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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
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
1 year ago
question for those with sight loss…….
can I ask of those that have experienced sight loss, has this been since your GCA diagnosis (and possibly already getting treatment) or was it part of the problem(s) that made you seek help….if you get what I mean ? I have had a “lazy” eye since birth, with limited vision (can’t see in detail) the other
can I ask of those that have experienced sight loss, has this been since your GCA diagnosis (and possibly already getting treatment) or was it part of the problem(s) that made you seek help….if you get what I mean ? I have had a “lazy” eye since birth, with limited vision (can’t see in detail) the other
Cfmad298601
in
PMRGCAuk
1 year ago
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Monopost eye drops
Is anyone in the UK having trouble getting Monopost single use eye drops? Pharmacist just says to ask for a different drop…not as easy as that when you’ve tried most available and they don’t lower pressure! So frustrating…don’t know what to do now.
Is anyone in the UK having trouble getting Monopost single use eye drops? Pharmacist just says to ask for a different drop…not as easy as that when you’ve tried most available and they don’t lower pressure! So frustrating…don’t know what to do now.
Charliecat123
in
Glaucoma UK
1 year ago
Trab after failed shunt
Hello. This is my first post so please bear with me. About a year ago I had a shunt inserted which I thought would be an end to my problems. After a lot of delayed appointments my IOP has started to creep back up, and my doctor has suggested a trab. My next visit is in 6 months, which I think is
Hello. This is my first post so please bear with me. About a year ago I had a shunt inserted which I thought would be an end to my problems. After a lot of delayed appointments my IOP has started to creep back up, and my doctor has suggested a trab. My next visit is in 6 months, which I think is
PeteJones
in
Glaucoma UK
1 year ago
RLS - Suboxone - PLMD
I have had RLS for years. Last year I weaned off ropinirole. In doing so, the doctor prescribed opioids. When I started Suboxone, I developed PLMD. Has anyone had this happen with Suboxone? Did nothave PLM before.
I have had RLS for years. Last year I weaned off ropinirole. In doing so, the doctor prescribed opioids. When I started Suboxone, I developed PLMD. Has anyone had this happen with Suboxone? Did nothave PLM before.
DogBella
in
Restless Legs Syndrome
1 year ago
timing of your medication monitoring blood tests
good morning all and thank you all for your kind and caring responses to my previous question. My query today is: has anyone ever found that having a blood test close to methotrexate day (or within two weeks of having a wee Drinkie…) impacts the liver reading? I normally ensure this doesn’t happen
good morning all and thank you all for your kind and caring responses to my previous question. My query today is: has anyone ever found that having a blood test close to methotrexate day (or within two weeks of having a wee Drinkie…) impacts the liver reading? I normally ensure this doesn’t happen
Bon1
in
NRAS
1 year ago
Weaning off Ropinirole
I am currently in the process of Ropinirole withdrawal. I was on 3mg per day having started on .5mg. My legs had started to play up as early as 11am in the morning, and I guess I was augmenting. My GP has put on Gabapentin 200mg at night and am reducing the Ropinirole by 0.25 each week. At the
I am currently in the process of Ropinirole withdrawal. I was on 3mg per day having started on .5mg. My legs had started to play up as early as 11am in the morning, and I guess I was augmenting. My GP has put on Gabapentin 200mg at night and am reducing the Ropinirole by 0.25 each week. At the
mickeyrose
in
Restless Legs Syndrome
1 year ago
Glaucoma - dealing with glare.
Hello, I was diagnosed several years ago. I use Monoprost drops in my right eye and had a trab in my left a few years ago. Left is getting worse slowly, right is quietly developing a cataract. I'm also bothered by blepharitis, dry eye and being aged 73 - lol. In other words, nothing unusual going on.
Hello, I was diagnosed several years ago. I use Monoprost drops in my right eye and had a trab in my left a few years ago. Left is getting worse slowly, right is quietly developing a cataract. I'm also bothered by blepharitis, dry eye and being aged 73 - lol. In other words, nothing unusual going on.
Quiet_Lin
in
Glaucoma UK
1 year ago
Lactobacillus reuteri , Mucuna Pruriens , and magnesium malate to treat RLS
Hello, Newbie to the forum wondering if Mucuna Pruriens is used by people on this forum? Magnesium Malate , which helps the iron cross the BBB? And Lactobacillus Reuteri? (Recommended for RLS by Dr. Will Davis)
Hello, Newbie to the forum wondering if Mucuna Pruriens is used by people on this forum? Magnesium Malate , which helps the iron cross the BBB? And Lactobacillus Reuteri? (Recommended for RLS by Dr. Will Davis)
Little_apple
in
Restless Legs Syndrome
1 year ago
Hello. I’m new here.
Hello RLS forum. I’m new here. I’m already learning a lot from reading your posts and responses. I could quickly tell that it is mostly women on this forum. It is a kinder and gentler place than the Parkinson’s forum with predominately older men. What a relief! I have anxiety which is greatly worsened
Hello RLS forum. I’m new here. I’m already learning a lot from reading your posts and responses. I could quickly tell that it is mostly women on this forum. It is a kinder and gentler place than the Parkinson’s forum with predominately older men. What a relief! I have anxiety which is greatly worsened
Little_apple
in
Restless Legs Syndrome
1 year ago
Moving on from a Tracheostomy
Sorry - another question from me. As it was a slightly different topic, I thought I'd start a new thread. My dad has had a trachy now for just over two weeks, following two weeks fully sedated on a ventilator due to pneumonia. He is much improved and breathing unaided for 36 hours so far. He is also
Sorry - another question from me. As it was a slightly different topic, I thought I'd start a new thread. My dad has had a trachy now for just over two weeks, following two weeks fully sedated on a ventilator due to pneumonia. He is much improved and breathing unaided for 36 hours so far. He is also
Pookyal
in
ICUsteps
2 years ago
myopic macular degeneration
I’ve been highly myopic from the age of 10 and as got older my right has reached -17 and my left eye -15.At the age of 25 I had a retinal detachment in my right eye which I was not educated a bout abd as I visited spec savers they diognosed me with elergic reaction and was prescribed eye drops and the
I’ve been highly myopic from the age of 10 and as got older my right has reached -17 and my left eye -15.At the age of 25 I had a retinal detachment in my right eye which I was not educated a bout abd as I visited spec savers they diognosed me with elergic reaction and was prescribed eye drops and the
Naveedulhaq113
in
Macular Society
1 year ago
Loss of central vision after starting to use Latanoprost
Hi everyone - great to find this community. I have been trying to find if anyone has had a similar experience to me. I have had high myopia since I was a child. Think I am about -13 to -14. My main issue started in 2008 when the cataract in my left eye thickened considerably. I then had cataracts
Hi everyone - great to find this community. I have been trying to find if anyone has had a similar experience to me. I have had high myopia since I was a child. Think I am about -13 to -14. My main issue started in 2008 when the cataract in my left eye thickened considerably. I then had cataracts
Ginger30
in
Glaucoma UK
1 year ago
Glaucoma suspect
I saw the consultant several days ago and am still a glaucoma suspect rather than having glaucoma as yet, though I will be monitored much more frequently and closely from now on by the eye clinic as the risk is going up. I have come to realise that my biggest fear is not of getting glaucoma and going
I saw the consultant several days ago and am still a glaucoma suspect rather than having glaucoma as yet, though I will be monitored much more frequently and closely from now on by the eye clinic as the risk is going up. I have come to realise that my biggest fear is not of getting glaucoma and going
Fran555
in
Glaucoma UK
1 year ago
drooling and excess saliva
We are trying to tackle a new issue that has come up for my hwp. Drooling. He just stands over the sink and the drool just chains out of his mouth pretty much all day long. His Neuro said her patients have tried everything to no avail. She is recommending botox injections into the salivary glands
We are trying to tackle a new issue that has come up for my hwp. Drooling. He just stands over the sink and the drool just chains out of his mouth pretty much all day long. His Neuro said her patients have tried everything to no avail. She is recommending botox injections into the salivary glands
slimweiss
in
Cure Parkinson's
1 year ago
How long before methotexrate 'kicks-in'?
I have been taking MTX for past 17 weeks ( last 2 weeks by injection) for treatment of uveitis. But I see no change in the inflammation and the recent FFA reveals that the inflammation is active . Do I need to wait more or will the rhumetalogist add another DMARD ( or even biologicals ) to speed up the
I have been taking MTX for past 17 weeks ( last 2 weeks by injection) for treatment of uveitis. But I see no change in the inflammation and the recent FFA reveals that the inflammation is active . Do I need to wait more or will the rhumetalogist add another DMARD ( or even biologicals ) to speed up the
Udupik
in
Vasculitis UK
1 year ago
Effect of thyroid dysfunction on N-terminal pro-B-type natriuretic peptide levels: A systematic review and meta-analysis
Papers regarding the impact of inappropriate thyroid hormone levels keep coming out. It would be a miracle if endocrinologists showed any evidence of having read them. And incorporated the lessons into their practices. [i]
Effect of thyroid dysfunction on N-terminal pro-B-type natriuretic peptide
Papers regarding the impact of inappropriate thyroid hormone levels keep coming out. It would be a miracle if endocrinologists showed any evidence of having read them. And incorporated the lessons into their practices. [i]
Effect of thyroid dysfunction on N-terminal pro-B-type natriuretic peptide
helvella
Thyroid UK
in
Thyroid UK
1 year ago
Hypermobility/HEDS recommendation?
Hi there. Thanks for taking the time to read my post. I posted on the EDS forum but it’s not very active and no response yet. I have recently been diagnosed with PoTs and have fibromyalgia and erythromelalgia. I’m in the watch and wait category I believe for auto immune inc lupus but at my recent autonomics
Hi there. Thanks for taking the time to read my post. I posted on the EDS forum but it’s not very active and no response yet. I have recently been diagnosed with PoTs and have fibromyalgia and erythromelalgia. I’m in the watch and wait category I believe for auto immune inc lupus but at my recent autonomics
Winter_night
in
LUPUS UK
1 year ago
The coenzyme nicotinamide adenine dinucleotide ( N A D H ) improves the disability of Parkinsonian patients
This is an old study. The coenzyme nicotinamide adenine dinucleotide ( N A D H ) improves the disability of Parkinsonian patients 1989 https://sci-hub.ru/10.1007/BF02263483 "The coenzyme nicotinamide adenine dinucleotide (NADH) has been used in an open label trial as novel medication in 34 patients
This is an old study. The coenzyme nicotinamide adenine dinucleotide ( N A D H ) improves the disability of Parkinsonian patients 1989 https://sci-hub.ru/10.1007/BF02263483 "The coenzyme nicotinamide adenine dinucleotide (NADH) has been used in an open label trial as novel medication in 34 patients
Bolt_Upright
in
Cure Parkinson's
1 year ago
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