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Please join us tomorrow, April 18th, for our first back to in person and also online Living Room
Hello, We're thrilled to be back in-person! If you live and/or are in the area, please join us for our first back to in person Living Room since our three year all virtual program from COVID-19. Please join us in our San Carlos office tomorrow. You can also always watch virtually on GO2's YouTube Live
Hello, We're thrilled to be back in-person! If you live and/or are in the area, please join us for our first back to in person Living Room since our three year all virtual program from COVID-19. Please join us in our San Carlos office tomorrow. You can also always watch virtually on GO2's YouTube Live
Michelezeh
in
Small Cell Lung Cancer Support
1 year ago
Please join us tomorrow, April 18th, for our first back to in person and also online Living Room
Hello, We're thrilled to be back in-person! If you live and/or are in the area, please join us for our first back to in person Living Room since our three year all virtual program from COVID-19. Please join us in our San Carlos office tomorrow. You can also always watch virtually on GO2's YouTube Live
Hello, We're thrilled to be back in-person! If you live and/or are in the area, please join us for our first back to in person Living Room since our three year all virtual program from COVID-19. Please join us in our San Carlos office tomorrow. You can also always watch virtually on GO2's YouTube Live
Michelezeh
Partner
in
Lung Cancer Support
1 year ago
T3 levels and oral thyroid hormones
This fairly recent review links up FT3 levels in the body with brain and pituitary gland activity. It shows that in T4-treated patients there may be insufficient T3 to prevent brain fog as well as other shortcomings. It also shows that tissue and circulating FT3 levels are closely linked so that blood
This fairly recent review links up FT3 levels in the body with brain and pituitary gland activity. It shows that in T4-treated patients there may be insufficient T3 to prevent brain fog as well as other shortcomings. It also shows that tissue and circulating FT3 levels are closely linked so that blood
diogenes
in
Thyroid UK
1 year ago
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hayfever medicstion
Hi there I need advice on hayfever med as I have open angle glaucoma . I’m allergic to blossom trees anc this usually starts end of feb I use to use Beconase but this is a steroid so a def no. I tried natural allergy inhalers last year but they don’t work. I need to take an oral med . Anybody who uses
Hi there I need advice on hayfever med as I have open angle glaucoma . I’m allergic to blossom trees anc this usually starts end of feb I use to use Beconase but this is a steroid so a def no. I tried natural allergy inhalers last year but they don’t work. I need to take an oral med . Anybody who uses
Salford49
in
Glaucoma UK
1 year ago
Bowel irrigation (Not "colonic irrigation")
I have obstructed defecation (anismus) which has not responded to biofeedback etc. The next step is at home bowel irrigation and I am just waiting for an appointment with the bowel nurse to issue me with the equipment. It would be helpful to hear of anyone`s experience with this. I don`t know which
I have obstructed defecation (anismus) which has not responded to biofeedback etc. The next step is at home bowel irrigation and I am just waiting for an appointment with the bowel nurse to issue me with the equipment. It would be helpful to hear of anyone`s experience with this. I don`t know which
janke
in
IBS Network
1 year ago
Notes on Updates and latest research from the ASH annual meeting.
MAZCD posted a good broadcast on "updates and latest research from the ASH annual meeting." I took some notes and figured it's worth a fresh post. https://healthunlocked.com/mpnvoice/posts/149382010/video-of-the-mpn-voice-patients%E2%80%99-webinar-london-30-mar-23-%E2%80%93-updates-and-latest-research-from-the-ash-annual-meeting
MAZCD posted a good broadcast on "updates and latest research from the ASH annual meeting." I took some notes and figured it's worth a fresh post. https://healthunlocked.com/mpnvoice/posts/149382010/video-of-the-mpn-voice-patients%E2%80%99-webinar-london-30-mar-23-%E2%80%93-updates-and-latest-research-from-the-ash-annual-meeting
EPguy
in
MPN Voice
1 year ago
Does Buspirone take time to work
I moved the actual question to the front. Lol. Too much rant. My question is: If any of you take buspirone, what were You told, please, as far as how it works? This is kind of a "poll" for my arsenal, not something I intend to use as medical advice. ***Were you told it takes awhile to work, and
I moved the actual question to the front. Lol. Too much rant. My question is: If any of you take buspirone, what were You told, please, as far as how it works? This is kind of a "poll" for my arsenal, not something I intend to use as medical advice. ***Were you told it takes awhile to work, and
Hidden
in
Anxiety and Depression Support
1 year ago
Possible Uveitis
Hello all - I'd welcome your input regarding possible Uveitis. As you'll see from my profile, I have a diagnosis of lupus. My main problems are fatigue and brain fog, joint pain, generalised aches and pains, raynauds, mouth ulcers, and recurring anaemia. I have always had dry eyes. About a week ago
Hello all - I'd welcome your input regarding possible Uveitis. As you'll see from my profile, I have a diagnosis of lupus. My main problems are fatigue and brain fog, joint pain, generalised aches and pains, raynauds, mouth ulcers, and recurring anaemia. I have always had dry eyes. About a week ago
Ophelia1
in
LUPUS UK
1 year ago
EMDR therapy for depression?
https://my.clevelandclinic.org/health/treatments/22641-emdr-therapy Anyone experienced EMDR therapy? Would you give it a try? Thoughts?
https://my.clevelandclinic.org/health/treatments/22641-emdr-therapy Anyone experienced EMDR therapy? Would you give it a try? Thoughts?
Renizzle2023
in
Anxiety and Depression Support
11 months ago
Visual field deterioration 6 weeks after cataract and Hydrus stent surgery?
I think that the sight loss area below my right eye has got worse between 31 Dec and now , 15 Jan. Had surgery 1 Dec. Has anyone else experienced this? Background : I was diagnosed with normal tension open angle glaucoma in July this year. My visual fields got worse between August and November, and
I think that the sight loss area below my right eye has got worse between 31 Dec and now , 15 Jan. Had surgery 1 Dec. Has anyone else experienced this? Background : I was diagnosed with normal tension open angle glaucoma in July this year. My visual fields got worse between August and November, and
Iona57
in
Glaucoma UK
1 year ago
New study just out (3/31/23) on natural therapies for tau aggregation (PSP included)
My father was recently diagnosed with PSP and I have been researching like crazy. I searched all 125 clinical trials on the Government website and all the pubmed articles and studies. This one just came out 3/31/23! It looked at all the studies that have been done on natural supplements, foods, therapies
My father was recently diagnosed with PSP and I have been researching like crazy. I searched all 125 clinical trials on the Government website and all the pubmed articles and studies. This one just came out 3/31/23! It looked at all the studies that have been done on natural supplements, foods, therapies
ShellTaylor
in
PSP Association
1 year ago
It's too much. All the medical procedures. Homesick. Getting into hospital on Monday
For my nose not mental health. But it's one hell of a time booking it all, going through all kinds of proffesionals. In Bulgaria something hurts you, you go to doc 1 , they send you to doc 2, they send you to doc 3, they send you to tests. You end up either okay or hospitalised or worse from all those
For my nose not mental health. But it's one hell of a time booking it all, going through all kinds of proffesionals. In Bulgaria something hurts you, you go to doc 1 , they send you to doc 2, they send you to doc 3, they send you to tests. You end up either okay or hospitalised or worse from all those
Against_the_current
in
Anxiety and Depression Support
11 months ago
Next treatment options available for advancing disease
I have completed all scans available to me and they show new metastatic disease throughout my skeleton. PSA @ 4.65 ug/L. The disease continues to advance while being treated with Zoladex and abiraterone. I have switched prednisone for dexamethasone and haven't had an updated blood test yet to see if
I have completed all scans available to me and they show new metastatic disease throughout my skeleton. PSA @ 4.65 ug/L. The disease continues to advance while being treated with Zoladex and abiraterone. I have switched prednisone for dexamethasone and haven't had an updated blood test yet to see if
Islandboy2021
in
Advanced Prostate Cancer
1 year ago
My Current Stack (What is in Yours?)
Fabnusasked me what my current stack was so I am sharing it here. Please remember I have not been diagnosed with PD. I have RBD and some other symptoms.
Also remember I have a HS degree, poor impulse control, and I am prone to bad decisions. Please do your own research.
The best place
Fabnusasked me what my current stack was so I am sharing it here. Please remember I have not been diagnosed with PD. I have RBD and some other symptoms.
Also remember I have a HS degree, poor impulse control, and I am prone to bad decisions. Please do your own research.
The best place
Bolt_Upright
in
Cure Parkinson's
1 year ago
Twitching running eye...
I have Hashimotos and wondered if any of you lovely people with this also have this happen to you.My left eyelid is kind of flickering and has been on and off for the last 4 weeks, it's not noticable if I look at it in the mirror but when I try sleep I can definitely feel it. Yesterday it was watering
I have Hashimotos and wondered if any of you lovely people with this also have this happen to you.My left eyelid is kind of flickering and has been on and off for the last 4 weeks, it's not noticable if I look at it in the mirror but when I try sleep I can definitely feel it. Yesterday it was watering
Diamond61
in
Thyroid UK
1 year ago
Spotlight on CLL - Nicole Lamanna, MD Wednesday May 24, 2023 1:00 PM to 2:30 PM EDT- sponsored by LLS- USA but open to all
Unlike other webinars I have posted recently, this should be easy to understand, especially for newly diagnosed and those not familiar with Med-Speak. Dr. Lamanna has a track record of explaining CLL and side effects, with a simple, caring & warm style. - Len - Nicole Lamanna, MD Director, Chronic
Unlike other webinars I have posted recently, this should be easy to understand, especially for newly diagnosed and those not familiar with Med-Speak. Dr. Lamanna has a track record of explaining CLL and side effects, with a simple, caring & warm style. - Len - Nicole Lamanna, MD Director, Chronic
lankisterguy
Volunteer
in
CLL Support
1 year ago
Prednislone and Anxiety
I've been reducing from 20mg pred since November 2022, currently on 11mg. Since Christmas I have had episodes of extreme anxiety, depression, mood swings and tearfulness. My Rheumy this morning suggested swapping to Betamethasone which does not cross the blood/brain barrier. However, when I researched
I've been reducing from 20mg pred since November 2022, currently on 11mg. Since Christmas I have had episodes of extreme anxiety, depression, mood swings and tearfulness. My Rheumy this morning suggested swapping to Betamethasone which does not cross the blood/brain barrier. However, when I researched
FleetRose
in
PMRGCAuk
1 year ago
ER+ PR+ HER2-
Hi, I am 5 1/2 years in remission for twice recurrent endometrial cancer. Currently, I am taking Ibrance and anastrazole, a MBC regimen because my cancer is more like mbc. Most of the research is on breast cancer, and now ovarian cancer. The medications and protocols trickle down to endometrial/uterine
Hi, I am 5 1/2 years in remission for twice recurrent endometrial cancer. Currently, I am taking Ibrance and anastrazole, a MBC regimen because my cancer is more like mbc. Most of the research is on breast cancer, and now ovarian cancer. The medications and protocols trickle down to endometrial/uterine
Merma
in
SHARE Ovarian Cancer Support
1 year ago
Relapse with blurred vison
Hi all All was going pretty well, managed to taper from 80 mg to 6 mg after almost 2 years (in april) after initial blurred vision/AF. Have not had any serious side affects or major relapses, one incident with raised CRP/ESR while tapering at 40 but markers settled. Then out of the blue today had
Hi all All was going pretty well, managed to taper from 80 mg to 6 mg after almost 2 years (in april) after initial blurred vision/AF. Have not had any serious side affects or major relapses, one incident with raised CRP/ESR while tapering at 40 but markers settled. Then out of the blue today had
Gilmor
in
PMRGCAuk
1 year ago
Update
Hola Gents, I have not posted in a while. MO started me on Zytiga; I was off that after 2 weeks. Mid-January I got a UTI. Took a vacay to Aruba. The day I finished antibiotics for the UTI, I tested positive for Covid. Spent 5 days in my hotel room. Just glad I had an ocean view room and a balcony.
Hola Gents, I have not posted in a while. MO started me on Zytiga; I was off that after 2 weeks. Mid-January I got a UTI. Took a vacay to Aruba. The day I finished antibiotics for the UTI, I tested positive for Covid. Spent 5 days in my hotel room. Just glad I had an ocean view room and a balcony.
MJCA
in
Advanced Prostate Cancer
1 year ago
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