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Read my charity evaluation of the best charity to donate to. I need to raise seed money and startup capital to start my business. I'm planning on becoming a binary options investor according to this website: http://www.60secondprofits.com/system/. This is a great binary options system explained by ex-stock broker turned independent trader Keith Jones. The basis of this free strategy centers around 60 second options, something that very few binary options platforms offer. The strategy is very sound, and what he shows you is how you follow a trend in the EUR/USD forex market and use a progressive buying strategy to capitalise on the small currency fluctuations over a .5 decimal base over the period of just 1 minute, so you can earn money from binary options very quickly indeed. Keith claims that this strategy has a 100% success rate (he averages $80 to $150 an hour profits).

Whilst testing out this free binary options system over a period of 5 days a reviewer was able to generate an impressive $6200 from a starting trade of just $5 and a bank of just $300. Quite impressive stuff I think you will agree. So what I need is $300 seed money and startup capital to get started. You can donate all or any part of this to my Paypal account by hitting the Donate link below. Or you could mail your donation to:

Brother Roger Bovee
PO Box 404
Wautoma, WI 54982

Thanks for helping because I really need the added income to provide for my ministry!

I really hate begging, but it's my last hope. I was working full time and just barely staying afloat with my basic bills (electric, rent, car insurance). I got injured at my work a month ago and haven't been able to return to work. It's doctor visit and testing over and over again. I am currently fighting to get workman's comp but they said it may be a while. I am a single mother and a 3 year old. She has medicaid and we get food stamps, but I haven't been able to get any other assistance.... either there's an extremely long wait or they're not taking applications. We also do not get any child support, her father is a deadbeat. I have no family to turn to either. I need help with my rent for just this month to keep a roof over our heads. It's $450 . Please help, any little bit will help. God bless.

I need to raise seed money and startup capital to start my business. I'm planning on becoming a binary options investor according to this website: http://www.60secondprofits.com/system/. This is a great binary options system explained by ex-stock broker turned independent trader Keith Jones. The basis of this free strategy centers around 60 second options, something that very few binary options platforms offer. The strategy is very sound, and what he shows you is how you follow a trend in the EUR/USD forex market and use a progressive buying strategy to capitalise on the small currency fluctuations over a .5 decimal base over the period of just 1 minute, so you can earn money from binary options very quickly indeed. Keith claims that this strategy has a 100% success rate (he averages $80 to $150 an hour profits).

Whilst testing out this free binary options system over a period of 5 days a reviewer was able to generate an impressive $6200 from a starting trade of just $5 and a bank of just $300. Quite impressive stuff I think you will agree. So what I need is $300 seed money and startup capital to get started. You can donate all or any part of this to my Paypal account by hitting the Donate link below. Thanks for helping because I really need the added income!

My father was diagnosed with Lung Canger, Stage Four a month ago. He worked all of his life to support his family and has always helped others out. Two months ago he thought he had a pnemonia and called his doctor to set up an appointment. She failed to find an infection and refered him to get further testing. The test results came back that he in fact has lung cancer and it has spread to his brain, liver, and lymph nodes. The cancer also caused extra fluid to accumulate around his heart which they drained. He just finished his first round of radiation treatment and is undergoing Chemotherapy twice a month. The doctors gave my father a prognosis of 18 months.
My parents have a mortgage and many of bills that are currently falling behind due to my father being unable to work. He was approved for Social Security Benifits but there is a 5 month waiting period with no exceptions and therefore he needs to wait until September to see his first check. I tried everything I could to see if there was an exception and the Social Security office told me that I would have to talk to my Senator. I plan on writing to him regarding this, but I know it will take a while before I hear back from any of them. Seeing my 56 year old father in such agonizing pain is hard enough, seeing my mother in a constant state of depression is extremly hard and trying to come up with plans to get fincancial help for my father seem to all be for nothing because he got not qualify for financial help due to my mothers pay. They dont put into consideration that they have a mortgage and a vehicle to pay for and with all of the doctors bills and presciption costs; they do not have enough money.
I am looking for any help that I can get. Any donated money would go directly to my father for his bills and mortgage payment. It would also go to presciptions and doctors visits so that he can continue to get good care. I have tried so many ways to find a solution to his financial problems and this is my last hope. This will save him a lot of additional stress. If there is any money that anyone could donate, it would be greatly appreciated.
We also do not know how we would come up with finneral expenses and such when the time comes. Any donations will not be used unless it is for my fathers healthcare, bills or for his funneral costs when the time comes. Thank you for your time and have a nice day.

My father was diagnosed with Lung Canger, Stage Four a month ago. He worked all of his life to support his family and has always helped others out. Two months ago he thought he had a pnemonia and called his doctor to set up an appointment. She failed to find an infection and refered him to get further testing. The test results came back that he in fact has lung cancer and it has spread to his brain, liver, and lymph nodes. The cancer also caused extra fluid to accumulate around his heart which they drained. He just finished his first round of radiation treatment and is undergoing Chemotherapy twice a month. The doctors gave my father a prognosis of 18 months.
My parents have a mortgage and many of bills that are currently falling behind due to my father being unable to work. He was approved for Social Security Benifits but there is a 5 month waiting period with no exceptions and therefore he needs to wait until September to see his first check. I tried everything I could to see if there was an exception and the Social Security office told me that I would have to talk to my Senator. I plan on writing to him regarding this, but I know it will take a while before I hear back from any of them. Seeing my 56 year old father in such agonizing pain is hard enough, seeing my mother in a constant state of depression is extremly hard and trying to come up with plans to get fincancial help for my father seem to all be for nothing because he got not qualify for financial help due to my mothers pay. They dont put into consideration that they have a mortgage and a vehicle to pay for and with all of the doctors bills and presciption costs; they do not have enough money.
I am looking for any help that I can get. Any donated money would go directly to my father for his bills and mortgage payment. It would also go to presciptions and doctors visits so that he can continue to get good care. I have tried so many ways to find a solution to his financial problems and this is my last hope. This will save him a lot of additional stress. If there is any money that anyone could donate, it would be greatly appreciated.
We also do not know how we would come up with finneral expenses and such when the time comes. Any donations will not be used unless it is for my fathers healthcare, bills or for his funneral costs when the time comes. Thank you for your time and have a nice day.

Hi,
We are a family of six that could use some finanical help.
We have 2 teenage sons and 2 yonger daughters.Last year I ended up
in the hospital ICU to find out I have type1 diabetes.My hospital bills
have reached over one hundred thousand dollars so far.Problem is I do not have
health insurance and now i have to buy insulin and blood testing supply's
every month that cost me hundreds of dollars. With all the new monthly bills
our household bills are just getting farther and farther behind. I feel like
I am a burden to my family. Its getting hard just to put food on the table.
If anyone out there could send a little help our way I would be so grateful.
God bless

I have an American girlfriend in the US who needs me desperatly right now. I had to come home to London to deal with some personal issues and we broke up for a brief time. Durring that time my visa expired and I need to get a new one. My girlfriend and I got back together a few weeks ago and she was planning to come here to me. She was recently in a bad car accident and she is not getting better. I have realized my mistake in breaking up with her all too late. Now I am desperate to get back to the states so that I can be there for her when she needs me the most. Please help me! I need $850 for all of the physicals, medical testing, and proper paperwork that I need to get done in order to qualify for a new visa. Anything you can offer as help would be much appreciated! Thank You!

Hi my name is Jeff I live here in NV. I’m not sure about this, I never been in such a need for money before let alone having to ask is not easy for me, I know a lot of people are struggling. Not too long ago we had the best economy in the US, now it is the worst. Getting a full time job here is almost impossible, my wife used to be an Accountant; I use to work as a service technician for a water company. My wife got laid off 3 yrs ago and now works pt. for Jack in the Box. I got laid off 2 yrs ago. It took me 6 months just to find pt. work for a Rent a Car agency. We managed ok using are credit cards hoping things would become better. We ended using all are credit and had to file bankruptcy. To make matters worse I ended up getting fired from my pt job, Due to a sleep disorder from depression and anxiety I have, I ended up crash testing too many of our rental cars. We are now 3 months behind on our Mortgage about $2400 And to top it off our home furnace went out 2 months ago we have nothing left for any expenses, its taking everything we have left to pay our bills and child support in which I refuse to get behind on my son and wife are my life, I just wish we could feel warm again. Our furnace could be repaired for about $2000 but any donation would be very grateful. Thank you so much Jeff

I've decided to try and get help through donations http://www.giveforward.com/unbreakmyheart and funding http://unbreakmyheart2011.blogspot.com/from outside sources since every doctor I've seen in 2 years agree that I need the leads to my ICD (defibrillator) replaced; but shuffle me back to the original doctor and wash their hands of me.

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 “extra” 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 – 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 “normal” 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.

I've decided to try and get help through donations http://www.giveforward.com/unbreakmyheart and funding http://unbreakmyheart2011.blogspot.com/from outside sources since every doctor I've seen in 2 years agree that I need the leads to my ICD (defibrillator) replaced; but shuffle me back to the original doctor and wash their hands of me.

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 “extra” 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 – 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 “normal” 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.

I am 38 yr old mother of 3 married for 17 yrs. Been with spouse 19 yrs total. Spouse is an alcoholic. I'm a disabled high school drop out with a GED. This past year spouse destroyed our marriage yet I'm stuck in this hell with no way out. I can't get disability or SSI. I have no income, savings or any way to support my kids. When I told spouse I wanted a divorce he was going to walk away & leave me with no way to pay the rent or utilities. Can't afford an attorney can't afford anything to be honest. I depend upon him for income. My list of health problems began at age 17 & have continued to compile since. Can not be treated for my medical conditions due to my hypersensitivity to prescription medications & allergies to opiates & codeine. My existence is utterly miserable!! I need a way out of this hell. Everyone deserves to be happy even me. I have to provide stability to my children so I live a lie day to day pretending to be his partner friend & lover. Honestly it is enough to make one have no desire to live. I am trapped in hell with 3 kids. I have been diagnosed with degenerative disc disease, fibromyalgia, restless leg syndrome, herniated T11-12, chronic tendinitis of the groin, eczema. I have very bad allergies with frequent allergic reactions to things in my environment and have no idea what they are. I will be allergy tested next week. The week after I start testing for lupus & kidney disease if nothing is found on scope test of my bladder. I stay sick get many things at one time & it takes me much longer to recover than normal people. There has to be a way out of this with some dignity. I was told by an SSI rep that I am one of those people that just falls through the cracks. There has to be hope for us down here for Christ sake there has to be

Thank you for even reading this because if you have then you are seeking to help people in need and you must have a wonderful heart. I have in recent years reached out to orphaned children in both Uganda and Mexico who needed me so I have no problems with asking for some help myself at this time.

After 3 years of back and forth with Social Security, I finally was approved for federal disability. Thankfully, I can move forward with testing and treatments to figure out what is causing the multiple symptoms disabling me. My sole desire is to get well enough to return to work in at least some capacity. Now I have some savings from back disability owed but not quite enough to finally purchase my own home. I am looking to purchase a modest home that is manageable for me in my condition. One that is safe and secure for me and my toy poodle who deserves something nice. Although I have enough for a decent down payment, my credit has suffered due to my inability to work. My medical bills went straight to my credit report as being unpaid while I waited for SSDI approval and Medicare approval. My credit score is below 600 and I cannot get a loan. I have $20,000 I can put toward my very first home ever. My goal is to get my $20,000 matched in order for me to purchase a small home/condo for approximately $40,000. My income is $955/mo and I still need to find suitable transportation also. My last vehicle was basically stolen by a predatory towing service and I was incapacitated at the time due to my disability and later was unable to afford retrieving the vehicle because of outrageous storage fees. Currently family members are taking me everywhere which can sometimes be more difficult than helpful. I A modest reliable vehicle is what I need. My individual goal is to become self sufficient and self reliant once again...get healthy and go back to work. Any help with the above items would be much appreciated. If I were in a better position I believe I too would be searching to help those in similar situations as mine.

Gratitude to all who are on this site!
In 2009 doctors and many others witnessed tiny fluorescent white little puff balls, I call them (They are actually rice grain shaped), emerging spontaneously from my skin by the hundreds,maybe thousands. I have been ill most of my life on and off, for at least 15 years with migraines 25 or more out of 30 days much of spring through fall. When the disease(es) is/are fully active, it is sheer unending torture...
Mild examples are that I got stung by a bee, and was relieved to see it was bee, not the disease..the other day for about 5 minutes, it felt like I had a pinl sticking into my back, antibiotic final stopped it.the itching, stinging, is unreal, intense . I have kept it subdued through alternative cures a.d mixes after anti fungal with antibiotic, yet it still persists, and spring and summer heat make it overactive.
It seems to come with this rustcolored mold that is now everywhere in the little camper I am living in. This rust colored mold also grows kn and in me, creating ...well, ill leave out all the gorey detsils..My family helped me to buy this new, in hopes living in good clean air would help. We looked at the mold under a microscope, and like the fibers that come out ogle, it is fibrous, not mold- like
To add to this, we looked at a slide I made of the fiber in 2009, and one of the fibers turned into a slug like thing while in storage on the microscope, and there is this strange black ink- like looking circle around it all.
my doctors are at a loss, as they don't know of any test to identify this. The fibers just came back as unidentified plant material. It is strange to see them emerge..it just blips right out of the skin in less than a second.
because my camper is now covered in this, no matter how much I clean, every rain the camper gets covered.
Whatever this organism had done to my body, I itch, well all the time. it gets worse when I touch people or old books, I cannot sit on fabric, I have to bring plastic with me wherever I go..
Even my bed is covered in plastic
This organism fights other organisms, even acidophilus!
This and my severe migraines led to finally sucumbing to the acceptance of needing help, which came immediately through disability.o
My goal now is to identify this organism(or group of organisms. I have to get the camper de- termed. I am so sensitive, even staying in people's homes is out of the question now.
I basically require a simple box,ee batbroomand kitchen with no carpete amper drapes, furnishings, unless all 3, etc. And living in Los Angeles, only h budget, the camper is the best solution right now. Help getting me out of this camper, help paying the cost of a company that will remove the mold/ organism, and help with paying for tests to identify this are needed most any experts in any of these areas, I guess if you donate a penny and leave your contact information through PayPal, I would be so grateful!
i' m seeing the infectious disease doctor in January...again though, they don't test, it seems for what I have
So my requests.
if there are any mycologists,, geneticists, mold remediation specialists, (to get my camper less toxic)
And any funds to send out samples to be tested (one place, parasite testing.com calls this neurocutaneous syndrome..and may be able to identify.. it just a swab test is $120!)
And I need to get myself into a place that is healthy for me...eventually it will either be a new camper or studio rented somewhere. For now, until get the mold out of this camper, I will not sell it.
So this is a tidbit of my story...I was a healer, then got too sick! I now channel some of that into healing art
Any help is appreciated! I am much toover- sensitive for any direct healing, I do appreciate intent/prayers out to the grater energy, beyond even consciousness that we are all a part of. I must reflect back any direct energy channeled through, and specifically deny permission for this( learned the hard way)
Thank you for taking the time to read this, for being at this site in the first place
May the world bring to you all you truly feel in your heart right for you!
Namaste
Laura
PS. My computer has been down, and writing this on a cell phone. Much as i tried to go back, I could not correct the typos!

This story is about my 13 year old son, Alejandro Jr. I will not be writing about anything that is sad or depressing, but about something that is wonderful and cause to celebrate. I am writing to share that my son has been accepted into the Fork Union Military Academy, located outside of Richmond, Virginia.

Me and my family are excited about this huge opportunity for my son. The road to get there was not easy however, but God answered our prayers. Alejandro Jr. has always been a very active child with an even more active imagination. As a baby, me and my wife would hear him play all night and could never sit still. During his elementary school days, his teachers would always remark how intelligent he was, but could just never sit still or not be a distraction to his class. What could I say, that is the way he was born.

But he went through elementary school on the honor roll each and every year he was there all the way through 6th grade. He was ready to go into middle school. When he entered into the 7th grade, things changed. There was a lot of bad influence and it started to affect my son because he has always been so innocent. His grades suffered, but he still scored in the top 97% of students in the end of the year state testing.

8th grade fared no better. He wasn’t the same anymore. He didn’t go to a good middle school. Lots of gangs and rumor has it drug dealing was going on there as well. His teachers didn’t care about him because he wasn’t doing the work, but he would still score 100 % on his quizzes and tests. His school wasn’t any help either. My son wasn’t being challenged, he knew the material, but he was not going to thrive in that environment, it seems he was getting harassed by his teachers and staff.

We wanted to remove him from that school as we had been fed up with the school district for a while now. We looked to see if there was an environment where he would thrive. After much research, we heard about the Fork Union Military Academy, which is an all boys military school. We took a look and my son loved it. This fits right in with his goal of joining the United States Marine Corps after high school.

We have been blessed that financial aid has covered roughly half of the tuition, but we are still in need of the other half, which is $10,000, which is due in 5 months. I am asking for any generous donation(s) that one may feel the need to contribute too. If you find it in your heart to do so, me and my family could not thank you enough and if you decide not to do so, thank you for your patience in reading about my son’s story. I wish a Happy Christmas to all.

This story is about my 13 year old son, Alejandro Jr. I will not be writing about anything that is sad or depressing, but about something that is wonderful and cause to celebrate. I am writing to share that my son has been accepted into the Fork Union Military Academy, located outside of Richmond, Virginia.

Me and my family are excited about this huge opportunity for my son. The road to get there was not easy however, but God answered our prayers. Alejandro Jr. has always been a very active child with an even more active imagination. As a baby, me and my wife would hear him play all night and could never sit still. During his elementary school days, his teachers would always remark how intelligent he was, but could just never sit still or not be a distraction to his class. What could I say, that is the way he was born.

But he went through elementary school on the honor roll each and every year he was there all the way through 6th grade. He was ready to go into middle school. When he entered into the 7th grade, things changed. There was a lot of bad influence and it started to affect my son because he has always been so innocent. His grades suffered, but he still scored in the top 97% of students in the end of the year state testing.

8th grade fared no better. He wasn’t the same anymore. He didn’t go to a good middle school. Lots of gangs and rumor has it drug dealing was going on there as well. His teachers didn’t care about him because he wasn’t doing the work, but he would still score 100 % on his quizzes and tests. His school wasn’t any help either. My son wasn’t being challenged, he knew the material, but he was not going to thrive in that environment, it seems he was getting harassed by his teachers and staff.

We wanted to remove him from that school as we had been fed up with the school district for a while now. We looked to see if there was an environment where he would thrive. After much research, we heard about the Fork Union Military Academy, which is an all boys military school. We took a look and my son loved it. This fits right in with his goal of joining the United States Marine Corps after high school.

We have been blessed that financial aid has covered roughly half of the tuition, but we are still in need of the other half, which is $10,000, which is due in 5 months. I am asking for any generous donation(s) that one may feel the need to contribute too. If you find it in your heart to do so, me and my family could not thank you enough and if you decide not to do so, thank you for your patience in reading about my son’s story. I wish a Happy Christmas to all.

On January 5, 2011, My mom was admitted through emergency for bleeding out of her rectum. At first they thought it was hemorrhoids, and further testing detailed that it was colon cancer. On 1/6/11, without much consultation or time to process my mom was in surgery to remove part of her colon. They removed about a foot of her colon, then did more testing to see where the cancer was. My mom was diagnosed with stage IV cancer, after it had metastasized to her liver. This was an unfathomable diagnosis, as no-one in my family had ever been diagnosed with cancer. They gave my mom six months to live. I could not accept that, and went on a search to help cure my mom. First we went to Mayo Clinic, where they thought they could help. My mom and I traveled there solo, much like we’ve done everything else in our life. She had a liver resection, to remove part of the liver that had majority of the tumors in it.

There I was sitting there in the waiting room, feeling very alone, while the two expert surgeons told me what they had done, and knowing it was a band-aid, hoping to have extended her life. I rejected that then, and I reject it now. I believe God for a cure, and for them to find no traces of cancer in her body, and I receive that which I’ve asked for. She is scheduled to have another round of chemo to hopefully kill what is left. The medical expenses have become unbearable.

I have done tons of research, so much so that I had to start taking sleeping pills to sleep at night. I know that there are ways to help my mom beat this disease, and I think I have found someone who can help. Unfortunately, her treatment protocol is $5900/week, for a minimum of four weeks. My mom is on disability, and I am currently collecting unemployment, as it was too difficult to travel with mom, and hold down a regular job. I have written letters to churches, charities, etc. I have to do whatever I can for my mom, she is my best friend, my brother, my sister, and the only father I’ve ever known.

Absolutely anything would help. Thank you so much, I appreciate your time.

im a 20year old female.ive been doing all i can to make the most out of my life. im tired and depressed and exhausted. i didnt finish my highschool education even though i should have pushed my self. but i never had any support from anyone. my parents divorced and my father was never around during my infancy. my sisters failed at there lifes as well. one raped and left pregnant at 16 and my other had drug problems and was literally at deaths doorstep at least twice as a teen.i haven't seen her in over 6 years. i experienced everything they went though and our family struggled so much. my mother was never around she only cared for her well being.left the family to find a man with money at one point to come back as a broken down women with no dignity. i dropped out of highschool at 12th grade and have been trying to get my ged but with how much it has been going up in cost its really hard to afford. i work two cities away with minimum waged job and live in a shitty apartment taking care of my brother and mother. barely make ends meat and im just frustrated with my how hard things have become. i want to higher my education to at least get a decent job that would improve my self esteem and also to give my brother the life he deserves. the life my parents never gave me. he is still young and doesn't understand most of whats going on.the worst part about the ged is that i live so far from the testing facilities so i try my hardest to find a center but transportation is a pain when most places are far away and i always have to take care of my brother whenever he is not in school. i need a car and just this test so i can at least have one chance to make things well, at for just this once i want to be able to not feel like an incompetent miserable fool.

Dear Sir or Madam,

As compared to some of the really sad and trying requests on this site mine seems so trivial. Unfortuneately I still need your help.
I sold one of my puppies last year to who I thought would be a wonderful home. I was wrong and my puppy has had to pay the price for my bad choice.
I do have a 100 percent take back on all my dogs regardless of age. Her owners just had a new baby and were not paying attention to her (Bella). Bella contracted a unrinary tract infection which they did not do anything about.
By the time they called me her temperature was 106 degrees and she was staggering. I drove two hours to pick her up at 10pm at night and took her to the Universtiy Vet Hospital close to my home. We arrived there at 3am.
It was a $2000.00 bill when they finally released her. If the owners had done their job it would have been $160.00 and 10 days of antibiotics. I have insurance on my guys but these people had nothing and they do not want to pay.
My husband and I are undergoing a seperation right now and I just don't have the $3000.00 this is going to come to when it is all done.
Bella is doing wonderful right now and I am looking for another forever home for her. She does have kidney damage and we are still testing to see how bad and if she is going to fully recover. Each of those visits is $150.00 and she needs to go once a month for a minimum of 6 months.
Please help and I thank each and everyone of you for reading my request and God Bless.

Regards
Cheryle and Bella

I am a 31 year old mother of 3.I have been without insurance for 2 years.I recently found a lump in my breast and I was able to go to a free clinic and get the testing I needed.I was diagnosed with breast cancer and need chemotherapy.I really can't estimate how much the treatments will cost but every little bit helps. Anything you could give would be very appreciated.Thank you!!!

54 yo female in accident while driving mom's car Oct 2008. Mom's seatbelt came loose and she ended up in floorboard. I was her only caregiver. She passed away Nov 2008. In Jan 2009 I woke up with right sided numbness. After mush testing a tumor was found that was pressing on spinal cord. It was surgically removed. Due to continued numbness and driving around 400-500 miles a week I had to do back out on disability. In 2010 I lost my job and benefits. In July 2010 I had a stroke but rehab helped me progress. Then I was brought home and left by myself with a weekly visit for dropping off groceries. My sister make my neurologist think I was unsafe and she got my disability check. She pays mortgage and utilities and gives me nothing. I paid my bills on computer while in rehab. Now with no money I would love to be able to get out for lunch and eat on occassion. I also need money for food and a pair of athletic shoes that fit properly since I am a diabetic. Please help me with any way possible for you. Thank you

I have over 10k in debt and can't seem to get ahead in life with all this debt I amassed as an 18 year old. Seven years later I still have most of the debt because of carelessness, being unemployed at times and new unexpected debt arising. I would like to go back to school and become a nurse but I have been finding it difficult to get the money to go back, and also finding it hard to apply for student loans because I am currently behind on the one I have now. So just testing this out, any help with be much obliged. Thanks much! And God bless.

I graduated from nursing school in the fall of 2010. I am a single mother I currently do home health aide work. I visit elderly people and help them clean bathe & get groceries. I have been able to send in my application for licensure but I have paid the 200 dollar testing fee for pearson vue. I would appreciate any donation. Feel free to ask questions .Thank You.

Hello,
I am a 29 year old Firefighter Paramedic. I lost my job about 9months ago. I have been continuously testing for departments. I have exhausted my savings/retirement. I never thought I would ask for help, but here I am asking you to please help. I have a 4yr old daughter and it is all I can do to get by with what I have. I am sinking and need a lifeline. Thank you for reading this. God bless.

Never did I think I would be posting something like this, but like many others in this time I find myself in need of some assistance. My husband, who has worked extremely hard top provide for our family, has found himself short of work. We started out own company 15 years ago and had done very well until the market crashed. During the crash we were in the process of building ourselves a home which we now live in but we lost a lot of equity in the sale of our old house and find ourselves in a tight situation now.

I have a college degree and have been looking for a job for 2 years, but because I have been a stay at home mom, home schooling my dyslexic son, the workforce seems to believe I am not qualified for even entry level positions. I have taken a job cleaning houses for $10.00 and hour. The little bit of extra money I am making is helping with everyday needs such as groceries and gas, but it does not go far. In addition to working part time, I am responsible for three children, my son, and my niece and nephew who live with us. I am also watching my neighbors little girls in the afternoons for some extra cash.

My immediate concern is that I injured my back in March of 2010. I have ruptured a disk which is sitting on the nerve to my leg causing excruciating pain. I was doing very well and was almost better until last week when I injured my back again, worse than the first time. I am unable to work my job or to watch the girls and now we have lost what little money I did make. I now have to have surgery, it is no longer an option, but because we are short on money and run our own business, we do not have any health insurance.

The hospital wants $5600.00 up front, the surgeon, $1600.00 and the testing for pre operation adds up to about $550.00. I can cover the $550.00 but as for the rest of it…

I have been tough for as long as I can, trying to avoid the surgery, but at this point the only way I can function is to take a lot of prescribed narcotics which then prevents me from driving.

I hope that someone out there could have some compassion for my situation and offer some help to me. The children are suffering and missing activities, my husband is stressed from working and taking care of my responsibilities, and I am feeling sad and useless.

My husband and I are constantly helping others who are less fortunate than us (i.e. my niece and nephew), but this time we need the help and only hope someone can reciprocate the favor. Thank you in advance for considering to help and I wish you well in all your endeavors.

http://www.giveforward.com/comingtogetherforcody

Please visit our page listed above to help Cody!

Our little Cody has not been well. Since he was just a month or so old he has had a problem choking when he eats. Around the time that he was eight months old we noticed he was having these choking episodes with much more frequency and they were becoming more severe. It got to the point where we were afraid to even give him a bottle without having the phone ready to call 911!

We took him to his doctor, who suggested we see a feeding specialist. And so began our journey.....

Right away Rosie (the specialist) noticed that Cody had trouble moving his tongue and chewing food. He tended to rush when he ate and that caused even more choking, but he was choking on everything- even just water. After a horrifying episode during one of his sessions, in which Cody choked on a piece of bread and turned blue, Rosie and Dr. Pepper (Cody's doctor) decided it was time for a Swallow Study.

During the study our little Cody enjoyed every last bit of barium as we watched him mash up food and try to swallow it. The speech therapist who was monitoring the test noticed that Cody's esophagus didn't seem to be moving quite right, he rarely chewed and had a lot of acid reflux going on. Aside from those observations, Cody had Oral Dysphagia as well. Those findings led us to an Upper GI Study that ruled out some really bad stuff, but Cody started having new symptoms. He was having difficulty breathing and had to be on nebulizer treatments, was increasingly grumpy, was gassy and had a very full looking belly that hurt so badly sometimes that he couldn't give us hugs. It wasn't long until he slowed down on his eating and Dr. Pepper decided it was time for a trip to Denver Children's Hospital.

In Denver Cody met a Pediatric Gastroenterologist and Pulmonary doctor who read his records and checked him in for several more tests. An Endoscopy and a Broncoscopy turned up a very nice looking esophagus (even the biopsies looked good!) but some pretty bad asthma. They placed a tube in his nose for another test called a PH Impedence Study to measure what was coming back up form the stomach and during which times it was happening. This was all very hard on our tiny little man. He had a horrible reaction to the anethesia which forced him to have to be hooked up to monitors. Anyone who knows our Cody knows what a busy little guy he is!

The results were confusing, though, because Cody had been on a medication that was supposed to help with motility and we knew it did SOMETHING for him- but with his great looking esophagus we weren't sure what it was helping with. If his esophagus was moving fine, why did a drug that was supposed to help it move make him feel a little better? The doctors decided to do a Gastric Emptying Study as well. Cody was NOT happy because he couldn't eat for yet another day. If you know our Cody- you know he loves to eat!

The next day we did the study and it didn't take long to get the results. In the time it takes the average stomach to empty, Cody's stomach had only emptied 7% of it's contents. The medication had been helping his little belly move. Unfortunately, it has some nasty side effects and he can't go back on it. They are currently trying him on a low dose of Erythromycin, which is the last medication available to treat Gastroparesis (Delayed Gastric Emptying), according to our medical team.

We soon got the results of the tube they placed in his nose, as well. Cody has a pretty big reflux problem, too. Since his belly is so slow to empty, his acid has no place to go but up. No wonder he is so grumpy. The constant flow of acid is also a huge trigger for the breathing problems he is having. They are now trying him on both Zantac and Prevacid- both drugs that have not worked well alone, but we are praying they will work better together.

We are trying hard to give Cody small meals throughout the day and to incorporate all the nutrients he needs, but its hard. With the delayed emptying we are supposed to avoid high fat and high fiber foods. We already have to avoid eggs, dairy, soy, berries and nuts due to allergies, so you can imagine what a challenge we have on our hands!

Cody's GI doctors have recomended 2-3 surgeries, including a feeding tube. Gastroparesis is a Dysmotility Disorder. There is a small chance he could outgrow this and there is also a small chance it is actually caused by something treatable- although in 60% of the cases there is no known cause.

In order to fully understand Cody's condition, why he has it and what all the options are, as well as how to care for him properly- we need to take him to Columbus, Ohio to see one of the very few Dysmotility Specialists in the country. We have no idea how long we'll have to be there or how much of this trip will come out of our pockets. Cody's insurance does not cover any travel expenses and will likely not cover any repeat testing he may need. He is currently on a modified diet and they don't cover the costs of any of that, either.


We are asking that our friends, family and anyone who is able come together to help us- both financially and spiritually. We need the finances to get us there and keep us going even when we can't work due to surgery or whatever may come; and we need your prayers and support to keep us strong as we try to manage this difficult and unfamiliar situation. We want so badly for our baby to feel better- he has brought us so much joy and is truely our little sunshine!

Thank you all so much for taking the time to read our story and for doing what you can!