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Wife is pregnant and both have been made redundant
Posted by PleaseHelpNeeded on 2012-01-25 14:58:43
My wife and I are expecting our second child in June, and last month were both made redundant from our public sector jobs.
Christmas which is meant to be a joyful time was nothing full of worries for both of us. The more my wife gets upset the more desperate I am, as I know the stress is no good for my wife or our unborn child. We have enough saved up for another two months but then nothing.
Please donate as much as you can and keep your fingers crossed for me, as I'm going for another interview next week.
Wife is pregnant and both have been made redundant
Posted by PleaseHelpNeeded on 2012-01-25 14:58:43
My wife and I are expecting our second child in June, and last month were both made redundant from our public sector jobs.
Christmas which is meant to be a joyful time was nothing full of worries for both of us. The more my wife gets upset the more desperate I am, as I know the stress is no good for my wife or our unborn child. We have enough saved up for another two months but then nothing.
Please donate as much as you can and keep your fingers crossed for me, as I'm going for another interview next week.
Wife is pregnant and both have been made redundant
Posted by PleaseHelpNeeded on 2012-01-25 14:58:42
My wife and I are expecting our second child in June, and last month were both made redundant from our public sector jobs.
Christmas which is meant to be a joyful time was nothing full of worries for both of us. The more my wife gets upset the more desperate I am, as I know the stress is no good for my wife or our unborn child. We have enough saved up for another two months but then nothing.
Please donate as much as you can and keep your fingers crossed for me, as I'm going for another interview next week.
lost my wife to car accident
Posted by needhelp025 on 2012-01-21 12:58:04
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.
hello, please, please, any help is greatly appreciated
Posted by needhelpsoon on 2012-01-13 17:58:43
Some background:
I am a mother of three wonderful children. I was married to their father for ten years, unfortunately. as with too many these days, it did not work out. I do not regret our marriage, for it gave me three wonderful children who are all almost grown now. 21, 19, 16. When we were married, we both decided it best for me to stay home with the children and raise them within our family, although this is pretty rare these days. Once we divoced though, I could only find manual type (cashier, inventory, stock, etc) work as I was married straight out of high school and did not try to go back to work until they were all in school. I did not mind working sometimes three different jobs in order to have full time hours yet work around the kids school schedule, son's physical therapy and the usual "Mom" stuff. People kept saying go back to school, but I could not figure out how to work three jobs, be the full time mom and dad and add school. Unfortunately five years ago I started feeling ill, like the flu that never went away. I kept working through it, with my kids being older as much as I knew I needed to be there, I knew I needed to pay the rent/bills too, so I started working split shifts at the grocery store. I'd go in at 6 am until 2pm, come home, be here for after school and dinner, then rush back at six and work until 11 pm. All the while I was getting sicker. I was hospitalized three times during this period. Unfortunately no one seems to want to agree with whats wrong with me, I have heard several diagnosis over the years, but RA is the one and only proven ailment, although they feel I have an overlapping autoimmune disease. I have no insurance right now, and hoping to get the state insurance soon, but I have a feeling treatment is a long ways away.
I did not want to go the ssdi route until I had no other choice. Too bad that's not how the system works. I, for the last three years have been dealing with such pain and illness, a "real job" became out of the question, so I'd work here and there, whenever I could get work and be able to do it, as some days are a little better than others. Believe me, nothing is below me, I'm happy to scrub toilets, clean dog poo, I will do anything legal to make it, most days now though I feel so bad I can't do much .Well, I have finally reached that "I can't do stage", just yesterday my daughter had to get me out of bed as I could not move. Problem is, SSDI takes up to two years to get, which I didn't realize, so now due to my inane pride, I am absolutely stuck. I just know if I can get on top of the important bills, I will be able to continue as I have (fingers crossed) until the SSDI is accepted, which I did finally file for.
More important than anything else, I need to get some food in the house for my son. I truly don't care if I eat, as long as its enough to survive, which believe it or not is very little. However, I want my growing son to be able to eat when he's hungry and have good healthy choices along with the occasional treat. My 19 year old is very self sufficient and has moved into her own apartment and after taking college courses all through high school is on the right track. My 21 year old moved out when she graduated high school and she too finished college and is self sufficient. (she has now moved back in with her daughter) That's why I only mentioned my son. I have plenty of clothes I can donate as he grew so fast, many very nice, and also more than willing to repay any amount, just can't promise when.
Please, any help at all, anything, is greatly appreciated. Food is first and there is a very cheap store nearby where I can grocery shop. Bills are secondary right now, so believe me, every bit helps. Thanks for reading my story and giving your time and any help you may be able to handle.
My Family is in need
Posted by needhelpsoon on 2012-01-02 11:58:29
I am a mother of three wonderful children. I was married to their father for ten years, unfortunately. as with too many these days, it did not work out. I do not regret our marriage, for it gave me three wonderful children who are all almost grown now. 21, 19, 16. When we were married, we both decided it best for me to stay home with the children and raise them within our family, although this is pretty rare these days. Once we divoced though, I could only find manual type (cashier, inventory, stock, etc) work as I was married straight out of high school and did not try to go back to work until they were all in school. I did not mind working sometimes three different jobs in order to have full time hours yet work around the kids school schedule, son's physical therapy and the usual "Mom" stuff. People kept saying go back to school, but I could not digure out how to work three jobs, be the full time mom and dad and add school. Unfortunately five years ago I started feeling ill, like the flu that never went away. I kept working through it, with my kids being older as much as I knew I needed to be there, I knew I needed to pay the rent/bills too, so I started working split shifts at the grocery store. I'd go in at 6 am until 2pm, come home, be here for after school and dinner, then rush back at six and work until 11 pm. All the while I was getting sicker. I was hospitalized three times during this period. Undortunately no one seems to want to agree with whats wrong with me, I have heard several diagnosis over the years, but RA is the one and only proven ailment, although they feel I have an overlapping autoimmune disease. I have no insurance right now, and hoping to get the state insurance soon, but I have a feeling treatment is a long ways away.
I did not want to go the ssdi route until I had no other choice. Too bad that's not how the system works. I, for the last three years have been dealing with such pain and illness, a "real job" became out of the question, so I'd work here and there, whenever I could get work and be able to do it, as some days are a little better than others. Believe me, nothing is below me, I'm happy to scrub toilets, clean dog poo, I will do anything legal to make it, most days now though I feel so bad I can't do much .Well, I have finally reached that "I can't do stage", just yesterday my daughter had to get me out of bed as I could not move. Problem is, SSDI takes up to two years to get, which I didn't realize, so now due to my inane pride, I am absolutely stuck. I just know if I can get on top of the important bills, I will be able to continue as I have (fingers crossed) until the SSDI is accepted, which I did finally file for.
More important than anything else, I need to get some food in the house for my son. I truly don't care if I eat, as long as its enough to survive, which believe it or not is very little. However, I want my growing son to be able to eat when he's hungry and have good healthy choices along with the occasional treat. My 19 year old is very self sufficient and has moved into her own apartment and after taking college courses all through high school is on the right track. My 21 year old moved out when she graduated high school and she too finished college and is self sufficient. That's why I only mentioned my son. I have plenty of clothes I can donate as he grew so fast, many very nice, and also more than willing to repay any amount, just can't promise when.
Please, any help at all, anything, is greatly appreciated. Food is dirst and there is a very cheap store nearby where I can grocery shop. Bills are secondary right now, so believe me, every bit helps. Thanks for reading my story and giving your time and any help you may be able to handle.
I will loose my apartment
Posted by christopherggreen on 2011-10-12 15:58:36
A few months ago I lost my job... Cut backs no fault of my own. I have been supporting my family through savings... And recently selling off my most vaulbile possisions. I don't have anything of vaule left... and my land lord has givin me a 72 hour notice. I have come up with most of it through family and friends, but I'm worried about next month. Electric will be shut off soon.
I have an interview next week... Fingers crossed.
If an angel is reading this. I could really use a maricle...
Please save my family and me
Please help, We're about to be homeless
Posted by weneedanangel on 2011-09-30 01:58:12
We're about to lose our home. I recently recieved a cut off notice for our utilities and in order to keep them on it will cost $181.61 the balance due however is $188.00. This will not matter however, because I don't have the funds to make the house payment coming due on the 12th of October. I am 399.00 short on the payment. The balance we owe on our home is $6,320.00. Once the house is paid off we will be able to pay $180.00 for lot rent instead of $580.00 for lot rent and house payment.. (Of which only $200.00 goes towards the balance if not paid in full - which is .32 more payments at $580.00 a month). If we can just get our home paid off we would be okay - even with child support garnishing 54% of my pay. By law Child Support Enforcement can garnish up to 65% of a payee's pay.
Just to be up front, I do have a job. Unfortunately I only work about 30 hours a week on average at minimum wage. I am very happy for my job, but after child support garnishes $478.00 a month from my paycheck we can barely make the house payment most months. I have filed for a reduction of child support, but they refuse to use my legitmate income, instead using the income I made previously when I was in a position to help others, and did so regularly. My employer has even filed an affidavit with child support enforcement stating they cannot offer me more then 32 hours and that I make minimum wage. I am curretly looking for a second job, or another job that pays better to take the place of the job I now hold. If anyone has any IT professional positions, please let me know as I would love to come work for you, or your company. That would be the best way to help us out.
My boyfriend would love to work, but he is disabled and currently has an application in with Social Security Disability, unfortunately it takes a long time for it to come through, and by the time it does we will have already lost our home. He was disabled 2 years ago last July when he was working on a wireless tower that was 80 foot tall. It collapsed under him and he is very lucky to have survived the fall, however, when he came down he landed on his ankle and the impact caused the joint to turn around backwards and upside down. He has had surgery for this, unfortunately it is still not right. He cannot straighten out his foot to walk. Because of shortening of the tendons on the inside and front of his ankle he is not able to balance or apply weight to the ankle for more then a few moments. And even that short amount of time causes him extreme pain. He tries to help around the house by doing chores such as mowing our small patch of lawn, but even that small chore takes him over 3 days to complete. My employer does not offer medical insurance, so we are without it. It makes it impossible to go to a doctor to help him get the medical assistance needed to 1. fix his ankle completely and 2. pain management. So he perseveres and does as much as he can.
Every day I have to try to get my 1984 Volvo 240 Station Wagon running so I can get to work that day. When I try to pull out onto the highway to go to work it bogs down like it is under water. It takes crossed fingers, prayer and much clutch/gas pedal manipulation for the car to pull out... and even more to get it to the speed limit. It is very scary because there is a blind corner that people speed around regularly and I'm just waiting for the day I get hit trying to pull out. Unfortunately we don't know what is wrong with it and do not have the ability to take it to a mechanic to see if they can do a diagnostic, much less pay to have it repaired. So if anyone is willing to donate their time and possibly parts to get the car up and running safely it would be greatly appreciated. It is the only legal vehicle we have.
I am trying to do odd jobs around town as well as sell jewelry that I make online and at a little shop here in Newport. It is hard because most months no one seems to buy my jewelry and the jobs are far and few between.
What is really sad is I know come the middle of October we will be homeless, my daughter's dog, Kenji and my dog, Nikki will have to go to the animal shelter if I cannot find them homes. I know I would not be able to care for them at all if we have no home in which to live. As it stands now, I haven't been able to buy them dog food for a few months, and the Animal Shelter in Priest River does not have any spare food for them, so they eat what we eat. the good thing is they are fat and very happy and loving dogs.
If you can help at all, even if it is a little bit ($1, $5 or even $10) - if several help out a little it will add up to a lot; it would be greatly appreciated, and once we're back on our feet, of course we fully intend to pay it forward by helping others.
Thank you for your time and consideration... God Bless
If you are able to help you can donate through PayPal.
Or if you have a job to offer me (18 years experience as an IT professional )
Single mom facing eviction...at the end of my rope PLEASE help...
Posted by sammi44 on 2011-06-30 07:58:43
Single mom facing eviction...at the end of my rope PLEASE help...
Posted by sammi44 on 2011-06-30 07:58:43
Single mom facing eviction...at the end of my rope PLEASE help...
Posted by sammi44 on 2011-06-30 07:58:42
Single mom facing eviction...at the end of my rope PLEASE help...
Posted by sammi44 on 2011-06-30 07:58:42
Single mom facing eviction...at the end of my rope PLEASE help...
Posted by sammi44 on 2011-06-30 07:58:42
Single mom facing eviction...at the end of my rope PLEASE help...
Posted by sammi44 on 2011-06-30 07:58:41
Victim of Brutal Dog Bite to Face!
Posted by valraeh on 2011-03-10 13:58:14
Thanking you in advance... ...for any size donation for these medical bills.
(Pic of Face): http://i100.photobucket.com/albums/m35/sassicash/Serious%20Dog%20Bite%20To%20Face/VICTIMDOGBITE.jpg
(Pic of Medical Bill): http://members.cox.net/timhebert/Medical%20Bill.Dog%20Bite.jpg
Money to be as creative as I can be
Posted by Dizkojockey on 2010-10-13 15:58:58
