Hey guys, hope you guys are feeling strong.

I think the cellcept may be finally working to an extent, yet im not even close to full power. I might be about half, yet its working more than usual i think...but with that is more side affects...is it worth having memory loss over?


Ive been having short term, and long term memory loss (long term like what i did yesterday) Short term like the other day i was driving down the road, and forgot where i was, and where i was going.

Ive also been having slurred speech and stuttering for the past couple days, and ive just been very confused, and dazed. Ive put in a call to my neuro, and usually they get back to me very fast, but its been two days and nothing has come of it yet. I cant be having this happen to me, what if i were to forget where my house is? Im 17, not an 80 yr old with alzhiemers. Honestly. But its not that bad, its just somethings i forgot, and with classes, its hard.

Has anyone else experienced this problem? Im sick of side affects. How do you deal with them? Ive started being able to deal with the MG to an extent, but the side affects are so hard.

But anyway, hope you feel well.

This is beyond side effects.

http://www.americanheart.org/present...dentifier=4742

Go look in a mirror and smile. Is there one side of your face drooping more? One side that feels weaker? A one-sided headache? Yes to any of those or the other symptoms from that website, which you already are describing, and you need to go to the ER. Actually, you need to dial 911. Why? Strokes need IMMEDIATE care. The sooner you get care, the better the chances of reducing the damage.

I am so tired of your doctors not taking this seriously. Side effects can kill you.

I'm past being concerned and have progressed to being ticked off (not at you). No one has even bothered to do an MRI or MRA. Enough already. Get some damn help.

Annie

And no offense, guys, but where is everyone else?

Tyson,
I experienced horrific memory loss also from Cellcept too!!! I posted about it a couple of weeks ago. It is incredibly scary so I completely understand your concerns. You should call your neuro back this morning and tell them you are having serious side effects!!! I saw my neuro about a week and a half ago and explained ALL the symptoms I was having. He said the memory loss was definitely med related. He felt like it was caused from the combo of cellcept and pred. He said it had also caused me to go into a serious depression. He took me off the cellcept completely and said it is time to get serious about getting me off the pred. I am down to 20 mg every other day. I can tell you I feel MUCH more clear headed since making these changes. I like you was forgetting things that I knew before like the back of my hand. I have a little dog I go see everyday at noon. I have been visiting him for 2 years and know their alarm code by heart. twice in one week I could not remember it for anything!!! The alarm went off and I had to call the owner. The second time was the one that almost sent me over the edge. I told my neuro I felt like I was living in a buble and everything was going on around me but I wasn't really there. I also like you mentioned had a fear of being in my car and forgetting how to get home. I don't want to scare you but this is very serious. One morning I was driving home and got so dizzy and sick I thought I was going to pass out. I had to call my husband and have him talk to me until I could get home. I was terrified I was going to pass out while driving and no one would know where I was. That is the day I stopped the cellcept. At the time I thought it was a reaction to Ambian but my neuro said it was from the med combo. Tyson get on the phone and INSIST they talk with you. If they can't squeeze you in for an appt have the Dr call you.
I am at the very same point as you where I would rather live with the weakness than the side effects of the meds. I didn't even feel like the same person anymore. Please also be on the lookout for major depression signs. DON'T ignore them. It is most likely from the meds and needs to be addressed immediately. My neuro didn't realize how severely depressed I was until he saw me. He went so far as to ask me if I was suicidal. I really think that and the memory loss together is what made him decide it was time to make some serious changes in my treatment. I am currently on 20 mg pred every other day. I am now taking 60 mg mestinon every 4 hours. It didn't work for me in the past but since the pred it definitely does. I can tell when it is time for my next dose. I am still taking a pill to help me sleep and Mirapex to help my legs relax at night and I hope to be able to stop taking the sleeping pill as soon as I am off the pred. Tyson please keep us posted. I am very concerned because I know where you're at and it is soooo scary!!! You may only be 17 but you know your body and when something isn't right. You may have to be insistent that they listen to you but you are your best advocate. I will check back later today for an update sweetie.
Kendra

Hey Tyson,

I'm not a doctor, but I seriously believe you need to be seen by one now while you are having these new symptoms. You mentioned in another post that one of your doctors prescribed an antidepressant recently. Have you started taking that in the past few days? Please put another call into your doctor if you haven't already, and ask to be seen right away. Make sure he/she knows of any new meds, if any, you're taking since you were there last. Let us know how you're doing.

Hugs,
Pat

Hey guys.

Kendra- sorry that you too are experiencing this. My neuro finally called back and I explained the symptoms to him(confused,memory loss, headaches) etc. He sugguested that I go to the er and get tested for meningitis. I have been here for 5 almost 6 hours. They did a ct scan of my brain and did a lumbar spine tap.

The ct so far has come back okay, and the lumbar hasn't come back.


I'm just tired, drowsy, confused and all that. I have 4 red lines on my thumb and my belly button is red and a patch of red on my abdominal area.


I hope you are all okay.

Tyson, They have to check your spleen! And your heart.

Do your doctors know about the red areas?

Do the lines on your fingers look like splinters (aka splinter hemorrhages)? Do your doctors know they are there? Damn. If you have subacute bacterial endocarditis, they won't know that without a transesophageal echocardiogram. A regular echo often doesn't catch it. It's where they look at your heart close up through your esophagus. A friend of ours had that. That most certainly can give you chest pain. And because your are immunosuppressed, an infection may not "show up" on CBC. It might on erythrocyte sedimentation rate.

And a HUGE sign of a spleen in danger is redness or a blue area around the belly button. Please be very careful, just in case. Don't move around too much or lift anything.

Other suggestions would be checking your platelets (CBC) and some clotting factors.

It makes me so mad that these doctors ignored you. You should've gone in last night. This kind of stuff you can't mess with.

I hope they will check everything out now. It's not nothing, that's for sure. I hope you'll be okay. Let us know. So much for staying off the forum for awhile!

Annie

http://emedicine.medscape.com/article/896540-overview

What I find completely NOT hysterical is that DUKE came up with the revised criteria for diagnosing SBE.

http://www.fpnotebook.com/CV/ID/SbctBctrlEndcrdts.htm

Tyson, I know the ER is not a fun place to be, but I am sure glad you are there. Make sure not only the nurses know, but the doctors about the red areas. Also, tell them about the horrible pain you were having going from your hip to your chest area. I hope they finally get to the bottom of what's been going on. Hang in there kiddo, we're all here for you. Feel better and let us know how you're doing when you can.

Big Hugs,
Pat

I was also told that I was having anxiety attacks, that it was all in my head and that I needed therapy. This was BEFORE my MG dx. I was having chest pains as well. Turns out I had thymoma and because of some other complications, it was causing the pain in my chest. But the ER's solution was to tell me to "breathe in through my nose and out through my mouth and try and relax". It was so humiliating. Stand your ground. You know when something is off and even medically trained personnel may not recognize what is happening to you. When I had my thymectomy, I was the first patient that particular anesthesiology team had done that procedure on at the time. I tend to be a bit defensive about such occurances as having MG can be a lonely thing. Best wishes!!!