Guest guest Posted September 14, 2001 Report Share Posted September 14, 2001 Hello, I was wondering if any parents have children who are taking or have taken Effexor? If so, could you please post. Thank you so much, Heidi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 20, 2004 Report Share Posted September 20, 2004 Wendi, That is why went to the counsilor to begin with. The anxiety was getting so bad it was hard to function. The dosage I take is a rather low dose. The typical dose is about 40 MG per day and I take 20, or sometimes 10. Very often I will take 20 one day and skip the next. It usually takes about that long to start feeling the meds wearing off. I don't particularly like taking medicine, but it beats the anxiety. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 20, 2004 Report Share Posted September 20, 2004 I think there are a number of ways you can go on this. Certainly getting a DX will help because it will better enable you to get the treatment that you need and the treatment that will actually work for you. My question is, what treatment would work for you the best? Meds may work, but they are more or less a quick fix. A more long- term approach might be to develop some coping strategies that will help you deal with AS and life's issues. I suspect some of this may have to do with three kids running in three separate directions 24/7 and you having difficulty coping? Each new day will bring new challenges. So the question becomes, how ill you deal with them? More meds, or a different perspective and reliable behavioral approach? I think getting a DX would be a good point of departure, but I'd caution you not to jump to the meds too quickly without first examining if there is anything else you could be doing behaior wise to help yourself deal with the accumulating pressures. But then, since I don;t live your life, maybe I don't have enough of a grasp of the situation to provide an informed opinion about what ought to be done. Tom > The reason I'm going for a dx (if I can get up the nerve to actually mail back these forms now) is because of the anxiety and possible medication. I have found through research that people with any type of autism need to take very, very low doses of these meds. Sometimes an anti-anxiety med might be *causing* more anxiety simply because the dosage is too high. I know adults who do well on a child's dosage. > > Even knowing this, I feel frightened about going on to meds. I'm glad to be going to a psychologist first. I am very sensitive to most drugs and react badly to many, even antibiotics. But my anxiety is getting out of control - (getting? more like 'has been') and I'm having more and more meltdowns lately... and this has just got to be affecting my family! > > Wendi > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2004 Report Share Posted September 22, 2004 There was an article published recently that said there may be a physiological reason for depression. It has been found that many people who suffer from chronic depression have more nerves in a part of the brain than other people. I think this was the amygdilla (spelling) part of the brain. Oddly enough I can see the region anatomically but can't think of the name. Anyway, they have more nerves by as much as a third. This probably also applies to other conditions like anxiety. I think this is so because no matter what coping methods I try, the anxiety doesn't go away. The only thing that really works is the medication. Of course, its not bad all the time, just when a major stressor comes along. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2004 Report Share Posted September 22, 2004 Yes, I agree Tom. My GP wanted to put me on meds a while ago (and I didn’t even tell her anything!), and I refused because of what I said the other day. Doctors look at me and see a woman with 4 yr old triplets with autism and think STRESS and think that is the only cause, but I know differently. I’m not going to act like some saint and say my kids are not a cause of stress, either! But they are not the only cause of my anxiety. I had major problems before the kids came along (which I thought were ‘normal’ but everyone else did a better job of dealing with) and they just don’t see that. Why? I can’t tell them. Sometimes I want to, but the words won’t come out. So... that’s why I feel a dx is important. If anyone is going to help me, they need to know what they are treating! I said I’m glad I’m going to a psychologist – and that is because psychologists cannot prescribe meds. I don’t believe meds are the first solution. I don’t know what is, but I want to try other things first. Plus, my husband is very against me taking them since his friend’s wife went on anti-anxiety meds and tried to kill herself – off them she is not suicidal... he’s afraid I may get like that too. I don’t have time to experiment either! What if I take something and feel all drugged up? I react very strongly to meds, I was sedated a couple of times and the ‘normal’ dosage “just to relax you a bit” was way too much for me – I was out cold and the doctors were terrified because they couldn’t wake me up! (Ever wake up in an operating room with 10 doctors and nurses rushing around like maniacs, most of who were NOT there when you went to sleep, some of them screaming your name, with a look of complete terror on the anesthesiologist’s face? It happened at the dentist once too, with ‘sweet air’.) If that happens, how will I be able to function? What happens to the kids? I have help once in a while from relatives, but not all the time and I need to let them know in advance if I have an appt and need them to watch the kids. They live too far away to come over here without notice. I won’t even take migraine medication because I’m afraid I may not be able to function. There is nobody else to take care of my kids! Granted I’m not functioning very well with a migraine either, but at least I know I can function minimally. The coffee hasn’t kicked in yet, I hope I am making sense! Wendi Re: Medication I think there are a number of ways you can go on this. Certainly getting a DX will help because it will better enable you to get the treatment that you need and the treatment that will actually work for you. My question is, what treatment would work for you the best? Meds may work, but they are more or less a quick fix. A more long- term approach might be to develop some coping strategies that will help you deal with AS and life's issues. I suspect some of this may have to do with three kids running in three separate directions 24/7 and you having difficulty coping? Each new day will bring new challenges. So the question becomes, how ill you deal with them? More meds, or a different perspective and reliable behavioral approach? I think getting a DX would be a good point of departure, but I'd caution you not to jump to the meds too quickly without first examining if there is anything else you could be doing behaior wise to help yourself deal with the accumulating pressures. But then, since I don;t live your life, maybe I don't have enough of a grasp of the situation to provide an informed opinion about what ought to be done. Tom > The reason I'm going for a dx (if I can get up the nerve to actually mail back these forms now) is because of the anxiety and possible medication. I have found through research that people with any type of autism need to take very, very low doses of these meds. Sometimes an anti-anxiety med might be *causing* more anxiety simply because the dosage is too high. I know adults who do well on a child's dosage. > > Even knowing this, I feel frightened about going on to meds. I'm glad to be going to a psychologist first. I am very sensitive to most drugs and react badly to many, even antibiotics. But my anxiety is getting out of control - (getting? more like 'has been') and I'm having more and more meltdowns lately... and this has just got to be affecting my family! > > Wendi > FAM Secret Society is a community based on respect, friendship, support and acceptance. Everyone is valued. Always remember that. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2004 Report Share Posted September 22, 2004 , I can't say I've read the article, but if it's legitimate, it would certainly explain a lot about why it is AS people suffer anxiety. How many of us have spoken on this and other boards about super- sensitivity to light, touch, taste, smell, hearing, etc.? Obviously our sensitivities could be due either to a different construction of the nerve cells, or a proliferation of the cells themselves. I have read that folks on the autism spectrum have bigger (not necessarily better) brains than those not on the spectrum. Why our brains would be bigger is something I won't speculate on. But size- wise at least we are different. I think depression would come easier for AS people anyway simply because (aside from the annoyances many of us feel due to heightened senses) every moment that we interact among the NT world we must realize on some level that we do not entirely fit in, and we must also realize that the world that they have created for themselves and continue to control is not ideal for us. I do believe that if we lived in ideal environments and societies that had been created by Aspergians for Aspergians, the depression many of us experience would be reduced if not eliminated entirely, the idea being that though we have phisiological differences, the lifestyles we'd live and the habitations we'd live in would be built and suited to accomodate those differences, and so the stress normally associated with the NT world would be non-existent, and thus no longer and influential factor in our phisiological mindsets. But until that time, or until those things take place, we PERHAPS must unfortunately resign ourselves to the fact that medication MIGHT have to play a role in our lives indefinitely. Tom > There was an article published recently that said there may be a physiological reason for depression. It has been found that many people who suffer from chronic depression have more nerves in a part of the brain than other people. >I think this was the amygdilla (spelling) part of the brain. Oddly enough I can see the region anatomically but can't think of the name. Anyway, they have more nerves by as much as a third. This probably also applies to other conditions like anxiety. I think this is so because no matter what coping methods I try, the anxiety doesn't go away. The only thing that really works is the medication. Of course, its not bad all the time, just when a major stressor comes along. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2004 Report Share Posted September 22, 2004 “How many of us have spoken on this and other boards about super- sensitivity to light, touch, taste, smell, hearing, etc.? Obviously our sensitivities could be due either to a different construction of the nerve cells, or a proliferation of the cells themselves. ”I have read that folks on the autism spectrum have bigger (not necessarily better) brains than those not on the spectrum. Why our brains would be bigger is something I won't speculate on. But size- wise at least we are different.” Tom and I believe what Tom is saying above is related to the theory (and I am paraphrasing badly) that the brain makes more connections than it should...the brain is supposed to ‘learn’ which connections to use and then the unused connections dye off, but in brains of people with autism, all the connections are being used (=larger brain). If I can find the article I read recently, I will post it. They are also finding this in people with sensory processing disorder (SPD - used to be called sensory integration dysfunction) – which explains all the hyper- and hypo-sensitivities people on the autism spectrum have. Consider a light touch activating many nerve pathways in the brain instead of just one like people without SPD have happen. Motor planning issues have been explained by this as well, stating the possibility that the brain is using the ‘wrong’ pathways to retrieve motor plans so the person can’t do things he has already learned. SPD researchers have been theorizing this long before they found it in MRI studies. Some people with autism hear words, but at times they have no meaning. Auditory input going through the wrong pathways? It doesn’t surprise me one bit about them finding this so with anxiety and depression as well. Same stimuli as a person without the extra connections, different internal reaction due to more connections firing! Oh dear, I feel a research obsession coming on... now it is later and I’m really hooked... if you don’t see me for a couple of days, that’s where I’ll be logging my internet time! I’ll let you know what I find out! Aside: Why do these things hit me just before I’m needed elsewhere? It is so frustrating! I have to go get my daughter (who goes to preschool half-days) off the bus now. All I can hope for is my daughter wanting to nap after lunch so I can indulge myself a little before the other 2 get home (insert anxious giggle here). Wendi Re: Medication , I can't say I've read the article, but if it's legitimate, it would certainly explain a lot about why it is AS people suffer anxiety. How many of us have spoken on this and other boards about super- sensitivity to light, touch, taste, smell, hearing, etc.? Obviously our sensitivities could be due either to a different construction of the nerve cells, or a proliferation of the cells themselves. I have read that folks on the autism spectrum have bigger (not necessarily better) brains than those not on the spectrum. Why our brains would be bigger is something I won't speculate on. But size- wise at least we are different. I think depression would come easier for AS people anyway simply because (aside from the annoyances many of us feel due to heightened senses) every moment that we interact among the NT world we must realize on some level that we do not entirely fit in, and we must also realize that the world that they have created for themselves and continue to control is not ideal for us. I do believe that if we lived in ideal environments and societies that had been created by Aspergians for Aspergians, the depression many of us experience would be reduced if not eliminated entirely, the idea being that though we have phisiological differences, the lifestyles we'd live and the habitations we'd live in would be built and suited to accomodate those differences, and so the stress normally associated with the NT world would be non-existent, and thus no longer and influential factor in our phisiological mindsets. But until that time, or until those things take place, we PERHAPS must unfortunately resign ourselves to the fact that medication MIGHT have to play a role in our lives indefinitely. Tom > There was an article published recently that said there may be a physiological reason for depression. It has been found that many people who suffer from chronic depression have more nerves in a part of the brain than other people. >I think this was the amygdilla (spelling) part of the brain. Oddly enough I can see the region anatomically but can't think of the name. Anyway, they have more nerves by as much as a third. This probably also applies to other conditions like anxiety. I think this is so because no matter what coping methods I try, the anxiety doesn't go away. The only thing that really works is the medication. Of course, its not bad all the time, just when a major stressor comes along. > > FAM Secret Society is a community based on respect, friendship, support and acceptance. Everyone is valued. Always remember that. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2004 Report Share Posted September 22, 2004 Sorry, I meant “die off” opps -----Original Message----- From: Wendi unused connections dye off Quote Link to comment Share on other sites More sharing options...
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