FIGHT FOR MIKE

FIGHT FOR MIKE
FIGHT FOR MIKE

Thursday, August 29, 2013

DAY 4 OF TREATMENT

Thursday, August 29th



Hello everyone!  Thanks for tuning in.  Today Mike had his usual around of treatment.  He had another massage which he states has left him pretty sore.   He had an added treatment which consisted of laying on a table with some sort of vibration.  I am not sure what that does.  Will have to find that out.   Dr. Weber has today and tomorrow off.  He said he has to give a speech  and is visiting his daughter.  However, his wife who has been on vacation was to be here today and tomorrow.  We did not see her at all today.  Dr, Weber said that one of them always has to be here.   I knew that his wife was also some sort of doctor, but I was not sure what she practiced.   We were told by another patient that she is an anesthesiologist.

There is a girl here from Phoenix (Lindy) for her 2nd visit.   She is here for breast cancer.  Leah is from Wales.  She has a tumor in her groin.  Leah is very outspoken in her beliefs of different supplements to take or not take.  Because she has been dealing with her cancer for 3 years and it has not metastasized, I think she may have incite to what works.

After lunch today, we had some time before Mike's hyperthemia treatment (that is where he is now) at 4:40 PM.  We got up from the table and hightailed it over to the train station that goes up the hill.   We left at 12:30 to walk over there by 1:00.  We had on jeans, long sleeve shirts, and took fleece jackets with us because we were told it would be cold at the top.   We were walking pretty fast trying to make it in time. Mike said you might as well slow down because we are never going to make it.   We did decrease our pace a little bit, and as we rounded the corner, we could see the train still sitting there.  We saw that there were other people still heading into the station so we  picked up the pace, bought our tickets, and were able to make the 1:00 departure.  The tickets cost 59 euros which would be $78.12.   The view up the mountain was beyond breathtaking.  Along the way, you could see trails up the mountain with people climbing up to the top.   We also saw a couple of shack looking buildings which appeared to be inhabited.  I guess if you don't want any neighbors that is the way to go.  We got to the top and had to go through a tunnel to get outside.   The highest point is 1,838 meters which is 6030 .184 feet.  It took about 20 minutes to get to the top.

We came out to a platform where there is a restaurant and various different stairways to take you to other sites.  As we were walking around this area, here comes our dinner mate Chris.   Chris is from France. He was still waiting for dessert and drinking a glass of wine when we left the clinic for our walk to the station.   We could not understand how he made the train when we left before him and just made the train.  We come to find out, he found a short cut to the train station and actually made it there a minute before we got there. We never saw him on the ride up the mountain.

We walked up to a lookout and the view was more than amazing.  At this point, we were at the lowest of all the possible viewing points.  We then walked up to another viewing area to the Wendelstein church.  This church was built in 1889.  It is considered to be Germany's highest consecrated church.   Services are held here in the summer every Sunday, and a lot of couples say "I do" here.  From there, we started our ascent up the mountain at 1724 meters toward the top.  There were rambling trails that had secure railings.   The trails were very rocky interspersed with sections of stairs.   We went through a tunnel and had many different viewing points along the way.   It was unbelievable as to how all this was created on the side of the Alp mountains.   The brochure states that The Wendelstein was formed 230 million years ago from a reef of mussels and other deposits and due to the natural movement of the earth's plates, it moved from the Mediterranian region to Bavaria.   Along the way we saw crow like birds, which of course Mike had to take a picture of. I don't understand what the fascination was there with them.  They were like seagulls at the shore with people feeding them,   We were almost to the top when we saw Chris coming down from the top. Unfortunately clouds had rolled in a a little while we were there, and Chris said you really could not see a lot more than we could already see.  At this point, Mike was ready to call it quits for the day.   I cannot tell you how many stairs we climbed to get that far.  I wanted to continue on, but then was afraid it would take too long to climb back down to get the 2:55 train so we could be back in time for Mike's 4:40 hyperthemia treatments.    We went into the restaurant to get something to drink. Mike wanted coffee but he could only find a machine with cappuccino and espresso and he did not want that.   I got something called a cola mixture.  I was hoping it was something like Coke.  It wasn't the same, but it was OK.   I had some sort of strawberry dessert here so I would have something in my stomach to carry me over since dinner is smoked trout.  Mike wants me to have them bring it out for me, and he can then have a 2nd helping of the trout.

We rode back down the mountain with Chris.  Again, we just got on the train with 1-2 minutes to spare. We forgot about the train going back down left at 5 minutes to the hour.  Chris showed us the short cut he took to get to the station.   Now we could see how he beat us there.   That was just too funny.

We just got back to the room from dinner.  Mike ate my trout.  He really liked it.  I had fruit, toast, and yogurt for my meal.  We then stayed and spent time talking with Leah, Chris, and Christy who is here from Charleston, SC.  Christy is here for her first time.  She is dealing with a 2nd  round of ovarian cancer.   Mike also heard she has some sort of cancer in her upper chest.   It is now 8:25 PM.

I had said I was going to speak about the food we have had thus far.   I will discuss that at another time. Hope all is well back in North America.
 

 

Wednesday, August 28, 2013

DAY 3 OF TREATMENT

Wednesday, August 28th  

It is now 05:45 PM or as they say here  17:45.


We were told it rained like crazy last night.  However, the rooms are very sound proof so we did not hear a thing.  It is dreary out again - it has rained every day since we have arrived, at least once a day.  Oh well, our main purpose here at Marinus am Stein is for Mike's treatment, and at least we can have that done whether it is rainy or sunny!

Today Mike had his usual  treatments that he has had the past couple of days.  But today, he got an added bonus of a massage.  He came back from that stating he was loose as creamed corn. I never heard that expression before.   We met with Dr. Weber to go over Mike's regular blood testing.  Everything was basically good.  He did have two things that were off. There were 3 parts to the blood testing that pertained to the liver.  Two of them were within the proper range.  One was  a little high so Dr. Weber is going to add a supplement to Mike's infusion to help with that. His magnesium was  low, which he said was from the chemotherapy that Mike had, so he gave him a powdered supplement to take every day.  His white blood cells are up to 4900. This is up from the 3400 from his last testing done August 12th, the date of his last chemo treatment.

We went for a walk after lunch on a gravel path that runs right next to the clinic and goes up into the hills.  Along the way, we came across cave-like statues in the side of the hill with religious figures in them.   The walk up the hill tested our strength as there were many steps up the side of the hill.   We could both feel the muscles in our upper legs being put to work and our lungs gasping for air.  At least it was a good work out.   When we got to the top, there was a church and beyond that more cave-like shrines I think depicting different parts of the bible.  I know there were at least 13 of them.  We walked a little further from there and got to a point where you could look out to the many houses below and the rolling farmland.  It was really pretty.   The houses all have clay tiles on the roofs and balconies with huge flowing flowers hanging down from them.   Some of the homes are just covered on many sides with these hanging flowers.  We have been graced by the smells of being amongst farmland.  There is no getting away from it.  Last night we were even subjected to it inside the clinic.   It reminded me of being back home and going through Amish country.

Mike should be back any minute from his hypethermia treatment, and then we will be heading down to dinner.   Will list the food that we have had to eat since arriving here.   Mike is being some what adventurous in trying some new things.


 

Tuesday, August 27, 2013

DAY 2 OF TREATMENT

Tuesday, August 27th

Hello everyone back in the states and in Canada!  It is now 10:00 PM here in Germany - 4:00  AM back home.  Mike just came back from having a bio mat therapy done. This is directed at the the whole body.  Earlier today he had Mistletoe and Thymus injections.  He also had localized hyperthemia to his liver.  He had an ultrasound done earlier today,  and Dr. Weber could not find any cancer.  He was very excited about this.  I did ask about seeing the colon, and he said that you really cannot see the colon with the ultrasound.    This afternoon Mike will have the whole body hyperthermia.

Everyone that is here is sharing their stories and the information that they have acquired in things to do to beat cancer.  You realize that you are not alone in this fight.  Everyone also has the same feeling that it is a shame that you cannot have this type of treatment where you live.

Dr. Weber said next week there is a small Bavarian Festival near here that he said he would take us to.   Our friend, Jay in California, who was here last went to a festival that Dr. and Frau Weber treated him too as well.

I am finding out that you are not able to make comments on the blog without signing up.  If you would like to respond to the blog or just want to leave a message for us, you can do so at my email address:   munuam@yahoo.com or on Facebook.

Monday, August 26, 2013

DAY 1 OF TREATMENT

Monday, August 26th


This morning we went downstairs prior to breakfast and met with Verena.  I have spoken to her through email when I made the arrangements for our stay.  Mike had some papers to fill out so that Verena could put together his chart with all the records I previously sent here.   At that time, we greeted Dr, Weber as he arrived at the clinic.  He told us to have breakfast, go for bloodwork, and then meet with him to go over Mike's treatment plan while here.  He told us that Mike would have the hyperthermia, hot packs to the liver, oxygen therapy, Mistletoe injections,  ozone therapy, bio mat therapy, magnetic field therapy,  Vitamin B injection He will have a massage three times a week.     He was given some supplements to take here besides the ones he has been taking at home.

We have dinner mates who are here from France, Chris and Marion.   Chris has lung cancer which he was diagnosed just 5 weeks ago.  He and his wife arrived here last Thursday, but she leaves tomorrow to go back home.   We met Lloyd who is here from Florida, but unfortunately he left around lunch time.  He had a tumor in his mid section the size of a grapefruit, but his recent MRI showed it the size of a  golf ball.             There is a young woman here with her husband from England who has breast cancer.  We have only said Hello to them in passing.    It seems we arrived when new patients were coming in and other had finished their treatment and were leaving,

After Mike's early afternoon treatment, we went downstairs where they were having tea, coffee, and some sort of bread.  They have this afternoon tea every day.  We then decided to go for a walk.  The scenery is beautiful.   The mountains are not like back at home where there are foothills and then they gradually go up.  These mountains take straight off from the ground. The weather here is chilly.  We did put shorts on today, but wore a jacket which you then have to take off when you become warm from walking.  Of course, Mike had to check out the stream that runs by the clinic to see if there were any fish in there.  He said he should have brought his fishing pole.  Dr. Weber told us to have someone show us how to get to the train that goes up the side of the mountain, but we are going to wait until we have clear, sunny skies so we can really take in the view.

When we got back from our walk and came up to our room, we saw Dr. Weber.  He stopped us and had one of his employees go get Mike's bloodwork.    Mike's CEA level is now 14.31!!!!!!!!!!!!!!!!!   This is amazing since Dr,Wyshock back home told us the toughest part would be to get Mike's level down from the 56.1 level than it had been for it to come down from 23,000 to 56.1.  He said Mike will have an ultrasound here at the clinic tomorrow morning.

Mike got back from his hour long hyperthermia treatment, and we went down for dinner which was a spicy cheese salad with ciabatta bread and fruit for dessert.

So today, the treatment consisted of bio mat therapy, magnetic field therapy, ozone drip, oxygen therapy, hyperthermia.  Tomorrow and Friday, he will have Mistletoe injections added to the above.  His massage this week will be Wednesday.



OUR ARRIVAL IN GERMANY

Sunday, August 25th

We landed in Germany around 7:40 am to find it raining.  The flight was very good...Mike did fine.  He watched two movies which  I think kept his mind occupied. Neither of us were  able to sleep on the plane.   We were basically up about 21 hours. We had to go though customs which we did with no problem once we found the right area.  The next step was finding the area to claim our luggage and the way out of the airport,   We walked out to find our driver holding a sign with my name on it.   He was very nice, but unfortunately, he did not speak any English.   We did a lot of shaking our heads yes and smiling.   We had a slight detour on the way to the clinic, which the driver was not expecting.  We had to go some distance out of our way so that we could get turned around and back on the highway.   Due to the dreary weather and being tired, we both fell asleep on the drive to the clinic.  We made it to Marinus am Stein around 9:10 upon which we met Dr Weber as soon as we walked in the door.  Dr. Weber took care of our taxi fare  and spoke with us briefly.  He is very friendly and  most welcoming.  He told us that we needed to rest and that we would speak with him in the morning for Mike to have his blood drawn and to meet to go over his treatment plan. Danielle (RN) showed us around and found Richard who is here from Delaware.  We first spoke to Richard and his partner, Glen, when they were here in Germany in May for his first treatment.   We have been in contact with him by phone and email since he returned home.  He has given Mike good information about the things to do to help beat this cancer.   He has the same cancers that Mike has,   We then came up to our room and took a 1 hour nap.  Danielle had to wake us to tell us it was time for lunch, which is the big  meal of the day here.  As we were still very tired, we came back to our room and took a 3 hour nap.  Then it was time for dinner.  We were able to enjoy both lunch and dinner and have more conversation with Richard before his departure, Monday, 08/26.    After dinner we went for a walk.  Mike was in bed before 9:00 which is nothing new.









Saturday, August 24, 2013

AND THE JOURNEY BEGINS....

Saturday, August 24th

Mike and I are sitting in Newark Airport waiting for our 5:30 flight.  We made it here thanks to Gary and Clare with plenty of time to spare.   We got through security without any problems.   The inspector asked me if I flew frequently because I had everything out in the bins as it was supposed to be .  Will post again, next time, will be in Germany.
 


This is Mike, me, Clare & Gary McWilliams (Mike's bosses and great friends) who drove us to Newark Airport for our flight to Germany.   Without their love, support, generosity, and hard work, this trip for Mike would not have been possible.   Gary is the person who made us aware of the possibility of alternative treatment.  

Thursday, August 22, 2013

WHAT'S BEEN GOING ON SINCE 07/15/2013

Thursday, August 22nd

Immediately after having Mike's testing done, I sent the CT discs and reports as well as the CEA report to Dr. Weber in Germany for him to review.   We then heard back from him with the information we needed in order to book a 3 week stay in his clinic - Marinus am Stein Klinik.   We booked our stay for 08/25/13 through 09/14/13.     We fly out of Newark, NJ this coming Saturday, 08/24 at 5:30 PM and arrive in Munich, Germany on Sunday 08/25/13 at 7:40 AM.

This will be Mike's first flight.  He seems to be OK with this, although he never wanted to fly before, but you do what you have to do.  He will have treatment every day with a lighter schedule on the weekends.  Hopefully we will be able to get out and enjoy some of the scenery while we are there.     At the end of the 3 week stay, Mike will have testing done to see if he has had any improvement with the treatment methods that Dr. Weber uses.

We are both a little anxious about the flight and the unknown of going to another country so far from home, but we are excited as well  as hopeful for the possibility of complete healing.  This is what we have been hoping for and waiting for since we found out about this clinic back at the end of April/beginning of May.  It is now just about in our reach and becoming a reality.    Saturday is just around the corner.  Germany here we come.......... to Fight for Mike!

I know I have said this before in my postings on Facebook, but I want everyone to know how truly blessed we are to have so many great, supportive, and caring friends and family.  We want to thank everyone from the bottoms of our hearts for your donations in helping with the expenses involved with this trip and everything else you given and done for us - prayers, cards, well wishes, dinners, and for those of you who were there as a shoulder  to cry on.  G & C -we cannot thank you enough for presenting this opportunity to us and all your help in making this trip possible.

If you would like to leave any comment, you can do so by clicking on the red No Comment wording at the bottom of each posting.    Until my next post from Germany..............