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Offically "probably NOT" MG
I had my Hopkins appoint today. The neuro doesn't think I have MG--they don't know what I have..but nothing straight forward of course. The SFEMG and posititive modulating Abs are non-specific b/c I also have a bunch of other autoimmune and inflammatory markers that are elevated.
They drew a boat load of blood and now I have to see their pulmonary and GI docs..I don't know how long that will take. My J-tube has been clogging or pulling out ~every 2 weeks and my docs down here want me to get one surgically placed...I was hoping to have a solution to this swallowing crap before it came to that. I'm totally frustrated..and apparently there is nothing that I can do. :( |
Big moose size hugs to you.
Sorry about the news. I'm hoping the doc will be brave enough and aggressive enough to follow up and help you on this. |
Oh, Eeyore, I'm so sorry! I know you were hoping for something DEFINATE - Why can't the docs figure this out? I can't even imagine what you are feeling right now, but I am so sorry. Know that you are in my thoughts and prayers:hug: Erin
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Hi Eeyore,
:Sigh:consideryourself:hug: How very frustrating for you, I really truly do hope they find something with all the blood they took. Take care, and keep comming back here!! redtail |
Eeyore,
I am sorry. Please keep the faith and stay strong. I will continue to pray for you (for answers & improved health).:hug: Nancy Lee |
I am so sorry you may need to start all over. Gosh, it seems life just keeps taking turns. Maybe you will find out it's something that can be managed better. I pray this is the case. :hug:
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HEy there!
Hey there!I just wanted to drop you a quick note and see how you are today/........I cannot imagine how frustrated you must be and I am so sorry for you. Do the docs have ANY idea of what you have, if not MG? I just don't see why it's so hard to diagnose you and give you the medical treatment you deserve:mad:. I'm still inb the hospital - 5 days of plasmaphoresis and now 4 days if IV IG - I was pretty worn down - but I was thinking of you:) Take care and stay strong! Erin
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So far it seems that the only consensus is that it is autoimmune..the current debate is CNS, muscle or some whole body syndrome or a mix of a few of these.
The neuro at Hopkins wants me to hold off on my regular IVIG b/c she thinks that the low dose I'm getting (0.6mg/kg) is not enough to do anything anyway. My past experiences with skipping doses has not been good---we'll see what happens this time erinhermes--I'm sorry to hear you are still in the hospital..are you feeling any better? |
Hey there!I was so glad to hear from you - I've been worried about you.......I truly cannot imagine how frustrated you must be right now, but please know that I think of you often (and pray for you). When do the docs expect ANY results from the lab work? Why can't they figure this out? I just don't understand:(...............I'm still @ the hospital - 5 days of plasmaphoresis and now 4 days of IV IG - I felt great yesterday afternoon, but am WIPED today, prolly b/c they never let me sleep here......they wake me up to give me xanax - crazy!!!!!!!! Hopefully I'll be home Tuesday. We'll see........
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