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4200 Township Ave.
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Site last updated 05/08/2008

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Pete    Cathy

cathy haedt update...

THE HAEDT FAMILY IS REQUESTING THAT
NO PHONE CALLS BE MADE TO THEIR CELL PHONES
.

THEIR HOME PHONE NUMBER IS 805.583.8242

HER EMAIL ADDRESS IS fncncc3@yahoo.com


Thursday, May 8, 2008

Hi Everyone,

Thank you for making Ceci's birthday great!!!  she said she laughed every time her text went off!!  She had Stephen thinking the joke was on him and that it really wasn't her birthday. She did confess the truth and they both got a kick out of the situation.

Well, today the IV went in and was good without too much wiggling.  Yes Lord!!

Hopefully, I won't have a bad reaction to the one treatment today.  I will be able to use this IV tomorrow for treatment. Then will start early so we can leave around 2:00.  We are praying for a shortened time to get across the border.

A praise report here.  One of the patients brought her friend from Scotland to help her and the friend gave her life to the Lord!! We met the grandson of the founder of the hospital and he said people receive more than just treatment here,  they have staff and prayer warriors praying for all who enter this hospital to be touched by the Lord in all ways.  He is a very compassionate man.

They say that Mother's Day is a very big and important holiday here in Mexico.  The nurse said he is 18 hours away from his mom and can't be with her so he will be home Sat. and cry.  Another male nurse said the same thing about crying, so it really must be a big deal.

Happy Mother's Day to all the mothers reading this.  We will be going to my mom's in the valley and Ceci will be able to join us. I am looking forward to Sunday.

Bye for now. Be blessed,

Baldy locks
(my new name from Kelly M.)

Tuesday, May 6, 2008

Hi Everyone,

No treatment on Monday.  I am sure enjoying the food.  I have been eating lots and lots.

I have been feeling pretty good. Taking a nausea pill every day but only one compared to 3 a day.  Just got back from having my blood about 1/2 cup and put ozone in it and then put it back in. 

Also, can you help me for Ceci's 18th birthday, which is on Wednesday, May 7? Since we are in Mexico and won't be home for Ceci's birthday, I thought it would be fun to get a bunch of texts wishing her happy birthday.  Maybe even send a funny picture of yourself or dog or something. 

 Her phone is 805-551-3649. If you cant text you can email her at 8055513649@vtext.com and it will text her

She will be so surprised and feel so loved.

Thanks and I love you.

Cathy

Sunday, May 5, 2008

Hi There,

We made it to Oasis of Hope in Mexico in 3 hours.  Pretty good timing.  No problems finding our way.  We stopped before the border to get the insurance. $62 for full coverage.  I thought it would be about $20.  Inflation. 

Our room is on the same side of the building with the same view.  No progress on that building we can see.  I thought in 8 weeks being gone we would see some change but doesn't look like it.

Our director Vic was happy to see us and very happy with the good report.  I saw one of the Dr.s and she was so happy for us too.  I am smelling the good food and can't wait for dinner.  Today I was feeling nauseas so I felt it better to take a pill for it since I was traveling.  I am glad I did.  It made me feel so much better. 

Our direct line to our room is 1-619-690-8441.

Please be praying for big veins for the IV's.

I read this scripture this morning and printed it to hang on the wall in my room. 

I will extol the Lord at all times
His praise will always be on my lips.
My soul will boast in the Lord
Let the afflicted hear and rejoice
Glorify the Lord with me
Let us exalt his name together

Psalm 34:1-3

Thank you for your continued prayers,

Love,

Cathy

Tuesday, April 29, 2008

Following Friday's news about Cathy's PET Scan, she met with the Oncologist today, who declared her in COMPLETE REMISSION!

She is still doing another round of chemotherapy this week. She and Fred leave this Sunday, May 4, for another trip to Oasis of Hope Hospital in Tijuana. They will be there until Friday, May 9.

We will post contact information at Oasis when we have it!

Friday, April 25, 2008

4/23 PET: Cathy Haedt

IMPRESSION:
This PET scan is negative for any hypermetabolic foci. It shows
complete resolution of the multiple abnormalities demonstrated on the
prior study of 2/13/08, suggests complete treatment response (But we know the truth God Heals!!)

Praise the Lord!!!!!  I am so excited.  I will talk to the oncologist on Tues to see if I will have to continue the rest of the chemo. Wow I am so excited.

Thank you Jesus!!!!!  You are my healer!!!  I'm trading my sickness Yes Lord Yes Lord Yes Yes Lord Yes!!!!!!

Thursday, April 3, 2008

Hi Everyone,

Its been so long since I have been on the computer.  I would start feeling nausea's and so I would stop.  I believe I have worked through that now and enjoying reading email and surfing the net and playing freecell!

We got home on Fri the 15th of March and the Master Commission students were leading a service at Angelus Temple on Sat the 16th.   I didn't know how I was going to feel so I never made plans to go.  But Saturday I woke up after sleeping in my own bed which felt like a cloud, I felt so good I decided to go that night.  Rhonda and Ceci and Carissa Wolf and I headed to the service.  Ceci hadn't been there all week because she was sick and I made her stay home.  The students ran to Ceci when they saw her they were so glad she came.  They told me how much they just love her and how they have been praying for me.  Then they showed me these bracelets that they made that had "for Ceci" on them.  This was a reminder for them to pray "for Ceci".  It makes me feel so good that she has such a support for her from her peers during this time.  They recognize how hard this situation is for someone there own age.  Talking to the kids that night they shared with me how they lost a parent. They really can relate to Ceci in her situation. One of the songs they sang that night had the words "I'm alive, I'm alive"  I turned to Rhonda and said that's my new theme song!!  I was singing my heart out and jumping and praising God for everything he has brought me through.  It was such a great night. 

I went to church the next day and it was so good to see everyone.  I thank you all for your prayers.  It means a lot to me knowing that you are interceding and standing in the gap for me.

It was great to worship the Lord in singing that day.  I would get short of breath just standing with my arms lifted and moving around and singing my heart out to God with such thankfulness, but I didn't care.  I was tired afterward but a good tired.

On Monday Fred drove me to Kaiser in Woodland hills.  They told me I have to have a blood test before chemo.  I asked if I could use the same site for IV and where they take the blood.  No she said can't do that.  I was so sad tears came down my face I couldn't help just thinking of them poking me twice after my arms were so sore from Mexico hospital.

The gal called my name to take blood and I recognized her from when I was in the hospital at Kaiser and she didn't hurt me then.  So I told her my story and why I have tears because I couldn't take anymore pain.  She said don't cry and hugged me.  She used the tiniest needle and it didn't hurt!!  I was so happy I cried for joy and she hugged me again!

Fred and I are sitting in the waiting room for me to be called to have chemo and the nurse came out and says we don't have time to give you the chemo today because your blood results won't be in for another hour.  Fred stood up and through his magazine down and walked out and I was jumping for joy!!  I just wasn't ready emotionally to get poked and God knew it and helped me out.  The next day I was emotionally ready and I told her the nurse who gave me the IV that I have special veins and she took her time with me and she got it on the first try!! I said Thank you Jesus and she said that's right.  God is so good to take care of the small things that make me so happy. 

I came home and felt great.  I ate dinner and took my 15 supplements with it.  Then about 7:30 it hit me with not feeling very well.  I took a nausea pill and I didn't get sick but just didn't feel good.  The next day the IV worked again Praise the Lord. I got in the car after the treatment which was only an hour long this day and I felt like I had to lay back.  Came home and just laid on the sofa.  I was able to eat dinner and take my supplements and back to the sofa.  It was so nice that our dinner was brought to us from different families at church and made it easier for me to just eat without having to think about what to fix and have the energy to fix it.  Thank thank you for meeting that need!!  Like I say sometimes its just the little things that let you know God is with you.

The next day I didn't feel so good before and after chemo taking lots of anti nausea pills.  Came home and rested.  Still able to eat.  Friday the same thing. Saturday I was feeling better and noticing not as many nausea pills and Sunday was Easter and I felt I had been resurrected from the dead I felt so good!!  Went to church stood and praised the Lord in singing and had a great time.  Went to my moms and still felt good all day.  Cecil was able to come home and we enjoyed being with her. 

Fred took me to the Dr. on Monday and I felt good again.  She walked in and was so surprised!!  She was thinking before she saw me that she wanted to take a chest X ray but she listened to my lungs and just smiled and laughed and didn't know what to say except you sound so good I can't believe it and she hugged me!!  She asked how my breathing was and I told her only when I dance and sing during worship at church I do feel short of breath and she just smiled and said that's great!! 

The plan is 6 rounds of chemo every 21 days.  The next round is April 8th.  I will go the first day to Kaiser Woodland Hills and get an IV for 3 hours. The next 2 days I can just take a pill and not have to go to Kaiser and no IV!!! Then she is scheduling me to have a PET and CT scan the week of April 21st. Then I have an appointment with the Dr to go over the scans April 29th and Chemo that week. I have to go back to the hospital in Mexico soon for 6 days to get treatment.  I am not sure when I will go yet.

I am enjoying this week with no Dr. appointments and no chemo and no IV's and feeling great!!  Rhonda and I went to Northridge Foursquare church on Wednesday and surprised Ceci.  Masters Commission lead their youth service.  The worship was awesome and again I just sang my heart out to the Lord and I was jumping and raising my arms.  One of the other students told me later that when she saw me from the back dancing around she had to get up and move.  She said if you can do it so can I!  When we got there all the students were in a group and when they saw me they started clapping.  I turned around thinking who is behind me that I missed that they are clapping for. There was no one but me and it just made me feel so humbled that they would do that for me.  One of the other students told me about a vision she had and she wrote it down for me but she never mailed it.  So she asked if she could share it.  It was so right on and a confirmation for what I was feeling.  I just feel the hand of God on my life in everything I do.  Good and bad, up and down he is there.  I know he is close to me and never leaves me and I can do all things but when you walk those words out, its amazing.  My calendar today says 'My soul clings to you; your right hand upholds me. Psalm 63:8  and below there is a quote that says "There is a place where my spirit sings  In the hollow of God's palm.

Thank you again brothers and Sisters in Christ for taking time to pray for our family and care by sending cards, emails, meals, books, hats, blankets, wigs and flowers.  We really feel loved and card for by all of you and the Lord.

Love you,

Cathy

 

Saturday, March 22, 2008

It's been so long since I have been on the computer.  My brain had been trained to  sit at the computer I receive treatment for hours.  So I couldn't get my brain to be retrained that's its OK to be on the computer and not get treatment!  So brain, there is no treatment today, no IVs, no chemo. 

We left Oasis of Hope Hospital on Fri the 14th.  It was hard saying good bye to our new friends and prayer partners.  Cancer patients have a special bond.  We did get email address and phone numbers to keep in touch.

I left CD's and the scripture verses I had on my wall with Juanita, who was having a hard time.  She had such fear.  I prayed with her before leaving and she prayed for me.  She was waiting for results from an ultra sound and was scared for the report.  I called her Sat from  Simi and the results were just GAS and she needed to walk more!! Praise the Lord.  We were so happy for that news. 

We left Oasis of Hope around 1:00 and started for the border of Mexico.  The driver was so good and knew all the back roads.  It was so congested. 

There was another couple in the van going home also.  They were from Iowa.  He had a sarcoma in his cheek and went right away to Oasis last June.  He has been going back every month to receive chemo and treatments.  He said the last scan is the cancer is gone!!  He said he feels like plowing the fields again!!  Praise the Lord.  So they have been through this border crossing at least 7 times and never had any problems. 

We ended up going to another border crossing since the TJ one was 3 hours for us in a van with a special permit.  Yikes.  The other boarder we had to get out and take all our luggage and walk across the boarder.  The line was short and moved fast. 

Well we had all this luggage for 3 weeks of stuff and the other couple only had 1 suitcase a piece they were there for only 1 week so they helped us with our stuff.  Then they had a guy that made them open there supplements and get out the paper work and check it.  They said that's never happened before.  Then we had to walk a long ways (it was long for me in my condition) to find our driver.  At least we were in CA!!! 

Fred takes a walk to find him and brings him to us.  Fred and the driver got out of the van and the van started rolling forward and I yelled and Fred jumped in on the passenger side and through it into park.  He saved the day!!  I never saw him move so fast!!  Had the van kept going it could have hit someone or another car bemuses we were in a very busy area.

We  got dropped off at our parking lot and the driver thought he was still in Mexico and pulls right in front of another car.  We were so glad to be in our own car and driving.  I felt like kissing the ground!!

We got home around 9:00pm and Ceci and my mom and Dave and Rhonda were here.  They had flowers and balloons and cookies and banners welcoming us home.  It felt so good!!  Thank You Lord for the great experience of Mexico and for providing the funds for us to go and for bringing us home safely and for giving us such great support through family and friends.  Jesus is Alive!!

Cathy

Wednesday, March 12, 2008

Hi Everyone,

I missed writing yesterday.  I was hooked up all day and the Vit K and Vit C make me feel yucky!!  My head just swims.  Ceci called and wanted me to make a decision on something and I just couldn't even start to think.  It's so hard to imagine right now how bad it gets when I feel normal now.

I am waiting to finish treatment. 2 more today.  Fred just got back from lunch.  The "companions" went to lunch together at the health food restaurant. He got tortilla soup that was really good he said.  he then took a walk to the beach and took a picture of the south west corner of CA. Pretty cool.  I went to lunch without Fred and one of the other patients said she was talking with Fred earlier today and she can tell me everything he has done  on my van. Fred is getting pretty bored if he is talking to the female patients about working on the van! lol

Well, I received my prescription for supplements today.  Only 36 pills a day!!  They are so nice they even give you a sleek black new rolling suitcase with every purchase. Guess what, all your supplements fill the case!!!  You will not believe it to you see it. You know how many supplements i have on the counter now.  I think we will have to remodel the kitchen so I have room for the supplements!!!!

 Last night we had a healing service in the chapel.  It was so great being in a hospital praying for healings!!  We also went into other rooms that the patients could not get to the service and they still wanted prayer.  We are all from different denominations but came together as Christ's church.  Some prayed in tongues some had words for others, we all laid hands on the sick  and praised the Lord. My friend prayed for someone else for the first time.  It was a great night!!

 Love and miss you all,

Cathy

Monday, March 10, 2008

Debbie Becker sent me this today and wanted to share it with everyone.

Today I was reading my devotion and it was in Mark 4:35-41. Jesus was in the boat and he was sleeping. In the devotion, someone asked, how do we wake Jesus up when He is asleep in our boat in the middle of a storm? Well, they said, you don't wake Him up - You rest with Him! If He's not worried - don't you worry. His PRESENCE calmed the storm then, just as it will do now.

The disciples didn't need Jesus to awake. They needed to awake to the fact that God was with them. Knowing Jesus is in your boat with you will give you supernatural peace. Calming the storm is great but Peace in the midst of it is even greater.

I love you!

Deb
 


HI there,

I just finished checking the messages on the message center.  I am so sorry to miss your calls.  Sunday I was out side enjoying the sunshine. We were swapping stories of how good God is in our lives.  How He led all of us to Oasis of Hope hospital and did all these great things to get us here.

There are some incredible stories.

I went to devotional time this morning and we read Psalm 24.  We read it 3 times and personalized it and people shared how that made them feel or what the Lord may be saying to them through the scripture.  Then we had time for worship and prayer.

 A couple went home today from Washington.  She had breast cancer and was here on a follow up.  She is doing so well.  She home schools 4 children!!  God is doing amazing things in their lives. 

We also prayed for a wife whose husband had a very hard night.  We found out later that he did pass away.  But the good news is he came to the Lord on March 2nd 2008.  Just days before passing.  She doesn't really realize this good news since she is a new believer.  But we were all rejoicing knowing where he is spending eternity.

Well off to bed I just took my melatonin so it won't be long............

Love you,
 


"He does great things too marvelous to understand. He performs countless miracles."                     Job 9:10

I am feeling so good and normal today. It feels so good.  Except for the IV in my arm, I really feel good.  I had trouble this weekend with the cold and headache. I listened to 2 CD's my sister sent to me that are just healing scriptures and I felt so much better.

We did go to Rosarita Beach.  It's only 20 min away.  They dropped us off and we walked around the stores.  These people are very aggressive in their selling.  You can't even touch anything or look at anything and they are trying to sell you.  So we took a walk to the beach which was only a half a block away. 

As we are walking toward the beach I can smell horse manure.  Which was very odd.  I thought I would smell the ocean; no, I smelt horse.  Well it was like a circus on the beach with all the horses to rent food to buy and trinkets to buy and they are really geared up for spring break.  The music was pumping!!  You could feel it. 

They have men at the beach from the bars trying to sell you table space with chairs and umbrellas.  So we were bombarded at the beach with the same aggressive sales people.  When you rent their tables then you buy your beer from the bar they worked for.  It's quite interesting,  lots of guys waiting for the girls to come.  Can you imagine that place at night?  This was a huge stretch of the beach.  They say they will get 20,000 students that come in for spring break, and they sure cater to them.

When we got back we walked down the street from the hospital to a health food restaurant.  I was thinking it was a lunch counter or something small.  It's a huge restaurant with a view of San Diego.  Great menu to choose and the food was so good.  We walked back and I fell asleep for the night.  I didn't think I was that tired but the day wore me out. 

Fred had rented a movie from Blockbuster and watched in on the lap top with headphones so that worked good.  I was so worried or him to go out at night to return the video back to Blockbuster.  He wasn't worried and made it safely back.

Sunday, we woke up and another beautiful day except for this headache I had. I did everything to get rid of it, but it just wouldn't go away. 

We had church in the dining area.  I stayed and he was so on fire for unbelievers to come to know Christ.  He shared some of the struggles he faces here in Mexico when trying to share the gospel.  He says it's so dangerous here you can't even trust the police and that the only way to survive is prayer!!  He is a pastor at a local church here and is the son in law to the founder of Oasis Of Hope.

I took a nap after church and woke up a couple of hours later feeling better.  Fred felt better because he went and got another hamburger at Carls Jr.  He was happy.

We just sat and visited with others who are going through the same things.  Everyone is so open and hopeful in Jesus so it is so encouraging for everyone to share with others what the Lord has done for them to get them here and what he is doing while they are here.  Its amazing. 

Went to devotions this morning and we prayed for a woman and her husband that is not doing so well. They put him in the regular hospital.  They accepted Jesus since they have been here, which is a praise.

I am sharing my worships cd's with others,  I find it helps so much when you are having your treatment.

Fred is out for a walk right now.  He goes on these long walks and talks to people everywhere.  So when he gets back he has all these new stories for me to hear.

He has been so good to me.  I was reading 1 Cor. 13, the love chapter. Fred has been this man of Love to me. He has been so kind and gentle, not irritable (even though I have.) He hasn't given up hope or faith. He rejoices in the Lord with me and he is certainly enduring through this circumstance.  He has been LOVE to me.  I thank God for Fred.

Friday, March 7, 2008

What a great day!!  I woke up feeling so good I skipped to church!!  We had 2 worship songs and they read a love letter to us from the Lord with scripture.  It was beautiful. 

Then we said goodbye to a man who is off home to Scotland.  I forgot to give him my email to keep in touch with him. 

After church I went back to our room and Fred was still sleeping so I didn't want to wake him up and I went to breakfast.  He finally came down and he wasn't feeling well.  He is used to eating more protein from beef source and isn't getting that here.  I think he was so low from not enough protein.  He took a walk to Carls Jr. this afternoon.  He sure felt better afterward.

I was hooked up to a IV from 10:15am-6:30pm.  I was so happy when they took that IV out.  I started jumping up and down.  No more treatment till Mon.

After dinner we went out front of the hospital and were talking with some of the wives of husbands who are getting treatment.  They are having such a hard time with the "health food" they were talking all about the food they wanted to eat and laughing so hard how a piece of cheese could taste so good.  They then talked about all the hamburger places near there homes that they like.  They just went on and on.  They were so funny.  It was good entertainment. 

Fred signed us up to take a trip to Rosarita Beach.  We were suppose to go last week but couldn't because I wasn't feeling well.  The weather looks good for tomorrow so we will try again.

We found some egg crates for Fred's bed to make it more comfortable so hopefully he will sleep better.  I have been sleeping so well.  They give me melatonin at night and its suppose to help you sleep better.  It works for me.

Well off to bed. Love you all and thanks for the emails and calls.

XOXO

Thursday, March 6, 2008

I am driving everyone crazy today because I feel so good! I think that cold or flu thing really brought me down physically.

if you could see me know I am on the computer with one hand because the other is hooked to a IV. They have me hooked up to oxygen in my nose, I have head phones on, my granny glasses on my nose and my Aunt Jemimah head scarf on!  What a sight!!!

I have to be careful when singing with headphones on that I don't sing too loud. they may move me to the funny farm level!!

Fred is getting my lunch for me since I am hooked to IV. I only have 4 hours of treatment left!!

Wednesday, March 5, 2008

It's Wednesday and I am all done with treatments today.  Yahoo.  No IV's in my arm.  My left arm is so sore from yesterdays IV.  Hopefully it will recover enough for tomorrow.  I spoke to one person and they said I should have a port put in and then I talked to a patient who has a port and she said it hurts her all the time.  I don't think there is anyway around the pain and discomfort of the IV.  I just don't do well with pain and my veins are so hard to find.  I pray before going to start the IV that it will be a good vein and get it the first time.  In fact the nurse who starts the IV is praying too!!

The last 2 days have been so long with all the treatments.  The fluid hurts going in so they have to slow the fluid down where I can tolerate it so it takes forever.  They are very patient with me.

We missed devotions this morning being so tired I couldn't even get up. We did go to breakfast because I don't want to skip meals so I can have some kind of strength and food still tastes good.

Jorge and Geri Armenta came into the dining room and we were so surprised to see them.  They were suppose to come on Thursday, which is an all day long on the IV for me and I don't feel good, but they ended up coming today.  They stayed and visited with us for awhile and had to move on to Ensenada, which is a couple hours south of us.  Its a beautiful day out with the sun shining.  I felt like walking out with them to their car.  They have a secured parking lot which was nice for them. 

We went back to our room and took a nap because they gave me a treatment of b-17 which makes me fall asleep.  We went to lunch and then sat outside for awhile.  Fred is taking a nap and I am trying to catch up with everyone since I have been under the weather so to speak.

Thanks for all the emails and scriptures and prayers online.  If I don't answer them it usually because I don't feel good and my brain feels foggy.  I wouldn't make a good drug addict.  I don't like this feeling.

God bless you all.  I miss you!

Love,

Cathy

Tuesday, March 4, 2008

I have been hooked up all morning and noon and now they are getting ready to hook me up again.  They gave me something for my cold which has helped with headache and nose running so I am feeling better.  Just a long day on IV.  No treatments tomorrow. 

Fred is out taking a walk and he is being such a blessing and a big help for me.  There is a lady here whose husband comes later in the week.  I can't imagine doing this without Fred.  Thank you Lord...

I have had an awful time with the IV thing.  They don't want to work and then this morning the Vitamin K burns my arm so bad they slowed it down and it took forever to go through it.  I have 2 more Vitamin C and 1 Vitamin K and a Laetrile.  4 more and they are about one hour each if they don't burn.  They used an ice pack to give me some relief.  They don't want you to be in pain.

Sunday, March 2, 2008

Woke up this morning not feeling well at all.  Took medicine for nausea and thought that would help.  Breakfast was my favorite - whole wheat and buckwheat pancakes with nuts and strawberry sauce on it. Yummy.  But when you don't feel good food doesn't taste good.  I ate it knowing that this is my favorite breakfast but it didn't taste as good as I remembered it. 

The church service was held in the dining area.  Dr. Contreras spoke about perspective when given the word cancer.  He is very compassionate and you can tell he loves the Lord and people who suffer. 

We went outside since the sun was shining but I had to put my hood on so my head wouldn't burn.  I didn't bring any scarves with me cuz I didn't know that my hair was going to fall out while I was here.  Oh well, I am not the only one with no hair. 

We came back to our room and fell asleep.  We are both fighting this cold.  It's not very fun.  I would rather be outside walking in the sun but no energy to get out.

I hope and pray for us to feel good tomorrow so I can get treatment.

Thank you for the emails and the love and prayers.

Saturday, March 1, 2008

Well today was the day my hair decided to come out.  I wasn't thinking it would fall out yet.  Kaiser Dr. said after 2nd chemo treatment, which is March 17th.  I got in the shower and ran my hand over my head and it felt like a spider web in my hand. I couldn't figure out what was going on.  Then I saw a handful of hair. Now the worst part is I just paid $20 on Tues to get a really cute hair cut!! It only was with me for 4 days!!  Well at least I looked good when I got here.  I went down for breakfast after I got my hair all out and had to cut some of it.  I left it spiked in front.  One of the other patients called me GI Jane!! He is from Scotland so if you can imagine hearing it with an accent. It was cute.

Not feeling well today and Dr. said it could be the flu more than a reaction from the treatment.  The treatment makes your hands swell so I had to take my rings off before I couldn't move them.  We were going to take a field trip to Rosarita Beach but since I am not feeling well we called it off. 

We were able to get a chair for Fred to recline in.  His back was bothering so much because there wasn't a comfortable place to sit.  I asked for prayer for Fred's situation at devotion yesterday and by evening we had a chair for him.  The Lord even cares about the little stuff!!

Ceci went back to Masters Commission last night,  Rheanna took her for us.  Ceci had had laryngitis for 2 months and needed a break.  On break she got the flu.  We thought best for her to stay home till Fri. to recoup more.  Please pray for her to have good health to make it through the hard schedule they have to do.

Thank you for all your emails and prayers.  Can never have enough.

God is our refuge and strength, always ready to help in times of trouble.     Psalm 46:1

Cathy

Friday, February 29, 2008

From Cathy this afternoon:

Yesterday and today they took out a cup of blood and put ozone in it and then ran it through an ultra violet light before putting it back in.  It takes about 30 min. to do the whole procedure.  The gentlemen that does this is so on fire for the Lord and it shows.  There was no one else in there and we had a concert of Gospel music which he loves and SINGS!!  He was sharing his favorite CD and songs and just blasting the music and singing away.  It was so fun.  That kind of stuff just doesn't happen at Kaiser!

Went to lunch and it was so good.  Came back and they gave me a treatment at 3:40 called Perftec.  Its a new treatment that they have had good results with.  They do all these things to put oxygen into the blood so the Vitamin C treatment will turn into hydrogen peroxide and kill the cancer.  That's my version of what they are doing.  Well after an hour of treatment I started getting pain in my chest that was so bad they had to discontinue the treatment and gave me a shot of pain medicine. Which really helped relieve the pain.  So on Mon we will try it again and give it slower by IV and give me some other medicine.  Its a very important part of the therapy and I want to try again.  My friend only lasted 3min. before she had pain.  So I don't know what they are going to do for her.

During the perftec treatment they have me on oxygen.  When the perftec treatment had to be stopped they gave me by I V Vitamin C, then B17 then Vitamin C again.  That took about 2 hours.  I felt good afterward not like the chemo at home where you have to take medicine for nausea.  Right now I am hooked up to Vitamin K by I V.  Not sure what it does.

Well thank you all for praying for me and the emails.  It really helps me to feel at home.

Praise Report- The doctor at Kaiser came through with the copy of the scans I need without having to go through all the paper work!! My mom already picked them up and put them in the mail.  How's that for answered prayer!!  Praise the Lord!!

Jesus is the same yesterday, today, and forever! Hebrews 13:8

Love you all!!

Thursday, February 28, 2008

From Cathy this morning:

I went to devotions this morning.  They have a chapel on our floor and a couple come and lead devotions from outside the hospital. He played the guitar and we sang Come now is the time to Worship and There's no God like Jehovah.  When do you ever go to the hospital and get to worship?

They went around the room and asked what you were thankful for. It was so encouraging to hear the thoughts of others and I said I was thankful for my dad who financially supported me to be here. I asked for prayer for my dad that through this situation he would see Jesus in me and the hope and faith I have and that he would want to know my God. They anointed me with oil and prayed for healing and strength and then they prayed for my dad Glenn.  What an amazing hospital that takes care of your spiritual life.

Wednesday, February 27, 2008

This email came from Cathy tonight:

We did get out of the house at 4:00 am. and made good timing except we took the wrong freeway so it was a 45min detour.  We still made it  on time. The guy picked us up and got our visas for us.  We were in our room by 10:30. The nurse came in our room and drew blood and then they sent up food to our room.  Fresh fruit, eggs and fresh salsa, whole wheat pancakes, and banana protein shake.  Yummy!!

The doctor came to our room to get my medical history.  He really wanted copies of the scans I had last week but we only brought the reports.  Please pray that the Dr. at Kaiser will be able to get the copies for us. 

We went to a meeting explaining our follow up visits then Fred and I walked to the beach.  It was so beautiful outside. 

Lunch and dinner were also so yummy!!  It's my kind of food. They gave me 16 vitamins to take with dinner and 3 pills to take at bedtime.  WOW!  I am used to taking vitamins and maybe 16 for the day not just one meal.  Tomorrow I will have vitamins at  each meal. 

We have met some interesting people.  Fred just met a man and his wife from England.  She was diagnosed with lung cancer and not given much time to live.  In England with socialized medicine they would not even offer her chemo.  She found Oasis of Hope online and is still alive today.  Praise the Lord!! 

They have scripture in big frames on all the walls and they encourage you to seek the Lord in prayer for your healing.  It's a very peaceful place.  We have devotions at 8 am and I am looking forward to that time. 

They have cards with scriptures on them for you to pray for yourself. Even in our room there is a picture of a scripture plus I had printed some on colorful papers and hung them on the walls in our room.  We are off to bed since we got up so early.

Thank you for all your prayers and support. We love you all.

He sent His word and healed me, and delivered me from my destructions.    Psalm 107:20

Monday, February 25, 2008

This update comes directly from an email from Cathy:

I have been off oxygen since 5:30 pm Fri. and feeling good!! Huge relief.  It means to me that the chemo is already doing its thing.

Please tell everyone how much I appreciate their prayers, cards, flowers, gifts, phone calls and visits.  All these touch me in such a special way of love from them and our heavenly Father. I know I am not going through this alone.  God never leaves me and neither has my church family.  I love them all!!!

Looks like Wednesday the 27th we are leaving Simi Valley at 4:00am (dark thirty) and will drive to San Diego where we will park the car in a long term parking lot.  The Oasis hospital will have someone pick us up and drive us across the boarder to the hospital.  I will start treatment that day at 12:00.  How's that for getting down to business?

The number at the desk is 1-619-690-8400 and they will give you my room.

Mail can be sent to:
Fred and Cathy Haedt
c/o Oasis Hospital
P.O.Box 530478
San Diego CA 92153

Cell costs 99 cents a minute so we won't be using that and text cost extra too.  I will probably have withdrawals not texting.

We are taking a laptop with us to keep in touch by email.

Also you can come down and walk the beach with us!!

love you all!

Friday, February 22, 2008

Cathy's breathing has increasingly become better and better this week. She is still on the oxygen, but it's on a lower rate, which is good.

After research, prayer, and counsel, she and Fred are going to spend 18 days at a hospital that does Alternative Treatments that work alongside a patients chemo and radiation protocols. It's called Oasis of Hope Hospital, and is located in Tijuana, Mexico.

The plan is to leave for Oasis of Hope on Tuesday or Wednesday and return on March 14 or 15. Then, after 3 months, they'll go back for another stay for 5 nights.

While there, they won't be able to use their cell phones, but she will have a phone number to her room and have email access. We will post the phone number and address as soon as she is able to get it to us.

Saturday, February 16, 2008

4:30 pm — Cathy is now at home resting. The bone scan results also came back all clear!!

11:30 am — Cathy is waiting to be discharged from the hospital. She will go home with oxygen, however, at the moment, she is off the oxygen and holding her own. That's what we want and pray for!

Her MRI of the head and neck area came back all clear! Praise God! She is still waiting for results from the bone scan.

Friday, February 15, 2008

11:00 am — Cathy experienced more nausea this morning which was helped by medication. She was experiencing nausea again later in the morning and was waiting for more meds. Please pray for Cathy's body to be able to endure the chemotherapy.

She had an MRI of the head and neck area this morning and will have a bone scan done this afternoon. Both of those tests will lead to the staging of the cancer.

She will have her chemo tonight and hopefully go home tomorrow morning. Right now, it looks like she will have to go home on oxygen, as her oxygen saturation level is at 94-95 with 2 liters of oxygen flowing. Ideally, they want it in the upper 90's, and is best at 100. If she can't achieve that on her own, she will have to stay on the oxygen until she can.

Thursday, February 14, 2008

10:20 pm — Cathy received her results from the PET Scan from the Oncologist. It shows that the cancer is in the lymph nodes in the chest area (which they already knew), in the neck area and around the esophagus (which explains the hard time she has swallowing). There is also a "tiny" spot on her liver.

Further explanation reveals that the type of cancer Cathy has does not go away and is not curable. The best human hope they have is that the chemo and radiation will put the cancer into remission.

She will undergo another test on Friday that will tell them what stage the cancer is at. The Oncologist will not give a timetable because every person is different in how their body responds to the treatment and to the progression of the cancer.

The treatment regimen was also clarified. She will under 6-8 treatments (each treatment is 3 days in length) as an outpatient. Each round of treatment will happen 28 days apart. After the 3rd round, she will have another PET Scan to help determine how many more rounds of chemo and what type of radiation treatment will be recommended.

Cathy will receive her last chemo medication of this first round Friday night. She should be able to go home on Saturday.

Cathy and Fred are hope-filled and trusting God with this process. We believe wholeheartedly that God can heal anything, no matter what the doctor says! At the same time, the family is taking the news realistically and with great appreciation for healthy relationships and deep love for one another, and soaking in all the time they have in the future together.

Please pray for continued peace, strength, endurance, and reduced swelling of the lymph nodes and removal of any cancer in her body!

11:15 am — Cathy had a little bit of nausea this morning, but meds were able to help greatly and she is feeling fine now. She was able to eat a full breakfast.

Last night, she started her first round of chemotherapy. Each round goes for 3 days, so she'll have part 2 tonight and part 3 Friday night. Then, she should hopefully be able to go home Saturday.

The PET Scan results will be in on Friday. This will tell them if the cancer has spread anywhere else and what stage it is at. The treatment is the same not matter what the PET Scan results are.

She will receive 6-8 rounds of chemo, with each round administered 3 weeks apart (3 days chemo, then 3 weeks off, 3 days chemo, then 3 weeks off, etc.). Halfway through, another PET Scan will be done that will determine how radiation treatments are handled from that point.

For now, as long as Cathy feels she is able to handle it physically, she is still taking visitors. However, you may want to watch this webpage before visiting. If she lets us know she is not feeling well enough for visitors, we will post that here.

Please pray for strength and endurance for Cathy, Fred and Ceci as they face this battle.

Wednesday, February 13, 2008

This morning, Cathy and Fred met with the Oncologist, who had more information for them.

Cathy has Small Cell Lung Cancer with at least two masses that are pressing against her esophagus. She is undergoing a PET Scan this morning, which should tell them if there are any more masses anywhere else and what stage the cancer is at.

Today, she will be moved to their 4th floor, where she will undergo her first chemotherapy treatment tonight. Their main concern right now is to shrink the masses so that her airway is not restricted.

Cathy and Fred are taking visitors if you would like to go see her. She loves getting visits from people. She is at the Kaiser Permanente Hospital in Woodland Hills. Click here for a map.

Tuesday, February 12, 2008

On Sunday, we prayed together for Cathy Haedt. She had been having trouble catching her breath for over a week. An x-ray last Thursday resulted in a CT-scan last Friday that revealed enlarged lymph nodes that were pressing on her airway.

On Monday, she underwent a biopsy on those lymph nodes. Today she received the news that the cause of the enlargement is cancer.

12 years ago, Cathy was diagnosed with and treated for non-Hodgkin's Lymphoma. She has been cancer free since then.

While the doctor does not yet know what type of cancer she has, there are some very good signs at this point. One of those signs is that she is overall very healthy. There is nothing that indicates the cancer, particularly in her blood work. This is a good thing!

On Wednesday, she will undergo a PET scan, among some other tests, to help determine the type of cancer and the treatment options. She will be in the hospital at least until Thursday as she is receiving some IV steroids to bring more immediate reduction to the size of the lymph nodes. She is at Kaiser Hospital in Woodland Hills.