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Bronchiectasis.. just had an ear operation.. finding pressure of using aerobika and chest clearance difficult .. any advice ??
Any advice for chest clearance after a lengthy operation out there please . Am home but Ear still bleeding a little I’ve not missed a days chest clearance in nearly 3 years and finding it difficult / worrying to put pressure into my aerobika & doing autogenic drainage for fear it may cause my ear
Any advice for chest clearance after a lengthy operation out there please . Am home but Ear still bleeding a little I’ve not missed a days chest clearance in nearly 3 years and finding it difficult / worrying to put pressure into my aerobika & doing autogenic drainage for fear it may cause my ear
Phill1
in
Lung Conditions Community Forum
8 months ago
Starbursts from new glasses driving me insane. Can anyone help?
Hi, I recently got 2 new pairs of glasses, one with Transitions lenses and one 'plain'. There's been a lot of faff with the Transitions because I didn't like the frames, but right at the outset I noticed I was suddenly getting these epic starbursts on lights (with both pairs), particularly in the distance
Hi, I recently got 2 new pairs of glasses, one with Transitions lenses and one 'plain'. There's been a lot of faff with the Transitions because I didn't like the frames, but right at the outset I noticed I was suddenly getting these epic starbursts on lights (with both pairs), particularly in the distance
Chancery
in
Anxiety Support
8 months ago
Starburst problem with new specs
Hi, I don't have glaucoma, but I'm hoping someone might be able to help me here as I have been Googling my issue all night. So, sorry if this is completely off-topic for you guys! I recently got 2 new pairs of glasses, one with Transitions lenses and one 'plain'. There's been a lot of faff with the
Hi, I don't have glaucoma, but I'm hoping someone might be able to help me here as I have been Googling my issue all night. So, sorry if this is completely off-topic for you guys! I recently got 2 new pairs of glasses, one with Transitions lenses and one 'plain'. There's been a lot of faff with the
Chancery
in
Glaucoma UK
8 months ago
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update: Zanabrutinib vs Obenven (O&V)
We are praying for Gods wisdom (James1:5), and we’re leaning toward the Zanabrutinib. The infusions and time and distance will be impactful to my husbands work and he’s prefer to go the simpler route. We learned he’s still 13Q and TP53 negative and his lymph nodes are reduced (we have used ALT for
We are praying for Gods wisdom (James1:5), and we’re leaning toward the Zanabrutinib. The infusions and time and distance will be impactful to my husbands work and he’s prefer to go the simpler route. We learned he’s still 13Q and TP53 negative and his lymph nodes are reduced (we have used ALT for
Cb1391
in
CLL Support
8 months ago
Surgery and immuno suppressants
Hi everyone. I am due to have minor surgery on my wrist and have been asked by my surgeon to cease taking mycophenolate for a week before and a week after my operation (I presumed because of possible risk of infection?). I spoke to my rheumatologist about this and she considered it unnecessary to stop
Hi everyone. I am due to have minor surgery on my wrist and have been asked by my surgeon to cease taking mycophenolate for a week before and a week after my operation (I presumed because of possible risk of infection?). I spoke to my rheumatologist about this and she considered it unnecessary to stop
cheeselover342
in
Scleroderma & Raynaud's UK (SRUK)
8 months ago
Cimetidine
Hi, my doctor prescribed Cimetidine for my painful bladder, I have the impression that it exacerbates restless leg syndrome. I'd like to know your opinion before taking this medication. Thanks in advance.
Hi, my doctor prescribed Cimetidine for my painful bladder, I have the impression that it exacerbates restless leg syndrome. I'd like to know your opinion before taking this medication. Thanks in advance.
halperinchen
in
Restless Legs Syndrome
8 months ago
Using ChatGPT to help us understand tinnitus. Thoughts? Here's an AI Assistant I've created for understanding Tinnitus
Just a topic for debate but I'm interested in your thoughts and maybe your direct experiences with AI to understand tinnitus. I'm assuming everyone has heard about AI and ChatGPT and other Generative AI tools. GPT is short for Generative Predictive Text. It is what it states (a convincing) prediction
Just a topic for debate but I'm interested in your thoughts and maybe your direct experiences with AI to understand tinnitus. I'm assuming everyone has heard about AI and ChatGPT and other Generative AI tools. GPT is short for Generative Predictive Text. It is what it states (a convincing) prediction
daverussell
in
Tinnitus UK
8 months ago
Lipoid pneumonia
Earlier this year I had serious nose bleeds resulting in hospital admissions and cautery. Subsequently seen by ENT consultant who advised daily insertion of Vaseline into nostrils to prevent them drying out and possible further bleeds. Since then I found on the internet (various reputable sites)
Earlier this year I had serious nose bleeds resulting in hospital admissions and cautery. Subsequently seen by ENT consultant who advised daily insertion of Vaseline into nostrils to prevent them drying out and possible further bleeds. Since then I found on the internet (various reputable sites)
FormerT
in
Lung Conditions Community Forum
8 months ago
My journey
I wanted to share some things that have helped me over the years since my weight loss surgery in 2017. When I started this journey I had ballooned to 312 pounds on my 5'7" Frame. I was, and still am, an emotional eater...struggle with it every day.....what I've found that has helped me the most is
I wanted to share some things that have helped me over the years since my weight loss surgery in 2017. When I started this journey I had ballooned to 312 pounds on my 5'7" Frame. I was, and still am, an emotional eater...struggle with it every day.....what I've found that has helped me the most is
mizzou7016
Visitor
in
Weight Loss Support
8 months ago
oh dear oh dear
Okay so everyone, After getting so much help from here from you lovely people I have been on a good 3 to 4 week routine of upping my vitamins and supplements. It took me a good amount of time and advise off here to make sure of what vitamins to get and take etc etc. So I was happy and hopeful. Believe
Okay so everyone, After getting so much help from here from you lovely people I have been on a good 3 to 4 week routine of upping my vitamins and supplements. It took me a good amount of time and advise off here to make sure of what vitamins to get and take etc etc. So I was happy and hopeful. Believe
Demitria
in
Thyroid UK
8 months ago
Drugs.com FDA Investigating Serious Risk of T-cell Malignancy Following BCMA-Directed (CAR) T cell Immunotherapies
https://newsletters.drugs.com/l/HXdBAPWpNu8924jmwPHb3VvA/LQCEtlvhvlnyLNQoIP4Gfw/jLVV3dtGc2BI8hLRqrMq892g [i]"Although the overall benefits of these products continue to outweigh their potential risks for their approved uses, FDA is investigating the identified risk of T cell malignancy with serious
https://newsletters.drugs.com/l/HXdBAPWpNu8924jmwPHb3VvA/LQCEtlvhvlnyLNQoIP4Gfw/jLVV3dtGc2BI8hLRqrMq892g [i]"Although the overall benefits of these products continue to outweigh their potential risks for their approved uses, FDA is investigating the identified risk of T cell malignancy with serious
JerrysGirl3
in
CLL Support
8 months ago
Aortitis
I was diagnosed with non cranial Giant Cell Arteritis in September last year. So far I haven't managed to find anyone else with this condition because most people have the temporal version with the headaches.Mine is Aortitis which apparently is rare. I'd love to share experiences with someone else
I was diagnosed with non cranial Giant Cell Arteritis in September last year. So far I haven't managed to find anyone else with this condition because most people have the temporal version with the headaches.Mine is Aortitis which apparently is rare. I'd love to share experiences with someone else
Dance62
in
PMRGCAuk
5 months ago
Webinar: What causes photopsia and photophobia in patients with Stargardt and what impact does it have on their lives?
Flashing lights in vision (photopsia) or discomfort due to bright light or glare (photophobia) is often experienced by patients with Stargardt. However, little is understood about what causes these symptoms, their prevalence or the impact they can have on people’s lives. Omar Mahroo, consultant ophthalmologist
Flashing lights in vision (photopsia) or discomfort due to bright light or glare (photophobia) is often experienced by patients with Stargardt. However, little is understood about what causes these symptoms, their prevalence or the impact they can have on people’s lives. Omar Mahroo, consultant ophthalmologist
Carol_MacularSociety
Partner
in
Macular Society
8 months ago
Genetic therapy: for solid malignancy hopefully soon
ok, I post them also because they are fellow Italians! But the platform is very promising even if clinical use has been approved only for glioma and glioblastoma at the moment. But there are clinical trials going on for solid tumors, prostate included. https://www.genenta.com/wp-content/uploads/2021
ok, I post them also because they are fellow Italians! But the platform is very promising even if clinical use has been approved only for glioma and glioblastoma at the moment. But there are clinical trials going on for solid tumors, prostate included. https://www.genenta.com/wp-content/uploads/2021
Maxone73
in
Advanced Prostate Cancer
8 months ago
4 months post TT
hi everyone! I am writing because I wanted to see if anybody had similar experiences. I am four months post total thyroidectomy, and in the first month or so I didn’t really feel many or any symptoms. Now in the past two months, I feel like I am feeling more symptoms of hypothyroidism than I did, in
hi everyone! I am writing because I wanted to see if anybody had similar experiences. I am four months post total thyroidectomy, and in the first month or so I didn’t really feel many or any symptoms. Now in the past two months, I feel like I am feeling more symptoms of hypothyroidism than I did, in
Rfranzoni
in
Thyroid UK
8 months ago
Ruminating.
Age piles the years on one by one Yet we try to do as we've always done The body gets weak but the mind stays strong Maybe that's where we all went wrong We should perhaps throw caution out And rid ourselves of those fears and doubt Unshield ourselves and put it about Get really drunk and rage
Age piles the years on one by one Yet we try to do as we've always done The body gets weak but the mind stays strong Maybe that's where we all went wrong We should perhaps throw caution out And rid ourselves of those fears and doubt Unshield ourselves and put it about Get really drunk and rage
Donald_1931
in
Lung Conditions Community Forum
8 months ago
had uraine sample no infection had my bladder checked with gyno no prolase, just weak mussles ,
hi , in september 2022 i had a prolase bladder op felt fine after 6 to 8 weeks . then in september this year i had my gallbladder removed and i felt fine only noticed that i felt like a feeling of urgent to go toilet and bladder felt full all of a sudden . so i went doctors ask to do a water sample
hi , in september 2022 i had a prolase bladder op felt fine after 6 to 8 weeks . then in september this year i had my gallbladder removed and i felt fine only noticed that i felt like a feeling of urgent to go toilet and bladder felt full all of a sudden . so i went doctors ask to do a water sample
Mrshappyme
in
Pelvic Pain Support Network
8 months ago
Diagnostic Imaging Not Yet Enough for Biopsy-Free Radical Prostatectomy - MedPage Today, November 27, 2023
Biopsy-free PCa diagnostics would be welcomed by anyone who has had one or more needle biopsies. This article in MedPage Today summarizes the current status for the several methodologies being studied as alternatives. Good info for those currently on AS or just watching a rising PSA. From the lead-in
Biopsy-free PCa diagnostics would be welcomed by anyone who has had one or more needle biopsies. This article in MedPage Today summarizes the current status for the several methodologies being studied as alternatives. Good info for those currently on AS or just watching a rising PSA. From the lead-in
cujoe
in
Fight Prostate Cancer
8 months ago
PMR and brachial neuritis
It looks like I have developed a fairly rare condition called Parsonage-Turner syndrome (PTS), also called brachial neuritis. It started with terrible pain in the shoulder, so initially I thought it would appear in the other shoulder and be the beginning of a PMR relapse. But it is taking a different
It looks like I have developed a fairly rare condition called Parsonage-Turner syndrome (PTS), also called brachial neuritis. It started with terrible pain in the shoulder, so initially I thought it would appear in the other shoulder and be the beginning of a PMR relapse. But it is taking a different
dmart7
in
PMRGCAuk
5 months ago
Question to the collective
As mentioned previously, I was diagnosed (Prof H/Sheffield) as having the SCA7 version of Ataxia in 2014. I was put on a tablet,( DANTROLENE) that has been gradually increased from 1 X 25mg capsule to the current 3 X 25mg Just had a phone call about some physio I saw last year, and it was then kind
As mentioned previously, I was diagnosed (Prof H/Sheffield) as having the SCA7 version of Ataxia in 2014. I was put on a tablet,( DANTROLENE) that has been gradually increased from 1 X 25mg capsule to the current 3 X 25mg Just had a phone call about some physio I saw last year, and it was then kind
Butcherpete
in
Ataxia UK
5 months ago
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