Guest guest Posted January 8, 2004 Report Share Posted January 8, 2004 Hi and welcome to our group. You have other Aussies here whom I am sure will jump in if they are reading the posts. First it sounds like you have Hashi's (Hashimotos Disease), which is an autoimmune thyroid disorder and can cause the TSH fluctuations tht you mention, in addition to that tightness in your throat. Next, 1/2 grain of Armour is practically nothing. You need to be on much more to have any good effects. It is rare to see someone on less than 2 grains and who is getting the most they can get from Armour. Additionally, once you are able to increase, you need to do two things--first, take it sublingually, which means to allow it to slowly dissolve in your mouth, preferable a place where there is the least saliva. I, for example, do mine between the lower gums and inner cheek. And second, you need to divide your dose to at LEAST twice a day. I do 1 1/4 grain in the morning, 1 1/4 grain in the early afternoon, and another 1/4 grain at bedtime, for example. " Low basal metabolic rate " is just another name for being VERY hypothyroid, in your case. Yes, you could need adrenal support. Several of us are on Isocort-- check out the FILES section, go to the ADRENALS folder, and you will find information on it plus a great site to get it. Nutri-Meds also makes an adrenal support which some folks here also use and like. Hope this is a good start of information for you. Don't hesitate to come back with more questions or support. Janie aka ThyroDiva Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2004 Report Share Posted January 8, 2004 , Welcome to the group! One thing that is not thyroid related, but could be related to your seizures. You might want to check and see if you are consuming anything with aspartame (Nutrasweet - I'm sure it goes by other names in Australia). In people that are sensitive to it, it can cause seizures. It's usually found in diet soda and sugarfree items such as chewing gum. I learned the hard way about it. Dusty From: Tink To: NaturalThyroidHormones Sent: Thursday, January 08, 2004 5:36 AM Subject: time to jump in Hi everyone, I've been lurking for a few days, and I've learned so much from you all already; but I figured it was time to introduce myself and ask for your opinions on the stuff I'm trying to work out. I'm sorry this e-mail turned out to be so long. If you're sick to death of peoples' stories about unhelpful doctors and want to jump straight to the questions, scroll down to the 3 asterisks. I'm and I'm 26. In a few months time I will have been noticably sick for 10 years. I've been given various diagnoses during that time: iron deficiency anaemia in 1997; asthma, chronic fatigue syndrome and fibromyalgia syndrome in 2000; sleep apnea, arthritis, insulin resistance and epilepsy in 2001; hypoglycemia in 2002; polycystic ovarian syndrome and endometriosis in 2003. Some of the diagnoses have been right (there the ones like PCOS that I knew for years before I could get a doctor to do the proper tests), some like CFS have served a purpose, and some like the epilepsy were just plain wrong. After a year of medication that did nothing but make my life hell, my partner realised and pointed out to me the connection between my seizures and me not having eaten for a few hours. In a couple of hours of research I came up with the answer that the neurologists had missed for the last year: I figured I was hypoglycemic, and probably hypothyroid too. I changed my diet and the seizures happened much less often. So I went to my doctor with that evidence. He agreed with my diagnosis of hypoglycemia and agreed to me reducing the epilepsy medication slowly until it was out of my system. He's a GP, a CFS specialist, and he also has a good knowledge of natural therapies. He's the only good doctor I've found, and I've seen a huge number of them over the last 10 years. At the time my big concern was the epilepsy medication because I knew it was doing nothing but making my life hell, but I did more reading on hypothyroidism and was amazed at how it seemed to describe my situation. Early in 2003 I saw my sleep specialist who agreed that hypothyroidism may be a problem and ordered a blood test for me. I was so excited when I got the results back and found that my TSH level was at the very top of the normal range (3.7). Here finally was evidence a doctor couldn't ignore! I went to my CFS specialist with my results. He was happy for me too and hoped that this may be the cause for my health problems. However hypothyroidism is something he's not an expert on so he referred me to an endocrinologist. I chose the endocrinologist. I searched the internet and chose one who people said cared about them more than there blood tests. I actually e-mailed him and asked if he wanted me to get any tests done beforehand. He wrote back and said he thought it was best practice to order the tests once he'd seen me, and I thought that was positive. At the first appointment he just gave me a form for the blood tests. At the second appointment he was horrible. My TSH had dropped back to 1.9 (it'd been 2 months since the last test) and he saw nothing significant in my low free T3 level. I asked him why he thought the TSH level was so different and he said my thyroid problem had probably just been temperary due to an illness of some kind. I asked him to explain my other symptoms. He said iron deficiency anaemia can cause tiredness and insulin resistance causes weight gain. I said what about my other symptoms like cold intolerance, emotional instability, heavy painful and irregular periods and chronic fatigue just to name a few. He didn't have any explanation for those and I walked out and vowed never to go back. I couldn't understand why my TSH levels were so different and just couldn't bear thinking about the thyroid thing for a while. I was scared back into thinking about it a couple of weeks later when my skin became flakey. And I knew something had to be done when I got that tight feeling in my throat like someone had their hands around my neck and was squeezing hard. At this time I was reading a lot about hypothyroidism and came across a phrase that rang a bell. The phrase was " low basal metabolic rate " and I remembered it from when I was in my early teens and my stepfather said I should ask the family doctor why I get cold so easily and can cope with the heat when everyone else is complaining. So I asked her and that was the answer. " nothing to worry about " she said. I was absolutely furious! A couple of weeks later the tightness in my throat was hurting so much I just couldn't take it anymore, so I went to a local GP who I could get an appointment with that day and she referred me for an ultrasound of my thyroid. That happened a couple of days later and the report said my thyroid was slightly enlarged and I had a nodule. I was scared about what the nodule might be and I knew that it would take a couple of months to get into see a new endocrinologist so, reluctantly, I went back to the old one. Predictably, he was no help and the appointment was a complete waste of time and money. He could not have cared less about the nodule that I was so stressed about. He said you could go to a bus stop and half the people there would have a nodule. I said the difference was that mine wasn't there before. He said it probably wasn't serious and, even if it was cancer, we could do nothing about it for 6 months and it wouldn't matter. I said that at the very least it was evidence that my thyroid problems weren't temperary like he had thought and asked for the results of the latest batch of thyroid levels I'd just had done. My TSH was back up to 3 and he admitted then that things weren't stable and examined my thyroid. He didn't have much to say about it though and would've been happy to just " monitor things " . I insisted on medication and he would not give me armour but, for the sake of getting rid of me I think, wrote a prescription for oroxine (the Australian equivalent of synthroid. I went back to my CFS specialist and told him all about my bad experience with the endocrinologist and asked for a referal to a good one, and for armour in the meantime. He was happy to prescribe me the armour, but we talked about it and decided that I should try the oroxine first for 6 weeks. We both thought it probably wouldn't help but at least we could then tell the next endo that I'd already tried it - plus, in Australia, there's quite a substantial price difference and oroxine is much much cheaper. After the 6 weeks I was feeling no better and so he started me on half a grain of armour. This was meant to be a temperary measure until I saw the good endo. It was October by this time, and I was leaving in early November to spend a month with my partner who lives in the US. I tried to get an appointment with the endo before I left but he was booked up until the end of the year and they didn't have the diary for next year yet. When I got back home I called his office again, answered all their questions, and then they called me back a couple of days later and said they wouldn't take me because I don't have private health insurance. I asked my CFS specialist for a referral to another endo and, while I will go and see her because she's one of the best reproductive endos in the state, I think I need to approach my thyroid and adrenal issues in a different way. So I've found a GP who's also a nutritionalist and specialises in hypothyroidism and adrenal insufficiency. I feel like I need help dealing with this rather than doing it on my own because I feel so overwhelmed by all the stuff I've read about my various conditions I just don't know where to start, or how to approach things in a way that will demonstrate what's working and what isn't. *** So my appointment with the nutritionist is a week from today, and I'd like to get your opinions on a couple of questions before I see her: One thing is, I take my half grain of armour first thing in the morning, but at night I'm often hot, particularly my legs. I feel like I'm badly sunburnt, or like I'm radiating heat. Does that sound like it's related to a hyper state, or adrenal problems, or both? Another thing is that, for a couple of weeks now, I've been getting goose bumps every so often just on one part of my body like my lower leg or upper arm. Here in Australia we're right in the middle of summer so it's definitely not cold-related. I've never read about this anywhere. Has anyone ever experienced this? And do you know what the cause was for you? Also, I'm confused about adrenal insufficiency and exhaustion, and wondering which category I belong in. I have symptomes like taking a long time to feel awake in the morning (actually, it's usually not until the afternoon), startling easily, and having a very low tolerance for stress, but I also seem to be able to produce adrenaline when I need to. For example, I helped organised a weekend-long convention a year ago, and I felt better than I usually do all weekend and was able to get lots done; but as soon as it was over I crashed. By that I mean I collapsed on the floor, I could not respond to things for a couple of minutes although I was aware of what was happening around me, and I was completely exhausted and unable to do anything. Also it feels to me like, for me to have a productive day like anyone else, my adrenaline needs to kick in at a level that can't possibly be healthy. So for me to have a good day which is like everyone else's average my body needs to release the amount of adrenaline that most people only need in an emergency. Is this making sense? Thanks for reading, and for any suggestions or ideas you might have. . -- Tink: atink@... I'm not an angry girl, but it seems like I've got everyone fooled, everytime I say something they find hard to hear, they chalk it up to my anger and never to their own fear (Ani DiFranco) *Consider all www users: use, support and create text-friendly sites!* ------------------------------------------------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2004 Report Share Posted January 8, 2004 --- In NaturalThyroidHormones , Tink > > Thanks for reading, and for any suggestions or ideas you might have. > > . Hi and welcome! a few things come to mind here...I had severe hypoglycemia in my 20's...I took the five hour glucose tolerance test and shortly after hour 2, I flunked it bigtime..luckily, I was in the hopspital lab waiting area and fell on the floor and began to have a seizure..my blood sugar had dropped to 30 in a record amount of time...- they injected me with something and helped me get up - after that, I began Dr. Carlton Fredrick's Low Blood Sugar diet, cut out sugar and refined starches and found it helped me a great deal...such severe hypoglycemia is a definite symptom of adrenal exhaustion. People with burned out adrenals sometimes make excess amounts of cortisol which tends to keep them in a constant state of " flight or fight " even when they are not in stressful situations..their adrenals are stressed..eventually it vbecomes worse, when you are no longer able to " rise to the occasion " even when you do have a stressful situation or sudden fright..then your levels remain always low because the adrenals can no longer make much cortisol. Both states are considered adrenal fatigue or, more serious adrenal, exhaustion. But proper treatment can bring them back to a strong place - you can rest and recharge the adrenals most of the time..One other anecodotal thing...my friend's cocker spaniel began having seizures several times a week..she also had lots of skin problems...the doctor put her on 1 grain Armour daily (she was 38 lb.s went down to 16 lbs in 6 months and stayed healthy)- her seborrhea and her seizures stopped...after looking this all up on the internet, I found that seizures can often be halted with thyroid meds...not if you have a case of epilepasy..but when seizures begin for other reasons, this is something that works for many pets...why not humans too? I never actually had cause to look it up and see if this pertains to humans. Good luck finding your way back to health!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2004 Report Share Posted January 8, 2004 --- In NaturalThyroidHormones , Tink > > Thanks for reading, and for any suggestions or ideas you might have. > > . Hi and welcome! a few things come to mind here...I had severe hypoglycemia in my 20's...I took the five hour glucose tolerance test and shortly after hour 2, I flunked it bigtime..luckily, I was in the hopspital lab waiting area and fell on the floor and began to have a seizure..my blood sugar had dropped to 30 in a record amount of time...- they injected me with something and helped me get up - after that, I began Dr. Carlton Fredrick's Low Blood Sugar diet, cut out sugar and refined starches and found it helped me a great deal...such severe hypoglycemia is a definite symptom of adrenal exhaustion. People with burned out adrenals sometimes make excess amounts of cortisol which tends to keep them in a constant state of " flight or fight " even when they are not in stressful situations..their adrenals are stressed..eventually it vbecomes worse, when you are no longer able to " rise to the occasion " even when you do have a stressful situation or sudden fright..then your levels remain always low because the adrenals can no longer make much cortisol. Both states are considered adrenal fatigue or, more serious adrenal, exhaustion. But proper treatment can bring them back to a strong place - you can rest and recharge the adrenals most of the time..One other anecodotal thing...my friend's cocker spaniel began having seizures several times a week..she also had lots of skin problems...the doctor put her on 1 grain Armour daily (she was 38 lb.s went down to 16 lbs in 6 months and stayed healthy)- her seborrhea and her seizures stopped...after looking this all up on the internet, I found that seizures can often be halted with thyroid meds...not if you have a case of epilepasy..but when seizures begin for other reasons, this is something that works for many pets...why not humans too? I never actually had cause to look it up and see if this pertains to humans. Good luck finding your way back to health!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2004 Report Share Posted January 8, 2004 --- In NaturalThyroidHormones , Tink > > Thanks for reading, and for any suggestions or ideas you might have. > > . Hi and welcome! a few things come to mind here...I had severe hypoglycemia in my 20's...I took the five hour glucose tolerance test and shortly after hour 2, I flunked it bigtime..luckily, I was in the hopspital lab waiting area and fell on the floor and began to have a seizure..my blood sugar had dropped to 30 in a record amount of time...- they injected me with something and helped me get up - after that, I began Dr. Carlton Fredrick's Low Blood Sugar diet, cut out sugar and refined starches and found it helped me a great deal...such severe hypoglycemia is a definite symptom of adrenal exhaustion. People with burned out adrenals sometimes make excess amounts of cortisol which tends to keep them in a constant state of " flight or fight " even when they are not in stressful situations..their adrenals are stressed..eventually it vbecomes worse, when you are no longer able to " rise to the occasion " even when you do have a stressful situation or sudden fright..then your levels remain always low because the adrenals can no longer make much cortisol. Both states are considered adrenal fatigue or, more serious adrenal, exhaustion. But proper treatment can bring them back to a strong place - you can rest and recharge the adrenals most of the time..One other anecodotal thing...my friend's cocker spaniel began having seizures several times a week..she also had lots of skin problems...the doctor put her on 1 grain Armour daily (she was 38 lb.s went down to 16 lbs in 6 months and stayed healthy)- her seborrhea and her seizures stopped...after looking this all up on the internet, I found that seizures can often be halted with thyroid meds...not if you have a case of epilepasy..but when seizures begin for other reasons, this is something that works for many pets...why not humans too? I never actually had cause to look it up and see if this pertains to humans. Good luck finding your way back to health!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2004 Report Share Posted January 9, 2004 > Next, 1/2 grain of Armour is practically nothing. You need to be on > much more to have any good effects. Oh for sure. It was never intended that I'd stay on half a grain for very long. It was just to get me started. I'll discuss it with my new doctor on Thursday, but I'd be hesitant to go much higher without adding some adrenal support. > two things--first, take it sublingually, I've been wondering about that, but mine are actually capsules. > Yes, you could need adrenal support. Several of us are on Isocort-- > check out the FILES section, go to the ADRENALS folder, and you will > find information on it plus a great site to get it. I actually don't have access to the files section, but I'll do a search on Google and see what comes up. > Hope this is a good start of information for you. Don't hesitate to > come back with more questions or support. I'm sure I will. Thanks so much. . -- Tink: atink@... I'm not an angry girl, but it seems like I've got everyone fooled, everytime I say something they find hard to hear, they chalk it up to my anger and never to their own fear (Ani DiFranco) *Consider all www users: use, support and create text-friendly sites!* Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2004 Report Share Posted January 9, 2004 > I've been wondering about that, but mine are actually capsules. Capsules??? Armour is tablets. What are you taking? I see you are in Australia, so are these the compounded Armour?? > I actually don't have access to the files section, but I'll do a >search on Google and see what comes up. Tell me about this. The FILES are right on this site: http://health.groups.yahoo.com/group/NaturalThyroidHormones/files/ Are you not able to access that?? Janie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2004 Report Share Posted January 9, 2004 > I've been wondering about that, but mine are actually capsules. Capsules??? Armour is tablets. What are you taking? I see you are in Australia, so are these the compounded Armour?? > I actually don't have access to the files section, but I'll do a >search on Google and see what comes up. Tell me about this. The FILES are right on this site: http://health.groups.yahoo.com/group/NaturalThyroidHormones/files/ Are you not able to access that?? Janie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 12, 2004 Report Share Posted January 12, 2004 > Welcome to the group! Thank you. > One thing that is not thyroid related, but could be related to your > seizures. You might want to check and see if you are consuming anything > with aspartame (Nutrasweet - I'm sure it goes by other names in > Australia). Nope, exactly the same names for it here (though I do know people that have other names for it <grin>). I'm Blind, so checking labels is not an easy option. I probably avoid most of it though since I don't believe in using diet sodas etc. I figure diet in that context just means " we've figured out a way to sell our products to people who can't have sugar, by replacing it with a whole heap of stuff that's worse " . When you were learning to avoid it, did you see it in anything that surprised you? . -- Tink: atink@... I'm not an angry girl, but it seems like I've got everyone fooled, everytime I say something they find hard to hear, they chalk it up to my anger and never to their own fear (Ani DiFranco) *Consider all www users: use, support and create text-friendly sites!* Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 12, 2004 Report Share Posted January 12, 2004 > my friend's cocker spaniel began having seizures several > times a week..she also had lots of skin problems...the doctor put her > on 1 grain Armour daily (she was 38 lb.s went down to 16 lbs in 6 > months and stayed healthy)- her seborrhea and her seizures > stopped...after looking this all up on the internet, I found that > seizures can often be halted with thyroid meds... Fascinating! We'll see how I go once I raise my armour to a good level. . -- Tink: atink@... I'm not an angry girl, but it seems like I've got everyone fooled, everytime I say something they find hard to hear, they chalk it up to my anger and never to their own fear (Ani DiFranco) *Consider all www users: use, support and create text-friendly sites!* Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 14, 2004 Report Share Posted January 14, 2004 > I personally dealt with retinal changes, vertigo, and slurred > speech...all of which have cleared up since I quit using aspartame over 6 > years ago. It is in sugarless chewing gums and even used as a dusting to > give the initial sweet taste on some non-sugarless chewing gums. It's in > PepsidAC chewables and some other chewable meds and vitamins. Vitamins! Now there's something I hadn't thought of. I will check them out. Thanks. . -- Tink: atink@... I'm not an angry girl, but it seems like I've got everyone fooled, everytime I say something they find hard to hear, they chalk it up to my anger and never to their own fear (Ani DiFranco) *Consider all www users: use, support and create text-friendly sites!* Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 14, 2004 Report Share Posted January 14, 2004 > I personally dealt with retinal changes, vertigo, and slurred > speech...all of which have cleared up since I quit using aspartame over 6 > years ago. It is in sugarless chewing gums and even used as a dusting to > give the initial sweet taste on some non-sugarless chewing gums. It's in > PepsidAC chewables and some other chewable meds and vitamins. Vitamins! Now there's something I hadn't thought of. I will check them out. Thanks. . -- Tink: atink@... I'm not an angry girl, but it seems like I've got everyone fooled, everytime I say something they find hard to hear, they chalk it up to my anger and never to their own fear (Ani DiFranco) *Consider all www users: use, support and create text-friendly sites!* Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 14, 2004 Report Share Posted January 14, 2004 ... Would you mind telling us what your vision challenge is? Total blindness, partial? is it independent of thyroid or possibly linked? I'm legally blind in one eye, a genetic defect that my father also has... During an car accident I ruptured a blood vessel in my good eye. In order to make sure that it healed correctly I was given drops that would knock that eye out completely so that I could not see. The idea being that if I could not see out of it I would be more likely to rest it.... It worked, the eye healed perfectly... BUT for a bit over a week I was blind, running into walls... unable to see much more the vague shapes and light and dark out of the bad eye.... I had a taste of a place that I would never like to stay... but also gained a respect for what it's like to not be able to do things that everyone else takes for granted...... If I'm being too nosey... I apologize... I'm just a curious person. Topper () On Wed, 14 Jan 2004 20:50:49 +1000 (EST) Tink writes: > Vitamins! Now there's something I hadn't thought of. I will check > them out. Thanks. > > . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 14, 2004 Report Share Posted January 14, 2004 ... Would you mind telling us what your vision challenge is? Total blindness, partial? is it independent of thyroid or possibly linked? I'm legally blind in one eye, a genetic defect that my father also has... During an car accident I ruptured a blood vessel in my good eye. In order to make sure that it healed correctly I was given drops that would knock that eye out completely so that I could not see. The idea being that if I could not see out of it I would be more likely to rest it.... It worked, the eye healed perfectly... BUT for a bit over a week I was blind, running into walls... unable to see much more the vague shapes and light and dark out of the bad eye.... I had a taste of a place that I would never like to stay... but also gained a respect for what it's like to not be able to do things that everyone else takes for granted...... If I'm being too nosey... I apologize... I'm just a curious person. Topper () On Wed, 14 Jan 2004 20:50:49 +1000 (EST) Tink writes: > Vitamins! Now there's something I hadn't thought of. I will check > them out. Thanks. > > . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 15, 2004 Report Share Posted January 15, 2004 I would hate for you, or anyone else reading this, to think that your experience of not being able to see well for a week is even remotely like my experience of being Blind. , This post was very thought provoking. I had eye surgery from the Graves disease. Orbital decompression. Anyway, for over 2 years, I lost my ability to read, drive, think straight, etc. I was miserable. I had diplopia of 10. It is now 3. Thank God. None of the doctors said it would improve. Some people have more surgery, often not successful. I often wonder if this neuropathy stuff is more related to my eyes not in the sockets straight than the hypo-thyroid. Non the less, you are so correct. I will concentrate on Gratitude for what I can see, and not the downside. I have thought about total blindness and what it would be like, but it would still be a totally different experience than yours. I pray that you can resolve your hypo, that would lighten your load. Frannie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 15, 2004 Report Share Posted January 15, 2004 > I have thought about total blindness and what it would be like, but it > would still be a totally different experience than yours. Definitely. My understanding is that, as a general rule, acquiring Blindness is much harder than being born with it. My guess is that that goes for any disability or condition. > I pray that > you can resolve your hypo, that would lighten your load. That's really sweet of you. Thanks. Yep, I feel like my hypo has made things much more difficult for me than my Blindness ever has or will. . -- Tink: atink@... I'm not an angry girl, but it seems like I've got everyone fooled, everytime I say something they find hard to hear, they chalk it up to my anger and never to their own fear (Ani DiFranco) *Consider all www users: use, support and create text-friendly sites!* Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 15, 2004 Report Share Posted January 15, 2004 Hi, , I have somewhat of an idea of what you are expressing, but " not quite " , if you know what I mean. I was born " vision impaired " . I wore terribly thick lenses in my glasses from three years of age, yet I still could not see well enough to cross a street, go down stairs unassisted, etc. I had no depth perception whatsoever, so I was always bumping into things. At home, I could almost always be found under the dining room table -- it was safe there. I could not bump into things and there were no weird shapes to deceive me into thinking that they were people or objects. I was born in 1946 and in 1997, it was determined that I had acquired cataracts that needed to be removed. Both eyes were to be done, but my " good " eye was done one week ahead of the " bad " eye. Rather than create a situation requiring even heavier lenses, my surgeons opted to use lens implants and I now have two implants in each eye and wear really thin glasses as well. I always had thought that trees looked sort of like green lollipops -- rounded and irregular, but rounded. My first sight of a tree shocked me and it was just outside of the hospital where my first surgical procedure was done. Wow! The result has been more freedom, but it has a price. At first I was so distracted by how well I could see things that I could not drive the car. I had been driving with those thick lenses before, so I did know how and I was licensed. I gave up driving for about five months unless I absolutely had to go someplace important and my husband could not drive me there. Having Attention Deficit Disorder does not help the distractibility situation either, but things have improved. I know that our situations do not compare, but I can appreciate the " difference " . Dianne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 15, 2004 Report Share Posted January 15, 2004 Hi, , I have somewhat of an idea of what you are expressing, but " not quite " , if you know what I mean. I was born " vision impaired " . I wore terribly thick lenses in my glasses from three years of age, yet I still could not see well enough to cross a street, go down stairs unassisted, etc. I had no depth perception whatsoever, so I was always bumping into things. At home, I could almost always be found under the dining room table -- it was safe there. I could not bump into things and there were no weird shapes to deceive me into thinking that they were people or objects. I was born in 1946 and in 1997, it was determined that I had acquired cataracts that needed to be removed. Both eyes were to be done, but my " good " eye was done one week ahead of the " bad " eye. Rather than create a situation requiring even heavier lenses, my surgeons opted to use lens implants and I now have two implants in each eye and wear really thin glasses as well. I always had thought that trees looked sort of like green lollipops -- rounded and irregular, but rounded. My first sight of a tree shocked me and it was just outside of the hospital where my first surgical procedure was done. Wow! The result has been more freedom, but it has a price. At first I was so distracted by how well I could see things that I could not drive the car. I had been driving with those thick lenses before, so I did know how and I was licensed. I gave up driving for about five months unless I absolutely had to go someplace important and my husband could not drive me there. Having Attention Deficit Disorder does not help the distractibility situation either, but things have improved. I know that our situations do not compare, but I can appreciate the " difference " . Dianne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 15, 2004 Report Share Posted January 15, 2004 Hi, , I have somewhat of an idea of what you are expressing, but " not quite " , if you know what I mean. I was born " vision impaired " . I wore terribly thick lenses in my glasses from three years of age, yet I still could not see well enough to cross a street, go down stairs unassisted, etc. I had no depth perception whatsoever, so I was always bumping into things. At home, I could almost always be found under the dining room table -- it was safe there. I could not bump into things and there were no weird shapes to deceive me into thinking that they were people or objects. I was born in 1946 and in 1997, it was determined that I had acquired cataracts that needed to be removed. Both eyes were to be done, but my " good " eye was done one week ahead of the " bad " eye. Rather than create a situation requiring even heavier lenses, my surgeons opted to use lens implants and I now have two implants in each eye and wear really thin glasses as well. I always had thought that trees looked sort of like green lollipops -- rounded and irregular, but rounded. My first sight of a tree shocked me and it was just outside of the hospital where my first surgical procedure was done. Wow! The result has been more freedom, but it has a price. At first I was so distracted by how well I could see things that I could not drive the car. I had been driving with those thick lenses before, so I did know how and I was licensed. I gave up driving for about five months unless I absolutely had to go someplace important and my husband could not drive me there. Having Attention Deficit Disorder does not help the distractibility situation either, but things have improved. I know that our situations do not compare, but I can appreciate the " difference " . Dianne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 15, 2004 Report Share Posted January 15, 2004 >I always had thought that trees looked sort of like green >lollipops -- rounded and irregular, but rounded. My first sight >of a tree shocked me and it was just outside of the hospital where >my first surgical procedure was done. Wow! This just happened in 1997?? Wow, what a great story!!! I'm REALLY happy for you. Was it the cataract that was causing the near blindness all those years?? Why didn't they figure this out before 1997?? Janie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 27, 2004 Report Share Posted January 27, 2004 Hi, Janie! My eyes were deformed at birth. I was extremely near sighted and my corneas were such a mess that the astigmatism caused as much trouble as not being able to see things in the size they would appear to others. My glasses from the start of wearing them were extremely thick lenses -- enough to put a " permanent " dent on both sides of my nose. The cataracts were present at birth, but didn't seem to be having any effect on what I could see. Actually, as my doctors explained it, my vision was already so bad that there was no way to know exactly what was causing the problems. The only way to " fix " things didn't become available until lens implants because the preferred method for preventing extreme vision loss following cataract surgery. It is the lens within the eye that becomes clouded by cataracts. Before implants, a person with otherwise perfect vision would have " low vision " until it was corrected with glasses. You can imagine the problems for those who already had " low vision " . The necessity for putting implants in both of my eyes stemmed from the fact that correcting only the " bad " eye would have caused problems because the good eye would have had bigger problems working with the rest of my senses to maintain balance, etc. In other words, my vision would have been too distorted to help and would legally have caused the situation to deteriorate to the point of " legal blindness " , which the SSA (Social Security Administration) did not want to allow because they would have had to increase my disability payments. Medicare and SSA discussed the situation and determined that it would benefit both of them and be a better solution for me to have the implants done on both eyes and complete any remaining vision corrections with glasses and/or contact lenses. The lenses in my glasses are so " skinny " that I do not feel them on my face. Even better, the " dents " that had been caused by years of wearing heavy lenses in cumbersome frames have begun to go away! Yee Haw! I also had Ptosis as a result of a frontal head injury, so two more procedures were performed to lift the eye lids. It was sort of like having a face lift. The tissue around my eyes turned black and blue for awhile, but the results have been great. My vision before surgery was L- 20/100 corrected, and R-100/200 corrected. After all of the surgeries were done, it was L 20/40 corrected and R 20/80 corrected. Believe it or not, I was driving a car with the old corrections. When I got my new glasses, driving a car was almost a new learning experience. It has been an amazing journey. I am more than thrilled with the results. Dianne At 05:28 AM 1/16/04 +0000, you wrote: >This just happened in 1997?? Wow, what a great story!!! I'm REALLY >happy for you. Was it the cataract that was causing the near >blindness all those years?? Why didn't they figure this out before >1997?? > >Janie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 27, 2004 Report Share Posted January 27, 2004 Dianne, very inspiring story. Glad you shared it. Janie > My eyes were deformed at birth. I was extremely near sighted and > my corneas were such a mess that the astigmatism caused as much trouble as > not being able to see things in the size they would appear to others. My > glasses from the start of wearing them were extremely thick lenses - - > enough to put a " permanent " dent on both sides of my nose. Quote Link to comment Share on other sites More sharing options...
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