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Holly's Blog
Author: Holly Created: 10/3/2008 8:02 PM
This is a unique support group started because of my experiences as the spouse of a PKU adult. There is hardly anything out there for adults with this condition and nothing for their significant others. I do not want others to feel alone in the battle to keep a loved one healthy.

 The battle for formula coverage is one many of us are familiar with. Here is our side.

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 PKU picnic and Walk-for-Research time!

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With working a couple of jobs, it has been dificult to maintain this site and all the other things I do on the side. However, I had to stop in and share the great news. Owen is starting to put on weight again! It started with him deciding to start fixing up the basement. He wants a workshop down there and has been building shelves and counters. Then, it continued with that large snowstorm last weekend. He tried so hard to be outside shoveling and clearing paths, even though the effort sent his heart rate way...

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We have just seen first hand what it is like when a PKU adult gets ill. Now, you must remember that Owen has complications that many PKU adults do not have (chronic low weight and hypoglycemia). However, you are still dealing with a person whose body does not work the same way ours do. You cannot give them chicken noodle soup. With their limited diets, not feeling well and not wanting to eat because of it can be a bit more risky.

 

Last Monday, Owen came home complaining of chest congestion and...

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At the UVA picnic we signed up for a free box of the Loprfin rice. It came in and Owen LOVES it! It was really easy to measure and make. I served it with Tasty Bite brand Pubjab Eggplant. It is a spicy blended eggplant sauce that he likes. It made a fairly large meal, but he cleaned his plate. Looks to me like we will be ordering a case of the stuff. YEAH!

 

We went to the DC Green Fest today and came home with more samples and more recipe ideas. It was at the festival last year that we were given...

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We had the UVA PKU picnic a few weekends ago. It was great to see familiar faces and catch up on the latest and greatest. I did a presentation for Ryan's PKU Foundation and the NPKUA. It went well. However, it also was a wonderful example of why Diet-For-Life is so important. Visiting with us that day was the first baby diagnosed at UVA with PKU. He is now 60 and it was heartbreaking. The brain damage was very, very apparent, he is....well, he is very low functioning. It was so sad. There was a 19 year old who...

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It has been nearly a year since I stared this blog as a support site for the loved ones of PKU Adults. While it looks like there has been hardly any activity here, quite a few people have responded via my Facebook page or in person during various PKU events. Recently, I sent information to NPKUA and hope that they might link this page to theirs. The UVA PKU picnic is next weekend as well, and along with hte NPKUA survey, I will have cards out with the info for this blog too. Now, more than ever, is the time to show support for the adults with this condition. They are being left behind and so are the ones who love them.

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