Posted 6/26/2012 6:39 PM (GMT 0)
I had the Linx Op a year ago & thought members might like to hear how things are since then & now.
Prior to Linx I was on high doses of Ranitidine, bottles of Gaviscon Advance & handfuls of ant-acids. I had tried every PPI on the market, but could not tolerate the side-effects.
I had all the tests, Mannometry, Ph, Endos, & they showed I had a Hiatal Hernia 2cms & a DeMeester score of 31.4 ( normal is around 14.7 )
My diet was becoming more limited & I seemed to be belching acid every time I ate. I was having to sleep with the bed propped up & life was fairly miserable.
I was offered the Nissan, but every instinct was telling me it was not for me.
I read about Linx in a newspaper, after Lewis became the first U.K. patient to have the procedure, & immediately started to research the procedure. It seemed a good fit for me & I got in touch with the clinic.
After sending all my test results & an appointment with the Consultant, I proved to be a good candidate, & a few weeks later I had my Linx fitted.
No problem whatsoever with the surgery - except for me telling them I don't do well on Morphine, they gave me some anyway & boy did I feel sick when I woke up!! I'd say my biggest problem the following day was lack of sleep!
I went home with mild pain relief which I didn't need & proceeded to follow the post-op instructions of eating a normal diet - small bites & portions, lots of sips of water & chew very well before swallowing. I was eating very small amounts between 6 & 10 times a day which is what my system seemed to want. All was well for the first few days & them I started vomiting large amounts of mucus every time I ate. The food stayed in, but I could vomit sometimes 4 times during the course of 1 small meal.
I was also getting a lot of pain at the base of my right ribcage after eating.
I went back to see the Consultant at the 2 week point, ( 7 lbs lighter ) & they were convinced they vomiting was due to saliva 'pooling' around the Linx, & the pains were Oesophageal Spasms, both of which should settle down in time. More water throughout the day to flush through the saliva & Buscopan for the spasms was the answer.
At that point I was pretty low & have to admit to wondering if I'd made a very expensive mistake!!
I stuck with it though, after about 5 weeks, things suddenly started to improve. The vomiting & the spasms stopped & I was able to eat on a more normal basis.
At that point I was still on the Ranitidine etc having been advised to reduce it over weeks rather than days, & I started to reduce the dosage. Probably too quickly as I did get the dreaded rebound & had to start again!! But as time went on I did stop all but the occasional Ranitidine. Food was getting much more interesting as I was able to add more & more variety to my diet as the weeks passed.
So where am I now?
Meds - I still take some Ranitidine as I have 'Variant IBS' affecting my stomach & it seems to help.
Reflux - I still get some Reflux, but it's not acidic.
Sleeping - I bought a brand new bed a few weeks after the op & have slept flat since I got home from hospital.
Food&Drink - Pretty much a normal healthy diet. I don't eat much Red Meat or Bread but that's more to do with the IBS. Unlike a lot of Linx patients, I eat loads of Chicken - maybe my system has just got used to it over time. There is very little now that I would be nervous about eating outside of my IBS issues. Alcohol is fine - just my v v low tolerance of it theses days as I hardly drank anything for a couple of years or more!! Fizzy drinks are still a no no as the gas just makes life uncomfortable. The mantra though is still Chew Swallow Pause.
Day to day living -Generally I only know I have the Linx if I try to eat or drink too much too fast. Otherwise it's when I get a build up of gas that wants to come up which can be uncomfortable. I can burp & vomit if I have to & do a lot more than before I had the device.Exercise is not a problem. Overall I am very glad I had it done & would not want to go back to where I was a year ago. It was worth a few weeks of misery for me.
I'm obviously aware of more recent Linx patients who are not having a particularly good time of it at the moment & I wish them all a speedy improvement. These are only my experiences & it seems that no two people deal with it in exactly the same way. I hope this is useful.