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Oxygen Tags
My Mother Is Dying And I Cant Afford Our Bills!
Posted by Danielle1984 on 2012-05-20 10:58:43
my mothers name, then they found out my name was on the lease when we signed a special form cause my mother is on oxygen. At that point they said pay it or we will disconnect. I do not have any savings left or even a credit card to use. Plead help me ... I don't know what else to do but to swallow my pride and beg. If UT wws
Please help me help my parents with money for a place to live they do not have much money and I do not want them on the streets
Posted by Chuck2012 on 2012-04-27 14:58:04
help while off work
Posted by jwc23 on 2012-03-26 06:58:57
Air Conditioner Repair So I Can Get To My Medical Visits
Posted by steph68461 on 2012-03-16 18:58:40
My name is Stephanie. Following the death of both my parents in a car accident 5 years ago August my health has been in a steady decline. I suffer from neurological issues that will soon have me in a wheelchair, and advanced COPD that means I have to have Oxygen continuously. Yesterday I had to go the doctors in 85 degree heat without any air conditioning in my van. By the time I got to the medical center and tried to find this new doctors location I ended up collapsing twice between the walking and breathing. I weigh 83 pounds at 5'5" and I can't carry the oxygen with me when I have to exit the vehicle. Ultimately I ended up in the emergency room.
I live with my daughter and grandson of 6 years. My grandson was in the car when my parents were killed and suffered a major brain injury at 13 months. I'm happy to report though that after months of hospitalization he is right as rain and is mad at me currently ;o) because I'm on my computer which he adores playing with. My daughter suffers from PTSD since the accident my parents were killed in. She cannot drive without someone in the car and she was going to go with me yesterday but the heat was so bad that we were concerned about Gavin in the back in my black 1994 Ford Astro van. It was just way too hot for him and with her PTSD we HAVE to go through town to get anywhere or she will lose it so there would not have been any steady air flow.
It's been a long 5 years. My parents and I jointly owned a duplex. Their deaths were the beginning of the most miserable time of my life. When I divorced it was jointly decided that it would better if I lived in the upstairs apartment so they could be there for the kids while I worked. Over 16 years we became so close that their deaths nearly destroyed me. I paid for the last 15 years on the note of the house, my buy in and we all lived there incredibly content and happy. My parents were my best friends.
After their deaths during the mortgage meltdown, credit locks, and the economic fallout my career of 16 years was one of the first to go. I worked in the non-profit sector designing programming for inner-city communities with a specific focus on youth. So 8 months after their deaths the funding streams I used for the programming dried up and a job I loved disappeared.
Life insurance was enough to cover their debt with a little left over because they didn't carry much but in the end I lost my home of 16 years to the insurance company that covered my daughters son through work when they filed a $ 90,000.00 lien against my home. So 7 months after losing my job I also lost a home I loved. So I experienced 3 deaths within the span of a little over a year.
Because I was unemployed so long and had to use my cards to keep the lights on so to speak my credit is not good. So I can't borrow the funds or even charge a repair for the car.
I can no longer go to doctors visits alone. I'm too weak to walk very far without help and I can't carry the oxygen canister on my own. So I need my daughter for these visits.
Like anyone with severe health issues I'm buried in bills but what I really need help on is funds that will me to fix the air conditioning in my van which despite it's age runs like a champ. I have a physicians assistant who comes into my home to work with my but getting to the specialists has become real concern.
My daughter even with her PTSD has reached a point where she doesn't want me going alone. I was supposed to call her when I reached the doctors the other day when I collapsed the 2nd time and they took me to the specialists office I asked the receptionist to call my daughter. She didn't and she left my daughter terrified that something horrible had happened to me. I don't carry a cell I can't afford one. My daughter was getting better about both driving and me driving myself; because of this receptionist my daughter has now had a huge set back. I have to see that doctor again next week and I can't take them without air conditioning so what I'm going to have to do is make sure I find someone that sit with my daughter while I'm gone to help keep her anxiety level low. I don't have any choice I have to get there. I won't have anyone to carry my oxygen but I'm hoping I can in there.
Anything you can do would be greatly appreciated. I am more than happy to pay it forward as soon as I can. I have been a lifelong contributor to various causes and I know people are in dire straights right now. We all need help in one form or another. I would never ask if I could do this myself. Please forgive me.
If you would like to know more about the accident and my Grandson and his Grandmother who after losing her home and moving into a 3rd floor apartment made a terrible mistake in her depressed state go to http://ontheirway.vanderbiltchildrens.org/?article=7511 this a feature story Vanderbilt Children's Hospital did in their print and web magazine.
DESPERATE! Please help me!!
Posted by singlemumof2 on 2012-02-07 11:58:16
He had a lack of oxygen to his lungs and it was touch and go for several days! He had to have oxygen, ventilators, a feeding tube and was in HDU!
As a single mother to two young children, I am forced to work part time as I receive no help, financial or emotional from their father, who ran off with my best friend.
I currently owe £4,000 in medical bills and on top still have to pay my rent and food and day care for my two children, plus the excess in sitters I needed for my older child while the baby was in hospital.
please please please if you can, help me. I would never normally do something like this but I cannot see any other option! I have been turnt down for a loan as I do not earn enough and live in rented accomodation.
I promise as soon as I am back on my feet, I will donate every penny I can afford to other needy causes!!!
Please help pay my sons medical bills
Posted by singlemumof2 on 2012-02-07 11:58:10
As a single mother I can only work part-time and I receive no financial help from their father.
I still owe £4,000 in medical bills and they are threatening me with court action!!
PLEASE PLEASE PLEASE help me!!
I promise as soon as I am back on my feet, I will return the favour and donate.
Dissabled couple, married 49 years, and need some help.
Posted by willway on 2012-01-27 19:58:49
We own our home(free and clear)and are not destitute, but we do need help.
We are both dissembled, My wife is on oxygen 24/7 and, due to nerve damage to both legs, I cannot walk or stand for more than a few minutes at a time. I manage to get around by hanging on to things.
As we get older there are some things that need to be taken care inside the house.
We have asked for help from our County to install new windows and doors that I have already purchased, and have had on hand for the last few years. I have checked with Habitat in our closest city and there is no help available in this part of rural America. The siding on the house is decaying badly and needs to be replaced. We also have siding and roof damage from a large storm here last spring.
We managed to get a kitchen remodel completed last year, by a handy man who owed me some money. This makes it much more accessible for my wife and I.
I have the tools and the know how, but my body wont cooperate.
I have never asked for help before, and have always been there for anyone that has needed help, but I am no longer able.
Thanks for reading this old mans long winded beg.
willway
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.
Please help save my car
Posted by inneedofassistance on 2011-12-18 12:58:38
Please help save my car- husband & 2 kitties
Posted by inneedofassistance on 2011-12-18 12:58:29
I lost my I am qualified by getting to be too old I keep getting denied. I do not know what to do only have $50.00 left in my purse.
Please help me I am asking for $1.00 donation.
Help me save my life and home
Posted by Bigred53 on 2011-12-13 07:58:53
Please help I want to stay alive and well
Posted by Bigred53 on 2011-12-06 17:58:45
need help with my power bill
Posted by jenncherry on 2011-11-16 00:58:04
On oxygen and need a better life!
Posted by Quasishort on 2011-11-05 06:58:44
I was born with congenital scoliosis and only half a rib cage. Because of this, my lungs never fully developed past the age of 5. I never thought of myself as handicapped and always pushed myself to do anything anyone else could do, but of course I was at a disadvantage and never really could be normal. But I was full of energy and I was young so I didn't let it hold me back. I couldn't run very far without having to stop and rest, but I still got around fine. A few years back I came down with pneumonia. Eventually I got better but the damage was done. After a while, I could tell that my breathing was getting worse. Eventually I noticed swelling around my ankles and I would wake up with horrible headaches. When I finally went to the doctor to figure out what was happening, I found out I had pulmonary hypertension and severe sleep apnea. Now I have to be on oxygen 24/7 and on a bi-pap machine while I sleep. I'm 30 years old and living on social security.
I still dream of earning a living for myself, but in order to do so I need some equipment so I can work from home. I also need a car so I can be more independent and stop relying on family members to give me a ride when I need to get groceries or go run errands.
Any help would be greatly appreciated and put to good use. Thank you and God bless.
Losing home Please help
Posted by AbbysDaddy on 2011-09-02 05:58:08
-Jeremy and Abigail
My journey to Mayo Clinic
Posted by truluv98 on 2011-08-05 02:58:41
Single Mother Needing Help To Buy Car
Posted by samanthasocey on 2011-03-07 21:58:02
My Mom
Posted by daleray on 2011-02-14 05:58:58
Drowning in financial woes
Posted by frisky14 on 2010-12-28 02:58:58
I am lost and in desperate need of a MIRIACLE! "Pay It Forward".. God Bless!
Posted by payitforward on 2010-12-26 15:58:58
I am the sweetest, sensitive, charitable, loving, giving, God Fearing, non judgemental, lover, encourager lady.. Many of my closest friends and family call me an "Angel on earth"... But even Angels need help once in a while.. I'm usually the helper so asking for help is new and a bit hard for me to chew..
First let's start with: My name is Crystal H.. I am a 32 year old caucasion lady that lives in Colorado.. Native to Colorado. Growing up I excelled in school thus earning 4.0 average and constant Honor Roll. I did have College opportunities ect. but at that time I met a young man in college, football player and fell in love. I had a good paying job as an office manager and thought all was good.. It was for several years anyway..We married and At 23yrs. I gave birth to my miriacle baby whom was premature and weighed 2 lbs. 11oz. I was very ill at the end of pregnancy due to acute Eclampsia so she was born early emergency c-cection, flight for lifed to Childrens Hospital in Denver and I stayed in ICU for the first week.. Keep in mind due to circumstances I never was able to see or touch my daughter before they airlifted her to Denver.. Finally one week later my doctor gave me a two hour pass to beable to go to Denver and meet my new daughter for the very first time.. Words can't tell what I felt and the emotions I was feeling.. I still tear up recounting the events.. But yes after many tears, fear of touching or holding her due to her size and all that was hooked up to her I did finally get courageous enough to hold my new born daughter after a week for the first time.. Love at first sight! Chills are still going through my body as I write this.. Anyway's over time she improved and became much stronger. She was small but mighty. I was finally released from the hospital myself and spent all my time with her at Childrens Hospital until release day.. Brought her home at 3 lbs. 12 oz and had the ultimate baby learning/motherly instincts. With 4 yrs. of twice weekly physical therapy she grew out of her challenges, and has grown into an way above average intellence, beautiful nine yr. old.. Thank you God!!!
My next challenges were none to fun at all! My marriage became rocky.. He became abusive physically, emotionally and mentally.. After about the last 3 yrs. becoming so bad and scary I could not deal with his abuse or allow my daughter seeing such activity. So with that said I asked him to leave our home. He would not leave without a police escort, but finally was gone nonetheless.. I am NOT pro divorce at all so after the initial anger callmed down I did go to him asking him to please do counceling with me and let's really try to work this all out. He REFUSED! So after being with my ex husband twelve years we finally did divorce.. =(
Right after the divorce at the age of 30, I was rushed to the ER and diagnosed with Congestive Heart Failure. I was in ICU for over one week and spent several months at home on oxygen. But now since the divorce I was dropped from his insurance so I am unable to have the cardiovascular care needed and a heart valve repaired.. But I have faith one day I will beable to have this delt with.. Gotta believe!
Next was really NOT PLANNED or wanted but happened. I finally met a young man whom I started spending much time with. Due to my heart and lack of insurance I was not on birth control but did use condoms with him. Unfortunately a condom did break and yes I did become pregnant.. Three day's before Christmas last year I misscarried the baby and spent two day's in hospital due to D&C and my heart. I was released at Christmas and had a hard time dealing with the hormones, lack of support from the young man, failure in my parents eyes ect.. Just plain and simple was a hard time for me emotionally but I NEVER once let my daughter know of this and still have not to this day. She does not need to be scared any further than what she has already in life.
Now we come to current events.. Swear I have let my life become a soap opera and should right a what not to do and how to survive book for women.. sighhhhh.... Anyways. After being single for nearly a year and of course wishing I could meet a nice (preferably) Christian boy to date and enter into a relationship with a man whom I have known for several years who was a family friend while I was married came back into my life. This time he showed strong romantic gestures and over time did finally earn some trust n love with me. We entered into a relationship and it felt safe and comfortable since I'd known him so long, family new him and my daughter new him well already too..
I finally started becoming happier and was slowly gaining a little self confidence, and believing that things will end up working out finally afterall.. (Keep in mind due to lack of insurance and Heart Failure I was still not allowed on birth control pills like I wanted) we of course used protection always. But two times the condom came off in me.. I hoped all would be fine and I would not become pregnant, not at all wanting to repeat my first ordeal I had with my daughter plus now with my Congestive Heart Failure on top of it all pregnancy would NOT be good! I went to a local clinic and talked to a female doctor there and begged her if there would be anyway I could qualify for any free birth control that would not hinder my CHF.. Finally I had good news.. =) She said she would see if I could qualify for the low hormone Miranna and if I did she would implant it in my uterous for free.. This was to last for five years.. Yes one positive answered prayer. I went to my doctors oppt. as sheduled, they had me do an UA to make sure I was not pregnant before insertion and preped me for the procedure. Right before the Doctor was to do procedure the nurse came into the room and notified both of us that indeed I was pregnant.. My head swirled with confusion, fear, stress ect.. After talking to my doctor briefly about it, my history ect. I left the office and proceeded to go to my boyfriend to update him of the current events.. At the very beginning he sounded happy and positive, even eased my mind a little but about two day's later he up and left me. I have had my first ultrasound and as of yet the baby is alive and well. Strong heart beat. I am nearly two months pregnant, doctor took me off all my heart meds. due to baby. Still no insurance, applied for Medicade which really saddened me that I was at a point I had to do this.. Very humbling to say the least, and am alone, confused, many urging me to abort the baby but remember I am Christian and this is a hard concept for me to accept.. Currently unemployed, single mother, pregnant, no father support, lonely, desperate and really beginning to feel hopeless.. There is a high probability that the acute Eclampsia could repeat itself again as it did with my daughter and now I'm older than before. Not 23 anymore now I'm 32 with Congestive Heart Failure and Hypertension. Trying to support my nine year old the best I can and now so worried and fearful of what is to come.. Christmas just happened and it so did not feel like Christmas to me. Not much I could do for my daughter or my loved ones. I'm so scared of what the near future holds and how I will beable to deal with it, and be healthy enough to continue taking care of my nine yr. old. Need a good job but kinda feel it would be hard since I am so high risk I have MANY constant dr. visits. Neonatal parnatologist, my OB, and supposed to find a cadiologist as well to monitor me.. Medicade pending but no answer if they would accept me yet, bills piling up, and feeling out of control totally of my life right now.. Sad and confused that bf left me too.. I'm praying sooooo hard daily, nightly, looking on internet for at home jobs I could do but most end up seeming like scams, keep going to church in order to help try to keep me grounded and keep the faith that somehow it will all work out.. I sure hope I have not bored you to death, some may be pretty disgusted by my mistakes and situation, but I do hope nonetheless that maybe even just one person actually found this post, read it through, and maybe just maybe is in a posistion of life that they could and would be willing to help me out a little.. The whole "Pay it forward" campaign.. I fully believe in that and fully believe what goeas around comes around.. Regardless of the outcome I wan't to take a moment to wish everyone that took the time to read my post all the best to you and yours, full love and ENDLESS BLESSINGS to all!
With love and true sencerity,
Crystal H...¢¾
P.S. I don't have a paypal acct. sorry.. If you would like to contact me you may please do so via email at:
chedenskog@yahoo.com Please let me know you are from this site in the subject line so I do not assume you are spam.. Thank you and God Bless...¢¾
single working mother needs help
Posted by MelB on 2010-09-25 09:58:58
Please help single mother elderly father ill
Posted by MelB on 2010-09-24 13:58:58
Caring for my 84 yr old WWII vet, critically ill
Posted by MelB on 2010-09-24 13:58:58
