Wednesday, March 31, 2021

No Stomach No Problem? Really??

I really should have updated this on Monday. I’m so sorry I didn’t. 


After the MRCP I immediately met with my Dr. He could see what looked like to be a stone in the common bile duct. The only real option for somebody without a stomach is to have another surgery to get it out.  He reached out to some of his GI friends who do ERCPs everyday and they said ‘there is no way, that is extremely technical because of the anatomy’.  We talked for a while with him and felt a bit of a relief.  We know what’s going on. We know how to fix it. So I got on the OR schedule for Tuesday morning.  And Dr Davis said I could stay the night in the hotel as long as I was back at 7am. Which made me extremely happy. Matt and I walked back to the hotel - it’s about one and half miles. The weather was beautiful.  We got to see all sorts of flowers blooming and like I said I felt like a weight had lifted off my shoulders.  Got to the hotel, ate some dinner, took a nice shower, and went to bed. Sleep very well. Woke up before my alarm, which never happens by the way 🤣 And was ready to go. Packed up all my stuff prepared for another night stay in the hospital. 


We got through preop farely quickly and off to the OR I went.  This procedure was anticipated to only take about 30 mins.


As I was slowly waking up in PACU I start comprehending what people are saying a little more.  I hear somebody tell me I have a foley catheter.  Then somebody mentions a drain.  As most of you know, waking up from anesthesia can be a bit of a blur. I don’t know how or when I learned the surgery took 3 1/2 hours.  Or that I will go home with the JP.  The stone was nowhere to be found....again.  So my surgeon decided to do something to prevent a stone from getting stuck in the bile duct again. So we wouldn’t be doing this again in the near future.  Thank goodness!  I’m so grateful he made some decisions while in there to be proactive and not just decide to close me up.  


But what I do remember is a feeling of overwhelming despair.  Not that surgery didn’t go as planned. Not that I would need to go home with a drain.  Not about anything from today. An overwhelming despair that this is my life. And feeling like my life will forever be a medical mystery and there’s nothing I can do about it.  I described it to Matt, my mom and my Dr that it felt like I was in a downward spiral of a tunnel that just kept getting faster and faster and there was no way out. And the rest of my life was going to be this way.  In and out of the hosptial.  Always needing surgeries.  Not feeling how I want to feel - healthy!  I feel like normally I’m a pretty optimistic person and always looking for the good and positive in things. But last night I didn’t give a SHIT.  I know I said many things that scared and worried many people.  I told my Dr that I not mad at him or how surgery went. And I’m not. Everything he did while in there was thorough and understandable.  The stone was nowhere to be found....again.  So my surgeon decided to do something to prevent a stone from getting stuck in the bile duct again. So we wouldn’t be doing this again in the near future.  It all makes sense to me.  I told him I am mad at the world.  I told him he should be glad he wasn’t present 2 hours earlier when I was really steamed up. Matt, in his very rational mind, kept reminding me I just to sleep.  Dr Davis asked me if I wanted some Ativan to take the edge off emotionally overnight. I told him I didn’t. I said I need to work through all these emotions now while I’m having them since I can now (being here and not having much to do - well, other than heal up and all that’s involved with that). Better to deal with it all here than when I get back home and I’m with my wonderful kiddos.  He asked ‘are you sure? with an eyebrow raise.  I know he was worried about me too. When he left the room I took Matts advice and I slept.  I have no idea how long, but I know he sat in my room with me the entire time.  I have to add, in my fit of rage and despair, he really stepped up.  In ways I’ve never seen him have to do before.  In the moment I told him he was bossy, but I know he was doing and saying all the right things to help me.  


So after a good rest, I woke up more rational and feeling like everything is going to be okay.  I cried. I mean I’ve cried a lot. And that is okay. I was determined to let myself feel all the feels no matter what they were.  I’m still crying a bit this evening.  The sadness is not going to disappear in an instant. But I have really improved today. I got a REALLY good nights rest thanks to an amazing nurse. You can still be a thorough night nurse with good patient care and allow your patients to rest.  I woke up this morning still feeling pretty down and unmotivated. They forced me out of bed at 7am.  Sat in a chair for a few hours before doing much else. Several people, but mostly my mom and husband really pushed me. They told me ‘you know what you need to do to get out of there’. At the moment I didn’t even care. I didn’t care to get out of here. I would find myself just staring into space at times.  There was also a provider (one who actually kind of knows me by now) who came in to check on my pain and realized I wasn’t okay. He sat down with me. He took the extra 3 minutes to have a chat and be real. And he had many good suggestions. Acupuncture.  Massage therapy.  Guided imagery.  He asked if I was interested and I said absolutely but that I know their schedules are hard to work around. He said ‘it doesn’t matter.  I’m going there right now to light a fire’. And he did. Within 30 mins more people showed up at my door. Including a kind of counselor person. She sat and talked for about an hour with me.  It has been so validating to feel heard. Not one person tried to brush off how I was feeling. Not one. Every single person I’ve encountered today has let me feel my feeling. Has let me cry.  And because of that has given me hope.  I was never worried about healing physically.  I was extremely worried and still am a little about healing mentally and emotionally.  


But it’s nearing the end of the day here and I feel accomplished. I’m so many ways.  I went from not caring about much this morning. I mean, I had a foley and didn’t care. Yuck. To now being ready to say goodbye to the PCA and hello to oral pain meds. So hopefully tomorrow I can be discharged and stay the night in the hotel again with Matt.  I gotten lots of walking in today. My appetite is coming back to I’ve eaten a good amount. I’m still working on hydrating, but we can’t do everything at once, right. Glad I have IV fluids still. Haha. 


So just to wrap this up. Anybody going through a rough time. It’s okay. Let yourself feel all the feels. And if that becomes to much don’t be afraid to reach out to somebody. Anybody.  I know the best medicine for me right now is walking, talking to my family, laughing, and being able to at least see the outdoors.  But sometimes we need actual drugs to help us. And that’s okay too. Everybody is on their own journey. And we are all doing the very best we can. Let’s give ourselves grace and kindness...everyday.  ♥️

2 comments:

  1. Thank you for sharing your struggles. If you haven't been through some of these challenges it can be hard to relate to the feelings. I have been able to share with my sister who is also a seahorse. I got on rx after my tg because I found I just couldn't tough it out emotionally. I wasn't trying to avoid my feelings, I was overwhelmed by them. My son has this mutation too and it is very hard to 'be strong' for him. He is on the surveillance plan at nih but has been on rx for depression and anxiety since high school. Finding out that someday he will need to have his stomach out (most likely scenario) isn't helping his mood disorder. The worst part is that my sister has had a reoccurrance to stage 4. I am so mad and sad I have had to up my medication. I'll get through it but the whole thing just sucks! I need to cultivate more friends who will just listen and not tell me to put it in the past, move forward, etc. I'm glad I have seahorse friends and the cdh1 fb page to vent when needed.

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    1. Cheryl, I am so sorry I didn't see your comment until now. I have not been good about logging in here and checking for comments. I am so proud of you for taking the necessary steps to support your and your sons mental/emotional health. It's been over a year now. How are you two doing?

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