I have been avoiding writing an update for a couple weeks now. Last week was quite possibly the most emotional one I've had in this journey so far, and I'm only just starting to recover.
I met with my neurologist on Monday, to recap after my reaction to the Tysabri and my stay in the hospital. To sum up the meeting, we are now back to the drawing board with everything. I am looking for a new doctor, we are chasing a mystery diagnosis, we are trying a just-in-case treatment, we are ordering some tests...ugh. My doc isn't confident we have the right diagnosis, and every plan we have made up until this point has been tossed out the window. He is referring me to mayo clinic for a second opinion, and he is hoping a doc there can help us solve this puzzle. He all but quit my case, telling me that he still stands by the reasons he originally thought this was MS, but saying that nothing about this has progressed like MS at all. He said there are too many puzzle pieces that he doesn't know how to make sense of, and feels very strongly that I need a fresh set of eyes on my case.
I deeply respect his honesty, but I also feel completely lost and defeated. This feels like a cruel, never-ending labyrinth. I am so weary of all the uncertainty. I don't even care what the answers are anymore, I just want answers. And now I feel like I am facing this alone. I am sure there is a doctor out there somewhere who can make sense of this, but parting ways with Dr. Okuda is one of the most frightening things that could happen. He has been my champion, my constant voice of reason, the creator of all my strategies. Dozens of crazy symptoms could crop up, and I could stay steady because I knew our plan, and I knew our backup plan. And I knew that he would talk straight with me, tell me when something was a problem, tell me if he didn't know something, tell me if it was time to abort the plan. I guess that day has come.
The biggest mysteries at this point are that my lesions have been enhancing for a year (MS lesions typically stop enhancing after 6-8 weeks) and my lesions have failed to respond to every treatment we have tried. It's not to say we are facing the worst case scenario. It's just to say that nothing is a guarantee. All options are on the table, as far as a diagnosis. I am soooooo ready for this nightmare to be over. And instead, it's starting over. It's like someone just hit rewind, and the whole thing is about to play again. I just can't believe it. It's been a year, and we are standing back at square one. Strangely, today marks the one-year anniversary of my original square one. My first MRI, my first day in the hospital...it all happened on October 31st. It is so ironic, it hurts.
I have never prayed harder in my life. I just want this insanity to end. I'm taking a little break from being brave for awhile. As my friend Tara Schlappi Bodrero and her family say, I'm taking a "brave break." It's been awhile since I've had one of those, and I think it's long overdue. Still praying, still hoping, still walking forward, but I can't promise to be brave. Not for awhile anyways ;)
Thanks to everyone for your thoughts and prayers. I need them.
Hi Mandy,
ReplyDeleteI so do understand you- I don't have a diagnosis of MS, only a bunch of weird symtoms and unspecific small brain lesions plus 2 new gliosis that grew up in 3 months.. Your blog is very inspiting to me, it showes how to be optimistic and not to give up. I also would like to get answers why I feel so sick most of the time. Even the best doctor that I've met ( the fourth one) has no idea why I feel so miserable. Anyway I just think that medicine simply doesn't know everything about humans brain, and that's why the doctors cannot give us anwers. I will keep you in my prayers, and everyone else who is stuggling with diagnosis.
Greetings from Germany
Aleksandra
Mandy, I completely understand your heartbreak. Feeling so sick and consenting to endless invasive testing with the promise of getting to the bottom of things only to come up empty handed is so discouraging. I love the concept of taking a "brave break".
ReplyDeleteHowever you mentally frame it, you continue to process this uncharted territory and it's overwhelming emotional onslaught. You warrior on in the face of uncertainty. Thank you for making this journey a public one and bringing together a community of people who are outliers in experiencing atypical neurological journeys. We standby you from all corners of the globe sending you prayers, hoping for answers and healing.
Kim
Hi Mandy,
ReplyDeleteI am trying to reach you by email. Somehow I misplaced your original email in "cleaning" up my desktop. I did manage to write a post on your blog, which is a first for me, but would prefer if you could contact me via email. In the blog I recommended an article in this month's (Nov) Reader's Digest and a doctor by the name of Dr. Najjar NYU. YOu can find the entire article beginning on page l53. I also have some other info once I can email you again. Still praying, Karen Kelroy
Mandy,
ReplyDeleteI can only second what Kim and otheres have already eloquently said.
Sometimes we need to feel low. It's not self indulgent or a set back, it's just another way to gain prospective on what detection up is.
Take care! You are not alone.
H.M.