After the Passport America rally we decided to attend a rally of our Camping Friends. Some of our grandkids were out of school for the Easter Holidays so we planned on them joining us for the rally. There was a mix up with what days the grandkids would be able to join us, so I schedule doctors appointments in Houston. After the grandkids joined us we left to attend the rv rally up in Coldspring, Texas.
Here is a couple photos from the rally.
Sue, Austin, Weston with Trevor in the back. (with the Astros stuff) on our hiking trip.

After the hike, we sat around one of the trailers and enjoyed the each other’s company. Sue Yoder and Marvin discussing all the world’s problems! 

Marvin, Jodi, Gail and Darlene listening intently to Sue Yoder.

Ralph gives his approval.

Tom doesn’t quite believe all the lies that are being told.

The RV park and our camping friends had all kinds of activities for the grandkids and all attendees to participate in at the park. There was a scavenger hunt on the hiking trails, Easter egg hunt, bean bag baseball, volleyball, horseshoes, rental bicycles and a few others I can’t remember. We also had a potluck that the RV park had and they supplied the meat. It was all very good!
We left on Easter Sunday after the rally and headed down to Victoria, Texas. Our good friend Richard King, was having a heart catheter done on Monday and we wanted to be there for him and Patsy in case they needed anything or any help. Everything turned out well on his heart catheter, so we are still parked in his driveway.
Saturday we will be traveling with them to San Marcos, Texas where we will be attending an Allegro Club meeting. Tiffin’s Allegro Club is trying to start a San Antonio/ Austin chapter. Richard got a letter asking for him to attend and he invited us to go with them. We will see how that goes.
Health Update
For those that haven’t been reading my blog, I will try to get you up to date. I was diagnosed with pulmonary fibrosis back in November 2011. With the pulmonary fibrosis I found out that there is no cure (except lung transplant) and no treatment. A good friend of ours from our Lonestar Allegro Club put us in touch with a doctor at Baylor College of Medicine that was doing clinical trials for pulmonary fibrosis. So they had me do a pulmonary fit test, CT scan and echocardiogram on Monday, April 2. I then had my appointment the next day with Dr. Frost, the doctor doing the clinical trials. First off she informed me that my lungs were now at 25% capacity down from 50% capacity that I had back in December 2011. Since they were now at 25% I was not acceptable for clinical trials. She also said that it looked liked my heart had a myxoma/growth near one of the valves. In her opinion my lungs were too bad for heart surgery and the heart was too bad for lung surgery. Catch 22!! What a shock!!!
But she then said “I am not a cardiologist, so I want you to get a MRI and let a cardiologist looked at it” So Wednesday I had a MRI done that was supposed to last 1 1/2 hours, but lasted 3 hours instead! Apparently to take good pictures of my heart they needed from me to hold my breath. But they wanted me to hold my breath for about 20 to 30 seconds. First I had to take a deep breath, then blow it out and then hold my breath. Well there was no way I could to that. So they had to adjust how they were going to take the pictures with the MRI. Well after all that, they discovered that there was no growth in my heart but a large Eustachian valve. GREAT NEWS!!!
We have now been referred to a lung transplant team for evaluation. We now have a tentative appointment for Monday, April 16th to meet with them. The reason I say tentative is that they are having difficulty getting in touch with my case manager at Cigna, my insurance company. I sure don’t need them to be dragging their feet about getting me to meet the transplant team. Now once we meet with the transplant they have to evaluate me to see if I am a good candidate for a lung transplant. They want to make sure that when they do a lung transplant that the person that gets it has a good chance of survival (no other medical issues, cancers, heart disease, etc.) So the first hurdle is the insurance company approval, and the second hurdle is if I am a good candidate for the transplant. If I get approved as a good candidate that I am sure there will be many, many more hurdles to go through. 
They have also put me on oxygen for any exertion, like going shopping, hiking with the grandkids, washing the motorhome, etc. So that is something I am going to have to get use to.
I will know more next week and will post to let everyone know!
Until next time!