Rhabdomyosarcoma Survivors
Comments
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Hi my name is Jessica and I may be a help to you or not. I have most certainly not been a survivor of rhabdo since the 70's or earlier because I am only 16. But I have been a survivor for 10, almost 11 years. I was diagnosed in 1992 when I was only 5 1/2. Ever since, I have been a survivor. You are free to email me. I too am kind of interested in finding rhabdo survivors becasue I know how rare rhabdomyosarcoma is.
-airesgal787@aol.com0 -
Hi Jessica:rhabdogal05 said:Hi my name is Jessica and I may be a help to you or not. I have most certainly not been a survivor of rhabdo since the 70's or earlier because I am only 16. But I have been a survivor for 10, almost 11 years. I was diagnosed in 1992 when I was only 5 1/2. Ever since, I have been a survivor. You are free to email me. I too am kind of interested in finding rhabdo survivors becasue I know how rare rhabdomyosarcoma is.
-airesgal787@aol.com
My name is Juan Sanchez.
My nephew Cesar was just diagnosed with Rhabdomyosarcoma. He is 12 years old. When he was told by a social worker what he had he got desperate and inconsolable. This is so hard for all of us.
He doesn't have internet access at the hospital. But I would like to hear your story so I can
print it and give it to him. I would also like him to get in contact with you as soon as he gets out the hospital.
I signed up with an alternate email address. My regular email is jc-sanchez@comcast.net
Thanks and god bless you.
Juan Sanchez0 -
Hi Jessica,rhabdogal05 said:Hi my name is Jessica and I may be a help to you or not. I have most certainly not been a survivor of rhabdo since the 70's or earlier because I am only 16. But I have been a survivor for 10, almost 11 years. I was diagnosed in 1992 when I was only 5 1/2. Ever since, I have been a survivor. You are free to email me. I too am kind of interested in finding rhabdo survivors becasue I know how rare rhabdomyosarcoma is.
-airesgal787@aol.com
My name is Sungchan choi and I want to get your help if you can. What type of rhabdomyosarcoma did you have and in which part of your body?
Could you e-mail me to below address?
csc@innowireless.co.kr
Thanks in advance!!!
Regards, Sungchan.0 -
Hi all,AuthorUnknown said:Hi Jessica,
My name is Sungchan choi and I want to get your help if you can. What type of rhabdomyosarcoma did you have and in which part of your body?
Could you e-mail me to below address?
csc@innowireless.co.kr
Thanks in advance!!!
Regards, Sungchan.
My 3 and half year old son get embryonal rhabdomyosarcoma in the bladder. Is there any body who has knowledge on this and can help me in getting some advice?
Thanks in advance!!!
BR/CSC0 -
I am a survivor that was diagnosed in 84>??? i know its not 70's or before, but now i am 24, was 4 when it happened.. if that would help at all0
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Hi, My name is Stephanie and I was diagnosed in 1978. I was only 8 weeks old at the time. The cancer was in my bladder and surrounding lymph nodes. I was treated at Primary Childrens Hospital in Utah. I had several surgeries and rounds of chemo and then I became the first child to ever be given a radioactive implant for three days. Now I don't know if I was the first child anywhere to have had this or whether I was just the first at that hospital. I went into remission at the age of 3. I've stayed in remission ever since but have had a slew of various other illnesses that were either related or caused by the treatment that saved my life. Feel free to message me if you'd like to know more or just for some support0
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I'm a ARMS survivor! I was
I'm a ARMS survivor! I was first diagnosed in 2003 at the age of nineteen. I had a reocurrace in 2008 at the age of 24. It's tuff stuff, especially since it's a rare disease with it's own set of complications. We are a special group of people! At least, that's what I like to blieve!0 -
hi.. my daughter was treatedanamazon said:Hi, My name is Stephanie and I was diagnosed in 1978. I was only 8 weeks old at the time. The cancer was in my bladder and surrounding lymph nodes. I was treated at Primary Childrens Hospital in Utah. I had several surgeries and rounds of chemo and then I became the first child to ever be given a radioactive implant for three days. Now I don't know if I was the first child anywhere to have had this or whether I was just the first at that hospital. I went into remission at the age of 3. I've stayed in remission ever since but have had a slew of various other illnesses that were either related or caused by the treatment that saved my life. Feel free to message me if you'd like to know more or just for some support
hi.. my daughter was treated for rabdo in the bladder/uterus area.. she is 5 yrs out and cancer free but we are dealing with so many freaking other issues due to treatment.. did you ahve radiation? did you have any issues with puberty? having kids? fertility? bone growth? Emma has had screw put in her femurs to keep the balls from slipping of their growth plates.. and we are afraid of her egg count. heading to endocronologist at the end of the month.. hope her hormones are ok. but expecting some issues.. any light you can shed would help.. XO bless you..w1 -
Long Term Follow upemmabeansmom said:hi.. my daughter was treated
hi.. my daughter was treated for rabdo in the bladder/uterus area.. she is 5 yrs out and cancer free but we are dealing with so many freaking other issues due to treatment.. did you ahve radiation? did you have any issues with puberty? having kids? fertility? bone growth? Emma has had screw put in her femurs to keep the balls from slipping of their growth plates.. and we are afraid of her egg count. heading to endocronologist at the end of the month.. hope her hormones are ok. but expecting some issues.. any light you can shed would help.. XO bless you..w
Hi Emma's mum I'm not sure I can provide much insight as although I had RMS (embryonal) it was in my neck (diagnosed 1992 when I was 6 years old). I did however have radiation and have therefore been closely monitored for similar issues to your daughter so I'm happy to chat with you to see if I can help in any way. Feel free to email me on
sarahkie_smiles@hotmail.co.uk.
How did Emma's endocrinology appointment go?
Hang on in there...it isn't always easy having to wade through all the late effects...but there's lots of us to wade with you
Regards
Sarah0 -
RhabdomyosarcomaAuthorUnknown said:Hi Jessica,
My name is Sungchan choi and I want to get your help if you can. What type of rhabdomyosarcoma did you have and in which part of your body?
Could you e-mail me to below address?
csc@innowireless.co.kr
Thanks in advance!!!
Regards, Sungchan.
My grandson this cancer in his arm he's been in treatment for the last two years, today they told him that it slowed down but they do not give him a year to live please if anyone has had success in fighting this awful cancer please tell me where and how!0 -
Rhabdomayosarcoma survivor
Hi,
My name is William Cozzens. I am 39 years old. I am a rhabdomyosarcoma cancer survivor. I was diagnosed when I was one years old. I believe that I had treatments till I was five years old. I was diagnosed in 1975 and it came back in 1976. I had had radiation and chemotherapy. It was in the soft pallet of the nasal pharonix. As a result of the treatments I have stunted growth in the face and other parts of my body. However, I am happy to be alive. Feel free to contact me. I have never met or talked with any survivors any age or close who had this disease. William.cozzens@yahoo.com
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Illnesses brought on by treatmentanamazon said:Hi, My name is Stephanie and I was diagnosed in 1978. I was only 8 weeks old at the time. The cancer was in my bladder and surrounding lymph nodes. I was treated at Primary Childrens Hospital in Utah. I had several surgeries and rounds of chemo and then I became the first child to ever be given a radioactive implant for three days. Now I don't know if I was the first child anywhere to have had this or whether I was just the first at that hospital. I went into remission at the age of 3. I've stayed in remission ever since but have had a slew of various other illnesses that were either related or caused by the treatment that saved my life. Feel free to message me if you'd like to know more or just for some support
Hello anamazon,
I realize I'm replying to a very old post, and you may never see this, but I'm gonna give it a shot. I was diagnosed in '74, and the cancer was in the same area as yours. I've had a few sporadic problems over the years, but now, at age 51, those problems have become so frequent and severe, that I have had to stop working. I'd be very interested to know what kinds of problems other survivors are experiencing, and perhaps swap stories of things we have each found helpful. This site is a bit confusing to me, as it seems to be all over the place, and for the short time that I have been using this site, no one has ever responded to me replies or posts. So I don't even know if my requests are going through. If there is any staffer reading this, please advise. Thanks.
(I think I may repost this on a more general board...)
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Living with the consequences of treatmentMallard97 said:Rhabdomayosarcoma survivor
Hi,
My name is William Cozzens. I am 39 years old. I am a rhabdomyosarcoma cancer survivor. I was diagnosed when I was one years old. I believe that I had treatments till I was five years old. I was diagnosed in 1975 and it came back in 1976. I had had radiation and chemotherapy. It was in the soft pallet of the nasal pharonix. As a result of the treatments I have stunted growth in the face and other parts of my body. However, I am happy to be alive. Feel free to contact me. I have never met or talked with any survivors any age or close who had this disease. William.cozzens@yahoo.com
I was diagnosed in '74, although the cancer was not in the same area as yours. I've had a few sporadic problems over the years, but now, at age 51, those problems have become so frequent and severe, that I have had to stop working. I'd be very interested to know what kinds of problems other survivors are experiencing, and perhaps swap stories of things we have each found helpful. This site is a bit confusing to me, as it seems to be all over the place, and for the short time that I have been using this site, no one has ever responded to my replies or posts. I will shoot you an email, as your post is about the most recent I can find.
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Son with rhabdo, learning about late affects....Mobjack said:Illnesses brought on by treatment
Hello anamazon,
I realize I'm replying to a very old post, and you may never see this, but I'm gonna give it a shot. I was diagnosed in '74, and the cancer was in the same area as yours. I've had a few sporadic problems over the years, but now, at age 51, those problems have become so frequent and severe, that I have had to stop working. I'd be very interested to know what kinds of problems other survivors are experiencing, and perhaps swap stories of things we have each found helpful. This site is a bit confusing to me, as it seems to be all over the place, and for the short time that I have been using this site, no one has ever responded to me replies or posts. So I don't even know if my requests are going through. If there is any staffer reading this, please advise. Thanks.
(I think I may repost this on a more general board...)
Just wanted to say, I read your post. I agree this site needs some kind of maintenance or webmaster. Can't help with your particular question, but maybe you can help me. Where was your tumor located? Trying to find out any possible late affects of the cancer from anybody and everybody. If you don't mind of course. Thank you sir.
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Rhabdomyosarcoma of sternocleidomastoid muscle in neckMobjack said:Living with the consequences of treatment
I was diagnosed in '74, although the cancer was not in the same area as yours. I've had a few sporadic problems over the years, but now, at age 51, those problems have become so frequent and severe, that I have had to stop working. I'd be very interested to know what kinds of problems other survivors are experiencing, and perhaps swap stories of things we have each found helpful. This site is a bit confusing to me, as it seems to be all over the place, and for the short time that I have been using this site, no one has ever responded to my replies or posts. I will shoot you an email, as your post is about the most recent I can find.
I realize your post is 2 years old, but I am a long term survivor like you. My rhabdomyosarcoma tumor was located in my neck and found at age 8 weeks back in 1973. I am running into some problems now related to my surgery (they had to remove the entire sternocleidomastoid muscle on one side of my neck, which is causing me to have a fair amount of pain now as I start to age), combined with a lot of muscle atrophy in the areas where I had radiation. I have found that with regular weight lifting that I am able to regain some of the atrophied muscle, but within 3-4 days of missing a workout I rapidly lose muscle mass again. I have resigned myself to having to work out at least every other day to stay pain free, but I suppose there are worse activities I could have to do! At least it keeps the rest of me in shape!
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