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Implants Tags
Im a type 1 diabetic, and needs financial help for my teeth PLEASE!!
Posted by youngtype1diabetic on 2012-04-25 05:58:41
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-04-23 14:58:47
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-04-23 14:58:47
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-04-23 14:58:46
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-04-23 14:58:46
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-04-04 14:58:51
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-04-04 14:58:50
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-04-04 14:58:50
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-04-04 14:58:50
I have only one breast
Posted by ZIPPER on 2012-04-03 13:58:26
So one fake breast is still there and one is missing. The area is flat and crinkled and ugly. My insurance company won't pay for reconstructive surgery because they say another breast is not "necessary."
I want to have a husband and family, but having only one breast looks and feels horrible. Please help me get the surgery I need so I can move ahead with my life.
PLEASE HELP A BABY BOYS LIFE AND HIS MOTHERS HEALTH
Posted by 4mybabyboy on 2012-04-01 18:58:37
~i am having trouble finding a a good reliable job...due to my extensive surgeries and health problems(ONE example: i have to have my entire mouth reconstructed and full implants and jaw surgery....which i just cannot afford,but is life threatening)
my son and i are staying at my parents house until i can figure out a better way for us...however my parents have alot of health issues going on to...and they dont have the financial means to allow us to continue living with them for long...i found a beautiful home for us and our 2 dogs(who are sadly not w us until we find a home...and are not in the best of care...but its all i hhave:()...yet i cannot afford any of this rightnow...i want to go back to school....and raise my son the best i can....i need to provide love ,safety ,and security...i am sooo scared and overwhelmed...... if you have the means a dollar donation toward helping my family in anyway, would be deeeply appreciated and never forgotten.
I need money for boobies! ( . Y . )
Posted by ineedboobies13 on 2012-02-20 16:58:39
Save the Tatas <3
You can donate through paypal (brittanyyjones@gmail.com)
I know it seems silly, but it would greatly improve my self confidence. Thank you for taking your time to read this, and even if you don't donate to me, there are many other people on here who could use some help. If you have the money donate to someone. :)
I need money for boobies! ( . Y . )
Posted by ineedboobies13 on 2012-02-20 16:58:31
Save the Tatas <3
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-02-09 09:58:56
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-02-09 09:58:56
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-02-09 09:58:56
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-02-09 09:58:55
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-01-30 14:58:19
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-01-30 14:58:15
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-01-30 14:58:13
IN DESPERATE NEED OF PLASTIC SURGERY.. PLEASE HELP!!! WILLING TO EVEN DO A LOAN!!!
Posted by lovelyangel741 on 2012-01-30 14:58:13
catch 22
Posted by louissa on 2012-01-28 15:58:47
My problem is when I was 18 I had a breast augmentation (enlarged) as my confidence was 0.Luckily at this time my parents paid the bill.The implants are not for life they last at least 10m - 15 years,having had 2 children they have suffered slightly, I need them re-done, although most of you may think it's a vanity thing it's not.Even if I just had them taken out I would need to pay and then be left with nothing.My husband and I are doing our best, and as we have spent my operation deposit just to live.
please help x x x
I Want To Feel Like A Woman
Posted by BuildAnArmy on 2012-01-25 13:58:53
I am currently scrimping and saving to pay for breast implants so that i can feel like a woman as i put on my wedding dress and walk up the aisle to meet my husband to be. I currently have around £200 as i have little cash to spare at the end of the month now that we are saving for a wedding!
Please help me in any way you can, anything you can offer me will be greatly appreciated, thank you so much!
unbreak my heart....
Posted by brokenhearted on 2012-01-20 17:58:04
I'm raising funds for ICD replacement surgery, to go see a HOCM specialist (Dr. Craig Asher) at Cleveland Clinic in S. Florida and to have advanced testing through Vanderbilt Autonomic Center in Tennessee.
I don't want to admit I need help; I've always been a strong, independent person who took care of everything and everyone. In August 2009, my whole world changed. After my procedure, I applied for disability and was turned down twice and had to hire an attorney. I went from being "super" mom, wife & friend and care taker of an Autistic son to being the one who had to be taken care of.
So how did I get to the point I have to ask others for help? Shortly before Father's Day 2009, I fell and broke my foot. When it didn't heal, I went to my primary with a broken foot and came out with a broken heart. After the shock wore off from the doctor telling me that I was going to die if I didn't have valve surgery; I started asking questions.
I didn't quite believe him and thought he was over reacting when he told me I was going to die because I walked and ran 3-5 times weekly and even did strenuous yard work. I felt fine and have 4 children aged 9-26 and kept up with them and stayed very active in things they did; but I was a ticking time bomb just waiting for the right time for my heart to stop.
He sent me to several specialists who said I had nothing really wrong, just some mild valve problems associated with aging; which was a huge relief. Everything seemed normal except my EKG's; they showed I had a huge amount of PVC's (premature ventricular contractions) roughly 50,000 âextraâ heartbeats daily.
My heart didn't really beat fully; it only quivered like a bowl of jello day in day out. The problem with it beating like this is, the heart becomes very ineffective at pumping and your cardiac output drops and heart muscle damage can occur.
The cardiologist and electrophysiologist I saw did extensive testing and recommended more testing in the hospital. I went in for a sleep study, Tilt table test and EP Study with Ablation. The sleep study revealed I had moderately severe sleep apnea and my oxygen goes from 99% down to 73% at night making it very dangerous for me when I sleep.
The tilt table test was the first inkling that something dangerous was going on inside. I fainted and had no palpable pulse; which is a very rare thing to happen. I was diagnosed with Dysautonomia - Neurocardiogenic Syncope and Orthostatic Intolerance.
I then had an ablation to burn the extra pathways in my heart and get rid of the pvc's I was living with daily. I was told this would be a relatively easy process and given a 95% success rate to get rid of the extra beats completely but it never crossed my mind that anything would happen.
What preliminary tests failed to show, is the pattern and origin of my arrhythmias were in a very dangerous spot to ablate - the RV Apex â in the bottom thin underside of the heart.
During the EP Study, I went into cardiac arrest and my heart stopped completely with no rhythm they could shock (Asystole), some how it started again for a few minutes but then stopped again. They were able to shock me back to normal sinus rhythm and luckily, the third time it stopped; it restarted on it's own so I didn't have to be shocked again.
I was diagnosed with Polymorphic Ventricular Tachycardia; a very dangerous, life threatening arrhythmia. I stayed in the hospital for 4 days trying to find a cause and to be prepped for an ICD (implantable cardiac defibrillator).
It took a cardiac catherization to finally find the problem and to show I had HOCM (obstructive Hypertrophic Cardiomyopathy) and internal high pressures in my valves.
My regular EP had to go out of town after the first procedure, so his partner had to do the implant; he wasn't as skilled as my regular dr and botched the lead implants.
When they checked the leads the next day before releasing me, they found a problem with the lead placement but the dr said it was "ok" and sent me home. Since then, I've had nothing but problems with the unit and been told by several other EP's I need to have the leads replaced and the ICD could be causing part of my problems.
Doctors think my other problems are related to HOCM (obstructive hypertrophic cardiomyopathy) and Autonomic nervous system failure and when I faint, my heart stops briefly causing damage each time this happens.
After the procedure, my body started failing from the damage it sustained the 4 times my heart stopped. My original cardiologist told me I would be in a wheel chair and totally dependent on others for everything by the time I'm 50; which is daunting because in March I'll be 45 and I can't deny the facts - my body is failing.
I was put on 10,000g sodium daily, water/fluid loading, Midodrine (insurance won't cover it $312 - 30 day supply), Propanolol, Pantoprazole, pain meds, suppression hose and binders as well as having to stay supine the majority of the day - which caused my heart failure to worsen and my EF (ejection fraction) to go down.
Nothing the doctor's have tried has helped, I still faint and my heart stops on a daily basis and I never know from one day to the next if something is going to trigger fluid build up and I have an acute attack.
In June 2011 I fainted falling into the side of my tiled tub, lacerating the side of my head in the process, severely sprained my neck and suffered a concussion. After that episode, I became a bit more cautious with every move I make because the dr found declining neurological functioning and mild brain damage; he said any more falls could lead to permanent major brain damage.
With so many previous medical bills and co-pays, I can't afford the 20% co-insurance to have my ICD replaced and Mayo Clinic wants a $5,000 deposit up front even with insurance. My ICD alone is $125,000, leads another $30,000 and then there's the doctor and hospital fees; which I won't know the cost until the procedure is done.
Each heart rhythm specialist and cardiologist I see tell me there is nothing more they can do after going over my history and treatments; I have a long hard fight to go and I have to just be thankful each day I'm alive. Some days I'm really glad I made it through, other days when the problems and pain take over; I wish the dr's had let me die.
I developed PTSD after the procedure, panic disorder and extreme agoraphobia. I went into such a deep depression over my health issues, I was afraid I would never see the lighter side of things again. I finally went to see a psychologist who prescribed Lamictal and diagnosed me with Bi-Polar disorder which has helped greatly but I still struggle on a daily basis.
One day we were just the ânormalâ every day family and the toughest thing we had to deal with is a child with Autism. Then; our whole lives changed in an instant we were dealing with mounting medical bills, expensive prescriptions, tests, appointments, loss of income and dealing with the possibility of death on a daily basis.
You just never know what the day may bring, so keep those you love close to you and never take one second for granted.
From the bottom of my heart thank you - even if it's support to say hey; I'm here if you need to talk or I know how you're feeling.
unbreak my heart....
Posted by brokenhearted on 2012-01-20 16:58:37
I'm raising funds for ICD replacement surgery, to go see a HOCM specialist (Dr. Craig Asher) at Cleveland Clinic in S. Florida and to have advanced testing through Vanderbilt Autonomic Center in Tennessee.
I don't want to admit I need help; I've always been a strong, independent person who took care of everything and everyone. In August 2009, my whole world changed. After my procedure, I applied for disability and was turned down twice and had to hire an attorney. I went from being "super" mom, wife & friend and care taker of an Autistic son to being the one who had to be taken care of.
So how did I get to the point I have to ask others for help? Shortly before Father's Day 2009, I fell and broke my foot. When it didn't heal, I went to my primary with a broken foot and came out with a broken heart. After the shock wore off from the doctor telling me that I was going to die if I didn't have valve surgery; I started asking questions.
I didn't quite believe him and thought he was over reacting when he told me I was going to die because I walked and ran 3-5 times weekly and even did strenuous yard work. I felt fine and have 4 children aged 9-26 and kept up with them and stayed very active in things they did; but I was a ticking time bomb just waiting for the right time for my heart to stop.
He sent me to several specialists who said I had nothing really wrong, just some mild valve problems associated with aging; which was a huge relief. Everything seemed normal except my EKG's; they showed I had a huge amount of PVC's (premature ventricular contractions) roughly 50,000 âextraâ heartbeats daily.
My heart didn't really beat fully; it only quivered like a bowl of jello day in day out. The problem with it beating like this is, the heart becomes very ineffective at pumping and your cardiac output drops and heart muscle damage can occur.
The cardiologist and electrophysiologist I saw did extensive testing and recommended more testing in the hospital. I went in for a sleep study, Tilt table test and EP Study with Ablation. The sleep study revealed I had moderately severe sleep apnea and my oxygen goes from 99% down to 73% at night making it very dangerous for me when I sleep.
The tilt table test was the first inkling that something dangerous was going on inside. I fainted and had no palpable pulse; which is a very rare thing to happen. I was diagnosed with Dysautonomia - Neurocardiogenic Syncope and Orthostatic Intolerance.
I then had an ablation to burn the extra pathways in my heart and get rid of the pvc's I was living with daily. I was told this would be a relatively easy process and given a 95% success rate to get rid of the extra beats completely but it never crossed my mind that anything would happen.
What preliminary tests failed to show, is the pattern and origin of my arrhythmias were in a very dangerous spot to ablate - the RV Apex â in the bottom thin underside of the heart.
During the EP Study, I went into cardiac arrest and my heart stopped completely with no rhythm they could shock (Asystole), some how it started again for a few minutes but then stopped again. They were able to shock me back to normal sinus rhythm and luckily, the third time it stopped; it restarted on it's own so I didn't have to be shocked again.
I was diagnosed with Polymorphic Ventricular Tachycardia; a very dangerous, life threatening arrhythmia. I stayed in the hospital for 4 days trying to find a cause and to be prepped for an ICD (implantable cardiac defibrillator).
It took a cardiac catherization to finally find the problem and to show I had HOCM (obstructive Hypertrophic Cardiomyopathy) and internal high pressures in my valves.
My regular EP had to go out of town after the first procedure, so his partner had to do the implant; he wasn't as skilled as my regular dr and botched the lead implants.
When they checked the leads the next day before releasing me, they found a problem with the lead placement but the dr said it was "ok" and sent me home. Since then, I've had nothing but problems with the unit and been told by several other EP's I need to have the leads replaced and the ICD could be causing part of my problems.
Doctors think my other problems are related to HOCM (obstructive hypertrophic cardiomyopathy) and Autonomic nervous system failure and when I faint, my heart stops briefly causing damage each time this happens.
After the procedure, my body started failing from the damage it sustained the 4 times my heart stopped. My original cardiologist told me I would be in a wheel chair and totally dependent on others for everything by the time I'm 50; which is daunting because in March I'll be 45 and I can't deny the facts - my body is failing.
I was put on 10,000g sodium daily, water/fluid loading, Midodrine (insurance won't cover it $312 - 30 day supply), Propanolol, Pantoprazole, pain meds, suppression hose and binders as well as having to stay supine the majority of the day - which caused my heart failure to worsen and my EF (ejection fraction) to go down.
Nothing the doctor's have tried has helped, I still faint and my heart stops on a daily basis and I never know from one day to the next if something is going to trigger fluid build up and I have an acute attack.
In June 2011 I fainted falling into the side of my tiled tub, lacerating the side of my head in the process, severely sprained my neck and suffered a concussion. After that episode, I became a bit more cautious with every move I make because the dr found declining neurological functioning and mild brain damage; he said any more falls could lead to permanent major brain damage.
With so many previous medical bills and co-pays, I can't afford the 20% co-insurance to have my ICD replaced and Mayo Clinic wants a $5,000 deposit up front even with insurance. My ICD alone is $125,000, leads another $30,000 and then there's the doctor and hospital fees; which I won't know the cost until the procedure is done.
Each heart rhythm specialist and cardiologist I see tell me there is nothing more they can do after going over my history and treatments; I have a long hard fight to go and I have to just be thankful each day I'm alive. Some days I'm really glad I made it through, other days when the problems and pain take over; I wish the dr's had let me die.
I developed PTSD after the procedure, panic disorder and extreme agoraphobia. I went into such a deep depression over my health issues, I was afraid I would never see the lighter side of things again. I finally went to see a psychologist who prescribed Lamictal and diagnosed me with Bi-Polar disorder which has helped greatly but I still struggle on a daily basis.
One day we were just the ânormalâ every day family and the toughest thing we had to deal with is a child with Autism. Then; our whole lives changed in an instant we were dealing with mounting medical bills, expensive prescriptions, tests, appointments, loss of income and dealing with the possibility of death on a daily basis.
You just never know what the day may bring, so keep those you love close to you and never take one second for granted.
From the bottom of my heart thank you - even if it's support to say hey; I'm here if you need to talk or I know how you're feeling.
