting ms (RRms) Life is good, is it not? Let’s
RoyceNewton
in
My MSAA Community
5 years ago
Low Iron - Are my symptoms normal?
From the end of November last year, until the first week of January this year I was experiencing a weird feeling of dizziness, and generally feeling ‘out of it’. I went to my doctor, and they diagnosed an inner ear infection as they weren’t 100% sure, which required no treatment. My symptoms disappeared
From the end of November last year, until the first week of January this year I was experiencing a weird feeling of dizziness, and generally feeling ‘out of it’. I went to my doctor, and they diagnosed an inner ear infection as they weren’t 100% sure, which required no treatment. My symptoms disappeared
Hidden
in
Thyroid UK
5 years ago
MCV increasing / folate levels
Just a quick question. When my daughter was first diagnosed with vit b deficiency her MCV was 92.5. She has been on every other day injections for a few months but it has risen to 94.8 - should it not have decreased ? Her ferritin was also low so is it just that low iron was masking the result to start
Just a quick question. When my daughter was first diagnosed with vit b deficiency her MCV was 92.5. She has been on every other day injections for a few months but it has risen to 94.8 - should it not have decreased ? Her ferritin was also low so is it just that low iron was masking the result to start
Vicky2822
in
Pernicious Anaemia Society
5 years ago
Epsom Salts?
Hello - I was wondering if you could help me! I suffer from IBS C (constipation). To cut a long story short, 4yrs ago I went to my GP as my constipation had gotten worse. He basically told me about this FODMAP diet, gave me some leaflets and some sites to look at. Initially he said follow it for 3months
Hello - I was wondering if you could help me! I suffer from IBS C (constipation). To cut a long story short, 4yrs ago I went to my GP as my constipation had gotten worse. He basically told me about this FODMAP diet, gave me some leaflets and some sites to look at. Initially he said follow it for 3months
Ms1991
in
IBS Network
5 years ago
Still dealing
Hi yall been a while since i have been on here.. im in a much better place with my anxiety 2 yrs ago i was agoraphobic, i am still fighting anxiety but am able to live, i now have a job at a nursing home and am able to do things with my family, work is stressful so i am taking my valium everyday which
Hi yall been a while since i have been on here.. im in a much better place with my anxiety 2 yrs ago i was agoraphobic, i am still fighting anxiety but am able to live, i now have a job at a nursing home and am able to do things with my family, work is stressful so i am taking my valium everyday which
Wyominganxiety
in
Anxiety Support
5 years ago
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