Now, this post will be somewhat different from what I write usually. This time I will write about something many anosmics may struggle with especially in their early years, but this also concern so many others. It effects so many people worldwide and on some people, make a huge impact on their life. You can find it at schools, work and almost wherever you look. I'm talking about bullying.
Even as early as kindergarden, some kids get picked on. Some for no reason, and some for being different. And it is these kids, who gets picked on as early as in kindergarden, who keeps getting picked on when they start school. For some, it even keeps on going, to after school, work and even just by going outside. Some bullies go to so big lengths to make another person's life miserable. You can sometimes read about it in the newspaper, or hear it on the news. About kids who strike back at the bullies, and often gets their life even more ruined. Kids who commit suicide because of the bullies. This is how big of an impact bullying have on people. Of course, the stories you read about and hear on the news, is just a few of many. So many people struggle with their life, because there are people in it, who make it difficult. Now, as often as we hear these stories, we hear about solutions that the politicians and schools are enforcing. But the reality is, they can't stop it. There have always been bullies, and there will always be bullies! We just have to get better to take the bullies, and make them stop. Make them realize how much they are damaging the life of the one they are picking on. Now, very often people get picked on because they are different. So when you have an disorder like anosmia, bullies love that. If someone with anosmia, is willing to be open about their disorder and tell people what it is, very often there are people who will take advantage of it, and pick on that person.
I know this all to well. I have been struggling with bullies for 10 years. The 10 first years of my education, was years i spent, being bullied. Now, I am not saying I only was being bullied because of my anosmia. I know that is not true, because the first years, I didn't even know I had anosmia. Perhaps I was a strange little kid. Maybe I couldn't handle to be picked on very well. But why should that matter?! Why should a person be picked on, because they aren't like everybody else, in interest or other things? I think we should do more, to help the bullies, then the people who are being bullied! Not help them to bully others, but to help them fix their cause of having to bully others. Many people like to pick on others, to make themselves feel better. If they get help with themselves, maybe they don't have the need to make others feel miserable.
Now, living a bullied life can be difficult. I have first hand experience at that. When you grow up, being told you are no good, and whatever you try to do, someone is there to ruin it, you start struggling with low self-esteem. As far back as I can remember, I have had huge problems with my self-esteem. I couldn't raise my hand in class. I couldn't have lectures in front of the class, and much more. I am not trying to make my life sound so much worse then any others, but my point is that so many people struggle with these things. Bullying ruins life's!
Now, as I said, some people even commit suicide because of this. And also here, I have some experience. It's not something I am proud of, and not something I write about with ease, but I want you to know how much bullying can effect someone's life. I have struggled with suicide thoughts in the past. I have been dangerously close to ending my life. All this, because of the bullies in my life. Just that a handful of people, picking on a person and basically tormenting them, can destroy a persons will to live.
Today my story has changed, I no longer fight with those kind of thoughts and my life is better then ever. I am even so-what tankful for the hard times I have had, because that has thought me the value of true friends. I have now many friends and I don't get picked on anymore. I have got better self-esteem and now almost all my problems are gone. But it's not like this for everyone who struggle with bullies.
No one should have to endure this!
It has to stop!
- Marius
lørdag 21. januar 2012
søndag 15. januar 2012
Doctors... Those lovely doctors
Now, since anosmia is not a very usual disorder, the knowledge of doctors on the subject, reflects that. I have been back and fourth between some doctors for some years now. I have had two CT-scans and some other test. But just to get there, was a pain in the a** some times. I'm not sure how it is in other countries, but in Norway, anosmia is very unknown. My doctor once told me, that I am the sort of patient a doctor only gets once in a career. Which not actually helped my feeling of being alone. But that is how all the doctors I have met is, almost. Just by searching the internet for a few hours, I managed to find out some information, and my doctor didn't even know that! I had written down a few points on my phone, and basically sat at the doctors office and learned my own doctor about anosmia. At that point, I didn't have much information myself, but still. I think it's hopeless, that we go to doctors for help with sickness and disorders, and you can find more out yourself with a google search.
The second time I was at a specialist for ear, nose and throat, the first thing he said to me was. There's nothing I can do. There is nothing to do with this. He didn't even look at my file. He didn't ask me anything. I don't think he even said "hello" to me. He just blew me of and destroyed the last bit of hope I had built up since my last visit to the doctor. But in the time that has passed, I have accepted the fact, that I will never be able to smell. That is just how it is, and there is no point for me to be angry for it. If I at an age 17 start to get angry over that fact, I will grow up to be and angry and bitter man, and that's just pointless. But I think that the medical community have much to learn and to change.
You can sometimes read in the newspaper about a football club who bought a player for many millions of dollars. And still, there are many diseases and disorders who don't get the founding they need. I understand that there is an entertainment value and much money in sports, but why can't they at least put some of the money in to medical research instead. A single man is bought to a football club over 100 million dollars. And the medical research needs money. I don't see the logic in that. All the money used in football and other big sports. While 2% of the worlds population, lives with anosmia. That is approximately 140 million people worldwide. Maybe not a big number since we have crossed 7 billion people worldwide, but still a big number. Now the 2% that live with anosmia, is both congenital and acquired anosmics. If I am to consider the number for congenital anosmics, the number is even lower. Approximately 700 000 people are born without a sense of smell. There are cities much bigger than that. But just because there are few of us, I mean, we have the right to the same medical possibilities and offers as anybody else. I mean that we deserve, that research in anosmia receives founding. When people get anosmia, it can be the early sign of Parkinson's disease or Alzheimer's disease. So if there is done more research on anosmia, maybe we can get a better understanding on these diseases, which effect many people. Is there one thing I have learned while trying to find information about anosmia and things around this disorder, is that when it comes to medical research, the investors only put money, where they think they can make money. I understand that. There is not many people who will use huge sums of money to research something so little percentage have. But this is where I believe that governments or other funds or something should step in. Maybe there is not that much money to be made, but it may improve the life quality of the people who have anosmia. And isn't that what medical research, hospitals, doctors and medicine is all about? Not making money, but to help improving peoples life.
Now, as I mentioned, I have been back and fourth between some doctors and the hospital over the years. But I haven't got anywhere. A part of that, I think is because I live in Norway, a little country. Our medical technology is quite good here, but there is not many places for disorders like anosmia. I haven't found any. Not that I have tried so hard. I have been to my doctor many times, some of them by my own request. As I learn new things about anosmia, I go to my doctor and discuss them with him. I have been to a specialist two times, but the first was only to check for polyps, which can be a reason for anosmia, and the other was just to check my options. I have had two CT-scans, and I am not entirely sure what they were looking for. But all in all, I have got just as much information from that, as I have from the internet by searching on my own. One of my dreams, is to go to the US and find a research facility or a specialist who may know more then the doctors here in Norway. I want to try to help out with what I can. I will gladly take part in experimental treatments and so much more. Cause as I figure it, what have I got to lose? My sense of smell? I hope, that when I get a little older, I will make a difference in the anosmic world. I hope that there will someday be, maybe not a cure, but at least a treatment who can help the acquired anosmics. People like me, is a different case.
I was born without the nerves in my olfactory system. So the signals from my nose, can't get to my brain. There is no way to treat that. They can't make my nerves grow inside my nose. But maybe there will someday be a treatment who can help unborn children, who are still developing, get the nerves grown, from medical technology. If a fetus is about to become a child with anosmia, maybe a treatment will help the child grow what it needs. It is sort is a help to mother nature.
Might sound like a silly dream, but we are all allowed to have our own dreams! But I hope there will someday be more available information about anosmia. More trained doctors on the subject and more treatments.
We all have dreams.
Mine is to help anosmics as best I can!
- Marius
The second time I was at a specialist for ear, nose and throat, the first thing he said to me was. There's nothing I can do. There is nothing to do with this. He didn't even look at my file. He didn't ask me anything. I don't think he even said "hello" to me. He just blew me of and destroyed the last bit of hope I had built up since my last visit to the doctor. But in the time that has passed, I have accepted the fact, that I will never be able to smell. That is just how it is, and there is no point for me to be angry for it. If I at an age 17 start to get angry over that fact, I will grow up to be and angry and bitter man, and that's just pointless. But I think that the medical community have much to learn and to change.
You can sometimes read in the newspaper about a football club who bought a player for many millions of dollars. And still, there are many diseases and disorders who don't get the founding they need. I understand that there is an entertainment value and much money in sports, but why can't they at least put some of the money in to medical research instead. A single man is bought to a football club over 100 million dollars. And the medical research needs money. I don't see the logic in that. All the money used in football and other big sports. While 2% of the worlds population, lives with anosmia. That is approximately 140 million people worldwide. Maybe not a big number since we have crossed 7 billion people worldwide, but still a big number. Now the 2% that live with anosmia, is both congenital and acquired anosmics. If I am to consider the number for congenital anosmics, the number is even lower. Approximately 700 000 people are born without a sense of smell. There are cities much bigger than that. But just because there are few of us, I mean, we have the right to the same medical possibilities and offers as anybody else. I mean that we deserve, that research in anosmia receives founding. When people get anosmia, it can be the early sign of Parkinson's disease or Alzheimer's disease. So if there is done more research on anosmia, maybe we can get a better understanding on these diseases, which effect many people. Is there one thing I have learned while trying to find information about anosmia and things around this disorder, is that when it comes to medical research, the investors only put money, where they think they can make money. I understand that. There is not many people who will use huge sums of money to research something so little percentage have. But this is where I believe that governments or other funds or something should step in. Maybe there is not that much money to be made, but it may improve the life quality of the people who have anosmia. And isn't that what medical research, hospitals, doctors and medicine is all about? Not making money, but to help improving peoples life.
Now, as I mentioned, I have been back and fourth between some doctors and the hospital over the years. But I haven't got anywhere. A part of that, I think is because I live in Norway, a little country. Our medical technology is quite good here, but there is not many places for disorders like anosmia. I haven't found any. Not that I have tried so hard. I have been to my doctor many times, some of them by my own request. As I learn new things about anosmia, I go to my doctor and discuss them with him. I have been to a specialist two times, but the first was only to check for polyps, which can be a reason for anosmia, and the other was just to check my options. I have had two CT-scans, and I am not entirely sure what they were looking for. But all in all, I have got just as much information from that, as I have from the internet by searching on my own. One of my dreams, is to go to the US and find a research facility or a specialist who may know more then the doctors here in Norway. I want to try to help out with what I can. I will gladly take part in experimental treatments and so much more. Cause as I figure it, what have I got to lose? My sense of smell? I hope, that when I get a little older, I will make a difference in the anosmic world. I hope that there will someday be, maybe not a cure, but at least a treatment who can help the acquired anosmics. People like me, is a different case.
I was born without the nerves in my olfactory system. So the signals from my nose, can't get to my brain. There is no way to treat that. They can't make my nerves grow inside my nose. But maybe there will someday be a treatment who can help unborn children, who are still developing, get the nerves grown, from medical technology. If a fetus is about to become a child with anosmia, maybe a treatment will help the child grow what it needs. It is sort is a help to mother nature.
Might sound like a silly dream, but we are all allowed to have our own dreams! But I hope there will someday be more available information about anosmia. More trained doctors on the subject and more treatments.
We all have dreams.
Mine is to help anosmics as best I can!
- Marius
torsdag 12. januar 2012
Anosmia Awareness Day
A little while back, while I was searching the web for information about anosmia, I found this page on Facebook. Its called Anosmia Awareness Day. It's it the 23. February this year, and the the goal is to raise awareness about anosmia. The same thing I wish to achieve with this blog. There is over 1000 people invited to this event, but only 189 people are attending. I think this is so sad. I am glad there are non-anosmics out there who supports us, but there are some who are just plain cruel. Like this one girl, she posted on the event "What the heck is amosmia its not even. Real word??", How can a person write this, when the explanation about what anosmia is, is written in the description of the event? But, back to the point. The event is created by Daniel Schein. In my opinion, a great person! He tries to make the global knowledge and awareness about anosmia greater. The hope is that as many people as possible will wear red on the 23. February 2012. One of the hopes is to get some media attention, to get information and just the name anosmia out to people. So please, support this event. Wear red on the 23. February. Here is a link to the event, if you want to participate: http://www.facebook.com/events/225528220844596/
As I have written here before, I am a part of two online communities for people with anosmia. The first one I found was a group for us with congenital anosmia. Which means we are born with the disorder. The group was made by Kathryn Snyder LaFleur. A person who I owe a lot of thanks. Because of this woman, I found a place to talk to people in my own situation. Before I found this group, I was alone as an anosmic, in my head. I had never heard of anyone in the same situation as me. The doctors I have talked with over the years, knows less then I do about anosmia. They had never had a patient like me. So as far as I knew, I was alone. After 16 years alone, here it was. Now I don't mean that I was alone in life, but I had always had a slight feeling of being alone, since everybody else around me could smell. A group with others like me. When I joined the group, we were just over 100 people, now we are 122. So we are few, but thats the thing about congenital anosmia. There is not many of us. When I found the group, I struck down with tears, not my proudest moment perhaps, but the feeling of not being alone anymore, was overwhelming. All the people on the group have helped me to live with my anosmia. Just to know that there are more like me and to be able to discuss so many things with these people. It have made such a strong impact on my life. We discuss problems and experiences, thoughts and hopes. We give each other help with questions and, to me, are like a family. Even though we are spread across the world, I know some people have met up, had lunch and become friends. I sadly don't have this possibility, because I live in Norway, and I haven't found any other people with congenital anosmia here. I am pretty sure there are some here, but i can't find them. But I can not put in to words how glad I am I found this group. It has opened a whole new world for me.
Some months later, I found another group. The group is called "Anosmics of the world, unite!" and was created by Peter Lembcke. Another person who I owe thanks. This group has 693 members. That is almost 700 people with the same disorder as me. And since this is a group for people with acquired anosmia and congenital anosmics, there is a much bigger variety of people. But the feeling is the same. We discuss experiences and so much more. The only thing that is different, is that some of the people in the group talk about "phantom" smell. That is when all you smell all the time is things like smoke and burnt grass. It is your brain trying to work around the anosmia or something, I am not quite sure how it works. This is something that only effects acquired anosmics. I read about people who lost their smell for 2 years, but then it gradually started to come back, I read about people who miss certain smells, and I read about how people got anosmia. But all in all, we are all the same. We are the little percent of the population, who experience the world, scentless.
Now, for the final person I will mention in this post. Michelle Krell Kydd. She has a blog, http://glasspetalsmoke.blogspot.com/, where she sometimes write about anosmia. She has helped me so much with what she has written, to understand my condition more, and to accept it more. She is posting new articles and information all the time and really helping out the community in my opinion. She really fights for our cause.
Now as the final thing in this post. I want to thank all of the people who are taking the time to read my blog. I have got a lot of good response, both from friends, and people I don't know. It mean incredibly much to me, that people are willing to read what I am writing. Cause that means that people are learning about Anosmia! I have got questions from people who have known me for years, but didn't know of my anosmia. People in my class and people around me tell me that they read what I write. That makes me without words. The only thing I can think of writing is, thank you. It means so much to me, and I hope it also makes a difference to the anosmic community. We are here, and in my opinion, we have the same voice as every one else. So if you get the chance, listen, you might learn something or think of something you didn't think of before.
But, once again. Thank you all for reading this blog. Over 270 people have read this. And when I made it, I was hoping for maybe 50 people in total. But I also hope you take in, what you are reading. I hope you might learn something and maybe see things a little different perhaps. And remember, Anosmia awareness day, 23. February. Try to wear red and inform anyone who will listen, about anosmia.
- Marius
As I have written here before, I am a part of two online communities for people with anosmia. The first one I found was a group for us with congenital anosmia. Which means we are born with the disorder. The group was made by Kathryn Snyder LaFleur. A person who I owe a lot of thanks. Because of this woman, I found a place to talk to people in my own situation. Before I found this group, I was alone as an anosmic, in my head. I had never heard of anyone in the same situation as me. The doctors I have talked with over the years, knows less then I do about anosmia. They had never had a patient like me. So as far as I knew, I was alone. After 16 years alone, here it was. Now I don't mean that I was alone in life, but I had always had a slight feeling of being alone, since everybody else around me could smell. A group with others like me. When I joined the group, we were just over 100 people, now we are 122. So we are few, but thats the thing about congenital anosmia. There is not many of us. When I found the group, I struck down with tears, not my proudest moment perhaps, but the feeling of not being alone anymore, was overwhelming. All the people on the group have helped me to live with my anosmia. Just to know that there are more like me and to be able to discuss so many things with these people. It have made such a strong impact on my life. We discuss problems and experiences, thoughts and hopes. We give each other help with questions and, to me, are like a family. Even though we are spread across the world, I know some people have met up, had lunch and become friends. I sadly don't have this possibility, because I live in Norway, and I haven't found any other people with congenital anosmia here. I am pretty sure there are some here, but i can't find them. But I can not put in to words how glad I am I found this group. It has opened a whole new world for me.
Some months later, I found another group. The group is called "Anosmics of the world, unite!" and was created by Peter Lembcke. Another person who I owe thanks. This group has 693 members. That is almost 700 people with the same disorder as me. And since this is a group for people with acquired anosmia and congenital anosmics, there is a much bigger variety of people. But the feeling is the same. We discuss experiences and so much more. The only thing that is different, is that some of the people in the group talk about "phantom" smell. That is when all you smell all the time is things like smoke and burnt grass. It is your brain trying to work around the anosmia or something, I am not quite sure how it works. This is something that only effects acquired anosmics. I read about people who lost their smell for 2 years, but then it gradually started to come back, I read about people who miss certain smells, and I read about how people got anosmia. But all in all, we are all the same. We are the little percent of the population, who experience the world, scentless.
Now, for the final person I will mention in this post. Michelle Krell Kydd. She has a blog, http://glasspetalsmoke.blogspot.com/, where she sometimes write about anosmia. She has helped me so much with what she has written, to understand my condition more, and to accept it more. She is posting new articles and information all the time and really helping out the community in my opinion. She really fights for our cause.
Now as the final thing in this post. I want to thank all of the people who are taking the time to read my blog. I have got a lot of good response, both from friends, and people I don't know. It mean incredibly much to me, that people are willing to read what I am writing. Cause that means that people are learning about Anosmia! I have got questions from people who have known me for years, but didn't know of my anosmia. People in my class and people around me tell me that they read what I write. That makes me without words. The only thing I can think of writing is, thank you. It means so much to me, and I hope it also makes a difference to the anosmic community. We are here, and in my opinion, we have the same voice as every one else. So if you get the chance, listen, you might learn something or think of something you didn't think of before.
But, once again. Thank you all for reading this blog. Over 270 people have read this. And when I made it, I was hoping for maybe 50 people in total. But I also hope you take in, what you are reading. I hope you might learn something and maybe see things a little different perhaps. And remember, Anosmia awareness day, 23. February. Try to wear red and inform anyone who will listen, about anosmia.
- Marius
mandag 9. januar 2012
It's hard
A thing I often hear when I tell people that i can't smell, is that is can't be that hard. But that is just the thing. It is hard, and it can be dangerous too. People are so good at taking there sense of smell for granted. It's like this invisible thing that you don't think much of, until it's not there anymore. Smell is such a big part of your day, but you give it suck little thought. It is almost like a spoiled little kid with much money, they don't think on all the hard work that has gone in to making that money. They don't understand how it is, until they start working themselves. That is how I feel it is for most people today, you never consider how lucky you are, being able to smell. Ever since i realized that i can't smell, there has not been a day, that i have not thought about my lack of smelling. I think about it every day, that I am anosmic, and that I will never smell a thing in my life. As I mentioned, it also can be dangerous. Smell is associated with danger in many cases. If you live alone, or are staying home alone, and there is a fire while you are sleeping, you are as good as dead. When you are anosmic, you are unable to smell the smoke filling the room while you are sleeping. You can imagine the result. Also if there is a gas leak. All gas used in homes and construction and stuff like that, is mixed with a smelling agent, so that you can smell when there is a leak. Just by forgetting to turn of the stove, anosmics are risking their life. We can't detect the gas, until it is to late. This are common dangers for anosmics, but there are also things that is not lethal, but highly irritating. We can't detect spoiled food. I have found myself eating molded bread more times than I can remember. I am good at checking dates on food and looking for mold, but I still make mistakes. Luckily, i have not tried to drink old milk yet, but I now some anosmics have. These are just some of the things that make living with anosmia difficult. So please, if you are about to tell an anosmic person that it can't be that bad, don't. This is a situation were I actually can say, you can't now how it is, until you are knee deep in it.
Now for a more personal story from me. Well, it's not a story, i guess. More of a realization that i don't like. Since I can't smell, I will never be able to tell my girlfriend/wife that she smells good. I can tell her, but it will be a complete lie. I don't now what smelling good means! If i lend my jacket to the girl I love, when I get it back, I can't smell it to remember her. Important people in my life, that pass away, i can't remember their smell. I've learned that one thing that many people remember about people that have passed away, is their smell. I can't do that. When I get kids, I won't be able to smell my kids, maybe a weird thought, but i've thought it. There is so many things to experience, much of it with someone else. And I am missing out. When I get old, I can't think of old memories, because a scent reminded me of an old memory.
Every time I step outside, I wonder if I smell. I am always insecure about being around people in case I smell, and no one tells me. My friends who know about my disorder, will tell me if I smell, because they know that is what I want. I want to be told if I smell bad, instead of walking around smelling like a trash dump. Same goes for my clothes, I have to be good at changing clothes, because i can't detect if my clothes smells bad. I can keep this going, but you get the point. All the "little" things you take for granted every day, bothers me, every day. It makes me almost scared of going outside amongst people. In my room, if there is a foul stench, I can't tell. There was one time, my dog pissed under a chair I had in my room. It wasn't until a month or so later, when I moved the chair, I could see the stain. These are things I struggle with every day. And you don't make it any easier by telling me my life is easy. You don't make it easier by stuffing my face with things that smells bad and treating my disorder like a circus act. I am glad to prove that i can't smell, but not of you just want to see because you think it is funny to watch me smell your gym socks or shoes. And I will prove it once. ONCE. You don't need me to show you several times that my nose is nothing more than a sort of hood ornament for my face.
Think of what you do and say!
- Marius
Now for a more personal story from me. Well, it's not a story, i guess. More of a realization that i don't like. Since I can't smell, I will never be able to tell my girlfriend/wife that she smells good. I can tell her, but it will be a complete lie. I don't now what smelling good means! If i lend my jacket to the girl I love, when I get it back, I can't smell it to remember her. Important people in my life, that pass away, i can't remember their smell. I've learned that one thing that many people remember about people that have passed away, is their smell. I can't do that. When I get kids, I won't be able to smell my kids, maybe a weird thought, but i've thought it. There is so many things to experience, much of it with someone else. And I am missing out. When I get old, I can't think of old memories, because a scent reminded me of an old memory.
Every time I step outside, I wonder if I smell. I am always insecure about being around people in case I smell, and no one tells me. My friends who know about my disorder, will tell me if I smell, because they know that is what I want. I want to be told if I smell bad, instead of walking around smelling like a trash dump. Same goes for my clothes, I have to be good at changing clothes, because i can't detect if my clothes smells bad. I can keep this going, but you get the point. All the "little" things you take for granted every day, bothers me, every day. It makes me almost scared of going outside amongst people. In my room, if there is a foul stench, I can't tell. There was one time, my dog pissed under a chair I had in my room. It wasn't until a month or so later, when I moved the chair, I could see the stain. These are things I struggle with every day. And you don't make it any easier by telling me my life is easy. You don't make it easier by stuffing my face with things that smells bad and treating my disorder like a circus act. I am glad to prove that i can't smell, but not of you just want to see because you think it is funny to watch me smell your gym socks or shoes. And I will prove it once. ONCE. You don't need me to show you several times that my nose is nothing more than a sort of hood ornament for my face.
Think of what you do and say!
- Marius
søndag 8. januar 2012
To make a few things clear
Although, you might think that living with anosmia isn't as hard as many other disabilities. It is. For starters, we are told that we are wrong. If we tell a person that we can't smell, they often say "No, you must be able to smell something!". Do you realize how irritating that can be?! Do you walk up to a blind man and say "You must be able to see something?", do you think we are just bored or something, so we tell people we can't smell. Most people don't seen to be able to comprehend that a person can live a life without smell. We do exist, and we don't like to be called a liar, for a disorder we have. But there is also hope, some people are extremely understanding for what we have to live with. I am very open about my anosmia, I don't try to hide it, I have no trouble talking about it, and I have no trouble with answering questions about anosmia to poeple. But if you want to ask an anosmic person about something, please use your head. People ask us the same question again and again, and often it is stupid questions you should be able to figure out yourself!
I will try to answer as best I can, some questions I have heard many times, stupid and real. As most of you should have realized by now, no we can't smell, and yes that is possible. In my case that comes of the nerves in my head that are supposed to send information to my brain, about what my nose is picking up, that isn't developed. There is no medical reason towards why it didn't develop before I was born, but that's how it is. Just because you might not be able to taste anything when you have a blocked nose, doesn't mean we can't. You are used to have the full experience and when you don't have your nose to help, you tongue isn't sensitive enough to give you a tasting experience. At least for people like me, with congenital anosmia, it isn't the same. I taste a whole lot! My whole life, I have only had my tongue to sense what I am eating or drinking. Most of the time, anosmic people have a better sense of taste, because that is all we have. It's like when a blind person get great hearing. The human body knows how to adapt to your situation. So when you loose a sense, your body improves the rest. And if you ever have taken your shoe of and said "smell this", really? you think your radiated shoe will make any difference to us? Can't smell, means can't smell. We don't choose what to smell and what to not smell.
Another question I have heard a few times is "What do you do with deodorant and cologne?". There are many answers to that question, but in my case, I rely on the help of my parents and friends. When I am out to buy a deodorant, I need my mother or a friend to smell for me, then tell me if it smells nice or not. Not my proudest moments, but it has to be done. Some anosmics don't even use cologne because we can never know if it makes us smell nice, or horrible. I have even had a employee at a store were they sell cologne, eyeball me extremely when my mother just said without thinking "Well, I have to smell it for you, cause you can't smell". My parents have a great "relationship"with the fact that i can't smell and they are great at just "plomping" it out without thinking, and I am quite amused if that, since people always have this weird reaction to it. But back to the story. When this lady heard my mother say I can't smell, she gave me a look like I was a devil in her store. What was i doing there, buying cologne in her store, when i can't smell?!?
There are of course many other question, but if I were to write all the question out there, i think the letters at my keyboard would be gone from the keys by the time I am done. When I am writing this, I am talking for my self. I think some of what I am writing about concerns many others, but I am sure there are anosmics who disagree with me, but that is human nature.
I hope you have learned something about the questions that we who are anosmics face. And more importantly I hope you have learned a little more about how to ask a question anosmic. Think before you speak. You can use that every where in life. At least for me, I really appreciate the effort from a person, if they want to ask me a question about my anosmia. If they give me a thought out question, one that makes me think of my answer, that makes me happy. That the person takes the time to make a good question, instead of asking a dumb question that they could have figured out themselves.
Thoughts make a difference!
- Marius
I will try to answer as best I can, some questions I have heard many times, stupid and real. As most of you should have realized by now, no we can't smell, and yes that is possible. In my case that comes of the nerves in my head that are supposed to send information to my brain, about what my nose is picking up, that isn't developed. There is no medical reason towards why it didn't develop before I was born, but that's how it is. Just because you might not be able to taste anything when you have a blocked nose, doesn't mean we can't. You are used to have the full experience and when you don't have your nose to help, you tongue isn't sensitive enough to give you a tasting experience. At least for people like me, with congenital anosmia, it isn't the same. I taste a whole lot! My whole life, I have only had my tongue to sense what I am eating or drinking. Most of the time, anosmic people have a better sense of taste, because that is all we have. It's like when a blind person get great hearing. The human body knows how to adapt to your situation. So when you loose a sense, your body improves the rest. And if you ever have taken your shoe of and said "smell this", really? you think your radiated shoe will make any difference to us? Can't smell, means can't smell. We don't choose what to smell and what to not smell.
Another question I have heard a few times is "What do you do with deodorant and cologne?". There are many answers to that question, but in my case, I rely on the help of my parents and friends. When I am out to buy a deodorant, I need my mother or a friend to smell for me, then tell me if it smells nice or not. Not my proudest moments, but it has to be done. Some anosmics don't even use cologne because we can never know if it makes us smell nice, or horrible. I have even had a employee at a store were they sell cologne, eyeball me extremely when my mother just said without thinking "Well, I have to smell it for you, cause you can't smell". My parents have a great "relationship"with the fact that i can't smell and they are great at just "plomping" it out without thinking, and I am quite amused if that, since people always have this weird reaction to it. But back to the story. When this lady heard my mother say I can't smell, she gave me a look like I was a devil in her store. What was i doing there, buying cologne in her store, when i can't smell?!?
There are of course many other question, but if I were to write all the question out there, i think the letters at my keyboard would be gone from the keys by the time I am done. When I am writing this, I am talking for my self. I think some of what I am writing about concerns many others, but I am sure there are anosmics who disagree with me, but that is human nature.
I hope you have learned something about the questions that we who are anosmics face. And more importantly I hope you have learned a little more about how to ask a question anosmic. Think before you speak. You can use that every where in life. At least for me, I really appreciate the effort from a person, if they want to ask me a question about my anosmia. If they give me a thought out question, one that makes me think of my answer, that makes me happy. That the person takes the time to make a good question, instead of asking a dumb question that they could have figured out themselves.
Thoughts make a difference!
- Marius
lørdag 7. januar 2012
My story
After some thinking, I decided to start a blog about my life with anosmia.
For those of you who don't know, anosmia is a medical term for a person who lack the ability to smell. This can occur from several different reasons, but mine, is (i think) one of the more rarely seen types. There are two types of anosmia acquired anosmia and congenital anosmia. Acquired anosmia means that you got anosmia during your life, either from disease, trauma or medication issues. Congenital anosmia is the people who are born with this condition, they start their life in a smell less environment, and it stays that way trough their lifetime. Now that you know a little about what anosmia is, here is my story.
My name is Marius and i am 17 years old. I live in Norway, a small country that lies right beneath Russia and besides Sweden. I lived the first 10 years of my life, thinking I was as everyone else, but that changed. All though i didn't use much time thinking about it, I sometimes wondered why everything "smelled" the same to me. It was when I was making candles with my mother, from wax plates, that I got her to understand (and understood it much better myself) that I am unable to smell. From there on, I have never been able to look at myself as a normal person. I have a condition that approximately 0,01 % of the worlds population is born with, congenital anosmia. For me, smell is nothing more than a word, it has no meaning to me. It actually took me 6 years, to find a name for my condition. For 6 years, i knew i couldn't smell, but I didn't know what to call it. After i found the name anosmia, I also found some groups on Facebook for people like me. I have become a part of a small internet community for people with anosmia, both acquired and congenital. I am also a part of a group only for people with congenital anosmia. Before i found these communities, I had the thought that I was alone. I thought there were no one else like me. When i found the first group, i was overwhelmed with emotions, here they was. More people like me, sharing their stories and experiences. While reading the stories from people, it struck me how similar it was to my life. As far as I can figure, most anosmics have the same types of experiences trough life. I learned that most anosmics don't know that somethings wrong until there teens, or later. When you are young, your mind can not understand that your olfactory system doesn't work. You think that everything smells the same, that nothing has a distinct smell.
While growing up, I got a lot of problems because of my anosmia. I got bullied a lot, and I believe that part of that is because no know believes you at first when you say you can't smell. It has caused a lot of uncertainty for me. I had no idea if my breath smelled, or if my shoes was smelling real bad. These are just a few examples, but you can figure out some of the problems i have encountered. Today, I am very open about my condition, but it still bothers me. Probably more than i want to admit.
I have spent many hours trying to do research about my condition, but the more I learn, the more upset i get. Even though anosmia can have a huge impact one a persons life, the medical doesn't care. When you are born, the doctors check you for hearing and sight, but not smell. People never think of the fact that they are smelling, it is taken for granted. The possibility that a person can lack the ability to smell, seems to be unthought of for most persons. A survey shows, that out of the 5 senses, people think it that if you had to loose one, smell would be it. No one knows how much impact smell has on their life, before they loose that ability themselves. Thats another thing about anosmia, if you get acquired anosmia, you can't remember any of the smells you have smelled in your life. The brain doesn't remember smells, so if you loose it, you can't remember hot things smell. But you still know what you are missing. That is also clear for us with congenital anosmia. At least for me. I have done the research and talked to enough people, that I know what I am missing out on. People who get acquired anosmia, struggle with depression and loss of sexdrive. Much of the things in life that you think nothing of, is triggered by smell. The release of hormones, memories and even danger. There are more than that, but these are at least some examples. We who have anosmia, have to take extra steps to ensure our safety and just to live a normal life. We can't detect if the food we are about to eat, is rotten. We can't smell a gas leak or of something is burning. Just to walk outside the house, raises a question for us, do I smell?
Another thing about anosmia, is that we can't enjoy flavor. We can taste, but we cant enjoy flavor. Flavor is the combination of smell (the aroma of the food), and the taste of the food. We have only our tounge. If you ever have had a bad cold and blocked nose, you have probably lost all sense of smell and taste. Or so you think. You do actually taste, but you are just so used to flavor, that you can't register just taste. This is what we experience every single time we take a bite of what we eat or every times we drink something.
This is just part of my story, and i will try to tell more on how it is to live with anosmia. But please, think of what you have. And even more, think of what you are taking for granted. The thing you almost never realize is there, is the ting i wish for most here in life. Enjoy the experiences, explore the world of scent. Don't just forget that its there.
- Marius
For those of you who don't know, anosmia is a medical term for a person who lack the ability to smell. This can occur from several different reasons, but mine, is (i think) one of the more rarely seen types. There are two types of anosmia acquired anosmia and congenital anosmia. Acquired anosmia means that you got anosmia during your life, either from disease, trauma or medication issues. Congenital anosmia is the people who are born with this condition, they start their life in a smell less environment, and it stays that way trough their lifetime. Now that you know a little about what anosmia is, here is my story.
My name is Marius and i am 17 years old. I live in Norway, a small country that lies right beneath Russia and besides Sweden. I lived the first 10 years of my life, thinking I was as everyone else, but that changed. All though i didn't use much time thinking about it, I sometimes wondered why everything "smelled" the same to me. It was when I was making candles with my mother, from wax plates, that I got her to understand (and understood it much better myself) that I am unable to smell. From there on, I have never been able to look at myself as a normal person. I have a condition that approximately 0,01 % of the worlds population is born with, congenital anosmia. For me, smell is nothing more than a word, it has no meaning to me. It actually took me 6 years, to find a name for my condition. For 6 years, i knew i couldn't smell, but I didn't know what to call it. After i found the name anosmia, I also found some groups on Facebook for people like me. I have become a part of a small internet community for people with anosmia, both acquired and congenital. I am also a part of a group only for people with congenital anosmia. Before i found these communities, I had the thought that I was alone. I thought there were no one else like me. When i found the first group, i was overwhelmed with emotions, here they was. More people like me, sharing their stories and experiences. While reading the stories from people, it struck me how similar it was to my life. As far as I can figure, most anosmics have the same types of experiences trough life. I learned that most anosmics don't know that somethings wrong until there teens, or later. When you are young, your mind can not understand that your olfactory system doesn't work. You think that everything smells the same, that nothing has a distinct smell.
While growing up, I got a lot of problems because of my anosmia. I got bullied a lot, and I believe that part of that is because no know believes you at first when you say you can't smell. It has caused a lot of uncertainty for me. I had no idea if my breath smelled, or if my shoes was smelling real bad. These are just a few examples, but you can figure out some of the problems i have encountered. Today, I am very open about my condition, but it still bothers me. Probably more than i want to admit.
I have spent many hours trying to do research about my condition, but the more I learn, the more upset i get. Even though anosmia can have a huge impact one a persons life, the medical doesn't care. When you are born, the doctors check you for hearing and sight, but not smell. People never think of the fact that they are smelling, it is taken for granted. The possibility that a person can lack the ability to smell, seems to be unthought of for most persons. A survey shows, that out of the 5 senses, people think it that if you had to loose one, smell would be it. No one knows how much impact smell has on their life, before they loose that ability themselves. Thats another thing about anosmia, if you get acquired anosmia, you can't remember any of the smells you have smelled in your life. The brain doesn't remember smells, so if you loose it, you can't remember hot things smell. But you still know what you are missing. That is also clear for us with congenital anosmia. At least for me. I have done the research and talked to enough people, that I know what I am missing out on. People who get acquired anosmia, struggle with depression and loss of sexdrive. Much of the things in life that you think nothing of, is triggered by smell. The release of hormones, memories and even danger. There are more than that, but these are at least some examples. We who have anosmia, have to take extra steps to ensure our safety and just to live a normal life. We can't detect if the food we are about to eat, is rotten. We can't smell a gas leak or of something is burning. Just to walk outside the house, raises a question for us, do I smell?
Another thing about anosmia, is that we can't enjoy flavor. We can taste, but we cant enjoy flavor. Flavor is the combination of smell (the aroma of the food), and the taste of the food. We have only our tounge. If you ever have had a bad cold and blocked nose, you have probably lost all sense of smell and taste. Or so you think. You do actually taste, but you are just so used to flavor, that you can't register just taste. This is what we experience every single time we take a bite of what we eat or every times we drink something.
This is just part of my story, and i will try to tell more on how it is to live with anosmia. But please, think of what you have. And even more, think of what you are taking for granted. The thing you almost never realize is there, is the ting i wish for most here in life. Enjoy the experiences, explore the world of scent. Don't just forget that its there.
- Marius
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