Search
Search
About
Log in
Join
Experiences with
Conditions and diseases
Posts
Communities
94,949 public posts
Filter results
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
Bowel Disease Support
8 months ago
MRI results…how long to wait?
Hi guys, hope you’re all okay. So I had my pelvic MRI scan on Monday, it was awful as I was in the scanner for an hour and 10mins 😥. I stayed strong and got through it though as I know it was important. Just wondered how long you’ve had to wait for results (with nhs). My letter said up to six weeks.
Hi guys, hope you’re all okay. So I had my pelvic MRI scan on Monday, it was awful as I was in the scanner for an hour and 10mins 😥. I stayed strong and got through it though as I know it was important. Just wondered how long you’ve had to wait for results (with nhs). My letter said up to six weeks.
endowarrior12
in
Endometriosis UK
3 months 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
4 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Drops affecting eyelashes
I'm 41, had a combined trab & lens replacement in right eye 2 years ago and just lens replacement in left eye a few months later. Now the only drops I take are Dorzolamide timolol in the left eye, twice a day.I switched to the preservative free drops a few months ago but I think it's negatively affecting
I'm 41, had a combined trab & lens replacement in right eye 2 years ago and just lens replacement in left eye a few months later. Now the only drops I take are Dorzolamide timolol in the left eye, twice a day.I switched to the preservative free drops a few months ago but I think it's negatively affecting
LyndseyMoo
in
Glaucoma UK
3 months ago
Apixaban rash
Diagnosed with DVT 4 weeks ago and prescribed Apixaban for life. This is my 3rd DVT. No problems for weeks and then a rash, very itchy, has developed on upper chest and top of arms. Occasional clusters elsewhere too. Just looking for general comments please before seeking potential switch to warfarin
Diagnosed with DVT 4 weeks ago and prescribed Apixaban for life. This is my 3rd DVT. No problems for weeks and then a rash, very itchy, has developed on upper chest and top of arms. Occasional clusters elsewhere too. Just looking for general comments please before seeking potential switch to warfarin
Falcon9
in
Atrial Fibrillation Support
3 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
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
3 months ago
New Sufferer advice
Hi Everybody My name is Daniel I have had to call out for some help or advice from this community please. I had never thought something like this would start to completely alter my life. I woke up one morning.... and had this "yinggggggg" sound in my left ear... it was annoying but i just thought
Hi Everybody My name is Daniel I have had to call out for some help or advice from this community please. I had never thought something like this would start to completely alter my life. I woke up one morning.... and had this "yinggggggg" sound in my left ear... it was annoying but i just thought
dannyboy1973
in
Tinnitus UK
3 months ago
Insomnia and Felodipine ?
Hi everyoneI have been on Felodipine for several weeks now after trying many other drugs for BP. While I feel a lot better on these drugs my existing insomnia is now off the scale!. I am now averaging 3 or 4 hours a night and over the counter sleeping pills aren't helping much. My GP says she has ran
Hi everyoneI have been on Felodipine for several weeks now after trying many other drugs for BP. While I feel a lot better on these drugs my existing insomnia is now off the scale!. I am now averaging 3 or 4 hours a night and over the counter sleeping pills aren't helping much. My GP says she has ran
BobbyCollins
in
High Blood Pressure Support
3 months ago
EMBARK Study: Enzalutamide +/- ADT
Results of the EMBARK study was published this week (10/19/23) in NEJM. It compared high risk BCR PCa treated in 3 groups: Lupron ADT alone. Enzalutamide plus ADT. And Enzalutamide monotherapy. 5 year follow up for metastasis free survival. Results below. Interesting that Enza monotherapy (No ADT) was
Results of the EMBARK study was published this week (10/19/23) in NEJM. It compared high risk BCR PCa treated in 3 groups: Lupron ADT alone. Enzalutamide plus ADT. And Enzalutamide monotherapy. 5 year follow up for metastasis free survival. Results below. Interesting that Enza monotherapy (No ADT) was
MateoBeach
in
Fight Prostate Cancer
8 months ago
Weaning off Omeprazole
Does anyone have a treatment plan for a successful weaning off Omeprazole please? I want to start this process but am a bit scared as I stopped cold turkey previously and had horrendous issues. I understand that the drug makes the acid producing valve loose which further contributes to the issue causing
Does anyone have a treatment plan for a successful weaning off Omeprazole please? I want to start this process but am a bit scared as I stopped cold turkey previously and had horrendous issues. I understand that the drug makes the acid producing valve loose which further contributes to the issue causing
Pink_peach
in
IBS Network
3 months ago
Celiac testing and Obinutuzumab
So I am getting tested for celiac disease. I've known I had issues with gluten for years, and my grandma had it, but it never got that bad. Now I've had diarrhea for months and am losing weight - so it seems sensible to get it checked out. But I'm on V & O, completed the O infusions in July (about
So I am getting tested for celiac disease. I've known I had issues with gluten for years, and my grandma had it, but it never got that bad. Now I've had diarrhea for months and am losing weight - so it seems sensible to get it checked out. But I'm on V & O, completed the O infusions in July (about
Greenbunnies
in
CLL Support
8 months ago
Rhupus
I have rhupus which is lupus and severe rheumatoid. arthritis having both and it being aggressive there r only 1% to 2% in the world that ever have both I guess I was just the lucky one lol unfortunately this is the most painful disease in the world you get never get over less your bones hurt so bad
I have rhupus which is lupus and severe rheumatoid. arthritis having both and it being aggressive there r only 1% to 2% in the world that ever have both I guess I was just the lucky one lol unfortunately this is the most painful disease in the world you get never get over less your bones hurt so bad
Buglove22
in
LUpus Patients Understanding and Support
4 months ago
Is Cold Water Therapy (cold plunge) for metastasis to bones or lymph nodes beneficial or harmful?? Slow progression?
Any insight would be greatly appreciated. TA??
Any insight would be greatly appreciated. TA??
Longterm101
in
Advanced Prostate Cancer
5 months ago
Lupus diagnosis after taking hydroxychloriquine for 14 months
Hi guys, hope everyone is well. Since getting diagnosed with lupus last month one thing has been really bothering me... As bit of a back story I was diagnosed with RA a few years ago. Over the last 6-8 months I've been amassing a bunch of other symptoms which last month resulted in my RA diagnosed
Hi guys, hope everyone is well. Since getting diagnosed with lupus last month one thing has been really bothering me... As bit of a back story I was diagnosed with RA a few years ago. Over the last 6-8 months I've been amassing a bunch of other symptoms which last month resulted in my RA diagnosed
Diagnosis_Collector
in
LUPUS UK
4 months ago
Blood Test for MS Activity Gets FDA Breakthrough Designation
The US Food and Drug Administration (FDA) has granted breakthrough device designation to the Elecsys Neurofilament Light Chain (NfL) test for multiple sclerosis (MS). November, 2023
Made by Roche, the test is intended to be used as an aid in detection of disease activity in adults aged 18
The US Food and Drug Administration (FDA) has granted breakthrough device designation to the Elecsys Neurofilament Light Chain (NfL) test for multiple sclerosis (MS). November, 2023
Made by Roche, the test is intended to be used as an aid in detection of disease activity in adults aged 18
BettysMom
in
My MSAA Community
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
3 months ago
REMINDER! Harrogate Lupus Group - Coffee and Chat meeting - 2nd March 10.30am
REMINDER! Saturday 2nd March, the Harrogate Lupus Group will be meeting at 10.30am, at the Woodlands Methodist Church Hall, 71 Wetherby Road, Harrogate, HG2 7SG. We will be joined by Frances Pearson, who will be talking about her ideas on the Lupus Observatory. Everyone is welcome to join! If you
REMINDER! Saturday 2nd March, the Harrogate Lupus Group will be meeting at 10.30am, at the Woodlands Methodist Church Hall, 71 Wetherby Road, Harrogate, HG2 7SG. We will be joined by Frances Pearson, who will be talking about her ideas on the Lupus Observatory. Everyone is welcome to join! If you
michaellasmith
Administrator
in
LUPUS UK
4 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
3 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
3 months ago
1
...
53
54
55
...
100
Next page
10
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Thyroid UK
9675 results
Advanced Prostate Cancer
7870 results
Atrial Fibrillation Support
5392 results
View top 10 communities
Sort by
Most Relevant
Newest