Ξ December 31st, 2004 | → 0 Comments | ∇ Jay |
Well, Happy New year everybody! I hope yours goes safe and well, and please know you are in my prayers! I hope you all can continue to say prayers for us here and especially Jay. There is no new news this morning, but we will update you all this evening.
Here is Sheila’s email from this morning:
Dec. 31st Morning:
Happy New Years Eve!
There isn’t a lot to report yet. I called the ICU this morning and they said
the Doctor’s haven’t rounded yet. They said he is restless and wiggles a lot
(he was doing this last night too) but other than that there is no change.
I’ll send another email this evening. All of you have a very happy and healthy
New Year. Please know that your thoughts, prayers and concerns have been very
appreciated.
Sheila
Ok well, Please KUTPs!!!!!!!!!!!!!!! and Happy New Year!
Ξ December 31st, 2004 | → 0 Comments | ∇ Jay |
Before I start let me paste Sheila’s email from this morning:
Dec 30th mid-morning:
I called for an update this morning and other than receiving insulin for
unstable blood sugar all is the same. I am getting ready to head to the
hospital. Jay’s family is here but they are all sick with some sort of bug.
I’m trying to stay clear of them so that I can still see Jay. They are all on
antibiotics and hopefully will be safe to see him in a day or two.
Thanks,
Sheila
Ok, well as Sheila said we are all not feeling too well, but I must admit that I felt great this morning until after the shower loosened all of it back up and then I have the cleansing time each morning, heh. But I got a lot out and felt very good today except for the canker sores I have in my mouth. arrrggg….
We all slept in this morning and then my Dad decided he was going to stay at the house and so my mother and Sheila and I went to the hospital to make the 1st 1hr. visit time of 1:30 pm Eastern. I went in first with Sheila and to tell you the truth Jay looked a lot better than I had 1st thought he would. Now to the normal avg. Joe He would have looked horrible……but I see people in his state and a lot worse in my profession when I go visit them, and for people in his state he looked very good. But it is always hard to talk to someone who is so drugged that they rarely acknowledge your presence, but it sure was good to get to see him smile at Sheila when she joked with him a little and he even turned and faced me a few times to face where my voice was. The nurse said he will not remember anything during this time period, but it is nice to know even in a subconscious state your brother knows your voice, heh. Well, each hour long visiting time my mother and I would spend 30 mins each with him and Sheila would stay the entire time. In between times we would just hang out in the cafe or cafeteria, play UNO, or call family members to find out how they were doing. Over all the day went good, except my Dad did not get to see Jay, but I think he got some much needed rest….something I think I should consider.
But, I held Jay;s hand (after a good washing or two, heh….and Sheila and I would just talk to him telling him how great he was and how good he was being.
The Dr.’s when we first got there were very happy with a chest X-Ray they did because it looked like his lungs were healing up very good, and they were slowly taking him off the breathing tube during the day and I think they got him down to 40 % Oxygen…and I think normal breathing is something like 22% Oxygen. So, his lungs are healing and they think that he should make a complete recovery in his lungs too!!!!!! Great new Great news!!!
So…now I think we will get another day with the tube and maybe one more day in ICU to keep an eye on him and then hopefully back to the Cancer Ward to kick some cancer butt!
They are also talking about the bone marrow transplant form me will probably be several weeks if not months from now…so it looks like I will just be doing lots or pep talking this round, heh.
=================================
Tiffany got to Pitt just fine (other than talking to a crazy guy sitting next to her on one of her flights that said the words, drug traffic, Mexico, kill, bomb, and a few other nice ones…and he would often mumble to himself….but other than Tiffany sitting next to a crazy man her flight was great! She got in around 9:20 pm, and Sheila, momma and I drove to the airport right after Jay’s 9-10 visiting hour. We then all proceeded to the nearest WalMart to buy forgotten supplies that people need when they make emergency trips to see their brother/son/brother-in-law. And now we are all settling down for another evening and sleeping in in the morning to do it all over again. I hope to use Jay’s computer to write my sermon (or start it) tomorrow…so pray for us all and thank you for your love and care!!!!
Oh I almost forgot… Earl Blair called Sheila on her cell phone this morning as we were pulling into the parking garage….he is one of my heros and what a wonderful man of God….
Ok must go to bed…let me check of Sheila’s evening email is ready yet…that she is typing upstairs…..yep here it is:
========================
Dec. 30th evening:
Finally some relief.
Upon visiting today, DG and I were met by the respiratory Doctor so was excited
to tell us the Jay’s chest X-ray significantly improved over yesterday and that
they think they will be able to remove him from the ventilator soon. This is
the real first bit of good news. This was wonderful. Today, was a little more
conscience and would actually move a bit and he would open his eyes and every
now and then he would sort of respond to us. One time he tried to smile and he
would turn his head occasionally to see who was speaking. The nurses said that
they don’t believe he will remember any of it. They have started reducing the
amount he is requiring from the ventilator and it should be just a day or two
and he will be off of it. They will probably keep him for a short time for
observation in the ICU once he is removed. The Oncologist rounding today came
down and seemed very hopeful too. This was so refreshing since yesterday was
not so. They believe that it was the lymphoma that caused his lung problem
because the sample they took from the bronchial scope contained the cells. His
oncologist said that he believes a full recovery of his lungs and kidneys is
possible with time. This is very good news. Hopefully we’ll have more
tomorrow.
Jay is quite famous around the hospital and the Doctors love him. I had three
Doctors come up to me in the café today inquiring about Jay and they are not his
current Doctors. In fact one was a medical resident he had only 1 time months
ago but he left a lasting impression.
We were visited by a friend of ours today we haven’t seen in years and it was
very nice to see him. I know Jay is going to be thrilled to see him. Later
that night a friend came to play card with us.
After the 10:00 visiting hour we drove to the airport to pick up Tiffany. Jay’s
family is all here and DG and Teresa seem to have beaten there cold but Randy is
still sick and stayed home to rest today.
Well, it’s very late and we have another busy day tomorrow and I need to get
some sleep.
Take care everyone,
Sheila.
===========================
Please KUTPs!!!!!!!!!!!!!!! God bless!
“Where are we all going?
And why are we in a handbag?”
<-----saw on a bumber sticker in Santa Fe Typing...... on a...... ergnomic...... keyboard and it... is.... hard to type on....ugggg...... Well, my parents and I got here tonight very tired, and all of us are a little sick....wich is freaking frustrating, becuase I am not sure if I will even get to see him for a few days until we all get feeling better.... Well, Jay is back on the breathing tube and still in ICU and they say he will stay there for a few days...which I guess is good because that is forcing him to rest/sleep and it forces all of the family to stay away until three viewing hours during the day... 1-2 5-6 and 9-10 pm. This is good for us because it is forcing us all to stay here at his house and rest snd get feeling better! I know I need to feel better and so does all of the fam...except super woman Sheila, heh. Sheila says now that they think the cancer just came back with a vengence and went straight into his Kidneys and lungs, and his WBC count was very high and amzed the Dr.s.....They took off two backs of WBC and hiis WBC count is at a workable level. And he is now under medication to keep it low. He is on Dialysis and will have it off and on as needed. But the Dr. feel like the Kindey function will come back. They are more comcerned about the lungs and have his sidated to keep him on the respirator for at least two more days if all goes well. Please keep him in your prayers...... ====================== My Nanaw (Edwina Emert mother on my Dad's side) is also in the hospital with Pnumoia. She was taken to the hospital via ambulance yesterday and they got her temp down, but then it jumped back up and then the last I heard it is coming back down now. Please keep her in your prayers.... ======================= Tiffany will be traveling up to see Jay tommorrow, and that will be good for all of us because she is such a loving angel, but she is feeling like a warm buck of hamster vomit right now jjst like the rest of us....and believe you me traveling in airports when your sick is not a fun way to fly. Please Keep her in your prayers........ ======================= As some of you might know my father has the same wonderful balance problem that my grandmother has and the sickness is making that act up too (and man you should hear his cough....what a wing dinger that one is!!!!), and so we are all doing double duty taking care of each other and lifting each other up in prayers!!!! please keep him in your prayers....... ======================= Also, when we went to see Tiffany's family yesterday...her nephew Caleb had a 103.5 temp and was coughing up all kinds of phlem. They went to the Dr. and he is much better tiffany said...but please keep him in your prayers.......... ====================== Yep needless to say..........we are all in desperate need of your prayers and thank you all for each and every one of them!!! Please pass our info along to any prayer worriors or chains you can think og and keep the faith! We need all the support we can get! ====================== Going to much needed bed now! Thanks again...and please KUTPs!!!!!!!!!!!!! Here is all of Sheil'as updates on Jay...man she is good about this! Dec. 29th 3:00 AM
It’s 2:46 AM and I just received a call from the ICU Doctor and he stated that
they had to place Jay back on the ventilator. They said they truly had no
intention of removing him from it this morning but since he ripped it out they
would see if his breathing would return to normal. He said their original plan
was to leave him on it for at least 24 hours so that his lungs could heal. They
monitored him all day and he was not doing well breathing wise and this morning
it got worse so they had to place him back on the ventilator. He said I
shouldn’t be scared because they originally thought he needed more time on it
anyway and that this will allow him to get the proper rest. They said he was
showing signs of oxygen deprivation. They explained that the reason he was
allowed to come out of sedation this morning was because his blood pressure was
low and they didn’t want to risk that going any lower and that is why he started
to become conscience and pulled out the tube. The Doctor explained that this is
truly the best thing for him and that he believes over the next 48 hours they
will be able to remove it again and it should be easier for him to breathe but
that he truly needed this help this morning.
He will most likely be on the ventilator all day tomorrow which means he will
remain in ICU. Anyone planning to visit him will need to wait only immediate
family and clergy may visit during this time.
There is no where for me to set up a computer at the hospital while he is in ICU
and my wireless card for my IPAQ is on the fritz and my usual tech support is in
ICU so that will have to wait. You may have to wait until tomorrow evening for
an update. You of course my try cell phone but it may be turned off because I
am in the hospital (please leave a message and I will call you back
412-973-9476).
He will most likely be in ICU for the next few days. I still can not see him
until 1:30 tomorrow so I will be home in the morning if you need to reach me
724-853-0204.
Thanks, Sheila
Dec 29th mid-morning
I just spoke with Jay’s nurse in the ICU and he said that they are keeping Jay
very sedated and that his vital signs are good. He said his blood counts
dropped a bit this morning and he will be receiving a transfusion (which is to
be expected). He said the Doctors haven’t rounded yet but it is his
understanding that they would like him on the ventilator for another day or 2 so
that his lungs will have time to heal. I will be there to see him at 1:30 so my
next update will probably not come until late tonight. I’m probably going to
try and go to my work in between visits today because it is closer than coming
home and I need something to occupy that time.
If you need anything before then my cell number is 412-973-9476 (leave a message
and I will call you back). Again, Jay’s parents and brother will be arriving
this evening and Tiffany his sister-in-law will be here tomorrow. It will be
nice for him to have them here when they take him off of the ventilator and
sedation in a day or two.
Thanks,
Sheila Hollums
Dec 29th Afternoon
I just came from seeing Jay and he is still unconscious and on the ventilator.
They did another dialysis treatment today. They also put in an arterial line to
monitor his blood pressure continuously. The doctors say this is best for him
but it is hard to see him this way. I will be returning to the hospital for the
5:00 visiting hour.
Thanks,
Sheila
December 29th Evening
I went to see Jay all three times today. It’s really hard to see him like that.
He is completely unconscious and they have inserted a tube in his nose too for
giving additional medication. I got to speak with the ICU Doctor and he said
that Jay is labeled serious condition for the breathing issue alone. The Doctor
says his kidneys should make a full recovery over time but he may need dialysis
every now and then.
He could not give me a prognosis on Jay’s condition other than it is serious.
He did say that Jay almost entirely stopped breathing on his own last night and
that is why they did what they did.
I was able to have dinner with a friend in between visiting hours and it was
very nice.
The Doctor said he will have a better idea tomorrow once they run to the tests
to see if there is a change in his condition. I spend my time rubbing his feet
(about the only part of him that doesn’t have something attached) and telling
him I love him hoping that if he can tell I’m there he’ll be comforted.
His family should be here any minute.
I will write more tomorrow and hopefully it will be better news.
Sheila
=====================
Oh yeah, and it goes without saying……..Sheila needs your prayers too……….
Got to go. Love yall!
Ξ December 29th, 2004 | → 0 Comments | ∇ Jay |
Here is Sheila’s last email:
Jay was still in the ICU today and I could only see him from 1:30 to 2:30 and
then from 5:00 – 6:00 and then from 9:00 – 10:00. In between times I tried to
track down Doctors to find out what is happening.
Jay will be in the ICU until tomorrow because his breathing has not stabilized.
They will try move him back to the cancer ward tomorrow but no promises. They
told me that he removed the breathing tube on his own this morning quite
unexpectedly when the sedation started to wear off. He doesn’t remember doing
it. He had another dialysis treatment today and they got his white cell count
down enough (31,000) to do a chemo treatment this evening. He is really
frustrated being in ICU and can’t wait to get back to his normal room. Jay’s
parents and brother will here tomorrow so that should make him feel even better.
I’m off to get some sleep.
Sheila
Ξ December 29th, 2004 | → 0 Comments | ∇ Jay |
Yeah that is right Jay is still in ICU tonight. He is having probalems breathing as would be expected since they just went into his lungs and toyed around a little. but my mother said he was doing OK, and the Dr.s just want to keep him in there to keep an eye on him.
I am still flying out tommorrow out of Lubbock and go with my parents to see him. I hope that our presence will be something to lift his spirits. I am sure they are fine, but I am a little worried about him, heh.
Thank you again for al your preayers and I will try to keep you all posted as to what is going on…when ever I can get my hands on a computer. Thanks to my parents and my Aunt (I love you all three soooo much…..I will be able to make the flight up there along with my wife!!!!
My mother did say that he started the chemo again…but gave no other info at all…so that is the best i can give for now. Thank you for your time and prayers! but…….
KUTPs!!!!!!!!!!!!!!!!!!
Ξ December 28th, 2004 | → 0 Comments | ∇ Jay |
Hey I just checked my email and found out that Sheila has been updating us all via email so I thought I would share her version of all that I have been telling you:
In Date order:
December 27th morning:
Jay is in good spirits (I’m very proud of him) but he’s having a VERY tough time
physically.
His kidneys shut down yesterday and he will be undergoing kidney dialysis in a
few minutes. Unfortunately, fluid is now filling his lungs and he has a pretty
severe cough from it. They just took blood gases and he is on oxygen and an
oxygen monitor. They gave him a mild chemo pill last night to help bring the
white blood cell count down and it didn’t seem to help much. They are hooking
him up to a paresis machine now to remove some of white cells. He is also going
to get an LP, and MRIs (if he can stop coughing). The respiratory Doctor was in
and they may do a bronchial scope too. This morning they placed a central line
in his groin so that they can do the dialysis and paresis. He also had 2 chest
x-rays and a sonogram of his bladder. He has been very busy.
They gave him some miracle drug that eats away uric acid last night and they
gave solumedrol (steroid) this morning to help with his lungs.
The Doctor Kaplan (one of the oncologist here) came in and spent well over an
hour with him last night just talking to him, trying to put him at ease. He is
doing remarkably well mentally for all he is going through.
The Doctor told me that his white cell count (normal is 5,000 – his was
134,000), LDH (normal is around 500 and his was 52,000), and uric acid counts
were the highest he has ever seen. What is amazing is that his bone marrow
biopsy on the 13th was normal and his pet scan on the 10th was normal. This has
all happened in less than 10 days. The 23rd was the first day we thought his
symptoms might remotely be the cancer.
If I didn’t include his phone number here at the hospital it is 412-578-4450.
Again you can email me at shollums@dam.com if you need anything. I will be
working often online from the hospital so it may be hard to get through. Just
email me and I will get you a time you can call or I will disconnect.
I’ll keep you updated. Thanks Sheila
========================================
December 27th evening:
Things have changed since the last email. Jay is now in the ICU at West Penn.
They had to do a bronchial scope on him and since he was not breathing well they
have placed him on a ventilator. They are hoping to remove him tomorrow but I
am not allow to stay with him tonight since they are keeping him unconscious but
we are hopeful that all will be well tomorrow. The found what they think to be a
hemorrhage in his lungs due to the low platelet count caused by the cancer.
They took samples and they analyze it to see if it’s actually the cancer in his
lungs. I will email you tomorrow to let you know when he is released from the
ICU. They also did the paresis and kidney dialysis today. They are set to do
more paresis tomorrow morning while he is still in the ICU.
I will email all of you tomorrow to let you know how he is.
Thanks,
Sheila
===================================
December 28th morning:
I just got off the phone with the ICU. They still will not let me into see him
until 1:30 (unless they move him).
The good news is that he is no longer on the ventilator and is breathing on his
own but they told me that he removed the tube himself unexpectedly this morning.
They couldn’t explain to me if he came out of sedation early or not or how he
did it himself. They said he is doing well though. The Doctors have not rounded
this morning so they couldn’t tell me when he would be going to a different room
or if he would be staying in the ICU. I’m heading out to get him some things he
needs for the hospital and to put some pressure on them to give me more
information.
I will let you know as soon as he is released to a normal room.
Thanks,
Sheila
OK there you go. Hope all this information helps,and I can’t tell any of you how much your thoughts and prayers matter to us all!
Ξ December 28th, 2004 | → 0 Comments | ∇ Jay |
Well, all I can think about is the scene in the matrix where Neo did the same thing…but
Sheila called this morning and told us that the Dr. told her that as soon as Jay work up from the procedure this evening or morning (not sure) he ripped out his own breathing tube!!!!! This is funny, and scary, but this also means that all of the fears that he would never come off of the breathing tube are gone. He is doing very good and Sheila is looking forward to them sending him to a room today so she can go see him.
My parents and I are leaving this Wednesday to go see him and I will keep updating everyone on this blog…….because I know yall care so much and you need to focus your prayer just like we do. Thank you and sure do love all yall!!!!!!!
More updates coming soon……………KUTPs!!!!!!!!!!!
Ξ December 28th, 2004 | → 0 Comments | ∇ Jay |
Well, I talked with Sheila today, and Jay took a turn for the worse today. When we talk about 3:00 pm today Jay was in ICU unconscious and on a ventilator. They did a Bronchial Scope to him today and he should get the ventilator and breathing tube out tomorrow, but they would wait and see. The Dr. said the procedure went fine. They think three thing might have happened….
1) pneumonia
2) Fluid in his lungs due to renal failure
3) Or he could caugh so hard and the burkkitts (sp?) Lymphoma was getting in his lungs.
They sent the fluids off for testing.
Jay right now is in ICU and is only allowed to be visited by Sheila or anyone for one 15 mins at a time. The Dr. and Sheila agree that that is probably very good, because Jay has not gotten too much sleep in a while.
They did a phoresis (sp?) test that filtered out the Whit Blood Cell Count and the Dr. felt good about it…(but I don’t know why)
They can’t give him any chemo right now, because they have got to get his White Blood Cell count down to normal before chemo or his Kidneys would die on him. A normal White Blood cell count is 4,000 and as of this afternoon Jay’s white blood Cell count was 150,000.
One good thing is that his kidneys seemed to be making urine, so they are not totally shot and might bounce back from all of this, but they still have him on Dialysis to help his kidneys function properly.
They made the decision to have this proceed done kind of fast, but they had to make it fast. He was coughing so bad that he was not being able to breath even with a Oxygen mask.
His platelets count was very low 15. and They also thin that he might have hemorrhaged his lungs from coughing so hard, and then when his plateletes count was so low that the burkkitts Lymphoma would go in and cover up the hurt spot instead of the plateletes.
He has been having severe nose bleeds to top it al off. The Dr. was amazed at how fast the Lymphoma was coming back…His Cretan (sp?) level(kidney something), WBC count, and BUN # (kidney something) were all way messed up.
Sheila, said that the Dr. was giving lots of his time with Jay and doing the best he could for him right now.
Sheila said it is a difficult time right now, but his Spirits are up! it is al amazing, but Jay (and Sheila) are scared. Jay should have a hard time talking for a few days due to the O2 mask, and the breathing tube they will hopefully take out tomorrow.
Sheila has also, told me and my parents that we might want to come and see Jay on an airplane, because this s the worse that she has seen him since all of this happened.
so……………Tiffany and I will go see her parents tomorrow in Lovington and have Christmas with them, and then Wednesday we will all be traveling up to see Jay via VERY expensive airplane flights. (Thank you to Tiffany who spent the entire afternoon and evening booking flights for a family who just could not handle all the stress right now.
========================
We opened up presents with my grandmother and family tonight, and it was great as always even with Jay and Sheila hovering over all our thoughts and conversations the entire night.
I am not sure when we will be back, from seeing Jay. I thin that Tiffany and I will come back in about a week, unless we need to stay there longer. And I am not sure about my Momma and Daddy, they could be up there for a while. And who knows maybe after they stabilize him that I can still be used for a bone marrow transplant?
What ever the way, or what ever the time………one thing is for sure…………………….Jay needs your prayers now more than every, and I can not tell you how much they mean to us! Love you all and God bless!
Oh and yes I realize that my spelling is horrible and such, but I am very sick (went to get a Marcela shot and a Z-Pack, and cough syrup today, and I think my fever broke while we were opening up presents. So, I am extremely tired, but I just had to let you all know about Jay, and ask you all to be praying for him! Thank you soooooo much!
KUTPs!!!!!!!!!!!!!!!!!!!!!!!!!!!
Well, Tiffany and I called Jay Christmas day while we were driving to Floydada and we called Jay on the phone to tell him Merry Christmas! Jay sounded good, and told me that he got a brand new Pocket PC for Christmas!!! (and wow is it good…actually the best on the market made by Dell……)
But, during the phone call Jay said that he was still feeling sick. (This is normal actually considering that they knocked down his immune system to nil and he has to come all the way back to a healthy immune system. So we thought nothing of it……
Well, today we tried calling him @ home and no answer and then on his cell phone and it was turned off…..then not more than 5 mins. later Sheila called us (not even knowing that we called 5 mins before) and told us that Jay was back in the hospital and that they were worried about his kidneys…and then they got to looking at him closer and now it is about a 99% chance that he has the cancer back.
Yeah, that is right we all get to go another round in the ring with this cancer. But, this time it is a given that I will probably fly up to them and do the bone marrow stem cell transplant with my bone marrow stem cells.
We still do not have any idea about the time involved in this or exactly if the cancer is back, but all signs point to yes. I will of course keep everyone up to date here on my blog on how he is doing….
When we talked to him today around 6:00 pm Eastern time…he was feeling very tired and laying in bed while Sheila (the super dooper wife of a thousands strengths) was packing up their home to bring Jay and her all the stuff they need again for another round. They have him in the hospital as “short term”, but they don’t know how long he might stay. His Dr. is out of the country, and they were trying to reach him via cell phone. Jay patiently answered all our questions, and then at the very end of the phone call he asked to speak to me….and said……
“Hey D.G,……… I got something to tell you…………I have a better Pocket PC than you!”
Yeah, needless to say his Spirits are still great, but the frustration is very evident in his voice as well as my parents. but all in all, we will all get through this time, and I know that the ride just might be a little longer than we all thought it would be.
If he gets to go home tomorrow then we will all have our Christmas with my Dad’s side of the family @ our house and we will set up a live camera feed for Jay and Sheila to see and hear the gifts being opened that they gave us and the ones that we gave them too. If they are still at the hospital, then we will do what most people do and just pass the phone around, heh. All in all, it will be a very special day to have everyone close or closer by phone! Thanks!
KUTPs!!!!!!!!!!!
=============================================
Oh and tomorrow, Tiffany and my fam are driving up to Lubbock and get her blood test and see if her hormone level is good or if she will need to take some more to keep it at normal levels, so in that regard also……KUTPs!!!!!!!!!!!!
Thank yall, and God bless all yall!!!!!!!!!!!!!
Hey!!! I survive the Christmas Eve Services @ our church yesterday, and I wanted to give all of you a give from me but that seems hard to do since we are all on the internet together…so I thought I would put up my sermon from this year and the one from last year, as my gift from me to you. I hope that you all get a blessing out of them…
Oh there is something you should know about them. These two sermons were written for our “Blue Christmas Eve Service”. Which is a service for those people who Christmas is not a happy time of the year. Maybe they have lost a loved one and this is the first Christmas or an anniversary of a year without them, or what ever. Our turn out is not as big as the rest, but it is still good. Hope yall like these!
A Shepherd’s View
and
Illuminating the Darkness
(don’t forget that you need to DL (Download) Adobe Reader to view the sermons. The link to Download Adobe Reader is on the right sinde of my page over there ——>)
Merry Christmas Day and have a wonderful New Year! We are off to see the fam. so I am not sure when I will be back to blog…but I might try @ my parents home. Thanks! and God bless yall!
=================================
Oh during the break Tiffany will get a blood test to check her Perjesterone (sp?) level, and then we will be going to get another blood test on Jan. 3rd to find out if we are Pregnant!!!!!!!!! I don’t know how long the test results will take, but I might try to keep you informed or not….heh… I really haven’t talked to tiffany about when we want to let people know if we are pregnant or not…..I guess that is important to talk to her about, heh. So…..all that to say……. Please Keep Us in Your Prayers!!!!!!!! (KUTP!!!!!!)
Merry Christmas and Happy New Year!!!!!!!!!!!!!
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