tag:blogger.com,1999:blog-1693248672834423402024-03-13T14:06:52.894-07:00Eric DoverEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.comBlogger102125tag:blogger.com,1999:blog-169324867283442340.post-35049138690935424322011-02-27T13:01:00.000-08:002011-02-27T13:04:10.088-08:00Released from the transplant team.Friday, Feb 25th I was officially released from the Bone Marrow Transplant Team and referred back to the care of my Oncologist who I will see on Monday. Will also be off the main steroid drug by next Wed. Still on home IV's for one hour per day so it will be at least another week or two before they pull the central line from chest. I feel great, with basically a clean bill of health! (yet still closely monitored).Eric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com0tag:blogger.com,1999:blog-169324867283442340.post-54665355236218264802011-02-18T17:02:00.000-08:002011-02-18T17:24:14.494-08:00Doing much better.Sorry I haven't posted in a while. About 2 weeks ago I finally started having signs of improvement from the stomach virus. I am now back to eating normally and getting daily light exercise. Although I still get tired rather easy. I am down to just about 1-hour daily IV support now. The doctors have also started reducing my Prednisone steroid doses and stopped one other anti-rejection drug (MMF). IF things continue to go smoothly, I'll be off Prednisone in 12 days. This will be a big step as it has been the main drug for the past 4 months that suppresses my immune system (plus various other side effects). I am also on track to finally depart from the transplant team within the next week or two. Then, it will back to my regular oncologist and I should only have to go for a check up once every week or two. I imagine they will be pulling my central line out of my chest here pretty soon also. So, just crossing my fingers the next couple of weeks continue to go smooth. Thanks again to everyone for all of your support and help.Eric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com0tag:blogger.com,1999:blog-169324867283442340.post-60084205145057936622011-01-30T10:11:00.000-08:002011-01-30T10:12:03.189-08:00Trying to stay Positive.Trying to stay positive, but it's tough. I have basically been confined to my bed (or the hospital bed) on IV's for the the past 5 weeks. Hoping this stomach virus get's cleared soon so I can have a better month in February.Eric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com1tag:blogger.com,1999:blog-169324867283442340.post-13065768475853812542011-01-16T18:15:00.000-08:002011-01-16T18:32:42.646-08:00Still fighting this stomach virus.I am still fighting this stomach virus that has me down. I am on IV nutrition 20 hrs per day which gives me the nutrients I need. But, I am still quite weak. Several of my GVHD meds needed to be switch to IV because the pill were going right through me. So, it's a bit tricky and complicated to deal with this. Daily trips to the clinic and managing meds, IV's, sleep, etc. at home is a challenge. Toshiko is incredible how she can help me and manage Tyler all at the same time. Julie and Jackie came and help at the clinic both days this weekend and that was a big help (thanks Jackie & Julie!). My parents are coming also to help tomorrow. Thank you, thank you! And, my good friend & nurse, Kelsey at the clinic has taken care of me the past few days. I am so fortunate to have so many people who care for me.<br /><br />EricEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com2tag:blogger.com,1999:blog-169324867283442340.post-52646341157523546142011-01-14T07:28:00.000-08:002011-01-16T18:14:45.393-08:00In and out of the hospital again.Last Friday I had flu-like symtoms and ended up in that hospital again for 6 days. They first thought is was a stomach virus, then gut GVHD. Finally, after many tests they concluded yesterday it is NOROVIRUS, a stomach virus. So, they are treating for that now. I came home 2 days ago and going to the clinic each day for insfusions, plus on IV hyrdation and nutrient infusions myself at home. I lost 12 pounds and rather weak, but getting better.Eric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com0tag:blogger.com,1999:blog-169324867283442340.post-61712771817853473392011-01-02T17:20:00.001-08:002011-01-02T17:21:36.848-08:00Enthusiasm.Nothing great was ever achieved without enthusiasm.Eric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com0tag:blogger.com,1999:blog-169324867283442340.post-39254694992832179362011-01-01T10:19:00.000-08:002011-01-01T10:20:05.048-08:00Inspiration.The more difficulties one has to encounter, the more significant and the higher in inspiration his life will be.Eric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com0tag:blogger.com,1999:blog-169324867283442340.post-27048193054705337452010-12-31T08:55:00.000-08:002010-12-31T08:56:27.331-08:00Attitude.Nothing can stop the man with the right mental attitude from achieving his goal; nothing on earth can help the man with the wrong mental attitude.Eric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com0tag:blogger.com,1999:blog-169324867283442340.post-25212504331385047142010-12-29T20:45:00.000-08:002010-12-29T20:46:52.754-08:00Back home today.Back home from the hospital today. Finally can get a good nights sleep, then back to the clinic for blood tests and Dr. visit tomorrow at 8:00 am. How fortunate I am to have such a great bone marrow transplant team at SCCA watching over me so closely.<br /><br />EricEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com0tag:blogger.com,1999:blog-169324867283442340.post-19182774370284402202010-12-26T20:11:00.000-08:002010-12-26T20:23:56.978-08:00Still here in the Hosptial - feel fine (normal).Still here in the hospital. Feels more like jail since I am not allowed to go out of my room because they don't want this virus to spread. It's a bit frustrating because they say it's a serious virus, yet they still don't have any test result back from last Thursday's test to determine if I still have the virus or not! Normally, the result should come back the next day but the weekend and the holidays have delayed things. They are still doing the 2-hr treatment every 8 hrs so it is good that I am staying healthy with this treatment. My only symptom is a runny nose. I am exercising daily and eating lots and skyping with Toshiko and Tyler. They said the longest I would be here is 10 days. Hopefully I can get out a day early and be home for new years. <br /><br />EricEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com0tag:blogger.com,1999:blog-169324867283442340.post-48266417749384202362010-12-23T13:21:00.000-08:002010-12-23T13:30:52.223-08:00Back in the hospital.This week I have some very minor signs of a cold. A test came back showing it to be RSV - a respiratory virus similar to the common cold but at higher risk of causing pneumonia. The doctors concluded the safest thing to do is treat it now as a prevention so is doesn't spread to my lungs. The treatment is called <span id="SPELLING_ERROR_0" class="blsp-spelling-error">Ribavarin</span> treatment. It's done in the hospital 3 times a day, 2 hours each time. They put an enclosed clear plastic square "bubble" over the bed and run <span id="SPELLING_ERROR_1" class="blsp-spelling-corrected">ventilator</span> that <span id="SPELLING_ERROR_2" class="blsp-spelling-corrected">humidifies</span> the medicine and I wear a mask to breath it in. Not sure how many days I'll be here, but sounds like at least 5 days or so. I started last night.<br /><br />EricEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com0tag:blogger.com,1999:blog-169324867283442340.post-39852223694360011352010-12-15T17:30:00.000-08:002010-12-16T08:21:37.372-08:00Day-80 bone marrow test clear. No Cancer.The day-80 post-transplant bone marrow test came back clear today. Complete remission. This is the last bone marrow test the transplant team will do. The next bone marrow test will be sometime during the next year when I go back to my regular Oncologist.<br /><br />I still have skin rash issues as a result of <span id="SPELLING_ERROR_0" class="blsp-spelling-error">GVHD</span> but it seems to be getting better with the steroids. So, we are going to try tapering the steroids again and see how I respond. I had a Long-term-follow-up training course today in preparation to depart the transplant team. It was quite informative. I learned that <span id="SPELLING_ERROR_1" class="blsp-spelling-error">GVHD</span> could be quite possibly be hanging around for a year or so and also I really need to be cautious for basically 1 year as I am still on immunosuppre<span id="SPELLING_ERROR_2" class="blsp-spelling-corrected">sant</span> drugs. Also, my new immune system is still quite young. They have <span id="SPELLING_ERROR_3" class="blsp-spelling-error">lot's</span> of rules, and <span id="SPELLING_ERROR_4" class="blsp-spelling-error">do's</span> & <span id="SPELLING_ERROR_5" class="blsp-spelling-error">don't's</span>. I'll be getting all new immunizations at the one year mark (next Sept) also.<br /><br />I have reached a milestone this week. I could not have done this without all the incredible outpouring of love and support from my loving Family, Friends, Doctors, Nurses and one very special donor. It is simply amazing how many people have come together to cure me. Words cannot express how grateful I <span id="SPELLING_ERROR_6" class="blsp-spelling-corrected">truly</span> am.<br /><br />EricEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com1tag:blogger.com,1999:blog-169324867283442340.post-42190883693997500272010-12-12T20:22:00.000-08:002010-12-12T21:02:22.777-08:00Lots of tests this week......Starting with my day-80 post-transplant bone marrow test and spinal tap tomorrow. This is the last time they are scheduled to do these tests before releasing me from the transplant team - what a relief - they are not fun. Then, on Wednesday I have <span id="SPELLING_ERROR_0" class="blsp-spelling-error">Xrays</span>, dental exam, blood tests, Dr. meeting, and a Long-term Departure orientation class. Friday; med-photo's, CT scan, more blood tests. I am both excited and nervous about this week. While they are tests that are signifying the end of the transplant process, they are also tests where the doctors are checking very close for anything abnormal.<br /><br />Currently, in addtion to my other 13 daily meds, I am still on the high-dose <span id="SPELLING_ERROR_1" class="blsp-spelling-corrected">steroids</span> (70 mg of <span id="SPELLING_ERROR_2" class="blsp-spelling-error">prednisone</span>/day) because they are still trying to get my <span id="SPELLING_ERROR_3" class="blsp-spelling-error">GVHD</span> skin rash completely under control. Last Friday, they also started me on another drug (Mylophenolate) to <span id="SPELLING_ERROR_4" class="blsp-spelling-corrected">control</span> the skin rash which doesn't have as bad of side effects as <span id="SPELLING_ERROR_6" class="blsp-spelling-error">prednisone</span>. So, the plan is to hopefully start to taper the <span id="SPELLING_ERROR_7" class="blsp-spelling-error">prednisone</span> this week.<br /><br />The rash is getting better and and I just feel great. <span id="SPELLING_ERROR_8" class="blsp-spelling-error">Toshiko</span> and I were able to go to a friends birthday party Friday and also my company Christmas party Saturday night. We had a wonderful time. It was great seeing and talking with all of my friends there. It was a bit emotional for me as it has been almost exactly one year since my diagnosis and it just felt great to be among f<span id="SPELLING_ERROR_9" class="blsp-spelling-corrected">riends</span> and feeling somewhat "normal" again after such a very long, very tough year.<br /><br />EricEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com1tag:blogger.com,1999:blog-169324867283442340.post-35474687614290342022010-11-25T16:32:00.000-08:002010-11-25T16:50:33.873-08:00Happy Thanksgiving to all. Ski pic's - don't tell my doctors!!<a href="http://4.bp.blogspot.com/_cRl2Is_1CCs/TO8BFFF6w7I/AAAAAAAAAEg/1izn_lvI3No/s1600/75158_1477377809674_1090608433_31024385_7213750_n%255B1%255D.jpg"><img style="WIDTH: 320px; HEIGHT: 240px; CURSOR: hand" id="BLOGGER_PHOTO_ID_5543650853094343602" border="0" alt="" src="http://4.bp.blogspot.com/_cRl2Is_1CCs/TO8BFFF6w7I/AAAAAAAAAEg/1izn_lvI3No/s320/75158_1477377809674_1090608433_31024385_7213750_n%255B1%255D.jpg" /></a><br />Hi everyone. On Nov 23rd we had snow and sun at our house! I couldn't resist the temptation so went out and skied in our driveway while Tyler was on his sled! At just 60-days post-transplant, the doctor's probably wouldn't approve of this but it sure felt great to be on my skis again. We had a nice thanksgiving dinner today at my house with Toshiko, Tyler, my parents, and a friend from Japan. Today is my one day off from the Clinic today. Had spinal tap yesterday (just one more to go now) and lots of other blood tests. Will see the Nurse tomorrow again to assess my GVHD rash. It has flared up a bit since we started the tapering the steroids, so they are watching close and have slowed down the taper. I feel great and getting better every day. So much to be thankful for this year. Love to all my family and friends. More pics below...<br /><a href="http://3.bp.blogspot.com/_cRl2Is_1CCs/TO8A9w5OuQI/AAAAAAAAAEY/dAsBCD9DMO8/s1600/155945_1477405650370_1090608433_31024453_4701898_n%255B1%255D.jpg"><img style="WIDTH: 320px; HEIGHT: 240px; CURSOR: hand" id="BLOGGER_PHOTO_ID_5543650727413332226" border="0" alt="" src="http://3.bp.blogspot.com/_cRl2Is_1CCs/TO8A9w5OuQI/AAAAAAAAAEY/dAsBCD9DMO8/s320/155945_1477405650370_1090608433_31024453_4701898_n%255B1%255D.jpg" /></a><br /><br /><div><a href="http://4.bp.blogspot.com/_cRl2Is_1CCs/TO8A3GVyGjI/AAAAAAAAAEQ/J9xYoJpakm8/s1600/155945_1477405610369_1090608433_31024452_348046_n%255B1%255D.jpg"><img style="WIDTH: 320px; HEIGHT: 240px; CURSOR: hand" id="BLOGGER_PHOTO_ID_5543650612911151666" border="0" alt="" src="http://4.bp.blogspot.com/_cRl2Is_1CCs/TO8A3GVyGjI/AAAAAAAAAEQ/J9xYoJpakm8/s320/155945_1477405610369_1090608433_31024452_348046_n%255B1%255D.jpg" /></a><br /><br /><br /><div><a href="http://3.bp.blogspot.com/_cRl2Is_1CCs/TO8AwVCUM_I/AAAAAAAAAEI/hbhBaHpKG-A/s1600/155945_1477405570368_1090608433_31024451_2964025_n%255B1%255D.jpg"><img style="WIDTH: 320px; HEIGHT: 240px; CURSOR: hand" id="BLOGGER_PHOTO_ID_5543650496596947954" border="0" alt="" src="http://3.bp.blogspot.com/_cRl2Is_1CCs/TO8AwVCUM_I/AAAAAAAAAEI/hbhBaHpKG-A/s320/155945_1477405570368_1090608433_31024451_2964025_n%255B1%255D.jpg" /></a><br /><br /><br /><br /><div><a href="http://1.bp.blogspot.com/_cRl2Is_1CCs/TO8Ap5XEV0I/AAAAAAAAAEA/HoUqf26Vo6M/s1600/77159_1477392890051_1090608433_31024418_6947697_n%255B1%255D.jpg"><img style="WIDTH: 320px; HEIGHT: 240px; CURSOR: hand" id="BLOGGER_PHOTO_ID_5543650386088580930" border="0" alt="" src="http://1.bp.blogspot.com/_cRl2Is_1CCs/TO8Ap5XEV0I/AAAAAAAAAEA/HoUqf26Vo6M/s320/77159_1477392890051_1090608433_31024418_6947697_n%255B1%255D.jpg" /></a><br /><br /><br /><br /><br /><div><a href="http://3.bp.blogspot.com/_cRl2Is_1CCs/TO8AgapgZ0I/AAAAAAAAAD4/rInSwSyezxQ/s1600/77159_1477392850050_1090608433_31024417_2923567_n%255B1%255D.jpg"><img style="WIDTH: 320px; HEIGHT: 240px; CURSOR: hand" id="BLOGGER_PHOTO_ID_5543650223225595714" border="0" alt="" src="http://3.bp.blogspot.com/_cRl2Is_1CCs/TO8AgapgZ0I/AAAAAAAAAD4/rInSwSyezxQ/s320/77159_1477392850050_1090608433_31024417_2923567_n%255B1%255D.jpg" /></a><br /><br /><br /><br /><br /><br /><div><a href="http://2.bp.blogspot.com/_cRl2Is_1CCs/TO8AaOX04lI/AAAAAAAAADw/ByPSzLkVXj0/s1600/77159_1477392810049_1090608433_31024416_3355099_n%255B1%255D.jpg"><img style="WIDTH: 320px; HEIGHT: 240px; CURSOR: hand" id="BLOGGER_PHOTO_ID_5543650116850999890" border="0" alt="" src="http://2.bp.blogspot.com/_cRl2Is_1CCs/TO8AaOX04lI/AAAAAAAAADw/ByPSzLkVXj0/s320/77159_1477392810049_1090608433_31024416_3355099_n%255B1%255D.jpg" /></a><br /><br /><br /><br /><br /><br /><br /><div><a href="http://4.bp.blogspot.com/_cRl2Is_1CCs/TO8ASeIRuhI/AAAAAAAAADo/aIh2_MoOjI4/s1600/75158_1477377769673_1090608433_31024384_1070184_n%255B1%255D.jpg"><img style="WIDTH: 320px; HEIGHT: 240px; CURSOR: hand" id="BLOGGER_PHOTO_ID_5543649983641795090" border="0" alt="" src="http://4.bp.blogspot.com/_cRl2Is_1CCs/TO8ASeIRuhI/AAAAAAAAADo/aIh2_MoOjI4/s320/75158_1477377769673_1090608433_31024384_1070184_n%255B1%255D.jpg" /></a><br /><br /><br /><br /><br /><br /><br /><br /><div></div></div></div></div></div></div></div>Eric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com1tag:blogger.com,1999:blog-169324867283442340.post-91363708021970879612010-11-13T12:20:00.000-08:002010-11-13T12:45:00.823-08:00Day 49 since transplant.Today is the 49th day since my transplant date. So tomorrow I will be halfway to the 100-day mark which is when I am scheduled to be released from the transplant team and go back to general oncology doctor . That is also the time I am schedule to go back home. Although the doctors may possible let me return earlier. For now, they still say I am too vulernable to infection to return home full time. I have been have more frequent afternoon visits home though and it has been so nice spending time with Toshiko & Tyler as I feel better. <br /><br />Yesterday I had another spinal tap which went smooth - only 2 more to go! I am still having some GVHD issues with skin rashes. They are trying to get it controlled with topical steroids and photo therapy (like a suntan bed). This, in hopes that they can start tapering me off the Steroids pills which I have been taking for more than two weeks. These pills are effective, but dangerous as they are making my platelets drop and also greatly increase infection risk. There are other long term side effects possible also, so they want to start tapering soon. I am still feeling better with each day and feeling closer to "normal" every day. <br /><br />EricEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com1tag:blogger.com,1999:blog-169324867283442340.post-77280755157216278232010-11-05T12:48:00.000-07:002010-11-05T13:19:19.191-07:00One day at a time.Dr. appointments went smooth this week without any major issues. I am still on the Prednisone steroid to control the skin rash from the GVHD. This makes my metabolism very high which quickly reduces muscle mass in my arms and legs. So, they have me eating at least 110 grams of protein per day and I am still loosing weight so they want me to excerise my muscles as much as posssible. I am currently 146 lbs (my normal weight is 165 lbs). I am feeling better every day and recovering good.<br /><br />EricEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com0tag:blogger.com,1999:blog-169324867283442340.post-77985962772358120162010-11-02T19:51:00.000-07:002010-11-02T20:05:58.503-07:00Good day.Today I feel a bit better than the past few days. I was able to walk and eat more. I have been feeling a little better each day. It will just take time to recover. I am basically recovering faster than average. So, hopefully the "good days" will start outweighing the "bad days". They do have me on about 20 pills per day plus IV fluids which all contribute to how I feel. I am pushing myself to walk, <span id="SPELLING_ERROR_0" class="blsp-spelling-corrected">exercise</span>, and eat more which also will speed up recovery.<br /><br />EricEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com1tag:blogger.com,1999:blog-169324867283442340.post-16765437419095298112010-10-25T19:36:00.000-07:002010-10-25T19:55:17.406-07:00Complete Remission!The results of the bone marrow test came back today and showed "no evidence of previously diagnosed Leukemia". This is the best news. This proves the transplant was successful. It was pretty emotional for me because for 10 months there has always be some very small % show when they did that test. There will be 3 more bone marrow test over the next 60 days to check and make sure it is still working. I still have lot of recovery and other issues to work out over the next 2 months. I tested positive for Graft vs. Host Desease (GVHD). It's mainly rashes on my hands and arms. My hands are swollen and with lots of bumps making it difficult and painful to do simple tasks like opening a bottle of water. They started me on Steroids to clear this up. They said some GVHD is good because it helps fight off any possible residual desease. <br /><br />Thank you very much to everyone. I am overwhelmed with the amount of support from so many family and friends. I feel incredible loved by so many. <br /><br />EricEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com2tag:blogger.com,1999:blog-169324867283442340.post-41322004328254498632010-10-21T21:44:00.000-07:002010-10-21T21:57:50.639-07:00Bone marrow test tomorrow.Well, it's already been 27 days since the donor cells were transplanted into me. So, tomorrow I will have the first of 4 bone marrow aspirations to test and see how well the engraftment is working and also to check if there are any remaining residual deseased cells. The doctors today said all of my blood test show all of my organs are working strong and normally and my blood counts are very good. They said I am doing quite well. I do have some mild skin rashes on my arms that could be some mild GVHD (graft vs host desease). It is expected that I will get some GVHD at some point, and this is good because it helps fight off any possible remaining bad cells.<br />I am still rather weak and tired most of the time. For example; I get up and walk for 15 minutes, then need to take a nap for an hour. But I am feeling better each day. I am on IV fluids at home all day that I administer myself with a pump they gave me.<br /><br />EricEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com0tag:blogger.com,1999:blog-169324867283442340.post-18758569967187051462010-10-17T20:53:00.001-07:002010-10-17T21:00:54.410-07:00Happy Birthday!Today is my birthday. I am feeling better each day. I had a nice day. After my appointments at the clinic, I had several visitors. It was great to see and talk with everyone. I couldn't do this without all of the loving support I have from so many family and friends. My parents have been especially great - basically waiting on me hand and foot all day. I am still feeling quite weak and moving slow, but my blood count are all moving up quite well every day and this makes me feel better each day. Next, I have appointments for tests and procedures every day this week starting tomorrow. Things are going good.Eric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com2tag:blogger.com,1999:blog-169324867283442340.post-36129576887020166442010-10-14T21:19:00.001-07:002010-10-14T21:25:43.455-07:00Out of the hospital now.Yesterday I was discharged from the hospital. My counts are steadily rising and the doctors said everything else looks fine. So, they decided to discharge me early since there is less change for receiving an infection at home than at the hospital. This is all good news, yet is it quite a challenge because I still feel very week. I am walking quite slow and eating a bit more now. I had clinic visits today and will have more every day for a while. The support I am getting from all of my family is just amazing. I am fortunate.<br /><br />EricEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com2tag:blogger.com,1999:blog-169324867283442340.post-90978295440441813982010-10-09T12:58:00.000-07:002010-10-09T13:08:58.730-07:00Got Cells?Today the blood test finally showed my new white blood cells are starting to engraft! WBC today is 0.110 with Neutrophil count of 0.060. These should now start a steady incline which usually replicate fast. The best thing is I will feel better each as these counts continue to climb. The Neutrophil count needs to increase to safe level of 0.500 and I should then be OK to home (possibly next week). I am still rather weak so am working on eating and walking more.<br /><br />EricEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com1tag:blogger.com,1999:blog-169324867283442340.post-4682273264841725202010-10-06T13:50:00.000-07:002010-10-06T13:54:33.511-07:00I am hanging in there.This is very tough, but everything is going well. The Doctors say everything looks good and going as planned. Still lots of pain with the mucositis. I am still eating and walking each day. I should start feeling better as soon as the WBC's start coming in which should be within the next 7 days or so. <br /><br />EricEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com4tag:blogger.com,1999:blog-169324867283442340.post-58766860040562858022010-09-29T08:40:00.000-07:002010-09-29T08:48:45.233-07:00Morphine is becoming my friend.The mucositis has been causing quite a bit of pain. But I am learning how to manage it with morphine. I have still been eating and getting up and walking several times per day. Have to push myself sometimes, but generally I am doing good. The doctor said everything is going smooth and all of my counts for organ functions look very good. It's tough, but I am on the road (a long road) to recovery. Endurance and persistance are important so I am keeping up on all the things they suggest I do. I'll be out skiing before I know it! <br /><br />EricEric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com2tag:blogger.com,1999:blog-169324867283442340.post-44236738944249619012010-09-26T18:13:00.000-07:002010-09-26T18:23:31.514-07:00The new cells are in me now.Yesterday, the transplant of the new bone marrow cells finally completed at about 10:00 am. A total of about 9 hours. I was completely exhausted by the time it was finished. It was a tough feeling because I was so tired I couldn't sleep. I have been up all day and night with trips to the bathroom every hour for the past 2 days. However, I have been able to get some sleep in between. They tell me the mucositis should set in in the next couple of days. It is suppose to be rather painful and they will give me morophine. I have had lots of family and friends visit so that is helpful. Just taking one day at a time.Eric Doverhttp://www.blogger.com/profile/07691167510631670995noreply@blogger.com1