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Welcome Lyn, we are here for you and your husband, questions, or you just need to share your feelings with those that understand what you and your husband are going through. you will find both here, those of us with the disease, and those of us with

spouse/sig other that have it and need support, or answers to questions, etc. so I hope we can share our experiences with each other. Marla

" Fear less, hope more; Eat less, chew more; Whine less, breathe more; Talk less, say more; Love more, and all good things will be yours. " - Irish Proverb  

 

Hello everyone!

My name is Lyn Rebro. I am new to the Neurosarcoidosis Yahoo Group. My husband, is a disabled veteran of Desert Shield/Desert Storm who has developed several life threatening diseases including Sarcoidosis, Gulf War Illness (waiting for diagnosis), ITP (blood disease), Irritable Bowel Syndrome and Chronic Fatigue Syndrome. He spends a lot of time at the VA Medical Center in Minneapolis, MN going through various treatments. We have four children ages 18, 9, 7 and 6. I joined this website to site to be a source of strength and to allow you to walk with us on our journey.

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Welcome Lyn.

To: Neurosarcoidosis Sent: Mon, April 4, 2011 2:36:27 AMSubject: Re: New Member

Welcome Lyn, we are here for you and your husband, questions, or you just need to share your feelings with those that understand what you and your husband are going through. you will find both here, those of us with the disease, and those of us with spouse/sig other that have it and need support, or answers to questions, etc. so I hope we can share our experiences with each other. Marla "Fear less, hope more; Eat less, chew more; Whine less, breathe more; Talk less, say more; Love more, and all good things will be yours." - Irish Proverb

Hello everyone!My name is Lyn Rebro. I am new to the Neurosarcoidosis Yahoo Group. My husband, is a disabled veteran of Desert Shield/Desert Storm who has developed several life threatening diseases including Sarcoidosis, Gulf War Illness (waiting for diagnosis), ITP (blood disease), Irritable Bowel Syndrome and Chronic Fatigue Syndrome. He spends a lot of time at the VA Medical Center in Minneapolis, MN going through various treatments. We have four children ages 18, 9, 7 and 6. I joined this website to site to be a source of strength and to allow you to walk with us on our journey.

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I just got the email Lyn. You look like a wonderful couple. I am so sorry your husband is so sick. Please tell him Thank you for his service, I am so sorry it has cost him so much. You will find a great deal of realistic and good answers to questions you may have about the disease, treatments, good doctors, insurance, disability, etc. I'm sure I speak for all of us when I say we would be happy to help you in any way we can. Please also feel free to "let it all out" if you need too. Sometimes we all need to do it, and we don't want to worry our families sometime so we talk to each other. Connie (North Florida)

To: Neurosarcoidosis Sent: Sun, April 3, 2011 4:57:15 PMSubject: New Member

Hello everyone!My name is Lyn Rebro. I am new to the Neurosarcoidosis Yahoo Group. My husband, is a disabled veteran of Desert Shield/Desert Storm who has developed several life threatening diseases including Sarcoidosis, Gulf War Illness (waiting for diagnosis), ITP (blood disease), Irritable Bowel Syndrome and Chronic Fatigue Syndrome. He spends a lot of time at the VA Medical Center in Minneapolis, MN going through various treatments. We have four children ages 18, 9, 7 and 6. I joined this website to site to be a source of strength and to allow you to walk with us on our journey.

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