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fall firewood prices for self-advertisers? ?

firewood prices remain stable

Warstein (SP) What is happening to the firewood price? Is there enough wood? Fuelwood Deutschland.de looking for answers. Firewood is a firewood dealer Deutschland.de community.

who in January 2009 could offer as a dealer or firewood, working with a professional drying chamber or to buy dryers. Air-dried product usually am this time of year and especially in the middle of a cold spell is no longer available. Therefore: be careful with alleged "bargain", because in a strong demand situation is no one from his firewood under value.

prices below 68 euros for the bulk cubic meters were actually illusory, then the dealer. If you still get offered something ". Not check amount, type of wood and especially the dry wood dries well in the winter months, so there are no supplies," advised the Dealer.

on the safe side when it was offered by dealers, dried himself, for that would have no other situation than three months ago. The raw wood has not become more expensive and it gibe enough wood. Or: "Ask the retailer for alternatives to expensive beech, pine is often available to you to get warm over the winter."

way: "firewood this winter are not much more expensive, so it is not a problem now store even larger quantities," said Wood Germany.





The current price of firewood Bitz



Bitz / County Balingen, Baden-Württemberg (SP), the council voted in October 2008 from
of the log price and came to the decision that in the previous year at 47.50. Euro to remain VAT inclusive.





Current firewood prices in Driedorf



Driedorf / Westerwald (SP), the firewood prices 2008/2009 in the community Driedorf / Westerwald: The parish council has kept the price of firewood last year. Thereafter, for a cubic meter of firewood, brought along the way, 55,00 €, and for industrial wood / logs 44,00 € / payable fm. For logging residues, a price of 15,00 € will be fixed per rm. Firewood orders takes the community to 30.01.2009. The wood is invariably granted under orders to local citizens.





Affordable softwood in the Fichtelgebirge



County Wunsiedel (SP) in the Fichtelgebirge, the world is in order - at least for the current firewood prices. The private forest owners in the district currently require Wunsiedel 45-50 € for the room meters oven finished softwood. There, in the past five years, a price increase took place from about ten to 15 €. But the prices are in the Fichtelgebirge still well below those required in southern Bavaria.

But demand is rising: The city Wunsiedel required for the space meters from the urban forest such as from € 2009, two more than previously. Accordingly, for example, requires the cubic meter for coniferous wood fellers six euros excluding VAT. For two-meter commodity that can be removed from the forest, are 25 €, also without VAT due.

The current wood prices in Reutlingen

rise also in Reutlingen / Baden-Württemberg, the wood prices easy for plywood are the future 60 euros per cubic meter to pay (previously 58 euros), firewood long costs 52 euros per cubic meter (previously 50 euros). The County Forestry Department is proposing to the municipalities, laminated wood for 65 € per cubic meter long and firewood for 52 € per cubic meter (50 € orders of more than thirty cubic meters) offer.

The current fuelwood prices in

Lübeck in the Hanseatic city of Lübeck pay fellers for hard wood (beech, oak, maple) between 15 and 30 euros per cubic meter. 75 euros will cost the already chopped wood in the lumberyard. The high demand (an increase of 20 percent over the past ten years) has let the fire firewood prices in the Lübeck municipal forestry since 2005 by almost 100 percent higher.





firewood prices fall for fellers



Bad Salzungen / Thüringen (SP) The Bad lowers Salzunger Forest Service treated both the prices for finished Firewood and prices for assigned forest areas, from which one can get firewood. Last year, costing the hard yards recycled hardwood firewood 43 Euro, now it costs 40 €. Even advertisers paid so far 12 to 16 euros per cubic meter - now there are eleven to 15 €. The graduation is explained by the different distance of the proposed sections for forest road. For an area right on the way, 15 € charged per cubic meter, whosoever shall further into the forest, will pay 13 euros, for way more than 60 meters away from the path, eleven € per cubic meter to be recognized. The drop in prices is explained by the lower oil price.

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How fast time flies.
The Day 100 is approaching with giant steps. This coming Friday, another bone marrow biopsy is called for to control. Originally we had hoped that in the course of this anesthetic on day 101 also equal to the venous catheter is removed. However, since floating around still some old blood cells in the body of Philip the doctors do not rush and slow down a bit so our exuberant optimism.

Despite this, Philipp better every day. He comes slowly again physically forces and will increasingly enduring. Although he has repeatedly in the short term arge abdominal pain usually with diarrhea, sometimes with nausea on imaging, but these phases are less and take shorter and shorter.

The appetite and the taste will be better every day. Philip has again feel like cooking, Gusto right to food and the amount consumed almost every day is almost at 2.5 liters, and often about it.

The present about weekly inspections, the "lead" every time longer.
3 weeks ago has disappeared, the strict liability mask at home.
Then came the permission to eat fast food again.
Last week came the release again in a restaurant if it is not too crowded to consume freshly cooked foods.
We have taken advantage of the weekend were the same and steak dinner. ;-)))) Mhhhh
And now he has thrown himself at the Christmas market at Karlsplatz on a fresh potato pancakes. To which it had been longer an enormous gusto, and then a fresh crepes and a punch.

aaahhhhh does well, though still with a bit of a strange feeling in the neck anyway if all goes well, but finally participate in the "normal" life.
Last week was Phil in the morning and once in a supermarket.
Just like that, without a mask, because before only 5 people including staff were in the supermarket.
He has long stood in front of the shelves with the tea's and has savored, and smelled, and then opted for some new tea varieties. Finally, he drinks for almost 6 months, only the tea we get home. His orders are based on his blush, but really himself again choose .....

2 weeks ago we were on Thursday immediately after the St. Anna checkup once in school for a visit. (At that time, with a mask)
The joy was enormous. In the classroom community anyway, but even with the professors, the joy was clearly visible on his face. Since then Phil can not wait to finally more fully to be there. This short visit has motivated him enormously.

The control of the Hautärtzin has gone well this week. After initial worrying signs in the hospital now had the all clear that the information provided by the irradiation anscheindend enlarged birthmarks not all of them being critical, but should nevertheless be observed.

This week, it sure caught the dad with the flu. Thus, it was time again for some mask requirement, mostly for Dad. This has, of course, also reflected on the feelings.
Philipps immune system is to create a lot now, and is diligent in learning, but we do not take any unnecessary risks.

Even Philip learns diligently. Every day now the teachers for almost 2 hours to him. Each week, school work, he brings on strong again and is looking forward immensely to the school. The eternal one lessons he is already sick and tired - you can not gossip, do not cheat, so there are a full 2 hours of real concentration of the day. Unfortunately

We currently have no safe predictions, as far as the real start of school. Sun from the date 100 is heist, according to protocol, you can possibly, depending on blood count and development, begin again to think more to go among the people.
same time, but no one wants to, will concentrate Philipp, especially during this flu season, no unnecessary risk.
long story short text, we hope, especially Phil, the great hope, before Christmas at least half a day on the way back to people at any normal school day. And if everything continues by and by slowly but steadily developed positively, perhaps, be full again after the Christmas holidays there.

It is, then won with one or the other week to expect total failure to build, just like small children in the kindergarten pick up their immune system while a virus and a week are sick, it can also occur next year when Phil stepped up.

But first we are in spite of the catheter remaining hopeful, and we're thrilled to "healthy" Christmas.

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;-)))) days 75, Sunday, 11/16/2008

Hurrah, we are doing great.
Control on Friday was ok. all current values correspond to the "norm" of the 73rd of the Day

Philipp it's getting better every day. Since the weekend it is the motivation for moving even easier.
He was a few short trips by bike already, is relatively quickly exhausted, but it's fun again to be more active.

The thing with eating "normal" more and more.
Philip has been noticeable this weekend's appetite for food. Seen again on TV cooking shows, cookbooks and has schmöckert in this Sunday for the first time since August again cooked a complete meal. Although he had to insert a break after 30 minutes, but with fried wonton Kichererbesensuppe bags filled with sheep cheese were delicious. :-)
gave the evening, fried banana with rum and lime - wonderful.

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:-) gradually uphill

small way it goes every other day better.
between Philip has a constant, not so good day, to which he will also drink less and has little appetite.
But the good days are getting longer.

Philip is always in the mood for funny jokes, just needs more rarely a nap and now has written under the strict supervision of his teacher, the English home-school work.

On Friday we had an unspectacular control visit in the hospital. The blood count was ok and corresponds to the normal state in this phase of physical regeneration. Otherwise, no treatment, no Infussionen, watch only listen, and go after 3 hours back home. Phil has to take this opportunity once again brought the medical advice of Fast Food. Since the fast food chains very meet high hygienic requirements must be fast food since Friday authorized.
We were right out of the hospital at burger king - the last 3 months, Philip's first meal that was not cooked at home or in hospital at us, and so true .....

The next examination is scheduled for next Friday. Until then, Philip mask duty when he meets with other people. The only exception we are as a family. It is anticipated, but dropped at the last Friday of drugs for immune suppression and then really begin building the immune system. The other few tablets to swallow now that Phil has to have vitamins and folic acid to support of blood production. And the one or other protective drug for stomach

etc. We are all glad that Phil really even see them every day better. The skin on the hands and feet is still very tender and soft, but the hair sprout again and he is every day stronger.

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:-))))))) day 64 - Tuesday 4th November 2008

It is done, Phil can again sleep at home.

After the results of the puncture on day 60 (Friday 31.10.) Are quite ok, Philipp daily more and more eating and increased fluid intake especially the day he was on Tue 11/04/2008 by the hospital (final) released. Now, after three unsuccessful Anäufen, finally fix at home.

He is also really good at this time. He's bouncy, makes pulling your leg a lot, and is physically within the possibilities in a good mood.
Although he is very thin, but he has risen in the last few days of 1 kilogram. So the trend fits.

Now that he's home and he feels, I can say yes: The release has been announced late last week, but because of the many disappointments of the past weeks we have not dared to talk about it. ,-O


After more than two months, we may get used again to a "new" routine. We are a fully united family again. Hurraaaaaa.
breakfast together, chat together in the evening, watch TV and play without having to be on time in the hospital. Full Toll ;-)))

Phil also gets all right appetite, stows away goose with red cabbage and dumplings, bacon, lentils and other hearty stuff. The stomach tolerates it and the body needs it.

From today's perspective, we also now have renewed hope for the day 100, ie on 10
December, as planned, the next bone marrow aspiration to take the test and if by then everything will fit right in the course of this anesthetic the venous catheter back out. Then there's Christmas without the annoying Pommel without catheter care and already drain again, almost without restrictions. We all hope that it is now really going uphill. The points were made, the evidence available.
:-)

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:-) Day 56

It's slowly uphill

Since Saturday, Philipp has been the starting. By day clock from about 10:00 to about 21:00 clock.
It's much better than him in recent weeks, with output.
He starts slowly but kontiunierlich food.
was on Friday still si looks certain that he gets a stomach tube on Tuesday, since it is no longer an issue today. First, while Philipp small, solid food is increasing, and these reserves as well.
The weight falls continuously down further. Therefore, he must also
until further in the night to the hospital to get extra energy into the veins. Over the weekend he has lost over 2 kg.

is coming on Friday even the day 60 The day of the second bone marrow aspiration after the transplant. This is another major milestone on the path of healing, with very detailed investigator researches.

We are once again amazed at how quickly time passes, in 40 days is approaching the day 100, there could be - if all goes well until then - get out of the venous catheter again. And from then Philip could again start slowly in the "normal life" to increase share.
The current state makes us all courage and hope. Philipp really good mood, making jokes and enjoys time at home.
The appetite is growing every day a little bit, and so gradually normalize things.

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:-((( first, there is another, secondly, as you might think .....

It was only a short visit to Rabbit.
But one night at home and take a shower at home, has enjoyed Philip.

On Tuesday morning he has several times but then have to break so violently that he is voluntarily come back to the hospital.

Now it is watered again through the veins and also supplied with nutrients, as he has in recent weeks, quite lost weight.
The mood is understandably very disturbed.

Today Thursday he was with the rescue in a remote diagnostic center with CT.
Physically, he feels much better already a bit better, but still very muddy and exhausted.

Currently there are no predictions could be thought of when to go back to the home.
would be first important to Philip begins with the food, otherwise he will get next week a feeding tube directly into his stomach.

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:-)) Day 48, Monday 20.Oct.2008

It's done!

Philip was today officially released by the station 1A. :-)
rightly so, we still can not quite grasp.
allowed after exactly 9 weeks today Philipp sleep for the first time back at home.

After on Tuesday because of fever was no exit, and Philip was really frustrated, he has been granted on Wednesday despite fever output. He is just at home but better, and he tries to drink more at home than in hospital. It has effects on positive's mind and promotes healing when you are at home - quite unconsciously.
has just arrived at home but he really just asleep, until it again in the evening to the hospital had. On Thursday he went
but zune shirt better. He was in a good and has been drinking enough. We did but not much hope to be released, because we have now been disappointed several times.
It was uphill but now every day. The blood values entire constitution, in short, felt better.
But because of the fever of Tuesday now an antibiotic was administered, the next possible Entlassungetermin the Monday discussion.

wanted Sunday night Phil absolutely not the hospital. It cost us a lot of persuasion.

On Monday morning, then the joyful message of dismissal. All on-duty nurses and physicians have bye. It was exciting to put anything and nothing to forget. It collects a lot of 2.5 within months.

Philip was so excited that he has begun to break in the hospital.
Also on the way home, he has passed several times. The we have known now for no longer than a week.
Although he is now very weak and tired, the circuit may today not as true in the evening, the temperature rises just below the temperature limit.
But we are all overjoyed.

Philip enjoys after 9 weeks, the first night at home. He can hardly sleep with excitement, although he is very tired and dizzy. On the way from the living room to the toilet it is sometimes black before my eyes. He has short rest because of over-exertion. Does not now, we live in a huge loft, it's only a 90m ² apartment, Phil brings to his physical limits.

is now training and practice it, fresh air and slow movement increases. And do not forget to drink at least 2.5 liters. Today he managed to barely half.

On Wednesday there is a check-up in SZT-ambulance. First 2 more times a week, but hopefully only 1x per week, a short visit to the hospital. We can not wait.

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:-( (Tuesday, 10/14/2008

remains unplanned

The weekend was great. Phil has enjoyed the time at home, and increased the amount of fluids daily.
was on Sunday reached the magical 2-liter limit. ;-))

the evening when you check in the hospital there was renewed hope that he, on Monday, when he drink so much then allowed to sleep on Tuesday at home.

The anticipation was great, but as you can imagine it already was obviously different.

added Am Monatag afternoon Philip suddenly after a nausea attack beyond 38 degrees fever. So earlier than planned return to the hospital. In the evening the fever was gone.
It remains the hope for release on Tuesday.

But on Tuesday it is also different.
Philipp out at an early fever and may therefore not today.
So no output, and the release also brings back the auserhalb already so palpable been closer.

Philip is desperate and may finally be healthy again and sleep at home. I really understand it, since he only sleeps for 8 weeks in hospital, although the last 10 days was the day "starting" but it costs an enormous overcome in the evening (optional) go to the hospital. And at first, is also the starting day are deleted.

We practice patience, and try as little as possible to plan in advance, because it anyway every day standoff. :-(

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Day 37, Thursday, 10/09/2008

First it is different, as you think.
But first, the events this week in order.

This past weekend we all enjoyed. We have picked up Phil at 10:00 clock in the morning, and he first had to be back at 20:00 clock in the hospital.
It was super great. We played cards, are lurking just relaxing and have enjoyed the day. Philip takes 2-3 hours to lunch for his beauty sleep. The rest of the time he is fit and funny on it. On Sunday we learned
this situation, the whole week will be above TOR. ;-)
The first day in the evening but Philip is glad to get back to the hospital. Since the day he infusions without enough liquid increases, he feels the lack of fluid in the evening.
As of Tuesday evening, he might understandably not even the hospital.


Since the whole-body irradiation, however, several internal organs were damaged, need for regeneration of the body and are flushed properly, especially of the proposed mid-passion kidneys. Therefore, Philipp drink at least 2 liters a day.
does not sound much but is very beschwehrlich if you have absolutely no appetite and the taste buds are all confused. The production of saliva works well not really. Everything tastes different somehow, some grisly, some things differently than you have it in blush, some burning in the mouth, much tastes like nothing.


On Wednesday we had a termination (dismissal) Interview with the ärtzlichen team. If Philip to Friday drinks at least 2 liters, then he can sleep at home, that is, Dates of release. :-))
Big goals, because Philip provides just a brief liter, and of which he breaks out again a part, which really should not be included.

The conversation is uniformly very positive. It has grown all the new stem cells, and are developing very well.
The "new" blood production works very well. Of his total blood content in 2100 new cells, only 50 of his old blood cells are present. This is really great and glittering internationally very successful.
Additionally, only in Vienna, also with a very specific measurement compared with just these 50 white blood cells with the same types of new white blood cells. This is now at the various Chromosomes visible. In this particular measurement are still 70% old cells that want to exterminate the doctors now have to really go on the safe side. The immune-blockers is reduced to attenuate the nine cells to be aggressive and not zusehr. This could also result in a stronger GvHD.

On Wednesday we went to for a teacher, physio and Arztgespröch at 15:00 clock home, but instead were allowed to stay until 21:00 clock.
Philip was very tired and has slept through most of the starting time at home.

Although he at home with the lift in front of the apartment door to the garage to the car drives, and in after 15 minutes steps Hospital's, it is mostly from the transport so exhausted that he has to throw up.

On Wednesday evening he is quite at home played out and a little body temperature rises just above 38th

On Thursday, he sleeps in the hospital longer, so the teacher can only later to him. Before starting he would still need to cardiac echo and ECG because because of the great listlessness may suspect something at heart and ensure that everything is ok.

shows the morning then the real reason for the fatigue, he has diarrhea. This could now be GvHD, or a virus, or something else because he spent recent days against the constipation swallow a lot of stuff had to Darmbeschleunigendes. However, the fever would rather point to a virus, but because of the immune blocker was reduced (70% to eradicate the old WBC), it could be GVHD.

So today no exit, back to bed and to the infusion docked for irrigation.
And it looks like even on Friday, no home sleeper.

The good news for the day, however, that in the next specific measure last Monday, only 40% old WBC were present. The trend fits. ;-)
Even today's cardiac examination revealed a unaffälliges result.

On Thursday evening Philip was again significantly better mood than even for lunch. He had no abdominal pain and felt better. In the evening, he stows away even with large appetite, a small piece of fish and two Petersillkartoffel. Very highly spiced with fresh herbs and almost salty, but it it tasted good.

Hopefully it is now a small step forward again and there is now nothing in between, then it's the beginning of next week for a long time to go home.
1x weekly checks are first provided in the outpatient clinic.
On day 60 another bone marrow biopsy and then probably only every 2 weeks for control.
And on day 100, there is then only the latest of bone marrow and if by then everything will fit in the course of which the venous catheter back out. That would be sometime in mid-December, so for Christmas at home without the hassle Schläuchelwerk at the breast. ;-) Those are fine goals, right? And Phil could then schedule the time to start again from a "normal" life in the society to go back to school, go back normally to the cinema or in any restaurant. But until he is really fully fit again, everything can and should be eating it but still take 6-12 months.

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:-))))))) ) Day 31: Friday, 03/10/2008

Hurraaaaa, it goes home
Phil gets out tomorrow and on Sunday.
Things change very quickly here in Spiatal, and today is drann positve side. We are pleased and thrilled.

Saturday and Sunday mornings at 20:00 and only home only to sleep clock back to the hospital.

The cold is getting better, the WBC increased again and now (18:00 clock), he gets just one Erykonzentrat that he is fit for tomorrow's output.

We, parents have now got a basic education, as we have what we observe at home. Philip already knows the basic hygiene rules and measures best.

people, it's a big step. We're a little excited. But the team at St. Anna gives us the necessary security. Philip, while still Immunsupremiert but as far as stable, and it should be a starting to enjoy. So stay cool, and make no major Sogen.
may now be his immune system get used to the family, without masks, we will no longer recognize.

goes step by step Philipp back towards "normal life". :-))))

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:-I Day 29 Wednesday, 10/01/2008

Things keep moving.

In the course of anesthesia for the biopsy was Philip again set a feeding tube because he drinks and eats too little.
But already in the awakening he has again rausgesp ...

We were still cautious on Tuesday made the prospect that Philip can maybe go home for the weekend, then The situation changed again today.

He now has a cold. Not all bad, but still. Thus, the probe would now be a hindrance. Because he was still far too little and drink every day he continues to lose weight must be irrigated through the veins.

Now the cold may not propagate, otherwise there antibiotics, and not only up the nose flows may be placed the probe and the gastro-intestinal tract can be reactivated really. Currently the case is something.

because all the WBC are now needed for the virus, the blood comes back through each image a bit. WBC and HB fall, Phil is tired and exhausted, but should move, because he is now losing weight every day and therefore muscle mass. And he has but do not fancy.

So we hope that he recovers from the Wochenede, then there may be a few hours of starting.
With the dismissal we expect from today's perspective until the end of next week.

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:-I Day 27 Monday, 29/09/2008

The WBC slow uphill climb.
Fri 1370 Sat 1320

1280 Sun Mon
1500
On Friday, Philip onkoeigenen in the gym, one floor down.
had when returning it with the physiotherapist Problems access system.
No key, no card so no entrance fee. Only one other doctor has unlocked using a key switch for the lift station 1A. The intensive training had
Philipp weekend a mega sore and did not want to get out of the room. Instead, he has until midnight Looked remote.

Today, Monday, it was not so good. The circuit has played a trick. Philip was tired, had headaches and nausea and has slept a lot. The always too high blood pressure today was suddenly much too low.

increases the number of slow-to-swallow tablets. Good sign, we interpret this as the initial preparations to go home.

The symptoms of GVHD are less again, so has remained Phil saves the skin biopsy last week.

morning there is a bone marrow biopsy to verify the activities of the many new stem cells.

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:-) Day 23, Thursday, 09/25/2008

The WBC stabilize.
1020-930-1020 - now exactly 1000
The other blood values toil a little, the HB was now so low that another Erykonzentrat was necessary. But this corresponds to the protocol itself and is no cause for concern.

The doctors and nurse team is excited as Phil goes through the therapy. There were already happening here some 100 transplants, but as Determined and confident of victory, with so much ambition and courage is still no young maschiert through these difficult weeks.
Philip feels right flattered and enjoys the same time the new-found freedoms. ;-)
Today he has his lunch first time cooked himself. There was turkey breast with potato. Although he has not eaten much but this is quite normal, after the taste buds must re new form. There

infusions and irrigation it only in the afternoon and at night. In the morning, he tries to drink hard working, but this is still a little hard. Today there were at least already 400ml. If he manages 2.5 liters, he must go home, if not the motivation.

clear that such a tired trip in the station kitchen, makes sense now to ordinary Philipp sore muscles, he is glad to be watered again, even as some infusions are the him in the morning felt were missing. The lack of morphine will be very angry and nothing fits one.

But gradually he weaned himself from the "artificial" supply and is making good progress.
:-)

In the shower, there are already facilities. Only 2 washcloths instead of 5, and Philip may again with shower Nivea shower instead Betaisadona.

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:-(

Today is a sad day
The hare, Flecki died by Marie-Therese.
We have him in the evening found in the bushes and quickly organized a very moving funeral of a Protestant pastor in our magical forest.

Philipp it goes well so far, today he was for 30 minutes on the road course and then pretty much exhausted. The WBC fall, now it was only 930th But (still) no cause for alarm. For us in healthy people vary Leukos always a little bit.

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:-))))) day twenty

I can get out

Leukos 1020 at 11:30 and gave it to the first output. Eh clear - übern transition toward the kitchen, because much larger is not the station.
There will always be fine. No more coat care, just more plastic aprons and face masks for the visitors. swallow
No more nutrient solution into the veins for a vitamin tablet to, but I did after 45 minutes again rausgespieben. The whole room added afterwards smelled of vitamins, such as when dissolving a vitamin spray.

The redness of the hands of GVHD is now fixed. If it gets worse, I get cortisone tomorrow and it would be scheduled a biopsy of the skin - but only if worse. Before that, I fear me a little.

Today I received from the SVM-Team at WU a cookbook and a DVD. Thank you. Now I can already get a Guster, but this does not work with food ever so right. If I eat too fast or too much comes right out again.

otherwise we are happy without a word
philipp

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:-) Monday, 09/22/2008) Day 19 Sunday, 9/21/2008

Hooray, it goes uphill

Leukos multiply constantly.
Today, there are already 910 WBC. :-)
Although the other blood values are already a bit confused, yesterday was a necessary and Erykonzentrat Tromos today are already very low. But the overall condition is improving daily.

The pain in neck / throat are still very much already, but it is already the first hunger. Today Phil for the first time and again demanded a steak. The food was painful, the taste of each other, but he was full of happy to eat something real. While not much, but at least some small bit of meat and a piece of potato. Various spices we only weak or no exercise for Phil now totally intense, other he did not taste it. This should return to normal but in the next few weeks.

on the palms Philip has always burning redness that is not yet diagnosed as GvHD can be, but may represent the first signs already. The GVHD is important to see that the new cells work and eat up any remaining cancer cells, but too much should be borne by the effect, because otherwise no other organs too damaged.

goes but it tends to climb. Phil is pleased with the increasing improvement, and may make the initial "baseline" expect little more.

Today was again the grandmother and had to visit again until the whole Hygiene preparations learn. It was a nice afternoon. Once again Phil can speak normally and has no more pain in the mouth, the two have talked a lot.

expected following the quiet weekend Philipp on Monday full program. The teacher comes to physiotherapy has also logged. Philip is mobisisiert slowly and should be fit for his first outputs. That makes a lot of lying tired and worn, but tomorrow will be trained body and lungs.
Tuesday is probably the corridor of the station and if it continues to develop almost the end of weeks he may already be on the roof terrace. And in two weeks, then maybe even just get out of the hospital, once around the block.

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:-) Day 15 Wednesday, 09/17/2008

Hurra, the WBC will
Since the weekend, they increase daily
110-180 - 240 - 340-444

I'm doing better every day,
and I eat even more
Today I ate almost an entire glass Hipp
course, not the glass but the filling ;-)

The drinking was previously very well
Today I have already 3 Häferln
was drunk on Sunday, however I Urschlechter after half a mug already.
The painkillers will be reduced very slowly.

Otherwise I'm tired but well on it and play with my Ipod

Maybe I should go for a walk Monday or Tuesday already in the corridor and laugh.
laugh I can always, of course. ;-)))
This week I have physical therapy for muscle and strength building.
I hope it goes on uphill

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:-I Day Eleven: We are still waiting ....

..... Although the condition is improving every day of the oral mucosa, but really is the new blood production is not yet under way.

Phil can talk since yesterday. The mouth is still swollen, but he bravely tried already to start drinking. Throughout the day, he creates already a tea mug and today he has already tried a few spoonfuls of a hip mash.

The measurable blood levels are not higher. Today, the thrombosis have crashed so far, that once a bag was necessary. Despite the really very low platelets, the bleeding in the mouth and throat, but have almost ceased. A good indication that the work Leukos.

The HB is recovered for a time but, all things very slowly, maybe Phil can this low again catch himself.

According to the forecasts and experiences, 2-3 days after the appreciable effects in the mouth, the WBC also measurable present. We have been waiting for day 8, - they could then come on, we would not mind.

repeatedly Philipp allergic reaction. It is not known what, when and why.
on the skin are deep red, hot spots, which and itch severely.
enough sometimes some cream with a mix of a special lotion and benzocaine. For this purpose a Coolpad or even several. Sometimes the reaction is severe, then there a drug into the veins, which makes then very tired. Every touch of the skin is then very unpleasant, including the pajamas and the ceiling.

Because the stomach has apparently forgotten in the last 8 days to run properly, it is often given after Philipp 2 tablespoons Breinahrung again. Although he gets a drug and then however, the situation calmed down quickly, but mostly it is then also very exhausted.

with one or the other reaction and a little nap because of subsequent Exhaustion, the days are relatively fast.

Philipp urtapfer, asked the doctors to reduce the already analgesic dose and really tried everything to get fit again as quickly as possible.

He ordered the physiotherapist and trained on the exercise bike, he will (voluntarily) all Schülbücher here and asked for his teachers to zuverpassen not in school connection. Also for the teachers a pleasing picture, because many children while they are locked up in the clean room space not much want to know from the school. Only when it is really much better off and get the kids out of the room to the Staion they start again with the lessons. Philipp But as ambitious and begins now.

He tries to drink as much as possible, even if he often breaks out again.

He is on the station of the star and is highly praised by the entire team, because such an ambition is very rare. :-)

The next hurdle is less than 1000 WBC, he may face masks out of the room and move out on the station again. That could be about 1 week so far, depending on how long the WBC now still leave time.

The next stage will be at least 2 liters per day drinking, then he may for a short time back home.

From today's perspective would be the earliest in 2-3 Realistic weeks, many of the children were approximately 1 month before transplant, the Philip, in recent days gone home.

First, there is only day a few hours out, then the whole day and only the night in hospital and if it all goes according to plan, then perhaps he should sleep in about 3 weeks and again at home. So dear readers

fixed fingers crossed.

Finally, a summary of the statistics:
were 2 days ago it's exactly 6 months since Phil in therapy
In 2 days we introduced exactly 4 weeks on the 1A station
In 3 days we have 14 days after the transplant.

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:-I Day Eight: We are waiting .....

The situation is almost unchanged. The discarded Leukos range from 0.19 to 0.07 - 0.13 to 0.10. to suck

To grayish remains from the mouth, Philip has got now a suction hose, you know something like the dentist.
The jaws are pretty swollen, every hour makes Phil's oral hygiene.
Betaisadona then rinse with a Bepanthen solution and then with a special Spültee. Finally auspinseln still with a solution to the mouth.

swallowing is impossible. For several days, Phil is supplied exclusively through the veins of nutrients and minerals.

The HB value (hemoglobin) has now fallen so far that Phil has now received two ERykonzentrate. He was yesterday very tired and sleepy.

is now in the evening after the two did the same blood Ackerln much better. The
Schmerzmittelbypässe are now so well managed that Philip is largely pain free and has almost no allergic reactions at all.

let the bleeding in the mouth for a bit.
This is also equal to the overall feeling noticeably better.

weekend I set up the router staionären Internet access using a WLAN. Now, Phil from the bed with the i-pod read emails and download games.
Since today he has again (something) like to do such as i-pod and remote play shows. Although only a short time, but still. The awakenings are a little longer and manchmel is also a little speech. No complete sentences but at least one or the other word.
So aside from the (still) not measurable existing WBC, the overall condition is improving a bit. ;-)


As I write here in the hospital the diary - it's now about 18:00 clock, say the nurses that are now better in the course of the day the gums already, that's a sign that the WBC has already . work The first fresh produce Leukos go immediately available for the rehabilitation of the oral mucosa. Since they are not measurable but it works already. :-))

on the measurable Leukos have to wait about 10 days, so everything is still on schedule. We now hope to rise a bit properly before the weekend, because on the Monday there is a mega blood counts which also differentiated exactly whether they are old, male or female fresh WBC.

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:-I Day Five: Sunday 7 Sept.08

Things are changing so fast that we do not comply with the letter

I try to summarize the last 4 days or less chronologically.

Marie-Therese was discharged from the hospital on Wednesday afternoon.
She had terrible pain in the pelvic area, could hardly sit and go.
Even pain pills do not work really.
On Thursday, she had all day and night temperature rose to 38.5 degree fever. This was to come back in the hospital as unusual and worrying, so she had to control. To rule out any infections, the doctors would have liked to have had a drop of blood from her, but she would not even let a finger down. Now she takes
a preventive antibiotics 3 times a day. The pain may be after a very slow, they can already "normal" to go, but climbing stairs is still a painful, like sitting or lying.

One of the two injection sites had yesterday (Saturday) not looked quite as good, but slowly grow the two small holes to.

Meanwhile, I have heard of the assistants in the operating room nurses that visible while in the skin only a puncture, but by moving the skin is repeatedly stabbed in various parts of the pelvic bone to the necessary amount of bone marrow taken from. Therefore, the wound pain is understandable.

When Philip has steadily downhill since Wednesday. This corresponds in principle to the protocol designed to but still spectacular.

The WBC have halved every day since last Saturday, 13,000 on Saturday at 7500 on Sunday, up to 250 on Friday. Yesterday (Saturday) it was 0.1 - that is practically zero. Today is Sunday - the first ray of hope them to grow and increase to 0.19. Every Monday we checked in a special process whether it is his old or his new cells. Because our children have different gender one can see the light of the XY chromosomes.

All other blood values but are confused.

Philip began responding Wednesday to a lot of necessary drugs. First, the immune blocker that is necessary in order to prevent rejection. We then tried the drug but not the veins of the stomach to give, as is usually the allergic reactions are not as strong. Therefore, the probe, because swallowing from Friday / Saturday will probably not be possible. When Philip
it was different, the reaction to the drug in the stomach was much more violent.
red itchy patches all over, heat attacks and while shivering, the circulation mess, headache, and nausea.
an antidote worked relatively quickly, but it was gruesome hours.

Now he gets another immune-blockers which he tolerates well. Just because even the name "Prograf" So for the count. ;-))


But he has an allergic reaction to an antibiotic on Thursday genauo now necessary. Now try it with another agent and an antidote that is administered before, etc. .. The morphine dose was

daily since Wednesday increases, but is not (yet) in the acceptable range, say the sisters. Merhmals day he can give himself a bolus by pushing a button, which is an additional booster thrust. The machine keeps track of how many such bolus but it is limited, and the daily dose and the interval between the additional shares. Nevertheless, responding

Philip several times daily with a violent allergic reaction.
Hot head, red ears, cold fingers and toes, chills, nausea, high temperature, red itchy patches to awful in all parts of the body. We try different creams to relieve the itching. Philip is very brave, but sometimes he is losing patience because the pain too soon to be bad.
Until he notices the nurse or doctor to examine and a cure is complete until the drug works and relieves the reactions in such a process takes around 2-3 hours.
The last few days it was usually in the evening, always go home if I wanted just to clock 20:00.

Phil is very proud of his feeding tube, and sneezing is not many a ghastly thing-tasting drink to sound special. He is also very careful to not break, because he knows that this mithochkommt the probe.

covered with the blood values, the Tromozyten, these are the platelets. Thus it tends to bleed easily. On the skin caused red dots. The mucous membranes
have passed almost completely through Saturday. Flows from the mouth of bloody yellow phlegm.

lie by the few and the food has stopped the bowel to work.
same time pushes the stomach. We try it first with Zäpchen then it is but an inlet. The result is quite bloody. From the mouth of bloody saliva flows. The cheeks are swollen all feeling in the mouth is gone.

In the night from Saturday to Sunday, it happens.
has accumulated blood in the stomach. Blood can not digest the body itself, which collects in the stomach until it passes. At about midnight, then a portion of Ordet and come up with it - clear anyway - the feeding tube.
Thereafter there was an emergency measure a Trombokonzentrat in the veins - they are darurch somewhat increased but still far below normal, is probably still as a yellow blood Ackerman. At dawn, Philipp
has again thrown up some portions of blood.

But you have but the cause of the allergic reaction found. It is probably the morphine. Now he gets a cure but the analgesic effect of morphine is not affected, however, relieve the side effects. This means it is
but only for swallowing, is now stupid without probe with open mouth and throat mucous membranes. Bravely endures but Philipp these torments.

And we hope - get the WBC ;-)) they ensure safety on, and with increasing WBC, it is the body relatively quickly better. There

New gavage it first, because they are not through the open throat mucous membranes can be introduced. So it is now standardized to swallow, which is currently not possible. Even those parents
report on the station, situated a few weeks before us in the schedule that the kids about 2 weeks nothing, absolutely nothing to eat and drink.

This is not serious because the body is supplied with nutrients via the veins, but gefähöich for the intestine. This has nothing to do, and thrives on Bacteria and fungi that want to be busy, and can occur because of the location while silly ideas. This could be potentially hazardous under certain circumstances.

should also Philipp train his lungs. Through the many and are the least physical activity are not supplying the lungs to the recent peaks. This creates the risk of pneumonia. Therefore, the Spiro coach, but in the current state of Philip can not be used. He is much too weak to stand up straight and manages to pee. Now and then he sits up in bed, but that was already with physical training.

difficult situation when you pass neighborhood should do something but physically simply can not. Now we have to wait for the "fresh" WBC, things are more easier again, and hope that in the meantime, nothing bad with the bacteria. Fungi and viruses happens in the body.

You can still talk a long time from a successful transplant. Too many potentially hazardous phases remain to be overcome.

Next comes what is known as GvHD. This is a reaction of the new cells to the new home. Finally, the cells recognize the body of Philip as their own and not attacking him. As a health police they eat everything foreign. This can dissolve the skin, gets confused about the liver and some other organs crazy play. But to do more if the extent is.

Currently we are busy every day to reschedule who is, at what times for which child. Phil can be visited daily from 11:00 clock to go to bed by one of us. Marie-Therese tried it (Monday) morning with the first day of school and needs an afternoon care. In between, many things remain on the track. From shopping budget on food, maybe try to work, an organizational challenge. The communication and coordination is possible largely only through's cell phone, which is virtually impossible to telephone the hospital, due to hygiene measures. (See post from the past Week) In the evening we fall exhausted into bed to sleep but not because the head can not turn off.

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Day Two: Thursday 4 Sept. 2008

Today I received two times a stomach tube.

Because I'm responding to an important drug for the prevention of GvHD Abstossungseffektes allergic and I need the drug therefore can not be administered through the veins but only by swallowing.

Swallowing will work but in the next few days getting worse because dissolve the mucous membranes. Therefore I have agreed to morning call for a doctor that I, a probe is placed. The great advantage is that I no longer drink the juice the Moro, but I can explore yourself.

the afternoon I was just so angry, and when passing the probe came out with.

After 10 minutes recovery period have set myself the sisters very stress-free, a new probe. marvel

The nurses and doctors how great I did it. For 6 years they have seen no one, which the probe can be positioned so unkomliziert.

The nurses bicker Jende day in the morning about who should care for me.

do all beautiful to me ;-))

feeling.