Bruising/broken Blood Vessels Of Fingers - Also Central Retinal Vein Occlusion
Jan 19, 2015
I have had blood tests to investigate the central retinal vein occlusion I had in September. Apparently the tests were okay - slightly raised in one area but not bad enough for the haematologist to get back to me, when my eye consultant asked for advice. I commented that I. Bruise easily but my consultant said the raised level would indicate the opposite. The CRVO was caused by haemorrhaging in the eye. I quite often get bruising/broken blood vessels in my fingers - got one today on the middle section of my ring finger, by applying my handbrake! Does this make sense to anybody? I'm fed up of explaining this to the various medics I see, who just look at me with a bemused expression! Am I going mad here??
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I have been experiencing clogged nose without colds, Pain around the eyes, forehead, the temple, migraine headaches, dizziness and imbalance when walking. A visit to the ENT showed normal hearing, no ear blockage or infections, no sinusitis or nasal polyps. His diagnosis is Vasomotor rhinitis. He said the weather, temperature, wind blowing triggers my blood vessels to swell and thus cause those symptoms. Anyone experiencing these weird feelings? Its so debilitating and affects my daily activities.
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My calf and foot are swollen (the foot is the worst). I am just wondering what the chances are of this going down eventually or is it going to be like this for rest of my life?
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I have pretty bad anxiety but I've been noticing some strange things lately. Sometimes after being on my feet all day my left calf will burn and pulse with pain until i sleep and then its gone in the morning. had a blood clot test performed for it before and it came clear, although its happened even worse afterwards. my family does have a history of varicose veins/vein problems and yesterday i noticed a tender spot on the back of my thigh (left side) , about the size of a penny. it doesn't hurt unless pressed or moves. i didn't look at it until today, and the tender spot looks like a purple little circle at the end of a larger vein. the veins in my legs are pretty visible but they don't really pop up or anything. i do have this strange, painless, green mark on the backside area of my knee though. im just freaking out bc i cant identify this. im only about 20 but i've been fairly inactive the past few years due to my anxiety. i also get this pulsing/pumping feeling through my legs, esp the left, when im laying down but im aware that can be a symptom of anxiety. does this look like a bad vein... or perhaps a bruise i don't remember getting? its easier to see from far away. sorry, im freaking out.
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3 days ago an object fell on top of my foot and my foot became hugely swollen and I was in so much pain that I had to go to the hospital. They took an x-ray and told me it wasn't fractured, but the blood vessels in my foot had broken and I am bleeding internally in my foot (I'm also taking warfin for another medical issue). The dr. gave me painkiller and said nothing could be done except to wait for it to heal on its own. For the past 3 days I have been on complete bed rest and have elevated my foot and place ice on it every 2 hours. I am in extreme pain and my foot is still badly swollen and now I noticed 3 medium sized bumps on top of my foot. I am also taking blood thinner due to another medical issue, so my blood is thinner than normal, so it would take longer to heal. I can't even touch my foot as it is that painful and I haven't put any pressure on it. My family dr. told me that it could take 4-5 weeks to heal. Has anyone else gone through this??? Is there anything else I can do?
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On 31st, my boyfriend inserted it a little bit without a condom for just 2-3 seconds. He didn't come though and he hardly put 1-2 cm inside. After that he fingered me and we noticed a few blood stains. Initially I thought I was getting my period but it has never been a week early. The blood was bright red the first day and brown gooey the next day. Now I'm really confused if this could mean that my hymen broke or I'm pregnant.
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I did not bleed I just had a little drop the next day which scared me at first so I went to the doctors and they said I just tore my Hymen so everything was ok
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On 2/1/14, I broke my tibia (spiral, slightly displaced) and fibula falling off a motorcycle (not at high speed). OS said I didn't need surgery and on 2/3/14 I had a long-leg cast put on. I developed blood clots from the leg which shot to my lungs and OS removed cast early on 3/5. I am now in a walking boot, although I cannot bear weight just yet.
I'm worried about the bone not healing or fusing properly since I am no longer in a cast. Will there be longer healing times since I am no longer in a cast?
X-rays were taking on 3/3 and OS says the bones are back in place nicely but no fusion.
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I am considering a vasectomy, and according to the medical literature (see links to citations below), the recommended methods for vas occlusion are cautery and/or fascial interposition (preferably both methods).
However, I have consulted with two local urologists, and neither of them use either of these techniques. Instead, both simply do an excision and ligation, and one of them takes an additional step of folding back and suturing the ends of the vas deferens. Both physicians have very good credentials and are highly experienced.
Is it unusual for urologists (in the U.S.) to perform only excision and ligation without any cautery or fascial interposition, or is excision and ligation still commonplace and considered good practice? Is it important to perform cautery and/or fascial interposition, and should I therefore continue to look for a urologist who performs one or both of those techniques?
Note, I am particularly concerned about long-term recanalization (i.e., a year or more after the procedure). I know the rates of late recanalization are generally assumed to be low, but as I understand it, the true rate is difficult to ascertain due to a lack of systematic long-term follow-up.
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My 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?
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I have never really suffered from headaches during my life until now (i'm 29). There is no family history of migraines.
Out of the blue, after a family function 2 years ago, we got home and I noticed the image out of my right eye was 'cloudy'. I wear glasses so immediately thought my glasses were dirty. I got a shock when taking them off to find it was my eye! I was a bit concerned, then 30mins later I had the worst headache in my life. I had to go to bed early. At some points even the sounds of the TV from downstairs were making me feel sick. It was as if every sound and sense in my body had been amplified. I think there might have been a tiny bit of twitching but can't confirm now as memory of it is a little hazy.
I woke up the next day feeling normal again, and put it down to hangover or just a 'bad headache'. I went back to my daily job (work in IT) and didn't think anything of it. The same thing happened again about a month later, this time not a headache as much, more visual symptoms. After 3-4 hours it passed and I was back to normal again.
The frequency of them started changing from one every month, then around Jan 2013 one every two weeks, and since around June 2013 one every 7-10 days.
At this moment in time I am off work due to depression/anxiety (Since Feb 2014) and currently can get them every 2-4 days. Last week I had four in the space of 7 days.
What I experience now: The 'trigger' feeling that I know one is coming is slightly worrying; I can visibly see my pulse (vein shape) pulsing in my right eye's vision to my heartbeat. This goes on for about 15/30mins, then I start to get spots/lines/an 'arc' shape which will sometimes be there and sometimes now. I will also get moments of no vision in that eye 'black spots appearing over the central vision'.
When I read of people with 'ocular' migraines they note these symptoms usually leave after approx 1 hour followed by a blinding headache. My concern is the aura stays with me the entire course of the migraine - approx 6-9 hours. I believe I have 'retinal' migraines. Difference being I ONLY get the aura in my right eye. If I patch the right eye my vision is normal out of my left for the entire 9 hours. Also my head feels incredibly tight and sometimes will get a throbbing pain just above the tear duct on the right side of my noise.
I have had my eyes checked and been told the pressure is fine (no risk of glaucoma). Also my blood pressure is normal/high (bearing in mind I do suffer with anxiety/depression).
I am at my wits end trying to work out what triggers them. I have spent months cutting out caffeine/alcohol. It made no difference. I have also tried limiting my use on computers/phones whilst I am off work. No difference.
The only relief I have found is through exercise. I typically don't do any sort of intense daily exercise, maybe a 20min walk a day and household chores.
2 Weeks ago, I decided to start an exercise regimen. Did jogging/walking for about 45mins-1hr each day. I went approx 10 days without a migraine (usually it's every 2-3 days at the moment). I am wondering what in the exercise is causing this relief? Could it be hormonal or just a stress reliever?
I don't smoke and don't drink much alcohol any more. I do have a bit of a weak neck - maybe this has something to do with it? My main concern above all else is it's not your typical aura, I only get it in one eye.
I have also noted that I have never had a migraine before 1PM and after 10PM (apart from one rare occasion at 4AM when I was having a panic attack in bed). Something is happening between approx 2PM-10PM to trigger it, but I don't know what.
I'm a bit of a hypochondriac at the moment, thinking it's a brain tumour or i'm at risk of stroke. I wanted to get a scan but GP said "if you would have had a brain tumour since 2012 you would know by now" and suggested meds.
Does anybody else here suffer from their 'retinal' migraines, or can offer any support or advice?
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my 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.
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After 2 weeks from the surgery I developed Central Macular Edema, it manifested itself as a round gray spot on my field of vision and could not read also with the glasses because everything was blurred also because my right eye has still the cataract. The ophthalmologist prescribed me Acular to take together with M for another 2 months and asked me to go back for check up at the beginning of April. I was forgetting: last year I was found to have a slight macular degeneration, the dry type and she said not to worry. I would like to know from other people who had the same problem as mine. Is it likely that after 2 months I could be clear of it? Also anyone can tell me how long they have to wait before taking a flight abroad?
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Anyone out there have any information on central pontine myelinolysis , my 26yr old son has been diagnosed with this condition. He has been in hospital for 6 weeks and spent the last 4 weeks in intensive care, he went into hospital on Christmas eve after having seizures to do with alcohol withdrawal the first couple of days he was doing fine then things started to go wrong. He started to loose his balance he started slurring his speech and was getting very confused. He then lost his ability to swallow then started to slip into a coma at which point intensive care induced him into a coma and we were told not to expect him to survive. A week later he started to come round and could breath for himself but could only use his eyes,3 weeks later and he can communicate by blinking his eyes can squeeze my hand with both hands can wiggle his toes and can understand everything we say to him. We know we have a long way to go and don't know what the long term recovery is but would be grateful for any info from anyone who has come through this condition.
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I 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?
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it's been awhile since I came on this board but I know there is many helpful people here. I asked for an MRI of my cervical but neurologist ordered MRI of my Thoracic region.
There is a small hemangioma arising from the right aspect of the body of T6.
A small right of midline disc herniation at T7/T8. It mildly effaces the ventral surface of the cord.
There is a central disc herniation present at L1/L2. This herniated disc measures 11 by 7 mm. There is compression of the anterior sac.
Impression:
1. Small right of midline disc herniation T7-T8.
2. Prominent central disc herniation L1-L2.
My symptoms are pulsing pain around my bra line. Weird deep pains that is hard to explain. Either the inside of thighs or from buttocks to ankles. Feet feel heavy.
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what 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.
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I had am mri w/o contrast and the findings were:
C2-3, the central canal and neuralformina are patent.
C3-4, a diffuse disc bulge effaces the thecal sac. There is minimal narrowing of the neural formina.
C4-5, a diffuse disc bulge effaces the thecal sac. There is mild narrowing of the neural formina.
C5-6, there is a disc/osteophytic ridge with moderate narrowing of the central canal and neural formina.
C6-7, there is a diffuse disc bulge asymmetric to the left. There is mild narrowing of the central canal. The right neural foramen is patent. There is moderate narrowing of the left neural foramen.
C7-T1, the central canal is patent. There is mild narrowing of the right neutral foramen and moderate narrowing of the left foramen.
Conclusion:
diffuse disc bulges narrowing the central canal and neural formina as described, most pronounced from C5-6 through C7-T1.
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I am now over a year from retinal tear/ pvd with a mass of dark floaters/ cobwebs/ Weiss ring in my visual axis.constantly blurring my vision. Makes everything a struggle and exhausting. My ophthalmologist agrees they are extreme and is willing to do a vitrectomy - I am so tempted to get this done, but at the same time very apprehensive. Would love to hear any thoughts.
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I have problem with my legs, i have 23 and i'm not overweight i think i'm active. i already have treatment - sclerotherapy on one leg and now it's ok. Recently i sign up at the gym and i saw that if i'm do e.g squats or stand long time, some veins on my second leg, near tibia are getting protrusion and soft when touching. so i guess it's early stage of varicose vein.
Now i wonder what to do, wear some compression on leg while being on the gym and everything will be fine? or just let go going to gym.
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I had vein in right leg stripped on Xmas eve all went well and seemed recovery good but for last week or so I've noticed where bruising is on thigh I've got a lump which is sore and hot at times. Is this normal?
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