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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
Short Synatchen Test
Quick question, could someone help me with some vague results from the hospital. Have been taking Pred for a long time but with the help of Methotrexate injections I am down to 3 mgs (hurray). I had a short synatchen test a couple of weeks ago and Rheumatology Nurse rang me and babbled very quickly
Quick question, could someone help me with some vague results from the hospital. Have been taking Pred for a long time but with the help of Methotrexate injections I am down to 3 mgs (hurray). I had a short synatchen test a couple of weeks ago and Rheumatology Nurse rang me and babbled very quickly
Hollybee21
in
PMRGCAuk
4 months ago
Newsystem23
Not posted for a while, hope everyone is managing their lupus symptoms as best they can. I did think that using 50spf sun screen and taking hydroxychloroquine would keep my skin lupus at bay. However, I'm beginning to realise it is not just the sun and artificial light that my skin is sensitive to.
Not posted for a while, hope everyone is managing their lupus symptoms as best they can. I did think that using 50spf sun screen and taking hydroxychloroquine would keep my skin lupus at bay. However, I'm beginning to realise it is not just the sun and artificial light that my skin is sensitive to.
Newsystem23
in
LUPUS UK
4 months ago
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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
Newly Diagnosed
Hello, I’m new to this forum and was only diagnosed with SLE in late December. I’ve also got secondary triple positive antiphospholipid antibodies. I’m 26 and I’ve always lived a very active/outgoing lifestyle and have always tried to be healthy so it I’m finding it all a bit difficult to process.
Hello, I’m new to this forum and was only diagnosed with SLE in late December. I’ve also got secondary triple positive antiphospholipid antibodies. I’m 26 and I’ve always lived a very active/outgoing lifestyle and have always tried to be healthy so it I’m finding it all a bit difficult to process.
ChloeScotland
in
LUPUS UK
4 months ago
Chemo question
Hello everyone, I was diagnosed with stage 4 ovarian cancer a couple days before last Christmas so I am early in my journey and feeling very scared and discouraged. Since my tumor is too large, I can’t have surgery yet. I had my first taxol/carboplatin treatment last week. I had an allergic reaction
Hello everyone, I was diagnosed with stage 4 ovarian cancer a couple days before last Christmas so I am early in my journey and feeling very scared and discouraged. Since my tumor is too large, I can’t have surgery yet. I had my first taxol/carboplatin treatment last week. I had an allergic reaction
Buster98
in
My Ovacome
5 months ago
EXCESSIVE WATERING EYES
I have had normal tension glaucoma for about 12 years, I’ve had a variety of eye drops for 10 years and a Deep Scleretomy operation on my right eye 18 months ago which now needs a Bleb adjustment. For the last few years I have had a real problem with watering eyes which has gone worse in my right eye
I have had normal tension glaucoma for about 12 years, I’ve had a variety of eye drops for 10 years and a Deep Scleretomy operation on my right eye 18 months ago which now needs a Bleb adjustment. For the last few years I have had a real problem with watering eyes which has gone worse in my right eye
Ella59
in
Glaucoma UK
4 months ago
IOP question
Last month,after a allergic conjuctivitis treatment which includes steroids drop,I measured my intraocular pressure,it's 16 in both eyes.Today,I measured it again and it's 18mmHg.My eye pressure was measured at 10am, why is there a difference?
Last month,after a allergic conjuctivitis treatment which includes steroids drop,I measured my intraocular pressure,it's 16 in both eyes.Today,I measured it again and it's 18mmHg.My eye pressure was measured at 10am, why is there a difference?
Our-poor-guys
in
Glaucoma UK
4 months ago
Lupus Diagnosis
I haven't been online for some times, perhaps years. I don't think I have posted since losing my Mum in August 2021 and then I lost my Dad last year June. My health, not surprisingly, has been all over the place and under the following hospital departments: Lupus Rheumatology, General Rheumatology -
I haven't been online for some times, perhaps years. I don't think I have posted since losing my Mum in August 2021 and then I lost my Dad last year June. My health, not surprisingly, has been all over the place and under the following hospital departments: Lupus Rheumatology, General Rheumatology -
KeepingUpBeat
in
LUPUS UK
5 months ago
NHS London statement on Synnovis ransomware cyber attack
I am posting this using the NHS' own website version - it is covered across news sites as well. It seems it is having a major impact on blood tests - which might immediately affect some members. As well as the rest of the impact. [i]
NHS London statement on Synnovis ransomware cyber attack
[
I am posting this using the NHS' own website version - it is covered across news sites as well. It seems it is having a major impact on blood tests - which might immediately affect some members. As well as the rest of the impact. [i]
NHS London statement on Synnovis ransomware cyber attack
[
helvella
Thyroid UK
in
Thyroid UK
1 month ago
Any readers?
Would really appreciate recommendation for books linking autoimmune disease and trauma. Somebody I care about wants to read about it. Thank you. 😊
Would really appreciate recommendation for books linking autoimmune disease and trauma. Somebody I care about wants to read about it. Thank you. 😊
Pawsedagain
in
Thyroid UK
5 months ago
foslevadopa/foscarbidopa by sibcontaneous infusion
Living in the uk and having had Parkinson's for 24 years l was excited to hear about the new treatment foslevadopa/foscarbidopa for subcontaneous infusion which has been approved by the nhs fo use in advsnced psrkinsons for 900 patients.could anyone explain why this would be better than existing treatment
Living in the uk and having had Parkinson's for 24 years l was excited to hear about the new treatment foslevadopa/foscarbidopa for subcontaneous infusion which has been approved by the nhs fo use in advsnced psrkinsons for 900 patients.could anyone explain why this would be better than existing treatment
Rosieskeeper
in
Cure Parkinson's
4 months ago
Sudden Tinnitus
hi, joined this in hopes I’ve getting some help or suggestions I’m an avid concert goer, I absolutely love it and it brings me a lot of joy. I always wear foam ear plugs during them However, last September I developed a weird beeping in my left ear. Went to doctors, had hearing tests, done an MRI,
hi, joined this in hopes I’ve getting some help or suggestions I’m an avid concert goer, I absolutely love it and it brings me a lot of joy. I always wear foam ear plugs during them However, last September I developed a weird beeping in my left ear. Went to doctors, had hearing tests, done an MRI,
Concertluver
in
Tinnitus UK
4 months ago
Looking for advice to deal with pain and stiffness related to AIH.
I was recently signposted as this may be my diagnosis by a GP and I'm awaiting a consultant appointment with Rheumatology as appose to a liver specialist despite me questioning this. I have no inflammation markers on my bloods but I do on my antibodies and smooth muscle blood counts which his why it's
I was recently signposted as this may be my diagnosis by a GP and I'm awaiting a consultant appointment with Rheumatology as appose to a liver specialist despite me questioning this. I have no inflammation markers on my bloods but I do on my antibodies and smooth muscle blood counts which his why it's
PeterStewart
in
British Liver Trust
1 month ago
Taking K2 MK7
I’ve heard that taking K2 MK7 is good for your bones, but am not sure if it’s safe to take with Xarelto. Apparently it cannot be taken if prescribed to Warfarin but it’s unclear as to whether or not it’s safe with other anticoagulants. Can anyone clarify this for me?
I’ve heard that taking K2 MK7 is good for your bones, but am not sure if it’s safe to take with Xarelto. Apparently it cannot be taken if prescribed to Warfarin but it’s unclear as to whether or not it’s safe with other anticoagulants. Can anyone clarify this for me?
SnoopyJ
in
Atrial Fibrillation Support
4 months ago
How accurate is a visual field test?
Hello I am new to this site but have been a member of Health Unlocked for some time. I have had glaucoma in both eyes for approximately 11 years and was well controlled until about 3.5 years ago when I developed uveitis in my left eye (my worse eye for glaucoma). It was treated as an acute emergency
Hello I am new to this site but have been a member of Health Unlocked for some time. I have had glaucoma in both eyes for approximately 11 years and was well controlled until about 3.5 years ago when I developed uveitis in my left eye (my worse eye for glaucoma). It was treated as an acute emergency
Mitziecat
in
Glaucoma UK
4 months ago
Obesity Associated With Faster MS Disease Progression
[i]
Obesity in multiple sclerosis (MS) was tied to faster worsening of disability and an increased risk of physical, psychological, and cognitive decline, a prospective cohort study showed.
[/i] [i]
[/i]
https://www.medpagetoday.com/meetingcoverage/actrims/108992?xid=nl_mpt_DHE_2024-03
[i]
Obesity in multiple sclerosis (MS) was tied to faster worsening of disability and an increased risk of physical, psychological, and cognitive decline, a prospective cohort study showed.
[/i] [i]
[/i]
https://www.medpagetoday.com/meetingcoverage/actrims/108992?xid=nl_mpt_DHE_2024-03
BettysMom
in
My MSAA Community
5 months ago
Please check!
Earlier today I posted the link to the PBC Foundaton's Urso calculator. There are so many posts and questions relating to Urso that I thought it was important for everyone to make sure they are on the right dose. This 'calculator' is also available on the PBC app. Knowing you are taking the right dose
Earlier today I posted the link to the PBC Foundaton's Urso calculator. There are so many posts and questions relating to Urso that I thought it was important for everyone to make sure they are on the right dose. This 'calculator' is also available on the PBC app. Knowing you are taking the right dose
DonnaBoll
Administrator
in
PBC Foundation
5 months ago
NKF launches educational video series for lupus, lupus nephritis
“[Lupus]
and
[lupus nephritis] are complicated autoimmune
diseases
that require many tests and kidney evaluations because a combination of steroids and antimalarial therapies may be prescribed due to the body’s immune system actually attacking the body,” Joseph Vassalotti, MD, chief medical officer for
“[Lupus]
and
[lupus nephritis] are complicated autoimmune
diseases
that require many tests and kidney evaluations because a combination of steroids and antimalarial therapies may be prescribed due to the body’s immune system actually attacking the body,” Joseph Vassalotti, MD, chief medical officer for
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
7 months ago
Stomach symptoms with your IBS?
Do you have symptoms in your stomach? Besides perhaps the intestinal symptoms (constipation, diarrhea, gas)...do you also have symptoms in your stomach/upper abdomen? I have like a gnawing sensation almost feels like you are hungry but you aren't.... Does anyone experience this or any other upper
Do you have symptoms in your stomach? Besides perhaps the intestinal symptoms (constipation, diarrhea, gas)...do you also have symptoms in your stomach/upper abdomen? I have like a gnawing sensation almost feels like you are hungry but you aren't.... Does anyone experience this or any other upper
Catsandsunsets
in
IBS Network
9 months ago
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