Saturday, January 31, 2009
Saturday, January 24, 2009
Sunday, January 18, 2009
Wednesday, January 14, 2009
Tuesday, January 13, 2009
Sunday, January 4, 2009
Meghan thinks this if funny
Thursday, January 1, 2009
Happy New Year
Hi
Happy New Year everyone. We hope this year brings good things to you all. Last year was quite a year for Meghan. You can look back thru the blog and see all that she got to do, thanks to so many loving people. We got travel and meet some fabulous people. We hope this year brings everyone good health and happiness. Meghan says remember to smile at someone you don't know everyday. It just might make their day. She says a smile can make a world of difference and if we all smile more than there will be less grouchy people in the world. Pretty simple.
Love to all.
Happy New Year. Let's make this a great one.
Happy New Year everyone. We hope this year brings good things to you all. Last year was quite a year for Meghan. You can look back thru the blog and see all that she got to do, thanks to so many loving people. We got travel and meet some fabulous people. We hope this year brings everyone good health and happiness. Meghan says remember to smile at someone you don't know everyday. It just might make their day. She says a smile can make a world of difference and if we all smile more than there will be less grouchy people in the world. Pretty simple.
Love to all.
Happy New Year. Let's make this a great one.
Monday, December 15, 2008
POWER IS BACK
YAHOO!!!!!!!!!! Our power is back on. 5 days without power is a major challenge for Meghan.
Especially needing nebulizers, overnight feeds, and TV.
Thank goodness for a generator. We had our pellet stove, fridge, tv, and nebs hooked up to it.
Plus we had some friends come and stay with us as they had nothing. So all in all it was ok.
Especially needing nebulizers, overnight feeds, and TV.
Thank goodness for a generator. We had our pellet stove, fridge, tv, and nebs hooked up to it.
Plus we had some friends come and stay with us as they had nothing. So all in all it was ok.
Sunday, December 7, 2008
Meghan wants to help other kids.
Hi
Meghan wants to help other kids. She wants to make either a scarf, a blanket, or a pillow. So if you know of anyone that is getting rid of fabrics, yarns, pillow stuffings have them send them our way. She thought of this because when she has been in the hospital she has been given hand made blankets and they helped calm her so much and now she wants to give too.
Thanks for your time.
Meghan wants to help other kids. She wants to make either a scarf, a blanket, or a pillow. So if you know of anyone that is getting rid of fabrics, yarns, pillow stuffings have them send them our way. She thought of this because when she has been in the hospital she has been given hand made blankets and they helped calm her so much and now she wants to give too.
Thanks for your time.
Monday, December 1, 2008
12/01/08 Clinic Visit
Meghan had CF clinic today and her lung functions are
97% with a FEV1 1.90
This is the Best they have ever been.
WE ARE SO EXCITED.
97% with a FEV1 1.90
This is the Best they have ever been.
WE ARE SO EXCITED.
Wednesday, November 26, 2008
NH Make A Wish
Hi
If anyone is looking for tax deductions how about making a donation to
the NH Make A Wish foundation. You can call them at 603-623-9474.
You can go to the web site by searching NH Make a Wish.
They have make a tremendous difference in Meghan's Life.
Thanks Sue
If anyone is looking for tax deductions how about making a donation to
the NH Make A Wish foundation. You can call them at 603-623-9474.
You can go to the web site by searching NH Make a Wish.
They have make a tremendous difference in Meghan's Life.
Thanks Sue
Thursday, November 20, 2008
Exciting News
Hi
This is very exciting news for us. A pill that puts CF
into a remission is coming. Yes it is.
Sue and Meghan
Sunday, November 16, 2008
Saturday, November 8, 2008
Tuesday, November 4, 2008
CF Clinic Visit
YAHOOOOOOOOOOOOOOOOOOOOOOOOO
Lung Functions 92% and weight is up too.
This is great news. Meghan is very happy. She has been working really hard to get her weight up and with the lung functions back in the 90's it makes life alot easier. I am sure she will get more colds and we know there may be another visit to hotel CHaD this season but we also know it really helps. So Thank YOU CHaD. YOU ROCK. I just can't say enough about the nurses there. There are four that really made and still make a difference in Meghan. Becky, Megan, Jess, and Michael. Too bad two of them are traveling nurses. CHaD if you are listening you really need to do whatever it takes to keep them here. They are tremendous with all kids.
Megan

Jessica ,Becky, Melissa

Becky Boss
Lung Functions 92% and weight is up too.
This is great news. Meghan is very happy. She has been working really hard to get her weight up and with the lung functions back in the 90's it makes life alot easier. I am sure she will get more colds and we know there may be another visit to hotel CHaD this season but we also know it really helps. So Thank YOU CHaD. YOU ROCK. I just can't say enough about the nurses there. There are four that really made and still make a difference in Meghan. Becky, Megan, Jess, and Michael. Too bad two of them are traveling nurses. CHaD if you are listening you really need to do whatever it takes to keep them here. They are tremendous with all kids.

Jessica ,Becky, Melissa
Becky Boss
Michael
Monday, October 27, 2008
NH Baseball Dinner
The NH Baseball Dinner will be Nov 22 at the Armory in Manchester NH. You can get more info by going to the NH Fisher Cats web site. This is a fundrasier for CHaD.
This year there will be a video showed and Meghan is the Star. She will be telling what it is like to be a patient at CHaD. She interviews kids and Nurses. So come check it out. Also be watching for a tv commercial about CHaD with Meghan in it.
That's all for now.
This year there will be a video showed and Meghan is the Star. She will be telling what it is like to be a patient at CHaD. She interviews kids and Nurses. So come check it out. Also be watching for a tv commercial about CHaD with Meghan in it.
That's all for now.
HOME
Yes we are home now and back to the routine. Meghan is feeling better. She went to school today....Yippeeeee. I went back to work.....yahoo. We are still getting back into the routine of not being spoiled every second with all the attention as she gets at CHaD. Maybe I can borrow a couple of nurses. That is all for now.
Friday, October 24, 2008
Monday, October 20, 2008
Meghan receives a special award.
This evening Meghan was presented with an award from Children's Hospital at Dartmouth (CHaD). It goes as follows.....
In recognition of your outstanding support of CHaD's commitment to providing outstanding, compassuibate care fir tge region's children and their families, this certificate is presented to:
Meghan Richardson
She is very excited about it. They gave it to her because she is always willing to go anywhere at anytime and talk about the outstanding care she receives here at CHaD. This week while being and inpatient here she did a video that will be played at the NH Baseball Dinner on Nov. 22 and she spoke at a freinds of CHaD Board meeting.
I am proud of her.
Saturday, October 18, 2008
Monday, October 13, 2008
Miss NH Outstanding Teen Visits Meghan in the hospital.
Hello
Guess what? This is my friend Megan Lyman. She is Miss NH Outstanding Teen and she came
all the way up to visit me today. It was fun to see her. She knows what it is like to be here.
Thanks Megan for visiting me.
Love Meghan.
By the way I am doing a little better I will find out in two days if my lungs function is better.
Saturday, October 11, 2008
Oct CHaD Vist.
Friday, October 10, 2008
Hotel CHaD
Hello
The queen in spending two weeks here at "Hotel CHaD" aka Children's Hospital at Dartmouth. She is getting IV meds and some physical and respiratory therapy. Hopefully we won't be here in Feburary but I am not holding my breath. Well that is all for now. Just and FYI
The queen in spending two weeks here at "Hotel CHaD" aka Children's Hospital at Dartmouth. She is getting IV meds and some physical and respiratory therapy. Hopefully we won't be here in Feburary but I am not holding my breath. Well that is all for now. Just and FYI
Monday, September 29, 2008
CHECK OUT THIS FUN TIME I HAD!!!
The Mount Washington "Make A Wish" Boat Ride. This is now an annual event sponsored by LandMark and Delta Dental. Awesome fun fulled event for the Wish Kids.



Above are the Smiths with Meghan they had donated to the NH Make A Wish Foundation for the past 15 years. They are super nice loving and caring people that have helped numerous kids. Plus they are good dancers.
Next you have Maureen Cronin MAW Executive Board member and faboulous Wish Granter.
Last but not least in this row is Sarah. Listen to this. She is a Wish Kid, (obviously older now), Wish Granter, and Wish Donor. What do you think of that plus cancer survivor. Now that rocks.
Subscribe to:
Posts (Atom)