NeuroTalk Support Groups - Very weak and becoming very frustrated

I would like to share what my doc found. Hope it helps.

I had soooo many health problems 4 years ago. Muscle spasms, twitches, asthma from acid reflux, severe pain in sciatic nerves on thighs, bouts of weakness that made me feel my life's essence was draining out my abdominal region.

My Doc tested me and found that I had almost no hormones of any kind, except estrogen, since it's everywhere in our environment. Also low in Vit D.

So now I am on progesterone, testosterone, and armor thyroid and vit D. Graduated from being on pregnenolone, and dhea. He said it was from ADRENAL FATIGUE from years of unrelenting stress. Regarding the asthma from reflux, that was from a low thyroid, since this makes your muscles and ligaments weak. The stomach has a sphincter muscle.

Now I am mostly normal. But occasionally have hypoglocemia from the low thyroid. The meds help, not cure. Was told to eat protein. This did not work for me, but I discovered if I EAT OATMEAL with breakfast, even if I don't want to, I tend to avoid becoming weak throughout the day. If I miss and get weak, there is no fixing it the rest of the day.

God Bless. Hope you all get better.:)

Quote:

Originally Posted by sunflower1116 (Post 901294)

I am a 25 yo F who works in the medical profession and was extremely active. After a miserable and frustrating, yet mild, Winter 2011 in NYC I was finally diagnosed with MG- and also told I had had it for 15 years (I have had ptosis and double vision that long).

I know many of you have difficulty reading long posts so I will try to keep myself brief. I need some advice/help.

My diagnosis via SFEMG MS was also ruled out just as a precaution- and in some magic most likely never to be repeated in the history of medicine- 3 neurologists agree I have MG. As of now I am Sero neg and MuSk neg. My Thalmus is fine.

Initally I was put on Mestonin, but it made me weaker and I was hospitalized because I could not clear the excessive secretions in my throat. Even when we played with the dosing it didn't matter.

We started IVIG and initially I thought it was the miracle all the nurses were calling it, but 4 months later I still feel like crap; I am realizing that the IVIG in the hospital worked because I was laying in a bed not doing anything, and not in my real life.

At my last visit my neuro mentioned doing plasmapheris, but we ruled that out because I am Sero neg and MuSk neg- she stated there is one more kind of type to test me for (a genetic autosomal recessive) but it would require a muscle biopsy and her hospital doesn't do them she needs to send me somewhere and isn't sure where she wants to send me. She also said treatment would be radically different because the type doesn't respond to IVIG or plasmapheris; which is why she thinks this is the type I have, but we are going to keep doing the IVIG anyway.

Does anyone have any idea what the heck she is talking about? Does anyone have and suggestions for me?

I have already cut everything out of my life except for work & IVIG. I don't even walk up the stairs in my house anymore, I use a chair lift- which is actually extremely depressing for someone who used to walk up 5 flights to her office.

When all this started I wanted to get back to the "old me." Now I just don't want to be exhausted and feel like I am dragging 50lb weights on my limbs by 10AM anymore.

Sorry I ran on for so long. I appreciate all of your suggestions.