My Mom Has CIDP - Marie & Louise's Story
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- Опубліковано 19 бер 2020
- To learn more about GBS and CIDP, please go to:
www.gbscidp.ca/
/ gbs_cidpfoundationofca...
/ gbscidpcanada
#cidp
#cidpawareness
#livingwithcidp
#cidpsupport
#cidpadvocate
#patientadvocacy
#cidpfamilies
#cidpwarrior
#gbs
#invisibleillness
#autoimmunedisease
#chronicillness
#IVIG
#ivigtherapy
#gbscidpfoundation
#gbscidpawareness
#peripheralneuropathy
Thank you so much for sharing your story. I too was finally diagnosed in Jan 2023. I’ve since had 4 IVIG Infusions and it’s helping with my symptoms. God Bless !
Going for my first ivig in couple days hope it works
Beautiful, in all ways.🌹
Thank you, and all the best to these two lovely individuals.
It really is a beautiful story, and they make it so easy to empathize with each of their journeys. Rare Diseases affect the person diagnosed and their entire support circle as well. For everyone's sake we need to advocate for medical practitioners to learn more about these rare diseases so that a patient can receive treatment immediately.
Such a strong bond between this mother , daughter team. Both survivors from two very different points of view. Thanks for sharing such a personal story. I wish you many more happy years, with good health and laughter.
My dad is 85 years old and was diagnosed with CIDP 2012 and before being diagnosed he had 2 surgery’s that was not necessary. It’s been very hard for him and he only gets his IVIG treatments now every two weeks that keeps him able to walk a little.
@@davidwatkins2578 Stories like these break my heart, but I'm so happy to hear that he's getting IVIG treatments finally!
@@davidwatkins2578 Very sorry for you father. Did he have so spinal surgery? Sending thoughts of comfort to him, and loved ones.
Tamara Foxen he first had carpal tunnel surgery that didn’t help then the doctor said it was be a pinched nerve in his neck he got that surgery and continued getting worse. We were having to pick him up from falling to the floor before the neck brace came off. We new it had to be more serious and we found a doctor in Florida that diagnosed him correctly.
Where can I find treatment in the USA?
See a neurologist. I'm in San Antonio. Go to dr. TARBOX