Tuesday, October 27, 2009

Sinking In

We've done a little more reading about James's hearing diagnosis from yesterday, and the literature seems to give a less optimistic view of the condition than the doctor did. Specifically, hearing aids don't always work, because the neuropathy causes problems with speech perception (especially understanding words when there is other noise). There seems to be a very wide range of outcomes. I'm not sure why the doctor was more optimistic than the articles we read; I think he's someone on the cutting edge of research in this area, so I don't know if he was just trying to be reassuring to us or if he actually has had more success in treatment than previous work would indicate.

We're still a bit in shock over the whole thing. All of the digestion and ostomy issues were (and are) hard to deal with, but at least there was presumably a light at the end of the tunnel when they would resolve. But this has the potential to be a lifelong serious disability. Right now it feels like there's a dark cloud over everything; there's a cold feeling in my stomach that won't go away, and our hopes for some kind of normal life seem like they're being shattered.

Mike rightly points out that even if we don't have good outcomes for his hearing per se, there are likely to be technological solutions -- voice recognition software and the like -- that can go a long way in helping James. And medical treatments are constantly advancing, so we don't know what might be possible five or ten years down the road. In the meantime, we're going to keep talking to him just like always (because maybe something is getting through), but we're also going to try to learn about other ways we can help him and communicate with him.

One thing that makes me sad is that I feel pretty confident that he could hear at some point in the hospital. Even when he was only a few days and weeks old, he would regularly open his eyes at the sound of my voice. His nurses tell us that he startled in response to loud noises, and we all thought that the music on his mobile seemed to calm him. So I wonder if he lost his hearing somewhere along the way. Or if not, it makes me sad to think of all the times we talked to him and read to him and soothed him and it wasn't getting through to him.

On another topic, the lab results for yesterday were improved. His direct bilirubin was down to 3.8, and the other liver function test was also improved. His sodium is still on the low side, though, so we'll be giving him a higher dose of that. (Apparently it's not uncommon for people to lose sodium through a stoma, and the Diurel for his blood pressure can also cause sodium to be washed out.)

20 comments:

Ann said...

I wish I had the words to comfort you but I don't! However, I believe in God the Almighty and anything is possible with Him! Once again, I have to say, if I took to heart everything I read, I would not be here today! I am not saying that you should not read up on Jame's condition but I am saying BELIEVE that he is going to beat the odds! I am still standing on it! That pit in your stomach is being a parent and wanting the best for your children!

Maybe try to find a support group that deals with this hearing issue!

Also, I know when one is tired and you two have to be on the point of exhaustion, things seem much worse! I am certainly not trying to be light about this situation but James has beat so many obstacles already and I know he will beat them down the road too! And he is going to have Matthew to help him! If he cannot hear you there sure will be alot more smiling going on in the house and touching! That is not a bad thing! James will be alright and so will you, BELIEVE!

I love you all!

Ann

Tanya said...

Melanie

What Ann says is so true in so many ways. Wikipedia medicine doesn't always paint an accurate picture. And regardless, if I considered only what the statistics indicated, I wouldn't have Julian or Lucy. I'm hoping for the best for all of you.

Much love,

Tanya

Niki said...

There's always hope. Always.

Yvonne said...

I'm so sorry you're having such a hard week. Your intuition may be correct about James' early hearing; I know from C's newborn experience that some antibiotics and other drugs can be ototoxic, but when they're lifesaving, obviously there's a clear choice. (C had to have her hearing tested at 6 weeks b/c of this potential issue after a round of IV antibiotics). May not be relevant in James' case, but I know you like more information rather than less.

We have a great 'baby signs' book that we'll bring you as soon as we find it, and we had really good luck getting Charlotte to sign a little from a young age (before she learned to speak), and we'd be happy to share our experiences with you. I can't imagine how overwhelming all of this is - please don't hesitate to ask us for a help (or just some company to talk about non baby things, if you want).

Anonymous said...

Stop being so selfish! You should be happy that James is healthy and actually was able to leave the hospital. Do you realize how worse things could have been? You should know by witnessing what other families have gone through. You are doing the boys a huge disservice by feeling sorry for yourself.

Lovely Wife George said...

I don't think you're being selfish at all here, Melanie (and Mike! Not trying to leave you out!). This is a loss--a smaller loss than others, but still a loss--that must be mourned if you're going to move on to doing what you have to do. Take care of yourselves, cry it out if you need to, whatever it takes to cope emotionally with this new issue.

You are a strong bunch of humans, and you will figure out how best to handle all of this. So far you've done great. I know it's a huge disappointment to have so many things go wrong, but as a little cartoon alien once said, "it's still good." ::big hugs::

Christina said...

Wow, "anonymous" is a real prize. Who trolls a parent's blog?

I'm so sorry to hear about this setback. But he will be okay. He is alive, and he is at home. He may or may not have hearing loss throughout his life, but he has a loving family, and friends, to help him deal with it. And yes, medical advances will come, and there will be technological aids and solutions. Hang in there; it'll be okay.

Mike said...

Anonymous: There is some truth to what you say, but the gush of emotions in the 12 hours after dealing with the new 'normal' hardly constitutes a pity party, and I doubt we are doing James or Matthew a disservice by this short period of adjustment. And yes, we have thoughht about how lucky we are compare to the terrible things that happened to other babies in the NICU. But taking comfort in the misfortunes of others isn't very satisfying. Instead, we'll regain our equilibrium, love the boys unconditionally, and look forward to a happy future with one another.

Anonymous said...

Mike and Mel... you've been through so much up until this point, you deserve to have a little bit of a "pity party"... this blog is a forum for you guys to work out your thoughts, almost like a therapy session. Ignore the comments of people that obviously don't know you or love you.
KIM

Anonymous said...

Hi Melanie, Hi Mike. I've tried to keep up with your news through Dave & Emily & the blog. I'm glad both boys are home!! My thoughts/comments come to you as someone who loves you & as someone who has spent her life working with kidos with some kind of special need. You don't seem to me to be feeling sorry for yourselves - but concerned for James. Keep talking to him! Talk to him so he can see your face as much as possible. He'll have the opportunity to read lips & to pick up from your facial expressions (which is part of communication whether one has hearing or not). A lot of parents are using sign language with "pre-speech" kids to help communicate. Even if there is not a significant hearing loss, signing could be beneficial for both boys. And if there is a long term need for augmentative communication, you as a family will already be ahead of the game. Matthew will be learning it along with you 2 & James which is exactly what you want to happen. I know that you have 16 gazillion professionals telling you what to do right now. Many from the medical world. From my experience they are not always very realistic when it comes to "real world living" & what is good from an educational perspective. Hopefully someone has told you about Early Intervention services. Here in Ohio that is provided through each county's Bd. or Developmental Disabilities. Where I worked (did you know that I retired?)services include staff with education, speech, occupational & physical therapy expertise. Something similar should certainly exhist in your area. OK - I'm off my "teachable moment". Love to all of you!

Nora said...

I haven't read, seen, or heard anything that suggests to me that Mel and Mike are feeling sorry for themselves or being selfish- they are having the normal emotions that any parents would have. Everyone wants the best for their children and these new developments and not knowing are going to take an emotional toll. If "anonymous" can't see that, I am not sure why he/she is even reading this blog!

Ann said...

I am with you Nora! It is not selfishness at all but the "hurt" the parent feels for their child! For only wanting them to have the best! I have to believe that anonymous has his/her own pain to deal with or has not experienced the love of being a parent! Whatever, they are in a place that I would not want to be!

Mel and Mike, please do not let that one blogger keep you from posting because I need those daily posts! I am too far away to check in physically and I need to know how all are doing, good or bad. And if you cannot share your feelings on this blog, well, that is just a shame!

Love

Auntie Ann

Christina said...

I heartily second the sign language suggestion. It really is great for all babies, regardless of hearing. We did it with E, and it was great at reducing her frustration.

Plus it'd mean Matthew would know it too, which will be invaluable for James growing up if he does have hearing loss.

Again, hang in there. Have you thought about restricting comment access here? I think blogger has different settings that might help.

Anonymous said...

Mel and Mike,
You guys rock. You and your boys have been through so many highs and lows over the past few months. You are in my prayers every day, and I always marvel at the amazing strength and courage you have demonstrated through this trial. No one who hasn't been in your shoes has any place criticizing you. Keep your chins up and keep doing the best you can for your boys-they are so blessed to have you as parents!
Love,
Mary Beth

Unknown said...

I'm with Niki! Hope reigns.
Love, Mom

Melanie said...

Thanks so much to all of you for your support, love, and advice. It really means a lot to us. (And yes, we definitely plan to do the baby sign language!)

To Anonymous, yes, we are well aware that things could have been worse, and we are very grateful for having James home with us. However, one of the range of possible outcomes for the diagnosis that James has been given is an inability to ever understand or use spoken language. While we hope that he's not on that end of the distribution, I don't think it's at all unreasonable that we would be sad and scared about what this might mean for our son's quality of life. Those feelings don't preclude us from hoping for the best and doing our best for him no matter what the situation turns out to be.

Anonymous said...

Anonymous, everyone here has been too polite to tell you to go fuck yourself. Oops, not everyone.

Mike and Melanie, sorry to rough up the comments section thats apparently read by your family and friends. But I'm sure theyve heard cursing before, so I hope no one is too offended.

I happened upon this blog by accident and have been following your story. The danger of the internet, you get strangers cursing and idiots commenting anonymously. Your story has been really moving and I have followed it religiously. I had a difficult pregnancy and my daughter has had some health problems so I feel like your story is a little bit familiar. I'm so happy that your little ones are home. Cherish them and they will give you back all the love you can handle and more, no matter what the challenges

Melanie said...

Anonymous II, I like your style! :) Thanks for the comment and best wishes to you & your family!

Leigh Ann and John said...

Mike and Melanie, John and I are still following your blog every day and our hearts are with you. Pain can close you off but it can open you up, too - in a good way. Thank you for staying open with us. Your courage and honesty is inspiring. We keep sending good thoughts your way.

craig said...

A bit **hug**. Mike and Melanie, and James and Matthew, you're in my thoughts. As always.