So i finally urged my neuro into an appointment.

He somehow had no idea i was hospitilized from the crisis a few weeks ago..

But its been a month since my last plasmapheresis and it only lasts about a month for me, so i figured out thats whats making me so weak. And Otp w my neuro he doesnt think the pred. is going to work. So im going to see him tomorrow and see whether or not to stay on the pred. or do plasmapheresis again.

Im thinking the plasmapheresis is going to have to happen, because a month in and, the pred. isnt working hardly atall.

Im sitting here, after taking a nap and my arms so so fatigued im hurting just writing this. My breathing isnt good, its hard to take a deep breath in, and its just not the normal way of breathing.


I hope i dont get there and hes like, oh you look good, just go home.

I want him to see how bad i am right now. Yet time will only tell.

Hope you all are doing well.

Tyson,

I'm going to be damn serious right now, ok?

Please read this and anything else you can get your hands on.

http://www.myasthenia.org.au/html/treatments.htm

And you ABSOLUTELY HAVE TO bring up the fact that you are on both Pred and Accutane. A call to your pharmacist will let you know what effect Accutane has on Pred - maybe. The two are NOT supposed to be taken at the same time!!!! Even one day may be too much (you said you were only going to be on Accutane for a little longer, which can do lots of harm).

And you may be on too much Pred.

WARNING: Going off of Pred too quickly can cause an adrenal crisis. You can die from that.

Something is not adding up. Maybe switching to Imuran or another immunosuppressant would help but those can take a LONG time to kick in too.

The bottom line is that you need help now. And if someone doesn't refer you to a pulmonologist, they are idiots. You have to have some kind of objective marker for your breathing so your neuro can SEE that.

Stand up for yourself. You know your body and how you are doing. And be completely honest with your neuro (not that you wouldn't)!

Annie

I hate when doctors say we look good. I want to FEEL good. Ask him if his eyesight is so good that he can see your neuromuscular junction . . .

Listen to Annie.. mixing those two meds is bad, bad, bad and don't just stop taking pred, you must wean off of it.

Please let us know what the Dr says and I hope you start feeling better soon.

You may have left for your appt. already...if not good luck. I hope you made a list of everything you want to discuss with him, it helps me a lot. Will be waiting to hear how you made out.

Hugs,
Pat

Very good Annie! "Ask him if he can see your neuromuscular junction." I love that and it made me smile.

Tyson, listen to Annie. Hope that you get help soon. Take care ~ Melanie

Praying for you buddy and let us know how things turned out.
Simon

Hope it goes well Tyson.

I also liked Annies bit about asking if he could see your NMJ! Hilarious!

Love
Rach

Annie- I completely feel you on the Accutane and Prednisone aspect, yet they do know I am on it, and when I went in yesterday, they asked if I was still on it. They said it was not an issue...so should I still call my pharmacist? I see where your coming from.

Yet this is how my appointment went..

He did the usual testing, pushed on my shoulders, made me look at his finger, etc, tested my leg strength. Then told me he didnt think the prednisone was working, but still wants me on it another month just to make sure that its not going to work. Because the plasmapheresis is worn off as of now, and im having trouble getting up the stairs, and such. -just trying to clean my room today was hard...

Yet he discussed options of Cellcept and Imuran after this next month w the pred. not working.

For the short term, so i dont go into resp. failure, he is trying to get me set up with plasmapheresis next week for 6 sessions to help w the bad symptoms that im having right now.

Hes hoping that the thymectomy works, yet as you guys know it takes a while to see.

But the thing that he said that bothered me the most was; "with some patients, they can excersize and maybe they'll have a bum leg, or eye after, for thats all this disease affects them w. Yet, you arent allowed to excersize AT ALL. No yoga, no walking, no running, no lifiting weights, no nothing, for I think its a life or death situation here, and you need to take this very seriously. If you push yourself, or even walk too much, you could without symptoms, have your lungs shut down, and not have time to get to an ER, and die. This is uncommon, yet your a patient that has to deal with it.'

So that was hard to hear, as you know I WANT TO BE ACTIVE. Its so hard! UGH.

Its so hard seeing all my friends go play basketball, and club soccer that im supposed to be on, going to all these tournorments and stuff and having to watch. And sit home and be a couch potato.

He says, usually in the patients that he treats their usually 60, and dont care about being a couch potato. But i do. im 17. I want a life. Its hard going through a regular school day. But now knowing that this disease could kill me, ****** me off even more.


Annie- about the pulmnologist, I WISH he would listen. I asked my neuro at UNC, (different than my reg. neuro) for a referal, he said no, because i didnt need one. Though my reg. neuro is getting me set up with a specialist at Duke, hopefully soon. They will probably have a pulm team to check me out at that app. Yet i dont know when that'll be..


Thanks for caring everyone. Im trying to deal with it. But its so hard.

I hope you all are doing welll

Ok, Tyson -- I may get yelled at by some other members -- but, I'm gonna go out on a limb.

I know NOTHING about Accutane and Prednisone -- but, I trust what Annie has to say.

I taught jr. high and high school and was a school counselor for 28 years -- so, I'm pretty comfortable with people your age -- and I feel like I understand your frustration.

I think that your neuro is WRONG. I think that you are in an exacerbation, plain and simple -- and that IF you give it time, you will regain "some" of your normal life. (This is the part where other members might get mad.)

Stress is a "killer" for MG. As long as you are stressed/uptight/frustrated/angry, MG is in HIGH gear. Sweetie, since I have first seen you post, you have not ONCE been calm. Love you, love you, love you -- you are SUCH a NORMAL teenage guy -- but, this does NOT "meld" with MG.

If you can somehow figure out HOW to get some PEACE with this BEAST, I truly, sincerely believe that this horrible EXACERBATION will calm itself down, your antibody production will kick OUT of overdrive, and you will go back to some semblance of normalcy. Will you be 100%? NO. Will every day be "da bomb"? NO WAY!! But, you will more like the old Tyson. I truly believe that.

Now, how long does an exacerbation last?? Three months for me. So, I am telling you that PROBABLY -- you ARE gonna have to be a "couch potato" for the rest of the winter!!! If you do a REALLY good job -- and REST PEACEFULLY -- you "might" be able to start "being Tyson" again by the end of March.

I know that we get angry in here when docs send us to psychologists or psychiatrists -- but, sweetie, I FIRMLY believe that EVERYBODY would benefit from some biofeedback/visualisation/cognitive therapy -- if nothing else, it ROCKS just to have somebody LISTEN to all of your problems and KNOW that it will be kept completely confidential.

A good counselor or therapist could give you coping skills to keep you from getting frustrated about having to REST. You may already be seeing somebody because of your mom and dad -- if not, ASK your aunt and uncle if could see somebody for some relaxation techniques. You REALLY need them.

Again, I feel VERY optimistic about you -- and I am a pretty seriously bulbar MGer who has had some scary respiratory problems. When I am NOT in exacerbation, I'm able to build up to walking a couple of miles a day (I'm 53).

Jana- Why do you think my neuro is wrong? I know it seems bold of him to say that, yet is his job. Id like to think hes wrong also, but maybe hes not, and i need to be careful for i could get into alot of trouble with this progression of my symptoms.

I do have a therapist and go every week, yet theres nothing ive found except for excersizing that helps me with this. and with this new information, i cant even begin to do that.

So what next?

I believe im in having an exacterbation aswell, yet pred. should be helping me and its not. Thats why ive opted to see a specialist at duke or unc to see which strand I have.

I am getting an antibody test, my neuro thinks i may have the strand which is very hard to treat. So, saying that, this is where my trouble may be coming from

Thanks for your feedback