Showing posts with label videos. Show all posts
Showing posts with label videos. Show all posts

Thursday, March 6, 2014

2007 CMN Miracle Awards: Dr. Ignacio Ponseti


How cool is this? LeVar Burton (a.k.a. Geordi LaForge in Star Trek: The Next Generation) and Dr. Ponseti in the same video! As a huge Star Trek fan, I'm geeking out.


I wish I could have had the opportunity to meet Dr. Ponseti in person. What an amazing man. I'm so grateful for what he's done for Peter, and all the children with clubfoot.


Tuesday, September 17, 2013

My Meeting with Dr. Segal

Ack, I didn't intend for an entire month to go by without a new post! It's been a very busy month, tying up loose ends at work and getting ready for Tiebreaker's arrival. I'm full-term today so we're in the home stretch!

I've been intending to write a more thorough description of my meeting with the pediatric orthopedic specialist who will be treating Tiebreaker's clubfeet. I don't have a ton of time at the moment, so here's basically a condensed version of what I wanted to write in a Q&A format.

Who will be treating your baby's clubfeet? Tiebreaker's doctor is Dr. Lee Segal at Phoenix Children's Hospital.

How did you find him? The day we received Tiebreaker's diagnosis (May 17, 2013), I visited Ponseti International's website and found their list of preferred providers, as listed by location. At the time, Dr. Segal was the only Ponseti-certified orthopedist listed for the Phoenix area. (Since that time, another doctor at Phoenix Children's Hospital has become Ponseti-certified!)

I checked with my insurance company to see if he was in-network (he was) and if I needed a referral from my OB first (I didn't). I called Phoenix Children's the following business day, explained about Tiebreaker's diagnosis, and set up a consultation appointment for August 8, 2013. The receptionist who set up the appointment was very kind and put me at ease, assuring me that Dr. Segal had treated many children with clubfoot and did a wonderful job.

Prior to the appointment, I read Dr. Segal's CV and watched the videos about both him and the Center for Pediatric Orthopedics, as featured on the Center's website:







On August 8th, I arrived at the appointment promptly at 4pm... and ended up waiting for an hour and a half. Apparently there had been some emergency and Dr. Segal was running several hours late. Luckily I had cleared my schedule for the evening (except for coffee with a friend, which I was able to postpone) and I had some Kindle books to keep me occupied.

The staff was very attentive to me and apologetic about the delay -- a nurse checked on me regularly to update me on how much longer it would be (I was in the waiting room for about 45 minutes, and then waited in a consultation room for an additional 45 minutes). They offered me snacks and bottled water  as well (I declined the former -- too nervous to eat -- but accepted the latter).

Finally, around 5:30pm, Dr. Segal came in. He had several other doctors with him, including the other Ponseti-certified doctor, a student doctor, and another doctor whose function I can't remember. We sat and talked for about 30 minutes. I liked him immediately. He was very kind, very personable, and put me at ease right away.

He asked about Tiebreaker's medical history so far, how my pregnancy was going, what research I had done, etc. I offered him the DVDs I'd brought with me that contained the ultrasound images of Tiebreaker's feet, but he didn't feel it was necessary to see them, given that he'd received and read the ultrasound report. It was impossible, he explained, to judge the severity of the clubfoot based on ultrasound images; it was just best to wait until the baby was born and he could examine his or her feet personally. He also explained the treatment process and asked if I had any questions.

Of course, I did -- I had an entire list that I'd been compiling since May. These are the questions I asked, and paraphrased versions of his answers:

When do you recommend starting casting? Do you recommend beginning within days of baby's birth? Dr. Segal answered that he recommended starting casting within the first two weeks of the baby's birth, assuming the baby was otherwise healthy and doing well, but the exact timing was flexible depending on what the parents wanted.

He asked when I would prefer to start treatment, and I explained that I only had six weeks of maternity leave so I was hoping we could get the baby out of casts entirely by the time I had to go back to work. Given my short leave time, my preference was to begin as soon as possible. He said we could definitely work out a schedule to our mutual satisfaction once the baby arrived.

Baby wearing - I'm thinking of the Baby K'Tan sling and the Beco Gemini. Do you have any recommendations? He said he didn't have much experience with babywearing and advised me to talk to other mothers of kids with clubfoot for advice (I already had by that point, and the two slings I mentioned above were the most recommended by them -- I've already purchased one of each!).

Do we need to have a pediatrician for the baby, or can we continue to use our family practice doctor? He said that a family practice doctor was fine (assuming baby was otherwise healthy).

Tenotomy - do you perform the tenotomy under local or general anesthesia? Dr. Segal said that in a baby with unilateral clubfoot (when only one foot is affected), he used local anesthesia, but for babies with bilateral clubfoot, when both feet were affected, he preferred to use general anesthesia, since two tentomies at once could cause more pain, moving around, etc. 

What boots/brace combo do you recommend once casting is done? He recommended the standard AFOs and Ponseti bar as sold by MD Orthopedics. I asked about the Dobbs bar, and he said that it was an alternative option if the Ponseti bar didn't work well, but he recommends trying the Ponseti bar first as he's seen the greatest success rate with it.

Will we get boots & bar through this office or will we order them independently? He said that the office would help us with the ordering process at our last casting appointment, and that there was an orthopedics shop not far from the hospital that had clubfoot paraphernalia in stock, so likely we could purchase what we needed the same day. Eventually, he's hoping to stock them in PCH itself.

I think I asked additional questions but I can't remember them. :)

Dr. Segal gave me his personal business card and told me to e-mail him directly as soon as the baby was born, and he would take care of setting up our first casting appointment himself.

I input the information into my iPhone immediately, and it's a good thing I did. I put the card in a folder of materials (printed PDFs explaining about clubfoot, the treatment, the importance of following the bracing protocols, etc.) I'd been given at the outset of my appointment, and then I promptly forgot to take the folder home! (I had to rush to the bathroom after the appointment and I think I left them in there -- oops!) But I already knew that the PDFs were available on the website for download, and I had the business card info in my iPhone already, so I didn't worry about it.

I feel much more settled and confident knowing that we have a good care provider for the baby and a basic treatment plan in place. Now all we have to do is wait for the baby to arrive and our clubfoot journey will continue (and hopefully I'll post more often). :)

Friday, August 16, 2013

My Favorite Resources and Information about Clubfoot

I believe that information is power. Whenever I'm interested in anything, I research the heck out of it. Tiebreaker's diagnosis was no different. In the weeks following the initial ultrasound, I spent most of my free time doing scouring the Internet for information. I also had a lengthy e-mail correspondence with an online friend whose daughter has bilateral clubfoot. Here are the most helpful resources I've found.

Blogroll

On the right, I have a blogroll of other blogs of parents on the clubfoot journey. If you have such a blog and would like to be added, please leave a comment or e-mail me!

Books

I couldn't find many books about clubfoot written for the layperson (i.e., a non-medical professional). The Parents' Guide to Clubfoot by Betsy Miller is one of the very few available.


It was written in 2012 so the information it contains is very current, and it's available in paperback, for Kindle, or for Nook.

I purchased the paperback version because I only have the Kindle app for iPhone, and I thought any pictures or diagrams would be more easily visible in the paperback as opposed to my small iPhone screen. Also, there's a section at the back that contains a book for kids about clubfoot, and I thought it would be easier to read it to them from the actual book. If you have an iPad or an actual Kindle or Nook, though, I think the electronic version would be just as good.

It is an excellent resource, and I highly recommend it for any parent of a child with clubfoot or even for anyone who wants to learn more about the condition. It has helped me feel more prepared for our baby's treatment, and contains many success stories from other parents. She also has a chapter about finding a Ponseti-trained care provider, "red flags" to look for when interviewing care providers, and information about online support groups that will be helpful for any parent whose child's clubfoot was diagnosed prenatally, as Tiebreaker's was.


PDFs

The staff at Phoenix Children's Hospital Center for Pediatric Orthopedics, where Tiebreaker will be treated, gave me a folder with several concise, informational PDFs about clubfoot, and I was pleased to see they were also available at their website for download.

Support Groups Online

The best online support group I've found is the Yahoo! Group nosurgery4clubfoot (this group is also highly recommended in Betsy Miller's book). So far, it's been a valuable source of information, and it's great to be able to chat with other parents who are on the clubfoot treatment journey. 


Facebook group - Clubfoot is Treatable 


Videos

This page on Clubfeet.net contains six YouTube videos about clubfoot. The first four comprise a complete documentary about clubfoot and the Ponseti method of treatment -- I found these very informational and helpful. The last two videos are of various medical professionals discussion clubfoot and its treatment.

This video features the doctor (and the facility) who will be treating Tiebreaker's clubfoot! I met him for a consultation appointment on August 8 and was very pleased by his knowledge and his manner.



This is another video about the treatment of clubfoot by Phoenix Children's Hospital, the facility where we'll be taking Tiebreaker for treatment, and again featuring his or her doctor. It also contains interviews with several parents who had their children's clubfoot treated there.





This video was created for the University of Iowa Department of Orthopedics, where Dr. Ignacio Ponseti (creator of the Ponseti method of treatment) practiced, for the purpose of promoting Dr. Ponseti's work. This a great peek into the history of Dr. Ponseti's method and his success with it. It was made while Dr. Ponseti was still alive, and the director was able to meet with him prior to his passing.






Websites

There are a ton of websites relating to clubfoot out there, but these are my favorites:

Ponseti International - a must-visit for any parent. The first step in the journey to find a care provider should be their list of Ponseti-certified physicians. It's important to find a doctor who strictly follows the Ponseti protocol (and who, preferably, learned the method from Dr. Ponseti himself and/or at the University of Iowa).

MD Orthopedics - the go-to site for the "boots and bars" brace that all kids with clubfoot wear after the casting process is completed.

Footnote Film Project - there's a documentary in the works about the treatment of clubfoot; they're currently fundraising to film internationally. Looks like a neat project!

Tony Spineto, Clubfoot Triathlete -  Tony is an endurance athlete who was born with bilateral clubfoot. He seeks to encourage and educate children with clubfoot and their parents, and he's currently writing a book about his experiences.

To Parents of Children Born with Clubfoot - a message from Dr. Ponseti, hosted at the University of Iowa Children's Hospital site, discussing why it's so important to get a child's clubfoot treated properly.