Anyone experiencing something similar?
A community for people diagnosed with Dry Eye Disease (Keratoconjunctivitis Sicca) and the comorbidities associated with Dry Eye Disease (DED) like Meibomian Gland Dysfunction (MGD), Blepharitis, and Corneal issues. If one is not diagnosed with one of those issues then r/EyeTriage is the place to post your question or concern. Diagnosis and medical advice is not allowed in this community.
Anyone experiencing something similar?
Meibomian Gland Dysfunction (MGD) is a common eye condition diagnosed in the majority of those with Dry Eye Disease. Eye doctors disagree on how to treat it. Patients understandably are not sure how to treat it and have questions that deserve answers. This community is designed to empower people with education on treatment options for MGD and get those questions answered. It would also be good for you if you went to r/DryEyes that has 18,000+ members and a rich body of resources for you as well.
For people living in Germany
Meibomian Gland Dysfunction (MGD) is a common eye condition diagnosed in the majority of those with Dry Eye Disease. Eye doctors disagree on how to treat it. Patients understandably are not sure how to treat it and have questions that deserve answers. This community is designed to empower people with education on treatment options for MGD and get those questions answered. It would also be good for you if you went to r/DryEyes that has 18,000+ members and a rich body of resources for you as well.
For people living in Germany
A community for people diagnosed with Dry Eye Disease (Keratoconjunctivitis Sicca) and the comorbidities associated with Dry Eye Disease (DED) like Meibomian Gland Dysfunction (MGD), Blepharitis, and Corneal issues. If one is not diagnosed with one of those issues then r/EyeTriage is the place to post your question or concern. Diagnosis and medical advice is not allowed in this community.
I need advice
This is a science positive, evidence-based community for people to discuss Sjögren's syndrome.
What to do?
Meibomian Gland Dysfunction (MGD) is a common eye condition diagnosed in the majority of those with Dry Eye Disease. Eye doctors disagree on how to treat it. Patients understandably are not sure how to treat it and have questions that deserve answers. This community is designed to empower people with education on treatment options for MGD and get those questions answered. It would also be good for you if you went to r/DryEyes that has 18,000+ members and a rich body of resources for you as well.
Hi there, could this be TED?
For anyone suffering from TED - a rare auto-immune disease affecting our eyes. This community is a safe space to share resources to manage TED. Abusers and spam is banned and removed. By participating in this group, you acknowledge that this is a group of peers, not medical professionals or experts. Use at your own risk. We cannot diagnose you - do not post eye pictures for diagnosis. For emergencies, do not post in this group - call 911, visit urgent care or https://988lifeline.org
Eyelid swelling: what could be the cause?
Having a medical issue? Ask a doctor or medical professional on Reddit! All flaired medical professionals on this subreddit are verified by the mods.
Eyelid swelling: what could be the cause?
Having a medical issue? Ask a doctor or medical professional on Reddit! All flaired medical professionals on this subreddit are verified by the mods.
Eyelid swelling: what could be the cause?
Having a medical issue? Ask a doctor or medical professional on Reddit! All flaired medical professionals on this subreddit are verified by the mods.
Different methods of testing
Scleroderma is an extremely rare, chronic, autoimmune connective tissue disease which causes an overproduction of collagen in the body. Its most visible symptom is the hardening of the skin. It is not contagious, infectious, or cancerous. There is more than one form of the disease and it varies between patients. To date, there is no known cure. Treatments aim for the management of symptoms, and some are directed at decreasing the hyperactivity of the immune system.
Could this be sinusitis?
Welcome to the sinusitis subreddit. This is a resource for short and long term sufferers of chronic sinusitis. Please feel free to join our community!
Help
Welcome to the sinusitis subreddit. This is a resource for short and long term sufferers of chronic sinusitis. Please feel free to join our community!
Help
A subreddit for hooded eyed people to discuss hooded eyes and to find and share makeup tips and tricks.
Hilfe, weiß nicht mehr weiter
Eine Community für Beauty und Kosmetik. Alles von Make-up bis hin zur Haarpflege! Inklusiv und ausdrücklich LGBTQ-freundlich.
Confused
Scleroderma is an extremely rare, chronic, autoimmune connective tissue disease which causes an overproduction of collagen in the body. Its most visible symptom is the hardening of the skin. It is not contagious, infectious, or cancerous. There is more than one form of the disease and it varies between patients. To date, there is no known cure. Treatments aim for the management of symptoms, and some are directed at decreasing the hyperactivity of the immune system.
Swollen eyelids
Scleroderma is an extremely rare, chronic, autoimmune connective tissue disease which causes an overproduction of collagen in the body. Its most visible symptom is the hardening of the skin. It is not contagious, infectious, or cancerous. There is more than one form of the disease and it varies between patients. To date, there is no known cure. Treatments aim for the management of symptoms, and some are directed at decreasing the hyperactivity of the immune system.
Living with diffuse systemic sclerosis
Scleroderma is an extremely rare, chronic, autoimmune connective tissue disease which causes an overproduction of collagen in the body. Its most visible symptom is the hardening of the skin. It is not contagious, infectious, or cancerous. There is more than one form of the disease and it varies between patients. To date, there is no known cure. Treatments aim for the management of symptoms, and some are directed at decreasing the hyperactivity of the immune system.
Tell me your story
Scleroderma is an extremely rare, chronic, autoimmune connective tissue disease which causes an overproduction of collagen in the body. Its most visible symptom is the hardening of the skin. It is not contagious, infectious, or cancerous. There is more than one form of the disease and it varies between patients. To date, there is no known cure. Treatments aim for the management of symptoms, and some are directed at decreasing the hyperactivity of the immune system.
Any suggestions for hyperpigmentation?
Skin care is a pretty big deal, and we love subs like /r/SkinCareAddiction, however we felt there needed to be a sub that deals specifically with skin that's over 30. Share your questions, frustrations and triumphs!
Thoughts on spironolactone
For women who have experienced hair loss for any reason to come together, discuss hair loss, share their experiences, and seek support. Please read Community Info before posting.
Thoughts on spironolactone
For women who have experienced hair loss for any reason to come together, discuss hair loss, share their experiences, and seek support. Please read Community Info before posting.
Regrowth or breakage?
For women who have experienced hair loss for any reason to come together, discuss hair loss, share their experiences, and seek support. Please read Community Info before posting.