Child In Pain: migraine surgery

Showing posts with label migraine surgery. Show all posts

Wednesday, February 1, 2012

Migraine surgery, part 1

January 17th was The Day: migraine surgery for Harriet. Here is the list of all the procedures they did to my baby (well, she's 16 but will always be my baby!):

1. Bilateral endoscopic release of the zygomaticotemporal branch of the trigeminal nerve
2. Septoplasty
3. Turbinectomy
4. Bilateral decompression of the greater occipital nerve, partial resection of the semispinalis capitis muscle and bilateral subcutaneous flap to shield the nerve
5. Third occipital neurectomy

The surgery took almost four hours. When surgery was over, but before we got to see Harriet, the surgeon came out to talk with us. Everything went just as planned, and he also found a blood vessel on her right greater occipital nerve - one big source of her pain - so he removed the blood vessel as well.

Harriet went into surgery with her usual pain level of 9 on a scale of 1-10. She woke up from surgery with her pain level at a 5. When she said that, I gasped and started to cry, and then the nurses (who were FANTASTIC and took great care of all of us) started to cry too. Of course, as the nerves woke up over the next few days and we dealt with all kinds of post-op yuckiness like drainage tubes (ew!) and nasal tubes (ow!), her pain got worse... But the primary pain is related to her surgery and not her migraine.

That's right! She still has migraine pain but it is definitely BETTER. Better after a year and a half of constant, debilitating pain. Better after an army of neurologists told us there is no cure, she needs to deal with the pain because it will never end, she's just stressed, she wants attention, or (my personal favorite) there's nothing left to help her but psychiatry.

It is so exciting to even contemplate that Harriet might get back to a normal life.

The surgeon tells us it will take 3 to 6 months to know for certain just how much relief she gets, but the initial results are VERY encouraging. Her biggest complaint now is that her scalp hurts and is super-sensitive. This is a common side effect of the greater occipital nerves finally being decompressed - they get "angry" and cause more pain for a while. It hurts to let anything touch her head, which means she is only sleeping a few hours here and there, so she's exhausted. But this pain will pass, leaving Harriet with either a greatly reduced migraine or (prayerfully, hopefully) no migraine at all.

This has been a hard couple of weeks, but Harriet, her dad, her sister and I can tell that we have done the right thing. Now, we sit back and wait for the healing. I'll blog a little later about some of the post-op specifics and some of the things along the way that have surprised us about this experience.

Please, Lord, let this be it!

Monday, January 16, 2012

Is this it?

Well, I haven't wanted to jinx it, but it is finally here...

Harriet is having migraine surgery tomorrow. They are decompressing the greater occipital nerves at the back of her head; removing a tiny nerve branch near each temple; correcting her deviated septum; correcting a "paradoxical turbinate," or as I call it, a weird-shaped thingie in her nose; and, while she's on the table anyway, removing two moles from her back.

The surgeon is quite confident that this will give Harriet significant migraine relief. As in, this could stop the perma-migraine she has had for 18 months straight. She could go back to being a regular teenager who just gets migraines once in a while. She could get her life back!

I'm afraid to hope, but also afraid NOT to hope.

Recovery will be painful, not to mention gross. She'll have tubes in her nose for a few days, as well as drains COMING OUT OF HER HEAD (ew) that I have to change every four hours for the next 3 to 5 days. I picked up all of the post-op meds today, and will spend an exciting evening getting all of this stuff organized so I can manage my kid's pain without OD'ing her.

Some people wake up from this surgery and can already tell that the migraine is gone. Others take a few months as the nerves have to settle down after being compressed and in pain for so long. And some find out that the migraine stopped at the surgery sites but, surprise, they also need the forehead nerves done too (which we would have to do 6 months or more from now).

We are just praying, and hoping.

Maybe, just maybe... Maybe this is it!

Subscribe to: Posts (Atom)

Timeline: My Child's Pain

July 17, 2010: Harriet got a migraine – pain, light and sound sensitivity, nausea, the whole shooting match. She’s had them a few times before, so no worries – we just gave her her meds and put her to bed. But it didn’t work this time. Before the month is out, we’ll go to her doctor twice and the emergency room once, complete an MRI and bloodwork, and we’ll start chiropractic care.

August 2010: Still trying different meds and Harriet has to drop out of cross country. Another trip to the ER.

September 2010: Local neurologist has “tried everything,” including various meds as well as trigger point injections. Harriet is referred to a pediatric headache specialist.

October 2010: We give up on chiropractic, which only seems to be making things worse. Pediatric neurologist tries different meds and sets Harriet up with a pain psychologist and biofeedback. Bloodwork shows a CoQ10 deficiency.

November 2010: The migraine is worse than ever. A one-week hospitalization with meds that make Harriet throw up every 6 hours help her pain very little. By now, side effects from meds have made her lose about 20 pounds, and she was slender to begin with. We worry about her weight but continue to try everything the doctors recommend.

December 2010: We see a neuromuscular dentist, who diagnoses TMJ and recommends a $5000 dental orthotic that he says will help, so we get Harriet fitted for that. She mourns the fact that she can’t be on the basketball team this year.

January 2011: Small improvement with the dental orthotic, but not enough to improve Harriet’s quality of life. School is a struggle. Revolving door of meds gives Harriet terrible side effects, including panic attacks.

February 2011: Headache is getting worse again. Lots of missed school. We’re getting adjustments to the dental orthotic every two weeks.

March 2011: Harriet is frantic with pain. The pediatric neurologist admits her to the hospital again. A spinal tap shows nothing out of the ordinary. Five days in the hospital and nothing works. Another pediatric neurologist examines Harriet for less than 5 minutes and says, “There’s nothing left for you but psychiatry.” Harriet is inconsolable that there is no hope. They discharge her from the hospital with her pain at a 10 on the 0-10 pain scale, with no recommendations for what to do now. We decide to try going to Diamond Headache Clinic.

April 2011: A full week in the hospital in Chicago with the Diamond Headache Clinic. No new diagnostic tests, although bloodwork shows mild anemia. Harriet’s pain goes from a 10 to an 8. DHC puts her on an MAOI, which comes with all kinds of restrictions for diet and other meds that can have life-threatening interactions. We start cranio-sacral physical therapy to help with the muscle pain in Harriet’s neck, back and shoulders.

May-August 2011: No real improvement in pain, but the MAOI is making Harriet gain 10 pounds a month. She is stressing out about her weight and has stopped sleeping altogether. She stays up around the clock most days. Counseling helps us all deal with the stress of chronic illness. The one bright spot is physical therapy, which is really helping her muscle pain.

September 2011: Harriet is switched to a different MAOI, which resolves the sleep problems but the weight gain continues. No improvement in her pain. Our doctor leaves the practice at Diamond Headache Clinic so we wait to see a new one there in October

October 2011: We meet the new DHC doc: Dr. Personality. Her first question is, “How is the depression?” It goes downhill from there. At our insistence, Harriet is taken off of the MAOI. By now she has gained almost 60 pounds with no improvement in her pain, so why keep on this path? On our own, we take Harriet to an ENT, who says her “migraine” really sounds like occipital neuralgia to him. He does a nerve block in his office that gives Harriet the most relief she’s had since this started. ENT orders an MRI of Harriet’s sinuses and neck, and refers us to a local pain management doctor.

November 2011: Pain management doctor agrees with the occipital neuralgia (ON) diagnosis and does a more precise nerve block. More relief for Harriet. We start researching ON and find out about nerve decompression surgery. Dr. Personality scoffs at the idea of decompression surgery, saying it’s “too soon” … when Harriet has been in pain for well over a year. We ignore Dr. Personality and schedule a consult with Dr. Fancypants, a plastic surgeon who does decompression surgery, to see if Harriet is a candidate. We’ve stopped all meds except a muscle relaxer and Harriet is less of a zombie now.

December 2011: Another visit to Dr. Personality, who again asks about depression. When asked why she keeps bringing that up, she says, “Well… Harriet seems quiet.” We remind her that Harriet HAS A MIGRAINE. Undeterred, Dr. Personality wants to re-try antidepressant meds, and we refuse. We don’t schedule another appointment with Dr. Personality, and we go see Dr. Fancypants for our consult. He is wonderful, his nurse is wonderful, and he recommends nerve decompression surgery as well as sinus surgery. Harriet seems hopeful and encouraged for the first time in months and months. We hold our breath to see what the insurance company says.

January 2012: To our joyous surprise, our insurance authorizes coverage of Harriet’s surgery.

More updates to come…