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Chair Tags
Massage therapyst needs money for start a place
Posted by Lucho333 on 2012-05-07 20:58:23
I really appreciate your help.
Thank you and regards
Luis
Massage Therapyst needs money for a work place
Posted by Lucho333 on 2012-04-23 21:58:24
I really appreciate your help.
Thank you and regards
Luis
NEED HELP BAD
Posted by jlvHELP on 2012-04-20 08:58:36
Anyone if you can help, please please please help us. Anything will help. I've written Ellen so many times but she must think we are worth the help, old folks that we are.
Hi, Help me to find a job in UAE
Posted by rinu on 2012-04-19 00:58:04
Professional and personal success can only be achieved with dedication and Hard work. We all strive to achieve great heights of fame and glory.
But when you are faced with financial problems, it keeps you sitting on a chair asking yourself what will i do to make money for my travel.
As you all know, in order to get a job in any country first you need a visiting visa. Visiting visa has 1 to 3 months validity in some countries. After getting a visiting visa you need to travel to that country, stay there and search a job within the validity period of visiting visa.
If you are lucky you will get the job within days. But the cost of visa, travel, stay and searching a job in UAE or any middle east countries is too high.
Total cost of my visa, travel, stay and search is approx 15000 USD. i will pay you back all the money with in 1 year after getting a job.
My prayer to all of you is to contribute 1 dollar each so i can get an amount equal to 15000 USD and go for my search of job in Middle east.
In every prayer of mine i will ask for the happiness and prosperity of every living being on earth.
"May god help you all"
Please help me
master_rinu20(at)rediffmail.com
Thanks you dear friends i will pay back every single penny i got from you
John Griffith = 50$
Laura Gerrad = 100$
Thank you and may god bless you both
Hi, Help me to find a job in UAE
Posted by rinu on 2012-04-19 00:58:03
Professional and personal success can only be achieved with dedication and Hard work. We all strive to achieve great heights of fame and glory.
But when you are faced with financial problems, it keeps you sitting on a chair asking yourself what will i do to make money for my travel.
As you all know, in order to get a job in any country first you need a visiting visa. Visiting visa has 1 to 3 months validity in some countries. After getting a visiting visa you need to travel to that country, stay there and search a job within the validity period of visiting visa.
If you are lucky you will get the job within days. But the cost of visa, travel, stay and searching a job in UAE or any middle east countries is too high.
Total cost of my visa, travel, stay and search is approx 15000 USD. i will pay you back all the money with in 1 year after getting a job.
My prayer to all of you is to contribute 1 dollar each so i can get an amount equal to 15000 USD and go for my search of job in Middle east.
In every prayer of mine i will ask for the happiness and prosperity of every living being on earth.
"May god help you all"
Please help me
master_rinu20(at)rediffmail.com
Thanks you dear friends i will pay back every single penny i got from you
John Griffith = 50$
Laura Gerrad = 100$
Thank you and may god bless you both
Hi, Help me to find a job in UAE
Posted by rinu on 2012-04-19 00:58:02
Professional and personal success can only be achieved with dedication and Hard work. We all strive to achieve great heights of fame and glory.
But when you are faced with financial problems, it keeps you sitting on a chair asking yourself what will i do to make money for my travel.
As you all know, in order to get a job in any country first you need a visiting visa. Visiting visa has 1 to 3 months validity in some countries. After getting a visiting visa you need to travel to that country, stay there and search a job within the validity period of visiting visa.
If you are lucky you will get the job within days. But the cost of visa, travel, stay and searching a job in UAE or any middle east countries is too high.
Total cost of my visa, travel, stay and search is approx 15000 USD. i will pay you back all the money with in 1 year after getting a job.
My prayer to all of you is to contribute 1 dollar each so i can get an amount equal to 15000 USD and go for my search of job in Middle east.
In every prayer of mine i will ask for the happiness and prosperity of every living being on earth.
"May god help you all"
Please help me
master_rinu20(at)rediffmail.com
Thanks you dear friends i will pay back every single penny i got from you
John Griffith = 50$
Laura Gerrad = 100$
Thank you and may god bless you both
Help Us Start Over
Posted by openyourheart4me on 2012-04-14 13:58:58
Help Us Start Over
Posted by openyourheart4me on 2012-04-14 13:58:55
Massage Therapyst needs money for place
Posted by Lucho333 on 2012-04-13 12:58:57
I really appreciate your help.
Thank you and regards
Luis
(2) Black Bar/Counter Stools-$35 (Holyoke, MA)
Posted by loveforall on 2012-04-04 10:58:53
I am trying to raise money for a small vacation for my kids who really need some time away and so i am selling some things. I have (2) identical black stools that came from JC Penny's Makeup Dept. Very large and in great shape. They are 26" and have wide seats. Seats are upholstered in black and the backrest is grey vynil with the logo "Lancome Paris" on the back. Has a small tear on the back of one chair but can be easily fixed. Very unique stools. I am selling both for $60 or $35 each. If interested you can call me at 413-686-6302 and leave a message with your name and number and i will return your call within 24hrs. (Sorry no text). I can also email pics. Need these sold by April 10th. Thanks.
Need a chair
Posted by reliefwanted0224 on 2012-03-31 07:58:13
Need your help to continue to make people beautiful!
Posted by blackpearl68 on 2012-03-26 15:58:33
My hair salon is so outdated,my chair cushions are sinking down,shampoo bowls,floors are stained,and my styling chairs are breaking down!Would love to buy new equipment and keep my doors open.But I can barley pay my lease.Would love to remodel so I can raise my booth rental to the rate of the salons around me.Thank you so much for taking the time to read my letter.
In need of furniture for new apartment
Posted by Ulquiorra on 2012-03-21 16:58:28
I have no bed, no chairs, no table, or anything else for that matter, furniture wise and most unfortunately no money.
I am currently sleeping on a blow-up mattress that deflates while I sleep so I am laying on the floor when I wake up.
What I am hoping to find is:
A bed (bedding would be nice too)
A small/medium sized desk/table
A chair (or two)
Some pots and pans to cook with
Some paper plates/bowls and plastic utensils
A desk lamp
A floor lamp
anything at all is greatly appreciated
If you have any of these items and are willing to let me have them please contact me on my cellphone at 1(781)789-1983 (Call or Text).
I am currently located in Center Barnstead, NH (approx. 20miles from Concord and Rochester and approx. 40miles from Laconia) and am willing to come to you to pick up anything you're willing to part with that I can use (distance dependant).
I would like to thank you all in advance for your generosity
Help Please
Posted by bella123 on 2012-03-09 08:58:17
28 year old wheelchair
Posted by wheelchairsteve on 2012-03-01 18:58:08
Help maintain a place for our children.
Posted by Plfd5stargym on 2012-02-07 21:58:01
As someone who is in a leadership position at YourCompany, I know that youâre pressed for time. But please, could you give me your full attention for the next 30 seconds as you read this letter?
You see, the children at Plainfield 5 Star Gym would like to continue to have a place to call theirs this year. But you know how it is: government budget cuts, on top of too-small budgets in the first place, have combined to make it impossible for them to be able to do so.
Unless someone steps in to help them. And thatâs where you come in.
The benefits of being at Plainfield 5 Star Gym are priceless: teaching children about the wonders of self esteem and motivating them to learn about their ability to achieve goals with discipline is one of the best ways they can learn about themselves and develop their interests, leading to future careers in hundreds of fields.
By helping the children at Plainfield 5 Star Gym to be able to have a place to retreat , you are not just helping them, but youâre also investing in the long-term future health of your community and even your company. A healthy, well-trained workforce is the most valuable asset at any company, and by helping our children to have gym they so desperately desire, you will be planting seeds for future employees loyal to your company.
Not only that, by contributing you will also be receiving free advertising and positive public relations in the community. Thatâs because we will post your name in the program for the boxing events , as well as on any materials produced promoting the amateur events. To top it all off, we will have a âPartner Wall,â bearing the names of all the contributors to the gym, which will be prominently displayed at the boxing events itself.
By contributing towards the boxing gym in Plainfield you can help our children immeasurably, receive free advertising and promotion for your company and feel good about it all!
Would you please help? Weâre are out funds to pay the rent for our gym. We need to raise a total of $50,000.00, which will cover the cost of 50 children from the community to attend without cost, rent,equipment rentals,presentation tables and chair rentals, printed materials like entry forms and flyers .
Any amount youâre willing to donate will be greatly appreciated!
Please contact Rich Johnson at 908 447 7174 to find out how we can work together to give our children the best opportunities to succeed while giving your company the exposure it deserves for helping us out.
Hope to hear from you and thank you for your time.
Sincerely,
Rich Johnson
PS: In lieu of a financial donation, weâd be happy to accept any donation in form of donated items or services. Please contact Rich Johnson 908 447-7174 to find out what items or services will be needed to maintain a place for our children.
help me fulfill my dream and ride the waves
Posted by jexrex1098 on 2012-01-30 23:58:05
I am 25 and for my entire life, I have been fat. I don't mean this as in, a little on the chubby side; but obese. I can remember being in 5th grade, when our class had to get weighed and measured at the nurses office. The sinking feeling in my gut that came up when I weighed almost 200 lbs at the age of 10 is something that I don't think I will entirely forget.
Because of my horrible diet as a child (McDonalds, soda, you name it), I have spent my entire young life coping with being overweight and all of the horrible things that go with it: wondering if I'll fit in a seatbelt, wondering if I would break a friends bed or chair if I sat on it, or never being able to find a cute outfit to wear like all the other girls. When I was about 14, I was diagnosed with PCOS, which is cysts on my ovaries (contributing to my obesity, or as a result of, but they worked in tandem to make my life miserable). Without health insurance, I was never able to get this issue resolved, and with my poor diet, my weight increased. PCOS symptoms also include abnormal facial and body hair, which was (and to a degree still is) the bane of mine and any woman's existence. A woman should never have to feel so ashamed of her own body, and yet that is exactly how I've felt for as long as I've realized that I was different, and that looks mattered.
My highest weight as of 4 months ago topped out at 324 (thought I had reached 340 a year earlier but had lost some weight over a long period of time). Recently I began taking HCG (a hormone that helps regulate fertility and also helps with weight loss), and am amazed to report that for the first time in my adult life, I am 270 lbs. While this still is a lot, for me it is an incredible number to be at. Never in my life have I felt the fear of dying at 30 begin to be lifted, though I still have a long way to go.
So the point of my request: there are a lot of dreams I have that I feel like I am within reach of grasping. Some of them have already been fulfilled: I have been able to travel with my family, and this past year my parents helped me to finance a jeep. This is a huge one...I live on the west coast and have always wanted to live a surfer/beach lifestyle.
But how could a fat girl ever be a surfer? It's been my dream for the past 10 summers to learn to surf, with beaches only 15 minutes away. But every year, the fear stopped me, my weight stopped me, my inability stopped me.
I want this year to be the last year fear gets in the way.
With my weight going down, I've been trying to exercise. I've been attempting a modified version of P90X, and have been eating healthy and avoiding all the foods that got me where I am today. The problem is that financially, while I do work full time, I barely make enough to cover my bills (gas, car insurance, car payment, cell phone), and am not even able to help my hard working parents pay rent. So money for extras this summer is not really possible, but I CAN'T let another year go by without accomplishing this task.
I want to attend a surf camp this summer in San Diego, called Surf Divas. The problem? Surf lessons are expensive. I think to get me on the right path, I'd need at least 10 hours of lessons. At $82 an hour, thats $820.
The reason I want to fulfill this dream is to prove to myself and others that no matter where you've been, or how far your body is from being in shape, that the human body is remarkably capable of change. I would want to encourage anyone who doesn't think they are the right "type" to surf or do a sport that they can push their bodies to do things they never thought possible. And I sincerely believe that learning to surf will help me pursue my health and fitness goals long term, as well as truly set free the earth-and-sea-loving hippie that I keep snug and close to my soul. I live for summer and the ocean...and being able to ride a way would be life changing for me.
If anyone is able to donate or help support me in taking charge of my health and fitness...there would be no adequate way to thank you. I will send you a picture of me riding my very first wave as a token of gratitude, with a friendship bracelet made by me with a few shells from the beach strung on it. My way to say thank you for helping me to live a healthy life.
I'm a giver who rarely gets, but if you could change that, I would be most grateful.
<3
Motorcycle accident..please help
Posted by tadwisn on 2012-01-21 14:58:09
On September 28th, 2011
My husband Trevan had an accident on is his way to an Interview and he was going on Lucent to get on to the highway on C470 and was not able to see with the dew on the street and sun glare. He didnât see the car at the stoplights, going on to C470. Didnât know or see that it was stopped at the light. The sun was so bad that he slammed right into the person in front of him and went over the handlebars of the motorcycle and over the personâs car and was found underneath the car. The Paramedics found him under the personâs car and had to pull him out from under it.
I got a call about 8:15 am from the fire department letting me know that my husband was in an accident. I was so scared I was trying to get my son ready for school and get my daughter ready to so I could take him. I was told that he was taken to Littleton Hospital and that I can call over there and get info on how he is doing. Instead of me calling the ER the ER nurse called me and gave me some info about what they are doing and what ER room they are taking him to. They took some x-rays and he couldnât be moved because they were not sure about his back. So they did the x-rays in the ER. That is what the nurse told me that they were doing and that he was stable. The nurse also said if I could get to the hospital as soon as I could, it would be a good idea to come since the police and fire department was still there. I told her I would try. I called my mother in law to let her that her son was in an accident and I called my mom. There were other people that I called too. When I got there and I had to park so far in the back of the hospital that I had to ask for directions to get to the ER from the outpatient so I could be there with my husband. When I got there it was very hard to see what he looked like. He had a neck brace on and his left arm was all wrapped up like a present. He had a big gash on the inside of his right leg that was pretty wide and you could see the fat and it kept on bleeding. They would not take off the brace from his neck because they didnât know what else was going on with him. I met the ER doctors and they told me that he is in quite bit of pain, and that he was starting to not know what happened off and on. I tried to see if he could tell me himself but could not remember. One of the ER doctors was very concerned about the blood in his urine so they took him to another place in the hospital to do some more tests on him. My mom in the mean time called me and told me that she was on her way to be at the hospital with me for support, I told her that I really need some comfort and to keep it together. When she got here Trevan was not yet taken to get tested yet so my mom said hi to him and ask him questions. Then with the ER nurses came in to take him for the tests my mom ask the nurse what kind of test that they were going to do on him and they said it is to check for internal bleeding. When Trevan was taken back we went to sit in the waiting room in the ER. My mom kept asking me questions but I could not answer any of them, because I have not been told about any thing besides what the nurse told me on the phone before I got there. I ask the nurses that were still around theyâre about where his belonging were because I needed to know if his wallet and other things like ring and glasses was there. They handed me the beg that had his wallet and other things that they took off of him. I took the beg with me so I could go through it and see if every thing was still with him. His wedding band was in there his wallet was in there and socks and helmet was there too so I took it with me out to the waiting room. There was also a ticket that the police left in it too. My mom took a look at it to find out what all happened. It just said it was his fault but we didnât think it was his fault, but later on we did fine out it was his fault but we took care of it for him while he was in the hospital. While we were waiting Trevanâs mom came with my daughter to see him but he was still not back in the Trauma room. After a while they finally moved him to a room so we all went there. They took him to the ICU and we had to keep our hands clean at all times coming and going. Trevan was put on many powerful pain medicines for the pain. He was put on dilaudid and he was on that for a while but then he was inching so bad that they took him off of that and put him on morphine he was a little better but still was itching like crazy.
Doug and Jan drove out here on Wednesday night they didnât stop except for brakes and gas but they drove all the way through so could see Trevan. They arrived at the hospital at 3:30 am. Trevan didnât remember that his dad and step mom came to see him the first night. I told him twice that they were here and he just didnât remember it. Every one came to see Trevan everyday Doug and J, Karen and John Hager, Kehli, his mom Beverly. Doug and Jan were here for four days and they were here also for the surgery. We had a lot of people in the waiting room Beverly and our kids, me, and Doug and Jan. I was happy that I had that many people there with me because I was very upset.
October 1st 2011
Trevan had his surgery on both the pelvis and the humerus bone. The doctor started with his pelvis first he said it was the quick one and that Trevan didnât loose much blood with that one. Then the doctor moved Trevan to another table to do the other part of the surgery. He lost a little bit of blood when they did his surgery on the arm they had to give him two pints of blood. The doctor did come out to tell us the update as he did them and how everything was going. He showed us before and after x-rays. The doctor did a great job of fixing Trevan up. Then after the surgery was done he was in recovery room for about an hour and a half. They moved Trevan to his room afterwards and he still was not doing hot. He kept saying that the room was moving and it made him sick. He tried to keep his eyes closed but it made him even feel worse. He also kept asking for ice chips which I feed to him as much as I could. He was better by the evening, he didnât feel dizzy any more. Family kept coming to see him and tell him that they love him and pray that he will heal quickly. I stayed with him every night after the surgery to keep an eye on how he was doing. He didnât remember a lot of things, which in some ways it is good but in some ways it is bad. I think a lot of it had to do with the pain medicine that the doctors was giving him. A nurse told me that it could happen with the medicine could make you forgetful depending on what kind of pain medicine.
October 4th 2011
While Trevan was at the hospital he did fall. He hit his head agents the closet that was in his room. The nurses found him on the floor. They did say that when he fell he landed on his right side and that they donât think he hurt him self, but he did hit his head when he went down. I asked them if they were going to see if he did any damage, and they said that he didnât and couldnât do that much damage because the way he fell. I asked them if he hurt any thing else and the nurse they checked him over and asked him questions and didnât see any evidence that he had any more damage to what he already had. I asked to if they did any test to see. They said they didnât do any other tests on him because they didnât want him to be exposed to any more radiation from the x-ray machine. He was getting out of bed by his self with out any help, which he was not supposed to do that. That is why when he fell they put a bed alarm on his bed so they would know at all times that he gets up, for his safety.
October 5th 2011
During that time while he was a Littleton hospital they were trying to find a rehab place for him so he can start getting back on his feet. They did find one and they had him transferred from Littleton to Porter hospital. Before he left I told him that I would see him later that evening and so will his mom and kids. He said ok and they he was gone. That evening Beverly and the rest of us call daddy from his momâs phone to let him know that we are coming to see him but we were going to stop and get something to eat on the way up to the hospital. Then while we were eating at Wendyâs he calls me on my cell phone and asks if we were still coming I told him yes. I asked him did you even remember that we called you before and told you that we were coming he said no he didnât remember. While he was on the phone with me still we asked him if he wanted us to bring something for him. He said yes. We brought him a hamburger and a frosty. When we got to the Porter hospital and got to his room we noticed it was very small and odd shaped. He had a window but in the wrong place or the room was just in the worst place. It looked like a bad shaped L and had no flow to it. I asked Trevan on how he was doing and he said tired and in pain. I said you just been through a lot and it will take a while to heal. Then we gave him is food and let him eat while we also talked to the nurses that were taking care of him there. We also ask that if there was a way for a cot to be put in there so I could stay with him some of the times. They said yes that they will get one in the room the next time I come up to see him. I said thanks. They also had a bed alarm on his bed and his wheel chair that he was using. I am happy that they had that on there but the moment that he got up to use the urinal that the alarm went off. And he didnât feel comfortable with them always coming in and him not able to potty when he wanted too. When he is in the bed but keep it on when he is in the wheel chair because he could not remember to lock his brakes before he transferred form the wheel >chair to bed or just getting up to stand.
October 6th 2011
Trevan calls him mom to get my number to be able to call me. He talked to her for a while and he also asked if we were coming to see him, and also asked if we knew where he was. His mom said yes she knew and asked him if he remembered that we were the other night. He said no and also said that we werenât there to see him. Which we were there but he just didnât remember that we were all there his son and daughter me and his mom. He forgot the entire evening and event that we even were there to see him the night before. His mom said to him that we were all coming to see you again tonight so we will see you later. The same day I went to take our van to get the oil changed in it and found out that there was a clucking sound and they told me that it was not safe for me to keep driving it. They said about a week or two would be all I should drive it. I called my dad and asked if he knew any one that I could take my van to get an idea on how much it would cast to get it fixed. This was all the same day that I was going to see Trevan at the hospital. They didnât want me to drive it anymore until it was fixed. So Beverly had to take me back and forth to and from the hospital for a while. After Beverly got off work we all got in to the car and drove up to the hospital. We asked the nurses if there was any way for Trevan to watch movies other than watching TV all the time. They said yes and told us there is a TV, VCR that is on a cart that can go into their room to watch movies and only VHS tapes only no DVDâS. So mom went into the lunchroom and looked at all the movies and wrote down all the ones that Trevan would be interested in watching. After she was done she brought the list to Trevan to see and to know that he had choices. Then we went home and told Trevan that we will see him later the next day. Then said our good-byes.
October 7th 2011
There was a lot of thing going on this day that I donât want to go through again. I had to take my van to a place that my sister in law told me about. I made my appointment with them the day before and they wanted me to bring it back today and get it fixed. They even said that it was not safe at all. I left it with them to fix it in the morning. Then I came back home and had more things to do. I had to run around back and forth using my mother in laws car which was ok she was taking care of my daughter and my niece so I got thing done and I was able to relax a little bit. We all went to see Trevan that evening. We had to go and pick up my van after we picked up dinner. Then we left to see Trevan. When we got there into Trevanâs room he looked really tired and in a bit of pain. We got an extra hamburger so we gave it to him so he could eat it. Of course he at it all up. I changed the channel and found shreck the movie and we all watched that with Trevan. The nurse cam in to see how he was doing. He said that he needed more pain medicine, also needed to have his depends changed. The kids and grandma left outside the room while he was getting changed. After he got settled again the kids came back in and they were getting rowdy so I ask Beverly to take the kids home. They gave their daddy a kiss and left. That night I stayed with him and he kept on asking if the nurse had given him his pain medicine. I told him yes that they did give you your medicine. I asked him if even remembered it and he said no. He asked me 4 other times to while I was there. When it was time for him to have another dose of medicine I said to use the call button that is what it is there for instead of me always running in and out of his room to let the nurses know that he needed more medicine. I stayed with him all night it was very hard for me to hear. When Trevan would fall to sleep he would start dreaming and breathing heavy then wake up crying and then fell back to sleep. It would go on about 5 times at night. I think it was nightmares and when he wakes up he would not remember any of it.
October 8th 2011
The nurses were coming into see how Trevan was doing. He had his breakfast and pain medicine. After breakfast the therapist came in to take him to do some therapy stuff. He worked on the ramp with wheel chair going up and down with keeping control with his feet. The first round was 35 minutes. Then comes back and rests for a half-hour and goes again for 30 minutes. Then he came back and rested and had lunch. Then he went with another therapist and goes and has a shower, but after a while he came back. The nurses told me when they came back with Trevan that the cut on the inside of the right leg came open while they were helping him with his shower. He lost a little bit of blood but it hurt him quite a bit. So two nurses came back. One was pushing him and the other on putting pressure on the wound. When he was back in the room he looked like a ghost, and looked very tired. Then his nurse came in to put a different kind of bandage on his leg. By the end of the day he had color back in his face and was doing better. That day and evening he didnât know that I was staying with him. I was with him at the hospital since Friday night, to Sunday evening. I will be going home on Sunday night.
October 9th 2011
The nurses and doctors decided not to have therapy because Trevan gave them a scare. So they just let him rest and let the wound heal some more before he did any more. I watched him sleep and he has the bad dreams again all day, and all night. I woke up every time he had the dreams. I counted how many times he would wake up and go to sleep again. It was hard to hear too. When he did wake up I would ask if he remembered any of it. He would say No. I did let the nurses know what was going on with Trevan and also asked him to keep an eye out and check on him. I also asked them to keep a record of it too. I left the evening so I could take care of my kids the next day. My mother in law had to work and had to keep Sarah with me. I said my good-byes. I asked the nurses to keep me in formed on how he did through the night.
October 10th 2011
Trevan told me that he had therapy and that he was in some pain. He was up in the wheel chair and bed. He was learning how to put socks and underwear, shorts and shirt on by him self with out help and doing it all by with one hand. He did OK is what he said. It is hard for him to remember which arm to do in first. The nurses said try to remember left first than over the head than right arm. Then put your glasses on so you can see. He said he would try to remember. Then I went home. He also saw the doctor and asked for Ibuprofen.
October 11th 2011
I got to the hospital to see Trevan about 7ish. He looked tire but also happy to see me. He said to me when I can in âI was wondering when you were going to be hereâ I said I had to take care of the kids first. In the morning he did therapy then he has lunch and after he had lunch he did some more activities he had u ride outside and played scrabble to get his mind working on thinking. That is what he did during the day when I was not there to see him during the day Trevan had therapy and looked somewhat tired when I got there, he was also in his wheel chair. He ate all the tacos that his mom got for him. After we got done eating he was in a lot of pain. He asked for more pain medicine and he could not get any more ibuprofen. So they gave him percocet for the pain. All we did while I was there with him we talked and watched TV together. Was late when I left to go home and care for my kids.
October 12th 2011
I went to see Trevan about 7ish again. He did a lot of thing in the morning it was all written down so I knew what he did. Which he was to do every day for his memory issues that he has. He had breakfast then he had PT. He did exercises with his legs. ST. tested him it scored 20 out of 25 on the cognitive tests. Then he did some transferring using one leg, 2-½ lbs. on the other leg (right leg all weight and partial weight on the left.) After lunch he did the walker, wheel chair, shower, teeth and hair. All of this info that I keep getting is what he writes down for his memory reminder. I took a look at him and asked him how he is doing, He said he is in a bit of pain. A lot of pain was mainly in the arm. He asked for some pain medicine and he started to fall to sleep. So I told him that I would head home and take care of the kids. He said to tell them that he loves them. I said ok.
October 13th 2011
Just reading his report that he wrote. He did getting in to his wheel chair to go to the toilet, Independence Square and weight. That was his activities during the day and he also had another stitch pop and his leg started bleeding again. That is what he told me. It is covered with gaze. I was happy that they did put that on there to protect it better. He has been sleeping better. They arenât using the walker with the plate form because of his bad left arm. He is balancing so much better on his right leg which I am very proud of him. I noticed while I was there he didnât remember that he had his pain medicine which they did give it to him. But they could not give him any more until 9:15 PM. And it was about 8:20 PM when he asked for more pain medicine.
October 14th 2011
Trevan woke up around 5:45 am having pain in his arm and needed to be changed. Found out that Dr. Bess has not released him from putting more weight on his left leg. It will be 30% weight for a while. At a little bit after 9 this morning went for a wheel chair walk. He sat in the wheel chair and used his right foot to move him forward and his right hand also help him to move forward in the direction that he needs to go. He went around the hallway twice. Then after he did that he came back to his room, so after that another person came in and took him down to the shower. Both of us were in the shower room with the nurse getting him ready and helping him stand only on one leg. He could not put much weight on the left leg. After every thing was off the therapist helped him sit on the shower/ tub chair. We both helped him get cleaned up, but we made sure he did most of the cleaning up. He did well at listening to me and stayed seated until we needed him to stand to pull up his pants. He only used his right leg to stand on and his right arm to pull up. I told him if he comes home he is going to have to listen and wait until I can come and help him. I didnât want him to fall again and end up in the hospital again. After the shower we went back to his room to rest for a few minutes. Then he went to do more moving therapy. He did hopping on the right leg and using the parallel bars with the right arm to and from the wheel chair. Then he did some bumping up and down on the stairs. They would not do any more of them for a while because it tired him out so much. We did not know when he would be able to come home yet. We were going to have someone come by to take a look at the house and see if he can come home. Right now it is set for wed. But it is not set in stone. I am planning to stay the night again and leave about 8:15 am to watch my daughter. Then I will be back to stay with him again that evening.
October 15th 2011
This is what Trevan did for the day, leg/ hip exercises, control wheelchair up and down ramp. ST- did memory strategies, put a picture with info, and writing down notes. OT- watched him do his brushing his teeth, getting dressed, independence square (cashier, shop, and sandwich) memory. That is what he did and also found out he has a urine infection. He slept a little bit, was up having to go to the potty all night, had to remind him mot to put any weight on his left leg. He said that he was not but I doubt it. I was watching him. After he was done he was always putting weight on the left leg every time he pushed his butt back in the bed. I am very worried about that. I did tell the nurses to keep an eye on him that he was having issues with him having to pee all the time. Since he had the infection. They said that they would keep watch and see how he does through the night.
October 16th 2011
Trevan had a bad day at remembering this day. I just donât remember what he forgot because I was also very tired this day also.
October 17th 2011
We brought Trevan home to do the home inspection so we could find out what we all needed to do and what to get for the house, so Trevan can come home. We didnât want him to get injured any more than what he is now. When we got to the house the two nurses had to lift him and the wheel chair up the stairs since we didnât have the ramp up quite yet. We did tell them it would be up once we know what day we could get help. While Trevan was still sitting in the wheel chair he had to use the restroom. He did try to get in the restroom which he did do just fine, but when he was ready to get back out and into the wheel chair he almost fell in to the wheel. So they deiced not to have him use the small bathroom.
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.
donation needed - help handicap adult male bathing
Posted by smokie080650 on 2012-01-01 02:58:05
.
mother without job or resources to fund. my pride is not more important than my son's persuit of dignity and/or happiness.
.
please mail to: Fm. Luke/ P.O. Box 9673/ Trenton, New Jersey 08650 USA
new home
Posted by living4jesus on 2011-12-31 13:58:07
New First Time Mother Having A Baby Girl
Posted by pearladams30 on 2011-12-22 13:58:21
nursing pillows
burp cloths
bottles equipped with newborn nipples
bottle brush
insulated bottle holder for diaper bag
nursing bras
nursing pads for bras
breast pump
diaper changing pads
diaper rash ointment
waterproof pads for changing table
rattles
any small toys
dirty diaper receptacle
wipes
cotton cloths
small thermos to hold warm water (for cleaning babies younger than 6 weeks)
plastic wipes holder(for the diaper bag)
packages of newborn diapers
pack of newborn t-shirts
6 one-piece outfits that snap at the crotch(long-and short-sleeve)
pajama sets
pairs of socks
pairs of soft booties
pairs of stretch cotton pants
bibs
cotton sweaters
knit caps
sun hats
zip-up sweatshirts
baby hangers
hooded towels
packs of washcloths
infant bathing tub
baby nail clippers
soft brush & comb
rubbing alcohol
petroleum jelly
digital thermometer
bulb nasal aspirator
receiving blankets
cotton blankets
cradle or bassinet with cotton sheets
crib mattress pads
waterproof liners(one for the bassinet and one for the crib)
crib & mattress
glider(rocking chair and footrest
dresser
hamper
baby monitor with 2 receivers
changing table
cool mist humidifier or vaporizer
lullaby cd's or audiotapes
stroller
sun shields for car windows
portable playpen
diaper bag
sling or soft front carrier
bouncy seat
baby books
digital camera or camcorder
playmat with toys attached
squishy baby ball
HELP FOR MS PATIENT
Posted by inneedofhelp12579 on 2011-12-19 13:58:46
Homeless needs help.
Posted by twilhelmsatx on 2011-11-01 21:58:17
This is the organizations website - http://www.beatthestreetstexas.com/. This is where I am staying. I am using a house computer, I am selling my laptop to another housemate to raise a little money. It's the LAST SELLABLE item I had. I don't even have a fork or chair or anything. I know you read a lot of these articles begging for help, but I am speaking the truth. I have begged for help here in San Antonio and got one month's rent paid one time.
PLEASE, PLEASE Help. This is the response I send to the spammers:
Hello,
Thank you for spamming me. Here is my current situation:
1) I am a technically homeless person living in transitional housing. I owe, as of this writing, them $4700.
2) I have NO INCOME of any kind.
3) I have no bank accounts.
4) I have no credit cards.
5) I have one debit card with $0.24 ( Twenty-Four CENTS) on it.
What kind of help can I count on FROM YOU?
Thank You,
Terry Wilhelm
Again - What kind of help can I count on FROM YOU?
PS - I will testify in any court in the United States of America, under oath, that the above is my current situation.
