- Post a Beg
- View Begs:
- Help Pay Bills
- Money for School
- Medical Bills Help
- Family Crisis
- Save Your Home
- Money for Travel
- Help Paying Rent
- Money for Business
- Disaster Help
- Toy Donations for Kids
- Entertainment
- Need a Job
- Need Clothes
- Unusual Requests
- Charity Donations
- General Begs for Help
- Miscellaneous
Stuff for Sale
Tag Cloud
- FAQ
- Avoiding Scams and Fraud
- Cyberbegging News
- BegsList Blog
- RSS Feeds
- Privacy Policy
Muscle Tags
Please help me LIVE a little bit longer.
Posted by SweetLittleDoll on 2012-04-18 01:58:02
I have several cronic illnesses. Including scoliosis:Scoliosis is a sideways curvature of the spine that occurs most often during the growth spurt just before puberty. While scoliosis can be caused by conditions such as cerebral palsy and muscular dystrophy, the cause of most scoliosis is unknown. My scoliosis curve got worse, the spine rotated and twisted, in addition to curving side to side. This caused the ribs on one side of the body to stick out farther than on the other side. Severe scoliosis can caused back pain and difficulty breathing. In my case In severe scoliosis, the rib cage may press against the lungs and heart, making it more difficult to breathe and harder for the heart to pump.I also experience harsh neurological affects of Muscle weakness, Numbness and Abnormal reflexes. To save my life I had to have surgery.
Surgery involves correcting the curve (although not all the way) and fusing the bones in the curve together. The surgeon lays bone grafts across the exposed surface of each vertebra. These grafts will regenerate, grow into the bone, and fuse the vertebrae together. The bones are held in place with one or two metal rods held down with hooks and screws, helping to support the fusion of the vertebrae.I went through all this at age 13. But now with the onset of sevral more cronic illness complication from the surgery that once saved my life now slowly kill me.
Years later I began getting sicker and sicker by the time I was 20 my spine was degenerating causing horrible pain, I had to have my appendix removed, then gallblader went bad. We never dreamed these all had a common factor. Doctors just shook their head proclaiming :you are just so young for your body to be failing like this". Eventually it was discovered I have Lupus and severe arthritus. Lupus is an autoimmune disease, meaning that the body' s immune system mistakenly attacks healthy organs and tissue. Lupus can affect any part of the body, causing inflammation and damage in joints, skin, kidneys, heart, lungs, blood vessels, or the brain. More than 90% of people with lupus have skin rashes, often triggered by exposure to the sun, and about half have kidney and lung problems. Because lupus affects the joints, it is considered a rheumatic (arthritis) disease.
Upon this discovery things began to make sense. So doctors now knowing why began a body wide check up to see what all has been affected. One test was A bone mineral density (BMD) test measures how much calcium and other types of minerals are present in a section of your bone. Your health care provider uses this test, along with other risk factors, to predict your risk of bone fractures in the future and detect osteoporosis. Bone fracture risk is highest in people with osteoporosis. They found I indeed had osteoporosis at the age of 22. SO now My bones are weaking causing damage areas all over my body, but the most serious being in my spine. Now comes the arthritis/lupus, they see these damaged areas and my own imune system attacks. Eating at the damaged areas creating even more damage, which increases the area the lupus attacks. It is a vicious circle. I have now been treated with medication over 10 yrs. But they can only slow the illness there is no cure, and dure to my scoliosis and the metal rods in my back surgical treatment options are very limited.
The damage is so severe I was decared legally disabled by the age of 23. My only income is SSI. I have to support my children and I on 658.00 a month. Thank God the court issued my ex to pay my rent in lue of child support. I am asking for help to cover upcoming medical bills. In the last 14 months I have had 5 seperate kidney surgery. My right kidney is damaged and I will soon be having a 6th surgery. This one to remove damaged section of the tube that leads from the kidney to bladder. then they will reattach at a higher section of bladder. I will aslo be having several Jaw surgeries. Due to exposure to radiation, osteoperosis a excessive vomiting of stomache acid my teeth are breaking and falling out. The doctor needs to repair what they can and put in inplants for what they cant. This will slow the degineration of my jaw. Without this treatment my jaw is going to cave in. Currently I am only able to eat mushy foods. I have drastically lost weight and my body is stuggling to heal due to the stress, pain and infection. So I hunbly beg of you to help me 1.00 or 50.00 anything would help. These procedures will not only improve my quality of life but aslo help extend my time here on earth just a little ehile longer. I just want to be with my kids as long as I can.Whith each dollar you donate its like adding an hour to my life.....What would you give for a few more hours with the ones you love?
Please help me LIVE a little bit longer.
Posted by SweetLittleDoll on 2012-04-18 01:58:01
I have several cronic illnesses. Including scoliosis:Scoliosis is a sideways curvature of the spine that occurs most often during the growth spurt just before puberty. While scoliosis can be caused by conditions such as cerebral palsy and muscular dystrophy, the cause of most scoliosis is unknown. My scoliosis curve got worse, the spine rotated and twisted, in addition to curving side to side. This caused the ribs on one side of the body to stick out farther than on the other side. Severe scoliosis can caused back pain and difficulty breathing. In my case In severe scoliosis, the rib cage may press against the lungs and heart, making it more difficult to breathe and harder for the heart to pump.I also experience harsh neurological affects of Muscle weakness, Numbness and Abnormal reflexes. To save my life I had to have surgery.
Surgery involves correcting the curve (although not all the way) and fusing the bones in the curve together. The surgeon lays bone grafts across the exposed surface of each vertebra. These grafts will regenerate, grow into the bone, and fuse the vertebrae together. The bones are held in place with one or two metal rods held down with hooks and screws, helping to support the fusion of the vertebrae.I went through all this at age 13. But now with the onset of sevral more cronic illness complication from the surgery that once saved my life now slowly kill me.
Years later I began getting sicker and sicker by the time I was 20 my spine was degenerating causing horrible pain, I had to have my appendix removed, then gallblader went bad. We never dreamed these all had a common factor. Doctors just shook their head proclaiming :you are just so young for your body to be failing like this". Eventually it was discovered I have Lupus and severe arthritus. Lupus is an autoimmune disease, meaning that the body' s immune system mistakenly attacks healthy organs and tissue. Lupus can affect any part of the body, causing inflammation and damage in joints, skin, kidneys, heart, lungs, blood vessels, or the brain. More than 90% of people with lupus have skin rashes, often triggered by exposure to the sun, and about half have kidney and lung problems. Because lupus affects the joints, it is considered a rheumatic (arthritis) disease.
Upon this discovery things began to make sense. So doctors now knowing why began a body wide check up to see what all has been affected. One test was A bone mineral density (BMD) test measures how much calcium and other types of minerals are present in a section of your bone. Your health care provider uses this test, along with other risk factors, to predict your risk of bone fractures in the future and detect osteoporosis. Bone fracture risk is highest in people with osteoporosis. They found I indeed had osteoporosis at the age of 22. SO now My bones are weaking causing damage areas all over my body, but the most serious being in my spine. Now comes the arthritis/lupus, they see these damaged areas and my own imune system attacks. Eating at the damaged areas creating even more damage, which increases the area the lupus attacks. It is a vicious circle. I have now been treated with medication over 10 yrs. But they can only slow the illness there is no cure, and dure to my scoliosis and the metal rods in my back surgical treatment options are very limited.
The damage is so severe I was decared legally disabled by the age of 23. My only income is SSI. I have to support my children and I on 658.00 a month. Thank God the court issued my ex to pay my rent in lue of child support. I am asking for help to cover upcoming medical bills. In the last 14 months I have had 5 seperate kidney surgery. My right kidney is damaged and I will soon be having a 6th surgery. This one to remove damaged section of the tube that leads from the kidney to bladder. then they will reattach at a higher section of bladder. I will aslo be having several Jaw surgeries. Due to exposure to radiation, osteoperosis a excessive vomiting of stomache acid my teeth are breaking and falling out. The doctor needs to repair what they can and put in inplants for what they cant. This will slow the degineration of my jaw. Without this treatment my jaw is going to cave in. Currently I am only able to eat mushy foods. I have drastically lost weight and my body is stuggling to heal due to the stress, pain and infection. So I hunbly beg of you to help me 1.00 or 50.00 anything would help. These procedures will not only improve my quality of life but aslo help extend my time here on earth just a little ehile longer. I just want to be with my kids as long as I can.Whith each dollar you donate its like adding an hour to my life.....What would you give for a few more hours with the ones you love?
I Cannot Afford The Plastic Surgery I Desperately Need A Tail Implant Now.
Posted by goodkarma on 2012-03-26 02:58:56
Need An iMac To Start My Career
Posted by amieb05 on 2012-03-15 15:58:34
I'm a struggling graphic designer in need of a new desktop Machintosh. I'm aiming to raise $1300 to buy a new iMac computer so that I can start designing to complete my portfolio and start applying for work. My last computer failed on me during finals in school. Thanks to my school's computer lab, I was able to finish my work and graduate. That was back in NYC. I couldn't afford living there on my own and had to come to a smaller town to live with parents. I worked minimum wage retail to gain some money, but the physical stress forced me to stop working due to muscle weakness problem I have. A medical affliction caused by a tumor that has been affecting my energy and skeletal/muscle strength for about 7 years. It was hard getting through school with my condition. It was twice as hard having to work on my feet for hours in a retail environment.
Double my misfortune, I live in a place where jobs are hard to come by. A small town which has a lot of developing to do and jobs are far between. I need a car to travel to the nearest grocery store and can't depend on parents to transport me everywhere. This is why a job is so imperative. I'd like to feel fulfilled knowing I'm doing something for my future and earning money to buy my needs. I wish I had the equipment to start looking for work.
I want an iMac more than anything in the world. If I had my iMac, I could update my portfolio, do some online freelance work and help my parents with some bills. I could start applying for jobs from home and not have to rely on my neighbor's iPad to browse the internet. Whenever my family goes to the mall in the weekends, I pass by our local Apple store and I see people walking out of the store with large boxes containing their brand new iMac's, Macbook Pro's or expensive iPad's...and I get angry.
Yes, I know it sounds terrible and I know not everyone buying a computer is a rich business mogul or an overpampered kid whose parents can buy them whatever they want, and they never have to worry about whether they could afford it or not. But it hurts me to know I'm in such a position, that although I am an adult who should be paying her parent's bills, I can't even help myself because I'm unemployed. No thanks to my stupid weak body that can't take a lot of physical strain, no thanks to ending up in a town where I can't get anywhere without having to walk at least two miles, no thanks to not having my computer...
My name is not Amelia. That is just a screen name because I am too embarassed to reveal my real name. I'd be so grateful to anyone that can help me reach my $1300 goal. I know Mac's are expensive, but they are the industry standard in what I do. I would like a desktop because they are durable and longer lasting. They can also take a lot processing power for the heavy graphic work I do. If you can find it in your time to spare any change .25 cents, $1, $5, I'll be grateful 'till eternity.
Anyone who donates, be kind to leave an email so that I can send you something in return for your favor.
Thank you and God bless,
ameliab2005@gmail.com
Genuine Tresor Paris Bracelet $70
Posted by Fruitbasket2468 on 2012-02-23 15:58:33
Business and Tax Help
Posted by Peachy on 2012-02-10 02:58:39
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.
22 female single w rare tumor
Posted by isitoveryet on 2012-01-20 06:58:09
raising 2 grand children
Posted by gabe1903 on 2012-01-07 18:58:49
A WISH FOR MY DAUGHTER WITH CUSHINGS DISEASE
Posted by dolphinfanatic on 2011-12-13 11:58:01
Paying medical bills not covered
Posted by SpiritualBeing on 2011-11-30 17:58:12
Miracle Needed
Posted by kimbirdy on 2011-07-13 09:58:40
Miracle Needed
Posted by kimbirdy on 2011-07-13 09:58:39
Miracle Needed
Posted by kimbirdy on 2011-07-13 09:58:39
Miracle Needed
Posted by kimbirdy on 2011-07-05 11:58:01
Miracle Needed
Posted by kimbirdy on 2011-07-05 11:58:00
Miracle Needed
Posted by kimbirdy on 2011-07-02 11:58:21
Miracle Needed
Posted by kimbirdy on 2011-07-02 11:58:20
Miracle Needed
Posted by kimbirdy on 2011-07-02 11:58:19
Miracle Needed
Posted by kimbirdy on 2011-06-30 23:58:36
Miracle Needed
Posted by kimbirdy on 2011-06-30 23:58:35
Miracle Needed
Posted by kimbirdy on 2011-06-30 23:58:35
Miracle Needed
Posted by kimbirdy on 2011-06-29 00:58:08
Miracle Needed
Posted by kimbirdy on 2011-06-28 23:58:20
