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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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#16 | |||
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Hello again! IV IG is usually done through the hand or groin. It requires a BIG needle cuz' it is so thick and gooey, that's why I went with the PICC line - plus, my veins "blow" quite often since the roids kicked in.
IV IG is pooled plasma from about 1000 donors. It "masks" your symptoms for about 3-4 weeks. The cost is approx 10,000-15,000 per bottle. I get mine monthly for a while - 5 days @ 500 mL. It takes about 4-8 hours, depending on the flow rate. The plasma exchange (for me) is much harder. My line is placed in my jugular - after getting a lidocaine shot to "numb" the area - does not work! ![]() Of the 2, I much prefer the IV IG. It is much less invasive and (bonus) I get to go HOME every night! ![]() Both last around 3-4 weeks. Some people get them every month. Others get them done as "pick me ups" and are much less frequent. ![]() In any event, they both make you feel amazing. ![]() ![]() My MG is pretty bad and I need the IV IG therapy more often than most. I am so thankful to be able to get it! I am lucky in the sense that my neuro fights tooth and nail to make sure I am able to get it as often as needed! God has truly blessed me with an amazing neuro. Hope this helps a bit. Sounds like your neuro wants to get you "back on track" - and these therapies should help quite a bit! Big hugs! Erin Quote:
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Erin . |
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