Chroidal melanoma (Eye Cancer)
Comments
-
to melton8
Yes I had a very large tumor in my left eye.
I know what you are talking about with the anxiety and fear. On august of 2000 I had gone to my regular optomitrist to get new glass. I alway's get my eyes dilated. So to make a long story short the found a large 10mm in my left eye.
The only option they gave me was removal of the eye. Two week's later the tumor had grown to 15mm.
I am doing very well!!! Of course their is the follow up test. But after almost 3 year's I am still Cancer free.
I'm not saying it was easy. I had to learn alot of things over. Because you will lose your depth perception and with losing my left eye I had to learn how to drive again.
But it takes time and the Love of family and friend's.
I hope all is well with you. What have the Dr's decided to do? I know they sometimes they can use chemo or some other type's of things.
The depression is their I know but time will heal.
I actualy can say I've been there.
I have a prosthic eye. Every body say's it looks so real. I hope I've helped you out alittle. I know it's not easy but you can do it. I Hope you pray because I do! And it helped me alot. Please write me back because you are the first person I've been able to find that has this type of cancer. Maybe we can keep in contact.
Thank's and may God Bless!
Angelcake488430 -
A former colleague and friend of mine had this cancer (in her case, it was the right eye, and she also had to have it removed).angelcake48843 said:to melton8
Yes I had a very large tumor in my left eye.
I know what you are talking about with the anxiety and fear. On august of 2000 I had gone to my regular optomitrist to get new glass. I alway's get my eyes dilated. So to make a long story short the found a large 10mm in my left eye.
The only option they gave me was removal of the eye. Two week's later the tumor had grown to 15mm.
I am doing very well!!! Of course their is the follow up test. But after almost 3 year's I am still Cancer free.
I'm not saying it was easy. I had to learn alot of things over. Because you will lose your depth perception and with losing my left eye I had to learn how to drive again.
But it takes time and the Love of family and friend's.
I hope all is well with you. What have the Dr's decided to do? I know they sometimes they can use chemo or some other type's of things.
The depression is their I know but time will heal.
I actualy can say I've been there.
I have a prosthic eye. Every body say's it looks so real. I hope I've helped you out alittle. I know it's not easy but you can do it. I Hope you pray because I do! And it helped me alot. Please write me back because you are the first person I've been able to find that has this type of cancer. Maybe we can keep in contact.
Thank's and may God Bless!
Angelcake48843
I don't know if you're familiar with this website:
http://www.losteye.com
...but it might be of help to both of you. The man who runs it also lost an eye to choroidal melanoma, and there's a lot of information there on how to cope with all the issues involved.0 -
Thank You!aries75 said:A former colleague and friend of mine had this cancer (in her case, it was the right eye, and she also had to have it removed).
I don't know if you're familiar with this website:
http://www.losteye.com
...but it might be of help to both of you. The man who runs it also lost an eye to choroidal melanoma, and there's a lot of information there on how to cope with all the issues involved.
I Will check this web site out.
I have also been trying to find help to cope with this.
thanks again
angelcake488430 -
To all of you: I had laser treatment on left eyeangelcake48843 said:Thank You!
I Will check this web site out.
I have also been trying to find help to cope with this.
thanks again
angelcake48843
melanoma at Wills Eye in 1998 which seemed to have
gotten it all, but in 2000 they had to radiate it
with cobalt for 5 days. It worked fine until last
September 2004, when a technician for a local
opthamologist who was supposed to check me half
way between the long distance trips to Philadelphia, put eye drops in my eyes that blinded me for 3 days! Tthe sight never came back
because the retina is shot. Now I have just been
diagnosed with melanoma in the lung and Wed I find
out what the treatment is to be. They were very
surprised to have the pathology report be melanoma
because the cancer in my left eye is all dead.
I know what you mean about scared and depression,
because I am going through it too, but trying to act like I'm doing well because of my family. Good luck to you all. And have you ever done a
survey in the waiting room of your oncologist to
see which eye is affected. We have found more left eyes affected where I go. Isn't that weird?
suppo0 -
GretnaGranny;angelcake48843 said:Thank You!
I Will check this web site out.
I have also been trying to find help to cope with this.
thanks again
angelcake48843
09-15-05
To all of you: I had laser treatment on left eye
melanoma at Wills Eye in 1998 which seemed to have
gotten it all, but in 2000 they had to radiate it
with cobalt for 5 days. It worked fine until last
September 2004, when a technician for a local
opthamologist who was supposed to check me half
way between the long distance trips to Philadelphia, put eye drops in my eyes that blinded me for 3 days! Tthe sight never came back
because the retina is shot. Now I have just been
diagnosed with melanoma in the lung and Wed I find
out what the treatment is to be. They were very
surprised to have the pathology report be melanoma
because the cancer in my left eye is all dead.
I know what you mean about scared and depression,
because I am going through it too, but trying to act like I'm doing well because of my family. Good luck to you all. And have you ever done a
survey in the waiting room of your oncologist to
see which eye is affected. We have found more left eyes affected where I go. Isn't that weird?
suppo0 -
Eye Cancer
Hi, I was just diagnosed with a tumar under my retina by an eye doctor. I understand exactly what you are feeling. On Tuesday Oct 27 and Wednesday Oct 28 I go to Mayo for further tests. I pray they do not find any more. Until I get the results you and I must be feeling the same feelings. I will include you in my prayers !0 -
choroidal malanomaangelcake48843 said:to melton8
Yes I had a very large tumor in my left eye.
I know what you are talking about with the anxiety and fear. On august of 2000 I had gone to my regular optomitrist to get new glass. I alway's get my eyes dilated. So to make a long story short the found a large 10mm in my left eye.
The only option they gave me was removal of the eye. Two week's later the tumor had grown to 15mm.
I am doing very well!!! Of course their is the follow up test. But after almost 3 year's I am still Cancer free.
I'm not saying it was easy. I had to learn alot of things over. Because you will lose your depth perception and with losing my left eye I had to learn how to drive again.
But it takes time and the Love of family and friend's.
I hope all is well with you. What have the Dr's decided to do? I know they sometimes they can use chemo or some other type's of things.
The depression is their I know but time will heal.
I actualy can say I've been there.
I have a prosthic eye. Every body say's it looks so real. I hope I've helped you out alittle. I know it's not easy but you can do it. I Hope you pray because I do! And it helped me alot. Please write me back because you are the first person I've been able to find that has this type of cancer. Maybe we can keep in contact.
Thank's and may God Bless!
Angelcake48843
I also have had radiation patch on my eye after being diagnosed with a choroidal melanoma. Now I have lost my eyesight. please email me or email me on here..thanks, I do feel quite alone, and no one really understands.thanks.. jean.johnson@charter.net0 -
please keep in touch withgjstark said:Eye Cancer
Hi, I was just diagnosed with a tumar under my retina by an eye doctor. I understand exactly what you are feeling. On Tuesday Oct 27 and Wednesday Oct 28 I go to Mayo for further tests. I pray they do not find any more. Until I get the results you and I must be feeling the same feelings. I will include you in my prayers !
please keep in touch with me. it is so much easier to talk to someone who understands such a rare cancer. thank you!0 -
choroidal malanomajeanjewing said:choroidal malanoma
I also have had radiation patch on my eye after being diagnosed with a choroidal melanoma. Now I have lost my eyesight. please email me or email me on here..thanks, I do feel quite alone, and no one really understands.thanks.. jean.johnson@charter.net
jean, I was just told I have cancer behind my retina on may 28 2010. I was referred to the mayo clinic in Rochester. I am having surgery on June 21 to have placque radiation sewed to my eye and it will be left for 5 days and then I go back to surgery and have it removed.They say a 90 percent chance it will kill the cancer.I am a 62 year old female who like you am feeling very depressed as they tell me I will lose my eyesight in that eye also. Would love to hear from you. I live in mimmesota rosiepete0 -
choroidal melanomarosiepete said:choroidal malanoma
jean, I was just told I have cancer behind my retina on may 28 2010. I was referred to the mayo clinic in Rochester. I am having surgery on June 21 to have placque radiation sewed to my eye and it will be left for 5 days and then I go back to surgery and have it removed.They say a 90 percent chance it will kill the cancer.I am a 62 year old female who like you am feeling very depressed as they tell me I will lose my eyesight in that eye also. Would love to hear from you. I live in mimmesota rosiepete
RosiePete, I hope you are doing fine now.
I am a 34 year old woman. I was diagnosed with choroidal melanoma June 24th 2010. My tumor is too big for radiation and we do not want to risk the cancer spreading while we wait to see if the cancer is gone. I am having my right eye removed on Tuesday July 6th at the UW Hospital in Madison WI. My surgery will be exactly 2 weeks after my 1st eye check. My vision in my right eye was very blurry. The 1st doctor I saw referred me to another specialist because my retina was detached and I needed surgery right away. The 2nd specialist said that my retina was detached but there also was a tumor in my eye. Two days later, I was told it was cancer. I had never heard about eye cancer. The specialists and surgeon I saw are pretty confident in the surgery. I had the blood tests and X Rays, and the cancer did not spread. I feel lucky about that. It still feels surreal, like it's a bad dream and I'm gonna wake up and my eye will be fine. I am glad to be surounded and family and friends. It helps so much.
I am trying to enjoy my last couple of days before surgery. My husband does all he can to take my mind off of this.
I too was depressed and mad after hearing the news. After a couple of days, I decided to focus my energy on fighting this thing and keeping positive thoughts.
I will beat this!0 -
choroidal melanoma
I was diagnosed on June 30 2010. Course of treatment? Brachytherapy. It was such a shock we didn't ask all the questions we wanted to. I am scheduled for a myriad of scans and bloodwork on Tuesday. Preop with Anesthesia and Oncologist and Surgeon on Thursday and One week from Monday July 12 will be surgery. I have so many questions...like pain..I am allergic to many pain meds what can they give me? What kind of vision can I look forward to post procedure? When will life become somewhat normal again? Will I be able to drive? What are the side effects? What are the long term effects? What is the likely hood that this will come back again? What is the likely hood of metastasis later? I just need some answers. Anyone have any input? I am confident that My Lord and Savior will provide a way through this but the information I am seeing on the internet is incomplete (or maybe I am not searching correctly) Can anyone help me?0 -
Choroidal melanomaemptynestmom2009 said:choroidal melanoma
I was diagnosed on June 30 2010. Course of treatment? Brachytherapy. It was such a shock we didn't ask all the questions we wanted to. I am scheduled for a myriad of scans and bloodwork on Tuesday. Preop with Anesthesia and Oncologist and Surgeon on Thursday and One week from Monday July 12 will be surgery. I have so many questions...like pain..I am allergic to many pain meds what can they give me? What kind of vision can I look forward to post procedure? When will life become somewhat normal again? Will I be able to drive? What are the side effects? What are the long term effects? What is the likely hood that this will come back again? What is the likely hood of metastasis later? I just need some answers. Anyone have any input? I am confident that My Lord and Savior will provide a way through this but the information I am seeing on the internet is incomplete (or maybe I am not searching correctly) Can anyone help me?
Hi: A friend of mine who was over last night was telling me about her experience with eye melanoma (very rare). She was diagnosed last year and was told she would lose her eye. But luckily for her a new treatment became available in a clinical trial at Princess Margaret Hospital in Toronto (a world-class cancer facility) that did not involve removing the eye. She went for it, of course. If I understood her correctly, they do not remove the tumour but rather completely stabilize it and it does not grow. If you want me to find out more from her, let me know: cpearce@uwo.ca.0 -
I have a tumor in my right eyerosiepete said:choroidal malanoma
jean, I was just told I have cancer behind my retina on may 28 2010. I was referred to the mayo clinic in Rochester. I am having surgery on June 21 to have placque radiation sewed to my eye and it will be left for 5 days and then I go back to surgery and have it removed.They say a 90 percent chance it will kill the cancer.I am a 62 year old female who like you am feeling very depressed as they tell me I will lose my eyesight in that eye also. Would love to hear from you. I live in mimmesota rosiepete
I'm also a patient at Rochester. It was in November 2010 when I had surgery and then radiation. So far I'm doing fine. The tumor was in the front of my eye so I'm able to see but not good enough to read. I'm watching my diet and trying to just stay healthy. I'm going to return for a 6 month checkup and hopefully everything will still be fine. I wish that I could find someone with "Monosomy 3" but this is even more rare than the eye cancer itself. I live in northern Minnesota and I'm 58 and am trying to stay possitive that this won't end up in my liver. I welcome all the prayers I can get.0 -
It has been a year since Iangelcake48843 said:to melton8
Yes I had a very large tumor in my left eye.
I know what you are talking about with the anxiety and fear. On august of 2000 I had gone to my regular optomitrist to get new glass. I alway's get my eyes dilated. So to make a long story short the found a large 10mm in my left eye.
The only option they gave me was removal of the eye. Two week's later the tumor had grown to 15mm.
I am doing very well!!! Of course their is the follow up test. But after almost 3 year's I am still Cancer free.
I'm not saying it was easy. I had to learn alot of things over. Because you will lose your depth perception and with losing my left eye I had to learn how to drive again.
But it takes time and the Love of family and friend's.
I hope all is well with you. What have the Dr's decided to do? I know they sometimes they can use chemo or some other type's of things.
The depression is their I know but time will heal.
I actualy can say I've been there.
I have a prosthic eye. Every body say's it looks so real. I hope I've helped you out alittle. I know it's not easy but you can do it. I Hope you pray because I do! And it helped me alot. Please write me back because you are the first person I've been able to find that has this type of cancer. Maybe we can keep in contact.
Thank's and may God Bless!
Angelcake48843
It has been a year since I had my left eye removed,I did not get a Fake eye because the cost is crazy and you have to get them replaced every 5 years.I just would like to find a job with one eye it will be hard but life goes on.I do not have cancer anywhere else that I know of I feel fine and with no money can not afford to get the blood tests and x-rays.I am the first one in my family to ever have any kind of cancer and was glad Doctor told me smoking had nothing to do with it.I just wear one of those eye band aid type patches on my left eye.I am 55 and would love to be good for at least 30 years or more.0 -
Chroidal in Veteransmoonlady85 said:It has been a year since I
It has been a year since I had my left eye removed,I did not get a Fake eye because the cost is crazy and you have to get them replaced every 5 years.I just would like to find a job with one eye it will be hard but life goes on.I do not have cancer anywhere else that I know of I feel fine and with no money can not afford to get the blood tests and x-rays.I am the first one in my family to ever have any kind of cancer and was glad Doctor told me smoking had nothing to do with it.I just wear one of those eye band aid type patches on my left eye.I am 55 and would love to be good for at least 30 years or more.
I am new here-- My husband has been 3 years with CM. He is a Vietnam Veteran and we found interesting stats regrading Vets and this cancer...
as you all know the data from all sources say it is so rare..5-6 in one million...or about 1400 a year.
But we have information from the Freedom of Information Act that follows Veteran hospitals...
the rate was much higher than 1400 a year for Veterans alone----
the rate was 1900 Vets treated in the year 07, about 2100 treated in 08, about 2200 in 09 ,about 2050 in 2010 and about 1600 in 2011.
These numbers are not duplicated. These are occurances. The numbers are frightening for veterans.
I am looking for fellow veterans of my husband with this cancer.. Please contact me.
My husband was a pilot..he owned his own airline. He no longer flies. He now gets 50.00 a month in VA benefits. I know he is not alone. Please contact us.
Thank you0 -
choroidal melanomabrutz said:Chroidal in Veterans
I am new here-- My husband has been 3 years with CM. He is a Vietnam Veteran and we found interesting stats regrading Vets and this cancer...
as you all know the data from all sources say it is so rare..5-6 in one million...or about 1400 a year.
But we have information from the Freedom of Information Act that follows Veteran hospitals...
the rate was much higher than 1400 a year for Veterans alone----
the rate was 1900 Vets treated in the year 07, about 2100 treated in 08, about 2200 in 09 ,about 2050 in 2010 and about 1600 in 2011.
These numbers are not duplicated. These are occurances. The numbers are frightening for veterans.
I am looking for fellow veterans of my husband with this cancer.. Please contact me.
My husband was a pilot..he owned his own airline. He no longer flies. He now gets 50.00 a month in VA benefits. I know he is not alone. Please contact us.
Thank you
hi maam
i was recently diagnosed with choroidal melanoma while active duty in the navy, i am 24 years old and a Qm3 in the navy
i just had my radiation therapy (rad patch) last month, as of i am doing ok
my email is jamesviernes87@yahoo.com, if you would like to be in contact with me0 -
CM and veteransjamesviernes said:choroidal melanoma
hi maam
i was recently diagnosed with choroidal melanoma while active duty in the navy, i am 24 years old and a Qm3 in the navy
i just had my radiation therapy (rad patch) last month, as of i am doing ok
my email is jamesviernes87@yahoo.com, if you would like to be in contact with me
James- much luck to you. You are a very young man. I thank you for your service to our country as well.
I am looking into the high rate of incidences of this cancer among veterans. You are not yet a veteran but you are certainly adding to my list of our high rate of military identified with this rare cancer. My husbands friend (also a vet) did well with his radiation. My husband had a much larger growth and needed the eye removed. May I ask where you have been stationed during your time in the military?
If there are any other veterans or active duty I would love to hear from you.
Continued luck to all of you.
brutz@pasco.k12.fl.us0 -
I has been a year since-moonlady85 said:It has been a year since I
It has been a year since I had my left eye removed,I did not get a Fake eye because the cost is crazy and you have to get them replaced every 5 years.I just would like to find a job with one eye it will be hard but life goes on.I do not have cancer anywhere else that I know of I feel fine and with no money can not afford to get the blood tests and x-rays.I am the first one in my family to ever have any kind of cancer and was glad Doctor told me smoking had nothing to do with it.I just wear one of those eye band aid type patches on my left eye.I am 55 and would love to be good for at least 30 years or more.
Hello Moonlady85
yes the fake eye is expensive. My husband did get one...he is a veteran though so the VA helped him out. i thought he would wear a patch he surprised me. But what his Dr. did say is that this eye of his can last much longer than 5 years. However his Dr. also said that women tend to get new ones more often. He needs to take it out and clean it. BUt as long as his eye lids are tight enough to hold it in he will remain with the same eye. I wish you continued luck in your job search I feel as though you may need to ask in the event you are not employed as to your lack of obtaining the job. You know they can not discriminate based upon your physical appearance.0 -
chroidal melanomabrutz said:Chroidal in Veterans
I am new here-- My husband has been 3 years with CM. He is a Vietnam Veteran and we found interesting stats regrading Vets and this cancer...
as you all know the data from all sources say it is so rare..5-6 in one million...or about 1400 a year.
But we have information from the Freedom of Information Act that follows Veteran hospitals...
the rate was much higher than 1400 a year for Veterans alone----
the rate was 1900 Vets treated in the year 07, about 2100 treated in 08, about 2200 in 09 ,about 2050 in 2010 and about 1600 in 2011.
These numbers are not duplicated. These are occurances. The numbers are frightening for veterans.
I am looking for fellow veterans of my husband with this cancer.. Please contact me.
My husband was a pilot..he owned his own airline. He no longer flies. He now gets 50.00 a month in VA benefits. I know he is not alone. Please contact us.
Thank you
I am a vietnam vet and My dr is ssspects chroidal melanoma in my right eye,
one more ultra sound to confirm to be next week, I am in shock from this diagnosis
of something I know very little, I am 66 yrs old and thought I was fairly good shape
I need help and any comments or encouragement out there. I am in state of Alabama.
I would love to here from anyone. jesse5150 -
melanoma in eyebrutz said:I has been a year since-
Hello Moonlady85
yes the fake eye is expensive. My husband did get one...he is a veteran though so the VA helped him out. i thought he would wear a patch he surprised me. But what his Dr. did say is that this eye of his can last much longer than 5 years. However his Dr. also said that women tend to get new ones more often. He needs to take it out and clean it. BUt as long as his eye lids are tight enough to hold it in he will remain with the same eye. I wish you continued luck in your job search I feel as though you may need to ask in the event you are not employed as to your lack of obtaining the job. You know they can not discriminate based upon your physical appearance.
I would like to know more of your husband experience and what was his diagnosis
jesse5150
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