Guest guest Posted April 18, 2001 Report Share Posted April 18, 2001 In a message dated 4/17/2001 11:52:12 PM Eastern Daylight Time, oh2bamermaid@... writes: > I've been led to believe that my Thyroid > problems are most probably caused by my Chiari. Mine is autoimmune related > and in my research and things I've read here at Wacma, I thought this was a > problem many of us shared possibly due to the csf pressure damaging or > supressing the pituitary gland. Am I wrong? > You could very well be right and yes, many with Chiari do experience thyroid/pituitary problems. The whole purpose of posting what I did was just for others to be aware that while their problems may all very well be related to having Chiari, we just need to explore all possibilites. Something else I was thinking about. Many (including ) are on various meds for pain relief, etc. We also need to keep in mind that sometimes, some of the symptoms one may experience may be related to their med or combination of meds. Good idea to always research the med that is being prescribed, especially if taking more than one med is involved. Some doctors do not take into consideration how meds work with each other (good and bad). Need to look at those side affects and interactions. It is just so important to look at the whole picture and all possibilites. Tory ('s mom) 18ys. old, craniofacial abnormalities, midline facial cleft, hydrocephalus, growth hormone (weighs 50 lbs.) and thyroid deficient, blind, severly delayed, choanal atresia, optic nerve hypoplasia, artificial tear duct, 12-P chromosome deletion, sensory integration disorder, latex allergy, probable malignant hyperthermia, ACM II w/30mm herniation, basilar impression. History of 43 surgeries. (and musically talented) SUCH A SPECIAL LITTLE GIRL! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 19, 2001 Report Share Posted April 19, 2001 Hi Tory and Everyone, Your absolutely right about blaming everything on chiari, granted some of the problems do stem from this disease, but not with everyone. A lot of our symptoms are similar, I don't doubt that. For instance, I thought my eyes were blurry because of the chiari, I went to the eye Dr. a couple of weeks ago and found out I have cataracts on both eyes, not chiari related. I had surgery on April 12, 2001 for my right eye, I let it go for so long thinking it was from chiari that my vision in that eye was 20/4000. This surgery will be repeated on my left eye April 30. I thank God my daughter insisted I go to an eye Dr., if I would have kept blaming it on chiari, I could have went blind, so I was told. Chest pains have to be watched carefully also, chiari does NOT cause chest pain. I read a lot of posts where chest discomfort was mentioned, please for your own safety have these pains checked out by your PCP. There are a lot of problems with chiari, many more than we'll ever know, but in the mean time just get some symptoms checked out by your PCP. Hugs & Prayers, Sharon Benedict Baltimore, land chiari ll ... first decompression '96' Second surgery waiting to be scheduled with Dr. Weingart, Supacuipital Craniotomy, Duraplasty, C1 Laminectomy Quote Link to comment Share on other sites More sharing options...
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