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Hollis in a coma, fundraiser, please help.

From; http://helpholligethome.blogspot.com/
Sunday, June 13, 2010
Update
Sorry it has been awhile since my last update. Holli had a swallowing test several weeks ago that she passed. She is now starting to get meal trays that we feed her. She is on soft and pureed foods with thicken liquids. Usually she take but only a few small bites of her meals but her therapist said that she is not concerned at the moment about how much she is eating but getting her use to the process. We are continuing to work with splinting her right arm. It is getting a little easier to do range of motion on her arm and she will relax it at times to about a 90 degree angle.
Last weekend I went to my parent's home and my childhood home town to celebrate my Dad's 90th birthday. We had a great family party. Holli called me while I was at the party and sang Happy Birthday to her Pappy!! It thrilled him as well as all of us there. When I got back this past Wednesday Holli had made me a water color sign ( with a little help) using her left hand that said I Love You. It was my welcome back present. I now have it posted on my fridge at home.
I still have not heard back from my appeal to her insurance company concerning her going to Shepard's Center in Atlanta. Hopefully I will hear something this month.
Holli's friends in San Fran are wanting to use the money they have raised recently for Holli to get massages. I am in the process of lining up someone to come out here to give regular massages. Her therapist here thinks this is also a good idea and should help the tone in Holli's arm and neck. She knows someone that I will be talking to real soon.
Posted by paigereno at 2:42 PM 0 comments
 
Help for Hollis

Hi - I sent some dollars in the hopes that they will somehow help. I wish for her a full and speedy recovery. Would love to know when there is a benefit for her. Would be happy to help.
 
Help for Hollis

Hi - I sent some dollars in the hopes that they will somehow help. I wish for her a full and speedy recovery. Would love to know when there is a benefit for her. Would be happy to help in any way I can.
 
:thumbup good on you Girl Curves
 
Woke up thinking about Hollis today-thought I'd give this thread a little bumpage but looks like Yana beat me too it :thumbup
 
From; http://helpholligethome.blogspot.com/
Saturday, June 26, 2010
Holli in hospital
Yesterday Holli started complaining about her left leg hurting whenever she would try to move it. Her left leg is her good side that usually she has no trouble in moving. Last evening we decided she needed to come to the emergency room since she has a history of DVT ( blood clots). When we got here after several xrays and blood work drawn we discovered that she had a urinary tract infection and that her blood level was too thin and running a fever. She was still having alot of pain in her left hip so the ER doctor had her admitted to the hospital. We got to our room about midnight and then at 2:30 AM she was taken to xray for a CT Scan. The CT scan showed fluid in her psoas muscle. The doctor said it could be either be due to a hematoma or abscess. Since her blood is too thin they are giving her frozen plasma today to thicken her blood so she can have that fluid drained tomorrow in xray. She is being given 3 different antibiotics and has a foley catheter in because her bladder was distended. We will be here at least several days depending on what they find from the aspiration of the fluid. Neither one of us got much sleep last night. I am having to sleep in a recliner by her bedside. The good thing is that speech, physical and occupational therapy are all seeing her during her stay here. I will keep you updated on her status. Please keep her in your prayers.
Posted by paigereno at 1:07 PM 0 comments
 
I've been out of the country for a couple of months and I see we are not stickied anymore. So the occasional bumpage is very welcome, and thanks for donating GirlCurves, I'll let you know if any benefits are coming up.
 
Thanks for updating :thumbup
 
From: http://helpholligethome.blogspot.com/
Monday, July 5, 2010
Discharged from Hospital
Today Holli was discharged from the hospital back to Madison Health care. She has a PIC line in that will stay for the next two weeks to receive IV antibiotics. Holli seemed glad to be back in her room but was very tired and just wanted to sleep so I left her alittle early tonight. I am needing some rest myself and hope to be able to recuperate in the next couple of days. I had forgotten what little sleep you get sleeping at the hospital. Thanks to everyone for your thoughts and prayers.
Posted by paigereno at 7:44 PM 0 comments
Friday, July 2, 2010
Friday
Today makes a week that Holli has been in the hospital. She had a rough night and day with pain and nausea. She is finally resting comfortable this evening and was able to eat some supper without any problems. Holli had a PIC line put in her left arm this afternoon so she can continue to receive IV antibiotics for several weeks after we leave the hospital. She continues to run a low grade fever that they have been unable to identify the source. When her blood cultures were drawn she had already received a couple of antibiotics which can mask anything that might be growing. The doctor talked like we will be going back to Madison Health care this weekend. I should know more tomorrow.
Posted by paigereno at 4:49 PM 0 comments
Thursday, July 1, 2010
Feeling Better
Holli is doing better. Yesterday she was very talkative and laughing but today is very quiet and sleepy. She is still running a low grade fever even though she is getting 3 different antibiotics. An infection control physician is now seeing her trying to find the source. Her blood count is slowly improving but is still not in the normal range but at least is holding. Heather stayed with Holli last night so I could get some sleep. I never slept the night before because Holli had a restless night. I am back now and will be with her for the rest of her hospital stay. We don't know how long that will be before she is discharged. I am thankful that she is improving. While we are here she is being seen by speech, physical and occupational therapy which is wonderful. They sat her on the side of the bed yesterday and is working with her left hand coordination to help her learn how to brush her own teeth and wash her face. Today when they came in she was too sleepy to be able to do much but hopefully tomorrow she will be more awake.
Posted by paigereno at 11:24 AM 0 comments
Monday, June 28, 2010
Hospital Day 3
Holli's color has been better today with her blood level improving. We waited all day for her to be taken to xray for her special procedure. We finally went down at 4:30. They called up to the room to say that she did very well with conscious sedation. They have inserted a drainage tube that is hooked up to a drainage bag located near her left groin. The drainage looks like blood instead of infection but cultures will be sent to the lab. Heather will be staying tonight and tomorrow day with Holli so I can go home and get a little rest and get ready to come back tomorrow evening.
Posted by paigereno at 4:11 PM 0 comments
Sunday, June 27, 2010
Day 2 Hospital
The doctor feels pretty sure that Holli has had a retro peritoneal bleed in the psoas muscle. Her hemoglobin and hematocrit dropped even more this morning so she is now receiving 2 units of blood and will also get some more plasma today also. Because her blood is still too thin she will go tomorrow to have the aspiration and drain inserted in xray. She ran a fever all night and they will continue her broad spectrum antibiotics. I can tell she is very weak because she is very quiet and sleeping alot. The nurses were in and out the room all last night giving plasma, starting another IV, drawing blood and doing vital signs. So it was another night of very little sleep. They did at least bring in a cot for me to sleep on. It brought back memories of St. Lukes Hospital in San Francisco of me sleeping on the cot next to Holli for almost 6 months. I will continue to keep you updated during our hospital stay.
Posted by paigereno at 9:12 AM 0 comments
 
Glad she's out. Being in is always tough on everyone.
 
Wow this has been a tough road for so many. Strong thoughts being sent.
 
Sorry for the long gap between updates.
From; http://helpholligethome.blogspot.com/
Sunday, August 8, 2010
Back in the Hospital
Holli was admitted back to the hospital this past weekend. For details please log on to caringbridge.org/visit/hollihawthorne where I have posted the latest on Holli's condition. Thanks. Diane
Posted by paigereno at 2:28 PM 0 comments
Diane has started using another website to keep us updated on her and Hollis' progress.
From; http://www.caringbridge.org/visit/hollihawthorne
Friday, August 27, 2010 5:20 PM, EDT
Holli went back to Madison Healthcare this afternoon. Her step-mom, Karen, stayed with her there this afternoon. I am still here at Baptist, just moved down to Doug's room to help take care of him. He moved to a regular room yesterday and looking and feeling better. They were able to remove the nasogastric tube this morning so that made his throat feel alot better. We were told yesterday that both the biopies from the colon and the stomach were cancer. Yesterday was a very emotional day for the both of us but our spirits are better today. I know that Doug has a rough road ahead of him from experience and I pray that the both of us will have the strength to face this new challenge. I ask for prayers for our family as we deal with Doug's cancer and Holli's recovery.


Tuesday, August 24, 2010 7:29 PM, EDT

This is the first time I have had time to stop for a deep breath in several days. Sunday Doug, my husband, went into a fast heart rhythm and had to be moved to surgical intensive care. They were able to convert him back to a normal rhythm but Doug's abdomin became very distended and he began to spit up dark brown sputum. He was in a lot of pain and could not get comfortable. Yesterday I spent all day at the hospital and was on the way home when I got a call from the nursing home that Holli's feeding tube was clogged and after trying for an hour was unable to get it functioning. They also noticed some blood in the feeding tube and was sending her to emergency room at Baptist. I turned around and met her in ER. The doctors were concerned that she might have some GI bleeding and admitted her to Medical Intensive Care over night for close observation. Both she and Doug had to have endoscopy this morning. Doug's was first and they found a large gastric ulcer and when they put in a nasogastric tube to relieve the severe distention and removed initally 1100 cc of fluid. He is resting so much more comfortably now and for the first time in two days he is able to sleep. Holli's endoscopy showed no bleeding and they inserted a new feeding tube. They are keeping her here over night and probably will go back to Madison tomorrow. Holli was moved out of intensive care into a regular room. I am spending the night with her. The good thing is that Holli is right above Doug's room, only 4 floors away. The nurses in SICU have been great letting me go in to see Doug whenever I can leave Holli. Now I have to wait for the pathology report on Doug's tumor. I thank everyone so much for your prayers. I have really felt them today.


Saturday, August 21, 2010 10:53 AM, EDT
Holli seems to be feeling better this week but still had one episode of vomiting and several of nausea. She keeps asking why she is there and what happened to her but when asked she remembers that she had an accident in India.
Thursday I had to take my husband, Doug, to the emergency room where it was found that he had a bowel obstruction due to a tumor in his colon. He had to have surgery last evening due to severity of the obstruction. Please keep him as well as myself in your prayers during this time. I will be going back and forth between him and Holli. He is going to have more testing done to check out some concerning areas in his abdomin and stomach. For his friends here in Nashville. he is at Baptist in room 8316. He took such good care of me when I went through my cancer surgery, now it is time for me to take care of him. All I can do is try to take one day at a time because I need to be with Holli too.



Monday, August 16, 2010 8:24 PM, EDT
Holli was transfered back to Madison Healthcare this afternoon. This morning she still had an episode of nausea but was relieved with medication and then she was in a good mood the rest of the day. It was great seeing her laugh and smile more today. Yesterday she had to be given medication for abdominal pain and nausea several times. They said it would take awhile for the erosins to heal in her esophagus and deuodeum. Her step-mom, Karen, stayed with Holli this afternoon so I could finally come home and get some rest. I only got about 3 hours of sleep last night so I felt I was running on fumes after 10 days at the hospital. I will be back out with her on Thursday. Heather, Dick and Karen will be taking care of her the next couple of days.


Saturday, August 14, 2010 1:58 PM, EDT
Holli had her endoscopy this morning. They found she had some erosins and inflamation of her esophagus and stomach. They also changed out her feeding tube to a J tube which goes down into the small intestines. She is being put on protonix to help heal her erosins and reduce the acid. Hopefully she will start feeling better soon. I think the plan is to hopefully get her back to Madison on Monday.


Thursday, August 12, 2010 8:36 PM, EDT
Holli's endoscopy was canceled yesterday due to her blood being too thin (at a critical level). It is now back down to a theraputic level. She is rescheduled for her endoscopy and changing of her feeding tube on Saturday morning. She still has occasional episodes of nausea and abdominal discomfort. Today she has not been as agitated. Her agitation corresponds to her being either in pain or not feeling well. She has had a very quiet day and has slept off and on. For the first time since we have been here she has not gotten mad when they did physical therapy. Tonight she complained of nausea and some leg pain but seems to be feeling better after given some medication. I always enjoy reading the guest book letters. Thanks to everyone for your words of encouragement. It means so much to me and helps give me strength.


Monday, August 9, 2010 9:01 PM, EDT
Today Holli had the Upper GI which did not show anything abnormal. She is now scheduled for Wednesday morning for an endoscopy to look at her stomach and her G tube that is used for her feedings and medication. Sometimes the bulb on the G tube can get out of position and cause nausea and vomiting. The doctor might change it to a different type feeding tube if necessary. Holli has not been in a good mood and has been very agitated. I am sure alot has to do with her hurting and not feeling well. I hope they can make her feel better so that hopefully she will get in a better mood and treat her caretakers better. Heather will come in the morning and let me go home for a few hours and then I will come back tomorrow night so I can be here for her procedure on Wednesday.


Sunday, August 8, 2010 4:55 PM, EDT
Holli is back in the hospital since Friday evening. Last weekend she began vomiting again and running a low grade fever. She was found to have a urinary tract infection and put on mild antibiotics until the culture results. Wednesday Holli was continuing to vomit and run a fever. Friday I brought her to the emergency room because she was not getting better. They found her lapase elevated and she was admitted for pancreatitis. That blood level has since returned to normal but Holli keeps complaining of abdominal pain and nausea but she has not run a fever since admission. They restarted her feedings and diet last evening. She has refused her diet and after drinking juice this morning became very nauseated again. She is scheduled for an upper GI series in the morning. Her doctor has also stopped some of her medications thinking they might be causing her problems. Hopefully the xrays tomorrow will give us some answers. Holli has not been the same since her last hospitalization. She will not be able to get stronger if we can not resolve this problem. Because she is feeling bad and hurting she has become very agitated with anyone that is trying to take care of her. I know that it makes it hard for the techs when Holli is mad and telling everyone she hates them. She even tells me that but I know it is her way of letting me know that something is not right.
On a positive note Holli got her first massage this past week and will continue to get them weekly. The therapist is working mainly on her right side and neck. By the end of the hour massage Holli was so relaxed. Hopefully with the botox and splinting the right arm this will hasten her progress. Please continue to remember her in your prayers.


Sunday, July 25, 2010 4:53 PM, EDT
Finally, after over 2 weeks, Holli is feeling much better. She has not had anymore rashes, vomiting or fever in the last several days. I have been so worried because we could not figure out what was going on with her. I am so glad she is over this set back. Holli has been more emotional lately wanting to know why she is here and that she does not understand what has happened to her body. I have had to constantly tell her that she was in an accident 17 months ago and had a brain injury. Her response is either "Oh, I did not know that" or she cries and tells me she is sorry that she had an accident. I reassure her that she has been slowly improving and that with hard work in therapy she will be able to get stronger so that I will be able to take her home. We have a new therapist working with her since Thursday that is going to do alot of teaching to the family so when therapy is not able to give Holli therapy we will be able to do it and not have her regress. I found out that the appeal was denied by Tenn Care on April 30th. They said that a letter was mailed but neither I or Madison Healthcare received it. I pray for guidance in knowing what road I need to take next for Holli. Our social worker is making a few contacts to different organizations to see if they will be able to help or guide us. Please continue to keep us in your prayers.


Sunday, July 11, 2010 6:21 PM, EDT
Holli has not had a very good weekend. Yesterday she started vomiting and developed a rash. Her IV antibiotics was stopped and today we tried another antibiotic per gastric tube. She developed another rash so that is now stopped. She is very quiet and just has a look on her face that she is not feeling well. I think she looks pale today. They are going to repeat her blood work in the morning. I hope she is not anemic again. I pray that soon she will feel good again and be happy once more. Her illness for the past several weeks has really taken a toil on her.



Monday, July 5, 2010 4:52 PM, EDT
Holli was discharged from Baptist Hospital today and returned to Madison Healthcare. She did not run a fever yesterday for the first time since admitted 10 days ago. She has a PIC line in that she will get her IV antibiotic for the next 2 weeks. I am so glad that she is feeling better and starting to laugh and talk again. Thanks everyone for your thoughts and prayers while Holli and family was going through this rough bump in the road.
 
Oh my gosh

I can't believe what you are going through. You are so strong! Please remember that there are many of us thinking of you a lot, although we may not say so.
 
Please let us all have some unified positive thought for this family and this amazing woman Dianne who seems to be able to keep coping.

You are not forgotten Dianne wishing well for you and your family.
 
Hi everyone.
Thank you all so much for your support of Hollis over the last year and a half or so.
I have decided that I'm not able to keep timely posts coming to this thread so I'm going to probably stop and encourage you to subscribe here if you would like to be updated when Diane posts a new journal entry. http://www.caringbridge.org/visit/hollihawthorne/journal
Feel free to bump this thread up yourselves if you want to post Hollis news.
Thanks everyone.
 
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