Interested in hearing people's symptoms and experiences with this. I had pvd of the left eye and sure enough 6 months later, right eye. Having problems dealing with it. When both eyes are affected, hard not to think of it 24/7. Would like to hear others stories.
View 1 RepliesI had a recent episode of flashes (left eye), so I went to the doctor and he did a thorough exam, and concluded that I was experiencing vitreous detachment (I'm 67). He explained that the flashes would soon stop, which they have. I only use reading glasses, but I've noticed some deterioration in my distance vision so I asked him about some correction. He gave me some contact lenses to try. The other day, I put them in, and I noticed that my left eye seemed worse with the contact lens in, so I took it out and just wore the right one. Now, I am more aware of some vision impairment (general blurriness) in my left eye for both reading and distance.
View 2 RepliesMy friend had retinal detachment after a hand stroke a year ago. First, his sight was 70%, then it came to 5%. few days ago now he had operation, and his vision is 20% now. Please, what are the methods for regenerating the photoreceptors and can something be done after such a long time?
View 1 RepliesI believe I have posterior bleph since it affects my Meibomian glands and I've had it for around 5/6 years, although I wasn't aware I had the condition until I saw a fantastic independent optician who also has it (note: don't both with any of the 'fast-food' opticians e.g. Specsavers - they haven't got a clue!).
Until recently, I never really had much of a struggle with it - it was generally more of an irritant, but recently it's become worse despite me upping the usual maintenance. My current routine involves the warming bag + cleaning with Blephaclean pads. There used to be an excellent product called Lid Care but they seem to have disappeared now unfortunately. Other than that, I take Omega-3 supps.
My symptoms lately are the usual e.g. soreness, grittiness, bright red lid margins, bloodshot eyes etc. However, recently I'm struggling a bit as I keep developing badly blocked glands that become a little inflamed and uncomfortable - is this quite common with the condition because I've never really had that? If so, does anyone have any alternative methods to counteract it?
Due to running excessively in the military, I believe my leg and feet injuries are related to Posterior Shin Splints and Posterior Tibial Tendonitis.
I am a female, 5'7, 160 lbs, and in the military.
I run approximately 15 to 20 miles a week.
I have high arches, and run flat footed.
I have hereditary varicose veins that have gradually become worse over time.
**5½ YEARS AGO** I dropped a three year weight class due to constant painful sores in both inner calves. The pain went away within a couple of weeks.
**2½ YEARS AGO** I received a second metatarsal hairline fracture on my left foot, due to an over excessive rucking competition (nearly 50 miles in two days, with zero training beforehand) I was volun-told to compete in a few days prior to the event. It healed within three months respectively, and the doctor had orthotics made for my feet. The orthotics worked great for walking, but instantly made my feet hurt while running. The problem continued to persist.
**2 YEARS AGO** I deployed overseas with my hairline fracture injury 99% healed. For most of the deployment, I did not experience any major problems. Towards the end, the unit conducted organized physical training, which included long runs. I started experiencing severe inflammation in my shins, inner calves, and swelling in my feet. The issue continued back home.
**1 YEAR AGO** I went to physical therapy when I came back from from deployment, and received deep tissue therapy for my shin pain. The deep tissue therapy helped my shins recover after each run, and the bumps on my shins started to disappear after each session (once a week). After my physical therapy sessions were completely over, I only had sensitive and tender shins after working out.
**½ YEAR AGO** When my unit increased the amount of running per week, I noticed the pains/sores were coming back in my inner calves. My shins remained tender, but the main focus was the pain in my inner calves. I went to the doctor for this issue, and they gave me a no running profile for a month. That was fine and dandy, until I came off profile and the situation became much worse than before. I played the “catch up” game to get back to how I used to be before I was on profile. In order to do this to my superiors standards, I had to to do this much faster and harder to achieve the results they were looking for. In doing this, the pains came back sooner, hurt more often, and did not require a hard physical workout to feel randomly throughout the day.
**PRESENT** Fast forward to present day, and now we run nearly every day of the week. Granted, most of the runs are now short runs, but now my pains are making any running absolutely miserable. I now have sharp pains starting from my inner calves, shooting up my legs, reaching the bottom of my knees. My inner calves are extremely sore and tender to the touch, even when I'm not running. I noticed just recently that I now have lumps/bumps on the bottom of both feet, in between the arch and heel (which I believe is called the Post Tibial Tendon). None of these issues are clearing up, unless I do absolutely nothing at all. But, once I start to exercise again, the pains and problems come back with full force. The bumps on my feet are not going away at all, I have had them for a few months and they continue to grow larger. So here are my questions:
1. Do you think I have Posterior Shin Splints and Posterior Tibial Tendonitis?
2. If not, what condition(s) do you think I have?
3. Do you believe these possible conditions can be fixed on my own, or should I see a doctor again?
4. I really cannot afford to stop working out, is there any low impact workouts that can keep me in shape if this turns into a medical issue?
Has anyone heard that HRT increases SS symptoms? I'm on a HRT in the form of a low dose patch. I've been experiencing dry/irritated eyes and read that HRT can make your eyes dryer in addition to the other risks associated w/SS.
View 14 RepliesI got hit in the eye about 18 days ago. Two weeks ago I started have flashes. Ophthalmologist said that I have swelling in the vitreous is this possible or is this just a PVD?
View 5 RepliesAn air bubble in the eye's vitreous appears black to the viewer. Truth??.
View 4 RepliesMy eye doctor saw something strange about my retina so she sent to a retinal specialist. After a 3 hour thorough exam he stated to me that sometime ago I had a detached retina and since I didn't notice, it healed itself. He stated that this do not happen often when a retina will heal itself. I have some damage but nothing very serious. There is a tiny blind spot when I look up but that is all. I feel very blessed that it healed because this should blinded me. Does anyone know if this has happened to anyone they know? I do have to be seen by the specialist every 6 weeks for a while. But considering the alternative...I have been blessed.
View 2 Repliesmy mother's age is 42, she had phacoemulsification last 5 years ago one right eye. on 15th January 2016 suddenly got whiteness in eye during cooking, after checkup from ophthalmologist he told the retina detached, we had a retina surgery using silicon oil but unfortunately the some amount of oil came out in inferior, that was removed after a month during the month she can see only 1 meter distance, when doctor dripped out silicon the cornea was swelled and once again another surgery was done after 7 days, now she can not see anything except a light is blinking in right corner of eye and sometime a blue sky color in eye, there is no different in eyes are open or closed. Is this possible that she can see again we are very upset because another eye is already dead since last 10 years. Or is there any possibility that we can change retina.
View 5 RepliesI have my 1st retinal detachment surgery 3 month ago with Scleral buckle and inject gas in my left eye. After the surgery sometime i see a dark spot on the upper right corner, which usually comes and goes. One time it appear and didn't go away but the dark area grow bigger and it has detach again (2 month after the 1st surgery) and i have my 2nd surgery 3 weeks ago with vitrectomy and silicone oil inject.
A couple of days ago i notice a dark spot (on and off) on the upper right corner of my left eye (same spot that the retinal re-detach).
2 days ago a notice a big dark area (2/5 of the vision field) on the upper center of my vision field. Sometime it was so dark i couldn't see my finger when i move it up to this area. But with outside day light i am able to see through a little bit (but still darker than other area).
I went to see my doctor immediately and he said the retinal look flat and alright in that dark area. He said there is a spot where the retina isn't completely re-attached yet but it is in the lower left side corner. I went to see another doctor and he said the same thing. And they all said the oil is clear.
But i haven't check with ultrasound yet.
I am still worry sick. Is it possible for the retinal to re-detach again with silicon oil still inside?
It is possible for the retinal to re-detach but Ophthalmoscopy doesn't pick it up?
Small but geometric -ish shape. This changes in 1/2 hour or more, the shape gets larger forming a getting larger approximate 'C' shape to the left of center. It is almost like me seeing a crude kaleidoscope . Eventually the thing disappears to the left. The shape seems to be of small triangles squares, anything 'sort of' geometric. I can see past it but still have to see the shape. Whichever eye I close I can still see it; close both I can see it! It has now cleared completely as I have not being looking at the sun or any strong light. Is it 'just one of those things' to be tolerated every now and then. I am 75 and in general good health
View 4 RepliesI'm late 5s,have had floaters since my 20s,back then they were small black or clear dots,fast forward,late fifties,now i've had pvds in both eyes,vitreous gel shrinks and pulls away from the back of the eye,now i have these clear to gauzy larger floaters,plus one large clumpy black one and I can't ignore them anymore. PVD is age related. I am just lucky enough to have these awful larger ones that can blur and obstruct vision. How does a person deal with it. Oh yes I also am starting to have dry eyes. Both also can cause hazy vision. Unless you've experienced it,no one else can relate
View 3 RepliesThe squint(left eye) had been developed at an age of 3 or 4 years I think... A cataract was also developed in it.. It had been ignored by me as I was not able to focus on it while seeing things... Cataract was recently removed(At an age of 18) by a laser treatment... But after the treatment also I had not get my vision back for my left eye (lazy eye).. I'm not able to see with that I now... Can I improve my left eye's vision...? If I can't.. Then how can I correct my eyes appearance... My left eye is little outwards from it's actual direction.
View 2 RepliesI have this squint since childhood. My eyes move outward. It happens a lot when I'm tired or try to look quickly at something, It was diagnosed early and I was asked to do a regular exercise with pencil. I had to Keep pencil in front of my nose and look at it and then slowly move the pencil forward and repeat it several times. The later I was given glasses and it improved it a little but then again it got as it was earlier. My vision is 6 by 6. But its just I don't have proper control over the muscles. They seem to be aligned but when I'm tired or move eyes they go outward. I wanted to know how it can be permanently corrected. It just disturbs me and I always feel a stress on my eyes. I have this irritation over eyes too and itching which makes it even worse. How it can be treated or it can be operated? I guess it would be easier with operation and I would go for it but I was asked to do exercise and told that it will stay but will get better, It was 30 degrees.
View 1 RepliesDoes anyone have either of these or know of someone who does and was able to go into labor naturally, were able to deliver vaginally? Or did it just end in an induction and C-section? If you did deliver vaginally were you able to get pregnant again without big complications? I have this and my doctor wants to induce because I am due tomorrow and I still haven't even softened, but I have a large chance even without inducing that I will have to have a C-section no matter. Every female on my mom's side has it and all had to have C-sections, except my mom who had my brother naturally and should not of and had to be artificially inseminated(sp) with my sister and I because she was not able to get pregnant on her own after.
View 5 RepliesAround 5 months ago out of nowhere, I started having immense headaches which at first I mistakened as just migraines or cluster headaches. I'm not sure how but I managed to endure the severe pain for 8 whole days by staying in bed (This was during exam break so I had no school). I've never suffered such a gratuitous amount of pain in my life! I could barely make it to the bathroom or even sit up to eat (I was 94.5 lbs after not eating for so long!!). After those 8 days I finally accepted the fact that it was not the typical migraine and was rushed to the emergency room. After going through numerous examinations with multiple doctors and specialists, I was diagnosed with posterior scleritis. It was really puzzling to hear that I had such a rare form of scleritis and at such a peculiar age since scleritis usually occurs at ages of 40-50 years. I was then put on 80mg of prednisone which relieved the pain. It was great at first but the heavy side effects eventually caught up with me. Anyways because of my condition, I was physically unable to show up for one of my exams although I wrote all the others while in such an insane amount of pain. I tried to explain why I wasn't able to attend but ended up getting yelled at and disrespected. I was deeply hurt and frustrated that the educators at my school didn't care for the health and safety of their own students ....
View 1 RepliesIs there anyone on the site who has had a Posterior Lumbar Interbody Fusion done.
I'm a little apprehensive about this op but I cannot stand the pain anymore, I'm now having problems peeing. God I can't believe I have to wait 4/5 months for this op and that's on the Urgent List.
Nobody understands when you tell them how much pain you're having, I'm so glad that I found this site as most people can sympathise with me.
Sorry for whining but I don't know how much longer I can cope with this Severe Pain & Numbness in my back and left leg and foot.
The doctor I saw today said he would do the reconstruction for my ruptured posterior tibial tendon as an out patient. That surprised me. Don't they usually keep you overnight?
View 14 Replieswhat this means! C5-C6: Posterior central disc osteophyte complex formation results in mild anterior effacement of the thecal sac. Endplate spurring and facet arthropathy results in mild narrowing of the right exit foramen.
View 3 RepliesI was driving on the highway last week. I started seeing flashing lights, shapes and lack focus, and disorientation. This has been something that randomly happens and I just sit down until it passes. After doing some research I know these to be either Auras or Simple Partial Seizures. This time on the highway I lost consciousness and woke up in an ambulance confused and soaking in urine. They suspected that I had a seizure while I was driving because of a bite on my tongue and history of seizures when I was a child. The hospital did a CT Scan which revealed something then an MRI the next day. The MRI showed that I have a 5cm cyst . That's bigger than a golf ball. I have my 1st appointment with a neurologist in a few days. Im so afraid...I don't know what to do. I've had to inform my job because I drive and travel everywhere for work. Its so hard to talk about it with people. I cant help but to think that I have had my last birthday.
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