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preservatives in B12
I have been reacting to subcutaneous SI and looking at what is in Panpharma B12 there is acetic acid sodium chloride sodium acetate. This is hydro. I have bought a lot of these and worry first if I can’t use them and secondly if all have this in them. Any advice please?
I have been reacting to subcutaneous SI and looking at what is in Panpharma B12 there is acetic acid sodium chloride sodium acetate. This is hydro. I have bought a lot of these and worry first if I can’t use them and secondly if all have this in them. Any advice please?
smg1950
in
Pernicious Anaemia Society
1 year ago
Lung nodule thanks every one who replied
I recently had a cardiac ct scan for chest tightness i have 3 stents stents the results showed that as well as copd which i also have there is now have a 20 mm lung nodule in my left lung Has anyone else have a nodule and how is it treated I have to have a repeat scan in 3 months and have been referred
I recently had a cardiac ct scan for chest tightness i have 3 stents stents the results showed that as well as copd which i also have there is now have a 20 mm lung nodule in my left lung Has anyone else have a nodule and how is it treated I have to have a repeat scan in 3 months and have been referred
Chrissca71
in
Lung Conditions Community Forum
10 months ago
Reactive Tinnitus - anyone else experience this
My T is very reactive and I have hyperacusis I have to wear ear plugs and ear defenders out n about I walked into a shop a few days ago ( for a few mins) without ear protection and the music has made my T go ballistic and changed tone to a higher pitch and more solid tone as well as being louder and
My T is very reactive and I have hyperacusis I have to wear ear plugs and ear defenders out n about I walked into a shop a few days ago ( for a few mins) without ear protection and the music has made my T go ballistic and changed tone to a higher pitch and more solid tone as well as being louder and
surviveT
in
Tinnitus UK
1 year ago
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Dangerous Supplement. Mucuna Pruriens. Dangerous side effects you must know.
Unregulated, no quality control, and may contain toxic poisonous contaminates. Lead, heavy metals, mold, fungus etc. Dosage is impossible to manage. Counter reaction to carbidopa levodopa is unmanageable and unpredictable. Makes combining it with real Parkinson's medications a night mare. Maybe just
Unregulated, no quality control, and may contain toxic poisonous contaminates. Lead, heavy metals, mold, fungus etc. Dosage is impossible to manage. Counter reaction to carbidopa levodopa is unmanageable and unpredictable. Makes combining it with real Parkinson's medications a night mare. Maybe just
Thal
in
Cure Parkinson's
2 months ago
Pembrolizumab & CLL
Greetings, has anyone got experience of taking Pembrolizumab while also having CLL. I have secondary lung cancer (non small cell) as a matatsisation of Squamous Cell Carcinoma.
Greetings, has anyone got experience of taking Pembrolizumab while also having CLL. I have secondary lung cancer (non small cell) as a matatsisation of Squamous Cell Carcinoma.
Meic13
in
Lung Conditions Community Forum
10 months ago
Late diagnosis of asbestosis
My Dad is 96 and has had progressive lung disease for many years. He's a non-smoker and I always wondered about the cause. On 16 October this year he was referred to a respiratory consultant for the first time. She took a detailed work history (again, the first one to do so) and we realised just how
My Dad is 96 and has had progressive lung disease for many years. He's a non-smoker and I always wondered about the cause. On 16 October this year he was referred to a respiratory consultant for the first time. She took a detailed work history (again, the first one to do so) and we realised just how
tchouli
in
Lung Conditions Community Forum
10 months ago
Picolax
Hi, I have done bowel prep lots of times over the years however I have always used moviprep so I know exactly what to expect as it goes through my system and I understand how it works especially with the volume of fluids it gives plenty of fuel to keep going all day and night however there is a shortage
Hi, I have done bowel prep lots of times over the years however I have always used moviprep so I know exactly what to expect as it goes through my system and I understand how it works especially with the volume of fluids it gives plenty of fuel to keep going all day and night however there is a shortage
MyStar86
in
Endometriosis UK
10 months ago
Tendon ruptures in hand due to long-term RA
I'm 67 and things have reached a chronic stage in my left, dominant hand due to several tendon ruptures affecting middle and ring fingers, which I can no longer extend. I'm now on the Orthopaedic surgeon's operating list, but I am very scared about how I will cope post-operatively, since I already have
I'm 67 and things have reached a chronic stage in my left, dominant hand due to several tendon ruptures affecting middle and ring fingers, which I can no longer extend. I'm now on the Orthopaedic surgeon's operating list, but I am very scared about how I will cope post-operatively, since I already have
dearpen1
in
NRAS
1 year ago
Robert
Robert was diagnosed with Parkinson’s in 2018 PSP in 2021 progression was slow at first. Last year Robert was walking with a cane and dragging his feet. In September he began to fall daily sometimes more. He got weaker every day and finally allowed me to call a rescue. What followed was a whirlwind
Robert was diagnosed with Parkinson’s in 2018 PSP in 2021 progression was slow at first. Last year Robert was walking with a cane and dragging his feet. In September he began to fall daily sometimes more. He got weaker every day and finally allowed me to call a rescue. What followed was a whirlwind
Wrski
in
PSP Association
9 months ago
Your bespoke prayer poem on faith and hope
Prayer poem for Elisabeth Linsdon on faith, hope and love It is in this, my hour of serious illness That of faith I have most need Then lord, be there to support me To Nourish my broken body And my hungry soul to feed Let my Faith and hopebe there to strengthen me when weak When with dark skies of illness
Prayer poem for Elisabeth Linsdon on faith, hope and love It is in this, my hour of serious illness That of faith I have most need Then lord, be there to support me To Nourish my broken body And my hungry soul to feed Let my Faith and hopebe there to strengthen me when weak When with dark skies of illness
JULIETstevens
in
Endometriosis UK
1 year ago
Occupational Therapy ‘drop-in’ event
Occupational Therapists play an important role in supporting people living with ataxia! We do occupations from the moment we’re born – they’re essential to living. They give our lives meaning and purpose, they shape who we are, and help us connect with others. This week is Occupational (OT) week!
Occupational Therapists play an important role in supporting people living with ataxia! We do occupations from the moment we’re born – they’re essential to living. They give our lives meaning and purpose, they shape who we are, and help us connect with others. This week is Occupational (OT) week!
wobblybee
in
Ataxia UK
9 months ago
Occupational therapy intervention for FND
Would anyone like to share their experiences of occupation therapy intervention for FND, especially in relation to the mitigation of shaking, vocalisations, and hypersensitivity to noise. How helpful did you find it?
Would anyone like to share their experiences of occupation therapy intervention for FND, especially in relation to the mitigation of shaking, vocalisations, and hypersensitivity to noise. How helpful did you find it?
Shimmyaway
in
Functional Neurological Disorder - FND Hope
10 months ago
wax treatments
having had an appointment with the specialist nurse yesterday I have been referred to occupational therapy for some help with my clawed hands. Really hoping I can get some positive help as I do suffer at times with pain and stiffness despite doing exercises. She also mentioned a wax bath treatment which
having had an appointment with the specialist nurse yesterday I have been referred to occupational therapy for some help with my clawed hands. Really hoping I can get some positive help as I do suffer at times with pain and stiffness despite doing exercises. She also mentioned a wax bath treatment which
Clangerscat
in
Scleroderma & Raynaud's UK (SRUK)
6 months ago
Paraneoplastic Syndromes and MPNs
This is a very interesting article on a topic I have not seen before. It caught my attention as I recall some on the forum reporting Myasthenia Gravis along with the MPN. I have experience intermittent hypercalcemia, but I do not believe this is due to a Paraneoplastic Syndrome. https://www.mympnteam.com
This is a very interesting article on a topic I have not seen before. It caught my attention as I recall some on the forum reporting Myasthenia Gravis along with the MPN. I have experience intermittent hypercalcemia, but I do not believe this is due to a Paraneoplastic Syndrome. https://www.mympnteam.com
hunter5582
in
MPN Voice
1 year ago
Allodynia
many contributors say that because of the different symptoms it is difficult to diagnose the exact Problem.this is because medical science isn’t yet quite up with the many problems of the body. Our Doctor advises that my wife no longer has Fibromyalgia. I’m not sure about that.one of the associated
many contributors say that because of the different symptoms it is difficult to diagnose the exact Problem.this is because medical science isn’t yet quite up with the many problems of the body. Our Doctor advises that my wife no longer has Fibromyalgia. I’m not sure about that.one of the associated
Vivtom
in
Fibromyalgia Action UK
1 year ago
Dry-Needling and Low Level Laser Therapy By Physios: Does this really work and can it worsen tinnitus?
I triggered tinnitus and hyperacusis over 7 years ago now. Luckily it always went eventually but as of about 4 months ago it seems as if it is here to stay and a lot worse. An otologist told me that areas I said gave me pain could be consistent with TMJ issues and that he worked with a physio who could
I triggered tinnitus and hyperacusis over 7 years ago now. Luckily it always went eventually but as of about 4 months ago it seems as if it is here to stay and a lot worse. An otologist told me that areas I said gave me pain could be consistent with TMJ issues and that he worked with a physio who could
PuddingChipsAndGravy
in
Tinnitus UK
1 year ago
ADHD-PI dad + ADHD-PH 4yo boy = Chaos
I’ll try to be brief. We both have ADHD with different classifications. All family goes to therapy. He takes Methylphenidate since 3 months ago and goes to occupational therapy. Also 1mg melatonin for sleep since he started those meds. He showed issues at school since over a year ago. Been kicked out
I’ll try to be brief. We both have ADHD with different classifications. All family goes to therapy. He takes Methylphenidate since 3 months ago and goes to occupational therapy. Also 1mg melatonin for sleep since he started those meds. He showed issues at school since over a year ago. Been kicked out
ADHDLatino
in
CHADD's ADHD Parents Together
10 months ago
Exercise at the bottom of the scale.
I thought I’d write up my experiences for those of us who are not going to go far or fast, either ever or anytime soon e.g. like me with mobility problems separate from the PMR. Set baseline I’m 67. I walk at all times with a rollator and have spinal curvature. My left leg is slightly twisted and
I thought I’d write up my experiences for those of us who are not going to go far or fast, either ever or anytime soon e.g. like me with mobility problems separate from the PMR. Set baseline I’m 67. I walk at all times with a rollator and have spinal curvature. My left leg is slightly twisted and
Mayadill
in
PMRGCAuk
1 year ago
She doesn’t act that way with me…
I’ve known since my daughter was 2 years old that something was going on, but everyone around me tries to explain it away. It seems like to them having ADHD and sensory processing disorder is the kiss of death and all is lost for her. Why do I have to over explain her symptoms and diagnoses? If I say
I’ve known since my daughter was 2 years old that something was going on, but everyone around me tries to explain it away. It seems like to them having ADHD and sensory processing disorder is the kiss of death and all is lost for her. Why do I have to over explain her symptoms and diagnoses? If I say
yum_yum
in
CHADD's ADHD Parents Together
11 months ago
An exhaustive study that offers hope that some types of activities can improve symptoms even as disease progresses
https://academic.oup.com/brain/advance-article/doi/10.1093/brain/awad325/7284004 ------- The article link above contains the entire pdf of the study results which is 44 pages. It might be hard to digest in a short time. I am providing here the analysis and summary of the study along with why the study
https://academic.oup.com/brain/advance-article/doi/10.1093/brain/awad325/7284004 ------- The article link above contains the entire pdf of the study results which is 44 pages. It might be hard to digest in a short time. I am providing here the analysis and summary of the study along with why the study
pdpatient
in
Cure Parkinson's
11 months ago
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