kasparov33
Premium
join:2007-05-04
Conover, NC
edit:
May 4th, @04:55PM
| [request] need email sent to my son who has cancer please!!
hi i have read here on dslreports for some time. as of last sunday we learned that my 12 year old son has cancer. he has been healthy with no major problems up until now. i dont know any of you but ask that you simply please just send an email saying hello and hope that he has a speed recovery. this may seem stupid but i would like him to receive over 100,000 emails. this may seem rediculous but i know how fast things can spread over the internet. this amount of emails would surprise him and make him feel great. the link is www.levinechildrenshospital.org. from there you click on email a child on the right. his name is micheal ybanez. again let as many people as you can send an email. if nothing more than a hello will do. thank you all and lets try for the 100,000 emails. i hope to post something on you tube later. my wife and i are just trying to bring as much happiness to him right now as we can. again thank you all and keep my son in your prayers. |
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deadmeat
Premium
join:2003-03-21
Sonoma, CA | Nice way to harvest emails. I mean how would he even read 100,000 emails? lol. |
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kasparov33
Premium
join:2007-05-04
Conover, NC | reply to kasparov33
i wouldnt expect him to read that many emails but just getting that many would raise his spirits and let him see just how many people care. the emails he gets are printed off here at the hospital and give to him. thanks. |
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deadmeat
Premium
join:2003-03-21
Sonoma, CA
| And the fact that the security certificate is for another website is rather fishy. I apoligize if I'm wrong.
The security certificate presented by this website was issued for a different website's address.
We recommend that you close this webpage and do not continue to this website.
--
"Keep your fundie guard up. They'll be looking to slip a shiv between your ribs first chance they see." |
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GanJa
Just Say No
Premium
join:2003-02-24
Crack House | reply to kasparov33
Seems like the real site is: »https://www.levinechildrenshospital.org
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I LOVE THE COUNTRY I LIVE, BUT HATE THE PEOPLE IN CHARGE. |
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CatSnak
Stick A Fork In Me, I'm Done
Premium
join:2001-05-06
Lakeside, CA | reply to kasparov33
Done!
You and your family will be in my thoughts and prayers. |
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kasparov33
Premium
join:2007-05-04
Conover, NC
| reply to kasparov33
sorry for the incorrect link. it is infact levinechildrenshospital.org. thank you for the correction.
my mind has been a little off lately. i am in no way trying to send anybody to a bad website and i will edit the post for the correct site. thanks again and let get the emails coming. |
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Masque
join:2001-12-04
Auburn, MI | reply to kasparov33
Done and may my prayers follow you all throughout this ordeal. |
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TwKs
join:2007-04-29
|  reply to kasparov33
Seems a worthy cause! I emailed your son. Its the least anyone could do to wish a kid the best and to help him stay positive. I wish you and your family the best. 
Also here is the direct link for the email form, which is secure: »https://www.levinechildrenshospital.org/···ilAChild |
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deadzoned
Premium
join:2005-04-13
Baton Rouge, LA
edit:
May 4th, @07:36PM
| reply to Masque
E-Mail sent. I'll be keeping your son, you, and your family in my thoughts and hoping for the best.
Please keep us updated on your son. |
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johnqpublic
Premium
join:2002-03-22
Xanadu | reply to kasparov33
John Q. Public has sent his best!
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veloslave
Geek For God
Premium
join:2003-07-11
Pleasant Hill, CA | reply to kasparov33
Email and prayers sent.
Great idea, thanks for posting this.
Please keep us up on how he is doing and remind us to send him another email now and then.
God Bless
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Mom was right...I need more FIBER> |
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ManMachine
Musique non stop
Premium
join:2006-07-10
t2p-2j3 | reply to kasparov33
I don't believe any of this. |
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Loker
Premium
join:2004-07-11
Fargo, ND
clubs:
| said by ManMachine  :I don't believe any of this. well some googling and that is a legitimate hospital site so I believe it now...
but when I sent the e-mail it said this...Thank you for sending an e-mail to a child at Levine Children's Hospital. Your message will be hand-delivered in the next 24 hours by a specialist from the Child Life Program.
If you try and get him 100,000 e-mails how many trees are going to be killed LOL
anyway good luck with all this and I am sure he will pull through!
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"While preceding your entrance with a grenade is a good tactic inQuake, it can lead to problems if attempted at work." -- C Hacking |
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pilotsr
join:2002-08-08
Troutman, NC | reply to kasparov33
Just sent my thoughts and prayers. God Bless you and your family.
-pilotsr |
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DirtyDeeds
Premium
join:2003-06-12
Akron, OH | reply to kasparov33
Sent ! |
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kasparov33
Premium
join:2007-05-04
Conover, NC
| reply to kasparov33
thanks so much for your quick replies. i was like man machine and didnt believe any of this either until the doctors said yes it is real. he has rhadomyosarcoma which usually affects young children. but at age 12 i have found out that is young enough also. the doctors said that in the last 4 days with radiation and some chemo treatments that he is more stable and has improved somewhat but it will take some time. and yes keep the emails coming. when he gets email from people he doesnt even know hopefully that will make him feel some better. i have read here at dsl for some years but never posted much until now. i have seen that most all of you seem to be nice folks by the way you post and even though i dont know you personally thank you very much for your time and consideration. well i need to sleep some and then see my son later. the doctors have him in a drug induced coma for the time being. they say he may be able to come off of that in the next few days so we will see. later all and keep em coming. |
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DirtyDeeds
Premium
join:2003-06-12
Akron, OH
 ·RoadRunner Cable
| reply to kasparov33
SARCOMAS
Sarcomas are rare types of cancer that develop in the supporting structures of the body, such as bone, muscle or cartilage. There are two main types of sarcoma: soft tissue sarcomas and bone sarcomas.
Soft-tissue sarcomas can develop in muscle, fat, blood vessels or in any of the other tissues that support, surround and protect the organs of the body. Bone sarcomas can develop in any of the bones of the skeleton but may also develop in the soft tissue near bones.
Soft tissue sarcomas
Soft tissue sarcomas are rare tumours. Their annual incidence is around 2-3/100,000, and they account for less than 1% of all malignant tumours. In paediatric age, however, about 8% of all tumours are soft tissue sarcomas.
Half of the paediatric soft tissue sarcomas are rhabdomyosarcomas, half constitute the heterogeneous group of the so called "non-rhabdomyosarcoma" soft tissue sarcomas.
RHABDOMYOSARCOMA
Rhabdomyosarcoma is the most common of the soft tissue sarcomas with approximately 5-6 children per million diagnosed each year. Most of them are younger than 10 years old. It is more common in boys than girls.
These tumours develop from muscle or fibrous tissue and can grow in any part of the body. The most common areas of the body to be affected are around the head and neck, the bladder or the testes. Sometimes tumours are also to be found in a muscle or a limb, in the chest or in the abdominal wall. Occasionally, if the tumour is in the head or neck region, it can spread into the brain or the fluid around the spinal cord.
Causes of rhabdomyosarcoma
The cause of rhadomyosarcoma is unknown. Research is going on all the time into possible causes of this disease. Children with certain rare genetic disorders, such as Li Fraumeni syndrome, have a higher risk of developing rhabdomyosarcoma.
Signs and symptoms
The signs and symptoms will depend on the part of the body that is affected by the rhabdomyosarcoma. The most common sign is a swelling or lump. If the tumour is in the head area it can sometimes cause blockage (obstruction) and a discharge from the nose or throat. Occasionally an eye may appear swollen and protruding. If the tumour is in the abdomen (tummy) the child may have discomfort in the abdomen and problems going to the toilet. If the tumour is in the bladder, the child may have blood in the urine and have difficulty passing urine.
How it is diagnosed?
A variety of tests and investigations may be needed to diagnose a rhabdomyosarcoma. These usually include a biopsy. This involves a small operation to remove a sample from the tumour to be looked at under a microscope. A biopsy is usually done under a general anaesthetic. Various tests may be done to check the exact size of the tumour and whether it has spread to any other part of the body. These may include:
# bone scan
# a chest x-ray to check the lungs
# an ultrasound
# CT or MRI scans
# blood and bone-marrow tests
Staging
The 'stage' of a cancer is a term used to describe its size and whether it has spread beyond the part of the body from which it originated. Knowing the particular type and the stage of the cancer helps the doctors to decide on the most appropriate treatment.
Most patients are grouped depending on whether the cancer is found in only one part of the body (localised disease) or whether the cancer has spread from one part of the body to another for example the lungs or bones (metastatic disease). The place in the body where the rhabdomyosarcoma started is also important information that is taken into account in the staging system.
Treatment
Treatment depends upon some patient and tumour characteristics such as the size of the tumour, the subtype (when examined under the microscope) its position within the body, the age of the child or young person and whether it has spread. The treatment of rhabdomyosarcoma usually includes surgery, radiotherapy or chemotherapy, or a combination of these.
If possible, surgery will be used to remove the tumour, however if it cannot be easily removed then it is often better to shrink it down with chemotherapy before attempting further surgery.
Chemotherapy using a combination of drugs is often given before surgery to shrink the tumour. Chemotherapy is the use of anticancer (cytotoxic) drugs to destroy cancer cells. Your doctor will give you more details about the chemotherapy that will be used.
Radiotherapy may be given to the area of the tumour. If the tumour cannot be removed with surgery the treatment will usually involve a combination of chemotherapy and radiotherapy.
Radiotherapy treats cancer by using high-energy rays that destroy the cancer cells, while doing as little harm as possible to normal cells.
Side effects of treatment
Treatment for rhabdomyosarcoma often causes side effects, and your child's doctor will discuss these with you in some detail before treatment starts. Any possible side effects will depend upon the particular treatment being used and, when radiotherapy is being given, the part of the body that is being treated. Side effects can include: nausea (feeling sick) and vomiting, hair loss, an increased risk of infection or bruising and bleeding, tiredness constipation and diarrhoea.
Late side effects
A small number of children may develop side effects many years after their treatment for a rhabdomyosarcoma. Longer-term side effects depend on the type of treatment used, and may include possible reduced growth, infertility, a change in the way the heart and the kidneys work, hearing problems and a small increase in the risk of developing another cancer in later life. If your child has received daunorubicin (and anthracycline chemotherapy) then your child may have a small risk of developing heart problems. He/she will have been monitored throughout treatment and following completion of this therapy.
Follow-up
Overall about two thirds of all children with rhabdomyosarcoma are cured, but the particular risks for your child will be discussed by your doctor. After treatment the doctors will regularly check the child to be sure the cancer has not come back and to look for any long term side effects of the treatment. After a while you will not need to visit the clinic so often. If you have specific concerns about your child's condition and treatment, it is best to discuss them with your child's doctor, who knows the situation in detail.
NON-RHABDOMYOSARCOMAS SOFT TISSUE SARCOMAS
This definition includes different tumours with different biology and natural history, some of which are more common in adults. These tumours can arise, generally as a soft part enlarging mass, anywhere in the body (most frequently in the muscles of extremities, less usually in the trunk or head and neck region). The cause of their origin is unknown, and researchers are studying possible causes: it is known that children with certain rare genetic disorders, such as Li Fraumeni syndrome or neurofibromatosis, have a higher risk of developing soft tissue sarcomas. However, the majority of soft tissue sarcomas are sporadic.
Usually, non-rhabdomyosarcoma soft tissue sarcomas are characterized by local aggressiveness. Metastases are rare at the time of diagnosis; when they occur, they are frequently localized at the lung. The propensity to metastasize is directly correlated to the grade of malignancy. Generally, low-grade tumours usually may have local aggressiveness but low tendency to metastatic spread. High-grade tumours have a more invasive behaviour with higher propensity to metastasize. Overall, the majority of patients with soft tissue sarcomas can be cured, even if the probability of cure depends on the degree of malignancy and the stage of the disease.
Diagnosis
The most common sign that leads to the diagnosis of soft tissue sarcomas is a growing swelling or lump. Other signs and symptoms depend on the part of the body where the tumour arises.
Various exams are necessary for the full diagnosis of soft tissue sarcomas. First of all, biopsy is needed for defining the histological diagnosis: a small sample of the tumour is taken and looked under a microscope, so that the pathologist can give the exact name of the tumour.
Then some tests are necessary to define the stage of the tumour (size, local invasiveness, spread in other part of the body): CT or MRI scan of the part of origin of the tumour, chest x-ray and CT-scan, abdominal ultrasound, bone scan are generally performed.
Knowing the particular type and the stage of the tumour is very important for deciding the most appropriate treatment.
Treatment
The treatment of patients with soft tissue sarcomas is complex and may necessitate multidisciplinary approach, including surgery, radiotherapy and chemotherapy. The treatment depends upon the type of the tumour and its grade of malignancy, the size of the tumour, and the possibility to remove it with a safety surgery.
Surgery is the mainstay of treatment. If possible, surgery will be used to completely remove the tumour. If the tumour cannot be completely removed without mutilation or functional sequelae, radiotherapy and chemotherapy should be used to shrink the tumour down and facilitate a subsequent operation.
Radiotherapy may be given to the area of origin of the tumour: high-energy rays can destroy tumour cells, but it is important to know that irradiation might cause late side effects (i.e. possible reduced growth of the irradiated part) that are difficult to foresee, but must be taken into account when the treatment strategy is discussed.
Chemotherapy is a combination of drugs that can destroy tumour cell with a cytotoxic mechanism. It is usually administered every three weeks: given intravenously, it can act against every tumour cell presents in the body, also against those spreading away from the site of origin of the tumour. Chemotherapy can be associated to nausea and vomiting, hair loss and increased risk of infection. With the exception of some particular histotypes, non-rhabdomyosarcoma soft tissue sarcomas are generally considered tumours with uncertain chemosensitiveness. But recent data would seem to suggest that chemotherapy may play a more significant role than is generally believed in some subsets of patients for which the risk of failure is high. Your doctors will explain you possible benefits and disvantages of the treatment choices.
»epssg.cineca.org/info.htm |
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Grethor
Today Is A Good Day To Format
join:2004-04-14
Puyallup, WA
clubs:
| reply to Loker
said by Loker :said by ManMachine :I don't believe any of this. If you try and get him 100,000 e-mails how many trees are going to be killed LOL How dare you all put a little boys recovery before a tree! 
e-mail sent. Trees be damned.  |
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nassaumike
join:2002-09-10
Westlake, OH | reply to kasparov33
Done...to hell with the trees.... |
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