Erin,

First IVIG was done over 2 days and was termed “loading dose”. It was done in an outpatient infusion center. I had a bad reaction to it and for other reasons, switched Neurologists. The new Neuro wanted to continue monthly infusions but lowered the dose (and switched brand) of IVIG given over 2 days each month. I don’t think it’s working. Those good days I’m having could just be typical MG good days. They don’t last long.

Regarding how I felt last night with not being able to swallow, it was the soft food (mashed potato consistency) which I could not get my throat to move! I could drink water and swallow dryer food. The slurred speech and tiredness were bad and I upped my dose of Mestinon, waited for it to kick in, then fell asleep. I had no breathing issues last night. Today, I’m so very tired, can’t walk or raise my arms. I’m feeling bad but I am not having trouble breathing, although if I push myself to move, I do have shortness of breath.

Barbi-girl

I guess the "loading doses" have gotten cut along with so many other things that are medical. When I began, I had 5 consecutive days in a row with a full dose, followed by one day a month. That was not enough, and I went to every 3 weeks, and eventually went to subq IG. It never really worked. I was a lot like you. I also took Cellcept for about 15 years.

The only thing that has worked for me has been Rituxan. That and Solaris really seem to be making some lasting difference in the lives of folks with MG. Personally, I've had 3 doses of Rituxan since January 2017, and am now on no other MG meds and also am 97% symptom free.

Keep looking for options! The more "failures" you have the quicker you may be able to try one of the "big gun" meds. In the meantime, be very careful. I'm sorry you, too, are suffering.

Barbi-girl, You can't wait until May for further treatments. If you are as bad as you say, a more urgent call to the neuro and/or a trip to the ER is in order. As these guys have said, if IVIG is not working, there are other treatments to try. Plasmapheresis can be done in the hospital.

Don't get to a point where you can't do anything (like even dial 911!). You need immediate care. Did you tell your neuro how badly you are doing? Some people need IVIG more often, or another treatment. To just drop something without adding something else is fairly dangerous!

Sometimes it helps to have another person speak for you. That might scare the doctor into action! But don't you be scared. Just get the help you need NOW.

I hope they can find a regimen that works for you!


Annie

Annie....I am going to send him a message tonight. He’s really good about responding to emails. I am feeling so bad today.

Barbie I'm going through the same thing. IVIG hasn't never worked for me. I just finished 10 IVIG's and nothing. Went to neuro he cut my statin (for heart stents) and I feel a LITTLE better but we are starting process for Soliras. Waiting for shot. He said Rituxan was too rough for me since my case is very complicated (4 different antibodies). I wish you the best. Best thing for me is no breathing issues. Keep us posted.
Prayers
Mike

I just sent my Neurologist a secured email and laid it all out, how my symptoms are getting worse plus I now have new ones. This is stressing me and the stress is a bad feedback loop for MG deterioration. I do not expect a response from him until tomorrow morning, but he will respond.

I didn’t mention this, but I also have fibromyalgia (over 10 years) and the stress of the worsening MG has caused a fibromyalgia flair and I’m in pain. Again, it is a bad stress feedback loop.

Since I’m seronegative MG, diagnosed by a positive SFMG, I don’t know what treatment will be appropriate for me. Is 6 months on Cellcept long enough to judge it’s not working? For sure, IVIG is not effective. Could the prednisone taper be the root of the deterioration? The last dose lowering was 3/16, so it seems unlikely. I’m due to lower again at the end of this week.

Barbi-girl

One more thing, my experience with the local ERs has been nothing short of pitiful. One ER physician asked ME what Myasthenia Gravis was and could I spell that for them. The other ER physician doubted I had MG (even though it was documented in my MR) and said I was having anxiety causing breathing issues so discharged me. I’m not putting myself through that again unless I’m close to death. It’s just humiliating and a waste of time.