Dear Friends and Family of ASDSurvivors,
As you well know, living with ASD can be very challenging not only for you but to your families as well. This organization was built with a view to helping you and your families to live up to this challenge by linking you up with people who share similar experiences and have succeeded in maintaining a positive outlook!
Explore more how our community had helped members face the…
ContinueAdded by Ben Munoz on February 22, 2012 at 6:59pm — No Comments
A heart disease can occur in any person. It can be genetic and can also be acquired during adulthood due to a lot of factors. Having a heart disease is never easy. There are a lot of things that you cannot do and some of your favorite foods can become a big no-no. At some point in life, we can say that having a heart disease is, perhaps, a bad luck. However, for a 5-year old Marty Viau, this is not the way it is. Despite having an Atrial Septal Defect since birth, he sees life so…
ContinueAdded by mary on January 29, 2012 at 9:07am — No Comments
ASD Survivors, Friends and Family,
As we begin a brand new year, envigorated with greater joy and compassion, we renewed our greater commitments to our community. BensFriends grew tremendously in the past three years, and we want to take this moment both to thank you and to make a promise to continue fulfill our mission: to ensure that everyone in the world with a rare disease has a safe place to go and connect with others like…
ContinueAdded by Ben Munoz on January 26, 2012 at 10:00am — No Comments
ASD Survivors, Friends and Family,
As we begin a brand new year, envigorated with greater joy and compassion, we renewed our greater commitments to our community. BensFriends grew tremendously in the past three years, and we want to take this moment both to thank you and to make a promise to continue fulfill our mission: to ensure that everyone in the world with a rare disease has a safe place to go and connect with others like…
ContinueAdded by Ben Munoz on January 25, 2012 at 10:00am — No Comments
ASD Survivors, Friends and Family,
We hope this message finds you well with high spirits and inner joy. We’re happy to inform you that our Atrial Septal Defect (ASD) community continuously been growing. And as always, we’re here to give strength and support.
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IN THIS ISSUE…
Added by Ben Munoz on December 19, 2011 at 4:50pm — No Comments
Were you told that your child should get and ultrasound to make sure they don't have an ASD. I was told it could be in the family. I know I shouldn't worry too much but it's hard not too while waiting for an appointment.
Added by Syl on November 19, 2011 at 9:41pm — 3 Comments
Well it's been 10 months since my procedure! Sometimes I still find this all so surreal. I am still having almost constant chest pain, now I have bradycardia recorded 39bpm one night, used to have tacycardia from atrial fibrillation and palpitations. Still very aware of my heart and it goes haywire when I lay down to go to sleep making it difficult to relax. Beats too slow, beats to fast, missing beats, thumping... Needless to say I'm not getting a great deal of quality sleep. Have an…
ContinueAdded by Diane M. on September 21, 2011 at 1:05am — No Comments
First I'd like you all to know it's been almost a year since Michael's ASD surgery and he is doing amazing. He was cleared by the doctor today to play football this year and he now weighs more than me and also taller than me. LOL Such a blessing that he is doing so well. Anyway, the main reason I am posting today is because I'd like to get defibulators put in at the school. I have been reviewing the cost and proceedures to get this done and it is going to cost about 14 thousand dollars to…
ContinueAdded by Kimberly Black on August 25, 2011 at 7:45pm — No Comments
Hi everyone, we took Alyssa to the cardiologist on Wednesday hoping for the best case scenario. Unfortunately, this is not what we got. They did another echo on her and found another hole. Because she has 2 holes and one is fairly close to a valve, they do not consider her a good candidate for catheterization. We are pretty devastated but trying to act as normal as possible in front of her. She will most likely have her surgery within 3 months. :(
Added by alyssasmom on August 19, 2011 at 6:28am — 4 Comments
So we took her back to the cardiologist on the 5th of August. He could not hear any murmur with his stethoscope, which was excellent news since last time he could hear it quite a bit. We did another ECHO just to see where everything was and to see if it had fully healed already or not. It came back that now instead of having a medium sized hole she has a tiny size and we go back in 2 years. Excellent news all around.
Added by 3Princesses on August 17, 2011 at 8:54am — 2 Comments
ASD Survivors, Friends and Family,
We hope this message finds you well, and that the first month of your 2011 was great. As always, we’re here for your support.
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IN THIS…
ContinueAdded by Ben Munoz on February 8, 2011 at 5:48am — No Comments
Does anybody have any experience with coumadin?
If so, why did they put you on it?
How has it made you feel?
Thanks.
Added by John on October 29, 2010 at 4:06am — No Comments
Added by Joy Bechdolt on September 16, 2010 at 8:11pm — 5 Comments
This community is all about helping. Helping yourself and helping others. Since many members have asked how they could help, we put together a list of ways you can help.…
ContinueAdded by John on August 23, 2010 at 2:30am — No Comments
We have some important information we are happy to announce!
As you all know we run support networks for people affected who have a…
ContinueAdded by michael Jones on July 15, 2010 at 9:53pm — No Comments
This community is part of the Ben's Friends network of patient communities. Learn more at bensfriends.org.
Patient Communities
Acute Disseminated Encephalomyelitis (ADEM)
ADHD/ADD
Adrenoleukodystrophy (ALD)
Arteriovenous Malformation (AVM)
Ataxia (International)
Ataxia (U.S.A.)
Atrial Septal Defect
Autism
Brain Aneurysms
Charcot Marie Tooth (CMT)
Chiari Malformation
Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
Crohn's Disease
Disabilities
Eagle Syndrome
Erythromelalgia
Fabry
Fibromyalgia
Glossopharyngeal Neuralgia(GPN)
Hepatitis C
Lupus
Multiple Myeloma
Myositis
Primary Sclerosing Cholangitis (PSC)
Psoriatic Arthritis (PsA)
Synovial Sarcoma
Trigeminal Neuralgia (TN)
Von Willebrand's Disease (VWD)
Other Rare Diseases
Dear Friends and Family of ASDSurvivors,
As you well know, living with ASD can be very challenging not only for you but to your families as well. This organization was built with a view to helping you and your families to live up to this challenge by linking you up with people who share similar experiences and have succeeded in maintaining a positive outlook!
Explore more how our community had helped members face the…
ContinuePosted by Ben Munoz on February 22, 2012 at 6:59pm
A heart disease can occur in any person. It can be genetic and can also be acquired during adulthood due to a lot of factors. Having a heart disease is never easy. There are a lot of things that you cannot do and some of your favorite foods can become a big no-no. At some point in life, we can say that having a heart disease is, perhaps, a bad luck. However, for a 5-year old Marty Viau, this is not the way it is. Despite having an Atrial Septal Defect since birth, he sees life so…
ContinuePosted by mary on January 29, 2012 at 9:07am
ASD Survivors, Friends and Family,
As we begin a brand new year, envigorated with greater joy and compassion, we renewed our greater commitments to our community. BensFriends grew tremendously in the past three years, and we want to take this moment both to thank you and to make a promise to continue fulfill our mission: to ensure that everyone in the world with a rare disease has a safe place to go and connect with others like…
ContinuePosted by Ben Munoz on January 26, 2012 at 10:00am
ASD Survivors, Friends and Family,
As we begin a brand new year, envigorated with greater joy and compassion, we renewed our greater commitments to our community. BensFriends grew tremendously in the past three years, and we want to take this moment both to thank you and to make a promise to continue fulfill our mission: to ensure that everyone in the world with a rare disease has a safe place to go and connect with others like…
ContinuePosted by Ben Munoz on January 25, 2012 at 10:00am
© 2012 Created by Ben Munoz.