UPdate..Lupus, CTDs, MS, MG, etc. Where I have been, Sorry I have not been able to be around.

I've been very sick since I last did a video. I just wanted to give everyone a quick update. I hope everyone is doing ok and apoligize for not being able to be around. I will try to do more vids from here on out.

Category:

Education

Tags:

• steroid
• steroids
• autoimmune
• autoimmune disease
• connective tissue
• MS
• Multiple Sclerosis
• SLE
• SLE Lupus
• Lupus
• Discoid
• discoid lupus
• skin
• Vitiligo
• skin disease
• scleroderma
• Sjogren's
• myositis
• polymyositis
• dermatmyositis
• dermamyositis
• undefferentiated
• chrone's disease
• chrones
• neuromuscular
• myasthenia gravis
• gravis
• MG
• crohn's
• psorisis
• yt:quality=high

[feawguita]

Glad to see you again Michelle!

Reason enough for us to celebrate with joy how beautiful you are.

Our love and hearts are with you always unconditionally. Just as long as you allow it. You are wonderful and beautiful and radiant. I know it. Strength and many blessing to you and family. Please accept our prayers.

Namaste.

[Michellemlm]

Thank you for always being so wonderful

[raclmtsu]

OMG Michelle, Steve has been telling me what a hard time you've been having, but even with that I had no idea. I can't imagine. You seem to have been poked and proded all over. Kind of like kicking a women when she's down. That'll teach me to whine about a little MS fatigue! I feel so bad for you. I hope my brother is taking care of you. You are his main concern. I can tell you that. I wish I could help.

[Michellemlm]

Youhave every right ot complain. my illness does not minimize anything anyone esle is going through... My daughter felt bad for complaining of a headache once... I asked her if knowing I was sick made her head stop hurting... lol... she said no, I said.. exactly.. so you have every right to acknowledge whatever you are going through.. One persons suffering does not ease the suffering of another's

I love you.

M

[AnotherSoulToClingTo]

also, do you have both lupus and MS too????? didn't know that was possible!

[AnotherSoulToClingTo]

i am so sorry! you look like you've been through the wringer! i hope better days for you soon. god bless.

[Shearhair1]

Bless you for sharing with us that are either beginning our journey or well into it. I have MCTD, hashimotos, fibromyalgia, and raynauds and the list goes on. Thank you for your videos Michelle.

[shenillap]

@NamekianPikkoro7 well your organs attack themselves and stop working properly and your blood even attack itself..it's not like when you get a bee sting or eat something that you are allergic to! where it is an outside force that is causing it!!

I believe it is more complicated!! i do think that diet and nutrition plays a big part in our lives!!

[shenillap]

@NamekianPikkoro7 well your organs attack themselves and stop working properly and your blood even attack itself..it's not like when you get a bee sting or eat something that you are allergic to! where it is an outside force that is causing it!!

I believe it is more complicated!! i do think that diet and nutrition plays a big part in our lives!!

[treappling1]

Michelle I am new to YouTube. I also have SLE and am in the same shape you are right now. I'm moon faced, on oxygen, home/bed bound. I wish we could talk privately but I don't know how to send a private message on here. If you feel like it check out my videos and page. Thinking of you.

[MsSweetladyjane]

Miss your videos sooooo much, pray that things get better for you.

[babble2leeza]

I hate to hear you have to get a port. They are the worst for infections. You and I could be twins. I was put on a hundread mg of prednisone and my weight shot up within weeks. I am now down to 25mg but still am huge. I can't take water pills. I miss my face and being active. It sucks when you need help brushing your hair. There is hope. My mother is 72 and went into remission when she was 50. I'm hoping it will happen to us. Just keep praying.

[jax252000]

I miss you, and am praying for you.

[NamekianPikkoro7]

I know this is a stupid theory/question, but I keep wonder, if lupus is basically where your body attacks you, like you were your own allergy, why don't they do a study with high doses of allergy medication is what I'm wondering, or if they have??? I mean, it's possible to be allergic to anything, like iron, which your blood cells are made up of...It just makes sense, on my end, and I'm just wondering how that would work. It must sound stupid though, sorry.